Consensus paper: current state of first- and second-line therapy in advanced clear-cell renal cell carcinoma. – UroToday

The therapy of advanced (clear-cell) renal cell carcinoma (RCC) has recently experienced tremendous changes. Several new treatments have been developed, with PD-1 immune-checkpoint inhibition being the backbone of therapy. Diverse immunotherapy combinations change current first-line standards. These changes also require new approaches in subsequent lines of therapy. In an expert panel, we discussed the new treatment options and how they change clinical practice. While first-line immunotherapies introduce a new level of response rates, data on second-line therapies remains poor. This scenario poses a challenge for clinicians as guideline recommendations are based on historical patient cohorts and agents may lack the appropriate label for their in guidelines recommended use. Here, we summarize relevant clinical data and consider appropriate treatment strategies.

Future oncology (London, England). 2020 Sep 23 [Epub ahead of print]

Peter J Goebell, Philipp Ivanyi, Jens Bedke, Lothar Bergmann, Dominik Berthold, Martin Boegemann, Jonas Busch, Christian Doehn, Susanne Krege, Margitta Retz, Gunhild von Amsberg, Marc-Oliver Grimm, Viktor Gruenwald

Division of Urology, University Hospital Erlangen, D-91054, Erlangen, Germany., Department of Hematology, Hemostaseology, Oncology & Stem Cell Transplantation, Hannover Medical School, D-30625, Hannover, Germany., Department of Urology, Eberhard Karls University, D-72076, Tuebingen, Germany., University Hospital Frankfurt, Medical Clinic II, D-60590, Frankfurt, Germany., Centre Hospitalier Universitaire Vaudois, CH-1011, Lausanne, Switzerland., Department of Urology, University Hospital Mnster, D-48149, Mnster, Germany., Department of Urology, Charit-University Medicine, D-10117, Berlin, Germany., Urologikum Lbeck, D-23566, Lbeck, Germany., Department of Urology, Pediatric Urology & Urologic Oncology, Kliniken Essen-Mitte, D-45136, Essen, Germany., Department of Urology, Technical University of Munich, Rechts der Isar Medical Center, D-81675, Munich, Germany., Department of Oncology & Hematology, University Cancer Center Hamburg & Martini-Clinic, University Medical Center Hamburg-Eppendorf, D-20246, Hamburg, Germany., Department of Urology, Jena University Hospital, D-07747, Jena, Germany., Interdisciplinary GU Oncology, Clinic for Medical Oncology & Clinic for Urology, University Hospital Essen, D-45147, Essen, Germany.

PubMed http://www.ncbi.nlm.nih.gov/pubmed/32964728

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Consensus paper: current state of first- and second-line therapy in advanced clear-cell renal cell carcinoma. - UroToday

Around Town: Life is a series of choices a look at California’s ballot propositions – VVdailypress.com

By Pat Orr | Special to the Victorville Daily Press

Tomorrow marks the start of mailing a ballot to every registered voter in California. And so it begins: The onslaught of mailers, ads, prevarications and outright lies that now constitute campaigns for our votes. If there was ever a year to do your own research, this is it.

The political parties want you to believe this is the most important election in our history, but they say that every four years. What can be important is that we have jobs, taxes, new government spending, crime and racial-preference laws before us in California to vote on.

The impact of the COVID-19 lockdown cannot be underestimated on the attitudes of California voters. Our nave view that the government knows what it is doing has been sorely tested even more than usual.

Proposition 14 is a straightforward request for your approval to issue $5.7 billion in new bonds to fund stem cell research. I ask why this is not funded by big pharma who, along with their academic research partners, will reap the profits from any breakthrough treatments? This bond will cost taxpayers $7.8 billion in principal and interest. Is it good for mankind? Yes, it could be. Is it good for taxpayers? You decide.

Proposition 15 is the attack on Proposition 13s property tax protection passed 40 years ago. Commonly called the Split-roll Initiative, it would revalue commercial property to generate millions from business property owners. This is one issue that the lock-down has helped clarify. This new tax law would cause more business closures and accelerate the departure of businesses who can escape. To intensify the issue further, new work-at-home rules are making large corporate offices obsolete. Couple that with the death of shopping malls and you have a looming business property foreclosure disaster that Prop 15 will only hasten. Voters have turned against 15 despite the hackneyed ads that claim, this is for the schools. Hey, schools are closed!

Proposition 16 is a weird attempt in this social climate to allow our state to legally discriminate in university admissions, public employment or contracting. We banned discrimination in California once. Now to fight racism, the liberals want to bring legalized institutional racism back. This will never stand up in court if it passes.

Proposition 17 would give 40,000 formerly incarcerated individuals now on parole the right to vote. Proponents see the inability to vote as an example of systemic racism because they claim that two-thirds of parolees are Black or Latino.

Proposition 18 will let 17-year-olds vote in primary elections if they will be 18 before the General Election. This will stop those pesky other parties, like Republicans and Libertarians, from getting a candidate in the top two primary ever again.

Proposition 19 will make it easier for those over 55 to transfer their property tax base to another home. This has overwhelming support particularly as we see so many folks displaced by wildfires this year that must rebuild or relocate. A yes vote is supported by Realtors statewide.

Proposition 20 makes crime a crime again. Theft valued between $250 and $950 will become a felony again if you vote yes on Prop 20. This may reduce the shoplifting plague that has been visited on retailers since the law was changed to allow offenders to steal up to $800 with a slap on the wrist. Every shop owner will vote yes on 20.

Proposition 21 is one more attempt to pass statewide rent control. It failed before and will fail again. Can you imagine there ever being any empty apartments to rent if there was rent control?

Proposition 22 is another issue totally reframed by the COVID-19 lockdown. It is the unions attempt to force independent contractors to become employees. Aimed at ride-share drivers and a host of other gig-economy workers, it is a naked attempt to get new union members. We all have become dependent on food, grocery and drug deliveries so there is zero chance this will pass this year. The value of letting people choose their own work life has become clear and essential for all of us.

Proposition 23 would require a licensed physician on-site at every dialysis clinic. This is good for the big chain clinics, not so good for places like the Victor Valley where the extra cost may force clinics to close.

Proposition 24 strengthens consumer privacy laws. This proposition creates a new state agency full of highly paid managers and unionized state workers to protect your personal credit information from being bought and sold. You decide if the return on investment is worth it.

Proposition 25 is an attempt to enable voters to end the catch-and-release game in the justice system right now. A yes vote keeps our cashless bail system in place under current state law. A no vote returns us to the system wherein the court sets bail requiring assets or cash to secure release until trial.

Meanwhile, every Victor Valley community has a local ballot issue to decide this year. Apple Valley (Measure 0) and Victorville (Measure P) are both asking voters to approve an additional 1% increase in the sales tax to be retained for municipal expenses like police, fire, parks and road maintenance. The impact of COVID-19 lockdowns on local sales tax revenue is significant. The state has signaled it will not be helping with any additional income, so it is either increase revenue or cut more services. We have always been a law-and-order-oriented region, so I expect both measures to pass.

In Hesperia Measure N is an attempt to modify land use and density rules to help keep Hesperia from becoming overbuilt and out-of-character projects from being built in the city.

Adelantos Measure R is a new tax on vacant land parcels that can range from $50-$600 a year depending upon how the property is zoned. I doubt investors or home builders are excited by the prospect of a new tax on unused dirt right now. Has the city made the case to voters they need the money based on past prudent spending?

Measure V is only for Spring Valley Lake residents and it would, if passed, create a new Community Services District. There are long-time residents on both sides of the issue. I expect the vote to be close and trust a majority of SVL voters have paid enough attention to really weigh the pros and cons of creating this new entity.

We all will vote on Measures J and K, which purportedly modernizes the County Charter (J) and imposes a one four-year term limit and salary reduction on our supervisors (K).You should know that J was put on the ballot by the supervisors, while K was put on the ballot by voter petition. Translation: These two may have conflicting provisions.

A yes vote on Measure U repeals the County Fire Tax for those folks living in County Fire Protection District Service Zone 5. The issue here is that many residents in this zone already pay fire fees to other fire agencies and the County sort of snuck up on this area and included it in their tax levy. You will know from your tax bill and your ballot if this issue applies to your property.

This commentary does not reflect the official position of the Daily Press Editorial Board or ownership.

Contact Pat Orr at avreviewopinion@gmail.com.

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Around Town: Life is a series of choices a look at California's ballot propositions - VVdailypress.com

Expansion Therapeutics Names Renato Skerlj, Ph.D., Chief Executive Officer and President – BioSpace

Oct. 5, 2020 12:30 UTC

Experienced life sciences executive to lead Expansion as it advances portfolio of medicines targeting RNA-mediated diseases into the clinic

SAN DIEGO--(BUSINESS WIRE)-- Expansion Therapeutics, Inc., a biotechnology company advancing transformative medicines to patients with RNA-mediated diseases, today announced the appointment of Renato Skerlj, Ph.D., as the companys new Chief Executive Officer and President, effective immediately. Dr. Skerlj will also serve on the companys Board of Directors.

This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20201005005251/en/

Renato Skerlj, Ph.D., CEO and President, Expansion Therapeutics (Photo: Business Wire)

Renato has a distinguished and proven track record in discovering and developing small molecule drugs for rare diseases which will be invaluable to Expansion as we move our programs targeting expansion repeat disorders toward the clinic, said Scott M. Rocklage, Ph.D., Founding Partner at 5AM Ventures, and Chairman of the Board of Directors of Expansion. Renato shares our vision to bring transformative therapies to patients with severe RNA-mediated diseases.

I am extremely excited about the potential of Expansions pipeline to deliver upon an unmet need for therapies that target a range of serious diseases caused by RNA. I look forward to working with the Expansion team to advance the pioneering work from the lab of Dr. Matt Disney to help patients suffering from these debilitating diseases, such as myotonic dystrophy, for which there are currently no approved therapies, added Dr. Skerlj.

Dr. Skerlj has more than 25 years of experience leading the discovery and development of disease modifying small molecule drugs to treat genetically defined rare diseases. He has authored 67 publications, holds 52 patents and has advanced multiple drug candidates into clinical development.

Most recently, Dr. Skerlj served as Chief Scientific Officer for X4 Pharmaceuticals, Inc., where he also was one of the companys scientific founders and co-inventor of its lead drug candidate, mavorixafor. Prior to joining X4, Dr. Skerlj held leadership roles in drug discovery and development at Lysosomal Therapeutics where he co-invented LTI-291, a CNS drug in clinical development for Parkinsons disease. Previous to that, he was interim Head of Small Molecule Discovery at Genzyme and part of the executive team at AnorMED, a publicly traded company that was acquired by Genzyme in 2006. Dr. Skerlj is an accomplished drug developer with two approved drugs; plerixafor, a CXCR4-targeted stem cell mobilizer approved by the U.S. Food and Drug Administration (FDA) in 2008, and ertapenem, an anti-bacterial approved by the FDA in 2001. Dr. Skerlj received his Ph.D. in synthetic organic chemistry from the University of British Columbia, and completed postdoctoral fellowships at the University of Oxford and Ohio State University.

About Expansion Therapeutics

Expansion Therapeutics is a drug discovery and development company pursuing the vast potential of small molecule medicines for RNA-mediated diseases. Based on exclusive worldwide rights to groundbreaking research from the laboratory of Matthew D. Disney, Ph.D., at The Scripps Research Institute, Expansion has assembled the intellectual property, know-how, and proprietary enabling technologies and tools necessary to facilitate the creation of potent and specific small molecule binders of RNA. Through this unique platform, Expansion is building a portfolio of novel RNA-targeted drug candidates with activity across a broad number of disease indications. The companys initial development focus is on therapies for patients with expansion repeat diseases who have limited and unsatisfactory treatment options. Expansion is relocating its corporate headquarters to the Boston, Massachusetts area and will maintain its research facility in Jupiter, Florida. For more information, visit http://www.expansionrx.com.

View source version on businesswire.com: https://www.businesswire.com/news/home/20201005005251/en/

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Expansion Therapeutics Names Renato Skerlj, Ph.D., Chief Executive Officer and President - BioSpace

League of Women Voters Releases Their Proposition recommendations – Valley Voice

The League of Women Voters has been fighting for Democracy for 100 years.The League is a non-partisan, non-profit 501(c)(3) educational organization, dedicated to encouraging active participation in government, and fostering understanding of public policy.

The following are their proposition recommendations for the November 3 General Election.

For more election information, go to VotersEdge.org

PROP 15 SCHOOLS & COMMUNITIES FIRST YES

The Schools & Communities First initiative will raise $12 billion every year for Californias schools, essential workers, and local governments. This will come by ensuring that all corporate properties worth more than $3 million pay their fair share of property taxes while protecting homeowners and renters, small businesses, and agriculture. This money is needed now more than ever and is critical to Californias recovery and reinvestment.

PROP 16 OPPORTUNITY FOR ALL YES

Affirmative action in state hiring, contracting, and education was banned in California by Prop 209 in 1996. Prop 16 will reverse that ban and allow schools and public institutions to take race, ethnicity, color, national origin, and gender into consideration when admitting students to colleges, hiring employees for public jobs, and selecting contractors for public projects. Equal opportunity programs are a time-tested way to fight systemic racism and gender discrimination by leveling the playing field and giving everyone a chance at good public jobs and wages and quality public schools. Prop 16 provides all Californians a fair opportunity in education, employment, and contracting.

PROP 17 RESTORE VOTING RIGHTS YES

Restoring voting rights to Californians who have completed their prison term is a matter of justice, equity, and fundamental fairness. Right now, nearly 50,000 people who have been released from prison and are on parole are denied the right to vote a right that is owed to every citizen and important to successful reintegration into the community. Our neighbors who are working, paying taxes, raising families, and rebuilding their livesdeserve a voice in the policy-making that shapes their lives. And including their voices will help California achieve a more representative democracy.

PROP 18 VOTING RIGHTS FOR 17-YEAR OLDS YES

Seventeen-year-olds who will be 18 by the next general election should be able to vote in primary and special elections. Prop 18 will give them that right. Young people are significantly underrepresented in Californias electorate.Allowing 17-year-olds to vote in primary and special elections will engage young voters while they are studying the issues in high school and have a strong interest in participation. Once voting begins it becomes a life-long habit. Furthermore, fairness dictates that people who will be eligible to vote in a general election should be able to help choose the candidates who will be on that ballot. Finally, many 17-year-olds are civically engaged and at the forefront of movements to improve the communities in which they live. We would all benefit from their voices at the ballot box.

PROP 19 PROPERTY TAX BREAKS NO

Prop 19 exacerbates an already inequitable property tax system offering tax breaks to people who do not need them. Providing tax breaks to homeowners over 55 who purchase a replacement home and allowing them to transfer their current tax assessment to a new home anywhere in the state does nothing to help low-income seniors or families struggling to find housing. This proposition would allow not just one, but three such transfers. Senior citizens are already allowed to keep their current tax assessment when they purchase a home of equal or lesser value.And while the plan to put state revenuefrom increased home sales into a fund to support firefighting may sound appealing, it will make it more difficult for the legislature to fund the states response to other natural disasters or public health crises.While Prop 19 eliminates a tax break for some property inherited by children from parents, this beneficial element is not sufficient to merit support.

PROP 20 ROLLBACK ON CRIMINAL JUSTICE REFORMS NO

Over the past decade, California has made progress enacting laws that reduce the prison population and create a more effective and equitable public safety system. Prop 20 would roll back many advances in criminal justice reforms and reinstate a get tough law enforcement system that believes longer incarceration is a solution to crime. It would make minor theft of some goods worth over $250 punishable as a felony. It allows the state to collect DNA from people convicted of misdemeanors like shoplifting and drug possession. Prop 20 sends California in the wrong direction at a time when there is forward momentum toward smart justice approaches that increase public safety and reduce costs to the state.

PROP 24 CONSUMER DATA PRIVACY NO

The League of Women Voters supports the protection of consumers private data. Prop 24 includes some beneficial elements, but we oppose due to the complexity of a 52-page initiative with impacts and nuances that are difficult for voters to discern and rollbacks to existing protections. Among the troubling aspects of Prop 24 is its expansion of pay for privacy through the addition of loyalty and rewards programs, allowing businesses to charge consumers more or provide worse service if they choose to exercise their privacy rights. The initiative also allows businesses to require consumers to direct each individual website and app not to sell information weakening the current legal requirement that companies respect a global opt-out for all services. These burdens are fundamentally inequitable, placing the onus on the average consumer to protect their own privacy. Working people dont have the time to do the paperwork and they cant afford to pay companies to respect their wishes. Finally, the initiative comes less than a year after the 2018 California Consumer Privacy Rights Act went into effect,before we have had an opportunity to see how the new law works or the legislature has had a chance to address any defects.

PROP 25 END CASH MONEY BAIL YES

A YES vote on Prop 25 is a vote to replace the money bail system with the use of pretrial risk assessment tools that focus on safety and flight risk. It is estimated that almost 46,000 Californians, a disproportionate number of whom are Black and Latinx, are being held in jail but not yet sentenced. Cash bail both criminalizes poverty and reflects the systemic racism that plagues our criminal legal process. California must move away from the money bail system to create a fairer and more equitable criminal legal system that balances public safety with the presumption of innocence. People who pose little threat to public safety should not be subject to losing their jobs, homes, and families simply because they lack the money to pay for release from jail while awaiting their day in court. While the new law that would go into effect with a YES vote is not perfect, it can be amended by the legislature.A NO vote, however, could enshrine cash bail and prevent future legislative action to curtail the commercial bail industry.

NO RECOMMENDATIONS ON OTHER STATE PROPOSITIONS ON NOVEMBERS BALLOT

PROP 14 STEM CELL RESEARCH NEUTRAL

While the League of Women Voters of California supports ongoing stem cell research, we are neutral on Prop 14 because of the funding mechanism used and because of the requirement for a supermajority vote to amend its provisions. Prop 14 would authorize the use of general obligation bonds to continue funding stem cell research through the California Institute for Regenerative Medicine (CIRM).However, general obligation bonds are designed for long-term financing of capital projects, purchase of facilities for public use, and repair or retrofitting of public facilities and structures not for funding specialized research by an entity that has little state oversight.Furthermore, the legislature is prohibited from changing the law without a 70 percent supermajority vote, thereby restricting state representatives ability to carry out their responsibilities. Finally, profits from intellectual property agreements could only be spent on CIRM-funded research treatments, limiting the states flexibility to spend funds on matters that might be more urgent.

PROP 21 LOCAL GOVERNMENTS & RENT CONTROL NEUTRAL

The League supports efforts to help resolve Californias housing crisis. We promote solutions aimed at increasing housing production in a sustainable, accessible, and equitable manner. Rent control policies are one strategy to address Californias housing challenges, offer tenant protections, and prevent displacement. Rent control may be an effective short-term solution but studies suggest that its longer-term impact may, in certain cases, stifle the building of high-density and more affordable housing.Some of the modifications in Prop 21 have alreadybeen addressed through recently passed legislation. Because there are benefits and drawbacks to rent control, the League has chosen to be neutral on Prop 21.

PROP 23 KIDNEY DIALYSIS CLINICS NEUTRAL

This measure will require operators of chronic dialysis clinics to have a minimum of one licensed physician at the clinic whenever patients are being treated, offer the same level of care to all patients regardless of how payment is being made, and make reports about dialysis-related infections to the states health department and the National Healthcare Safety Network (NHSN). There is disagreement about whether the presence of a doctor is always necessary or could exacerbate a doctor shortage, and over whether costs are manageable or prohibitively high. Furthermore, the League questions why voters should be deciding questions of recordkeeping and medical staffing. The uncertainty of the costs and benefits of the measure leads the League to take a neutral position.

PROP 22 RIDESHARE AND DELIVERY DRIVERS NO POSITION

The League of Women Voters of Californias positions do not cover the issues in Prop 22. We therefore take no stand on the proposition.

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League of Women Voters Releases Their Proposition recommendations - Valley Voice

What is the difference between ventilation and respiration? – EMS1.com

By Chris Ebright

You were taught from day one of taking vital signs to countrespirations. However, I am here to say that your stellar EMT instructor let you down because thats wrong. The same incorrect terminology is also written in numerous textbooks, on run reports, and spoken everyday between medical professionals. So now youre asking: OK, smartypants, then what is the proper term? The appropriate term, my fellow professionals, is, you count ventilations.

Arent these terms essentially the same? The easy answer is no. The harder question is: Well, why not? This installment of Back to the Basics discusses these physiological processes and how they differ. So please, read on.

Simply put, ventilation is breathing the physical movement of air between the outside environment and the lungs. Air travels through the mouth and nasal passages, then down the pharynx. Upon reaching the vocal cords, air flows into the trachea, transitioning from the upper airway into the lower airway. Here, it continues distally to the carina, then through the primary bronchi, various branches of bronchioles, and eventually arriving in the alveoli. This is inhalation. Air movement in a reverse pathway from alveoli to mouth and nose, is exhalation. Inhalation, followed by exhalation, equals one ventilation. This is what you observe (chest rise and fall) when determining the breathing rate.

A ventilation can only take place if the brainstem, cranial and associated peripheral nerves, the diaphragm, intercostal musculature and lungs are all functional. Combining the function of all these structures, the pulmonary ventilation mechanism establishes two gas pressure gradients. One, in which the pressure within the alveoli is lower than atmospheric pressure this produces inhalation. The other, in which the pressure in the alveoli is higher than atmospheric pressure this produces exhalation. These necessary changes in intrapulmonary pressure occur because of changes in lung volume.

So, how does the lung volume change? Quite simply, it is a combination of muscle contractions stimulated by the central nervous system, and the movement of a serous membrane within the thorax called the pleura. The pleura is made of two layers: a parietal layer that lines the inside of the thorax and a visceral layer that covers the lungs and adjoining structures (blood vessels, bronchi, and nerves). Between the visceral and parietal layers is a small, fluid-filled space, called the pleural cavity.

The initiation of ventilation begins with the brainstem, where impulses (action potentials) generate within the medulla oblongata, then travel distally within the spinal cord. The impulse traverses individually through cervical nerves three, four and five until just above the clavicle. Here, the three cervical nerves merge into one large nerve called the phrenic nerve, which attaches distally to the diaphragm. Imagine these two nerves resembling a pair of suspenders on the anterior chest. The delivered impulse from the phrenic nerve initiates diaphragm contraction.

The intercostal muscles are a group of intrinsic chest wall muscles occupying the intercostal spaces. They are arranged separately in three distinct layers (external intercostal muscles, internal intercostal muscles, and innermost intercostal muscles). The intercostal nerves that stimulate these muscles originate from the spinal cord thoracic nerves 1-11.

Inhalation is initiated as the dome-shaped diaphragm is stimulated. As it contracts and flattens, the thorax expands inferiorly. The internal and innermost intercostal muscles relax, while the external intercostal muscles contract from stimulus by the thoracic nerves. This produces an upward and outward movement of the ribs (similar to the movement of a bucket handle), and the sternum (similar to when pulling upward on a handle of a water pump). The fluid in the pleural cavity acts like glue, adhering the thorax to the lungs. Hence, as the thorax expands vertically and laterally, the parietal layer drags the visceral layer along with it, causing the lungs to expand. Adequate expansion of the lungs results in a decreased pressure within the alveoli. Therefore, when the alveolar pressure drops below atmospheric pressure, air rushes into the lungs.

Remember, inhalation requires a stimulus initiated from the central nervous system. Think of it like turning on a light. The light stays unlit until you flip a switch (CNS), releasing electricity and stimulating the components of the light bulb. As long as the switch is on and there is an impulse, the light stays lit. However, if you turn off the switch, the stimulus ceases, and the light shuts down. Exhalation is akin to turning off the switch, so to speak.

Thoracic stretch receptors constantly monitor chest expansion. Once an acceptable limit of expansion develops, they send a message to the central nervous system to turn off the switch. All the nerves stimulating diaphragmatic and external intercostal muscle contraction temporarily stop conducting. Consequently, the diaphragm and the external intercostal muscles relax, decreasing the thoracic volume like letting air out of a balloon. Assisting with this passive process, the internal and innermost intercostal muscles are stimulated. Their contraction pulls the ribcage and attached pleura further downward and inward, compressing the lungs and increasing the air pressure within the alveoli. Once the alveolar pressure exceeds the atmospheric pressure, air moves out of the lungs.

That is all there is to it simple, right? Adults normally ventilate between 12 to 20 times per minute, thanks to the autonomic nervous system. We do not even have to think about it! Nonetheless, what becomes a problem (and why EMS gets a call) is when the nervous system, the thoracic musculature, or the lungs become diseased or disabled. Here is a partial list of pathologies that impair ventilation:

Respiration is the movement of gas across a membrane. The gas exchange in the lungs is referred to as external respiration. The very thin membrane gas crosses is called the respiratory membrane, separating the air within the alveoli from the blood within pulmonary capillaries. Its structure consists of the alveolar wall, the capillary wall, and eachs respective basement membrane. A basement membrane is a thin, fibrous structure that separates the lining of an internal or external body surface from underlying connective tissue. Think of it like Christmas wrapping paper around a box.

Recall that adequate ventilation enables air to reach the alveoli and establish a pressure gradient. The alveolar pressure of oxygen typically ranges from 80 to 100 mmHg, whereas the alveolar pressure of inspired carbon dioxide is very low (typically 40 mmHg). Oxygen-depleted blood, transported from the bodys cells and back to the right side of the heart, is pumped into the pulmonary trunk and through the pulmonary arteries. Eventually, the blood makes its way through the distal pulmonary capillaries surrounding the alveoli. Oxygen within the pulmonary bloodstream typically has a pressure of 40 mmHg, and carbon dioxide has a pressure of 45 mmHg. These differences in pressure allow for diffusion of oxygen from alveolar air, across the respiratory membrane and onto the hemoglobin of red blood cells. Carbon dioxide diffuses off hemoglobin, crosses the respiratory membrane, and enters the alveolar space.

The result of external respiration establishes a hemoglobin oxygen pressure in excess of 100 mmHg, and a decreased pressure of carbon dioxide of 40 mmHg. The exchange of oxygen and carbon dioxide continues across the respiratory membrane until the equilibrium of each gas is established. Oxygen-rich blood then flows from the lungs via the pulmonary veins back to the left side of the heart. Here, it is pumped out through the aorta to all body tissues.

Blood flows from the systemic circulation, down through arteries, arterioles, and eventually to the capillaries. Capillaries are only large enough to accommodate one red blood cell at a time, and blood flow at this level is very slow. This maximizes the time for the release of oxygen and reabsorption of carbon dioxide. Cells require high concentration oxygen to function correctly. Thus, another membrane exchange of gas must take place between individual body cells and the systemic capillaries.

This transaction occurs with gas already within the body, so it is termed internal respiration. Organelles within a cell take oxygen and combine it with glucose, fat, or protein, and make energy (ATP) through a series of complex chemical reactions. The resultant waste product is a high concentration of carbon dioxide. So, as arterial blood flows into capillaries, an awaiting cell has low oxygen pressure (40 mmHg, typically) and a high carbon dioxide pressure (45 mmHg).

Oxygen that is attached to hemoglobin maintains a pressure of around 100 mmHg, and carbon dioxide a pressure of 40 mmHg. A diffusion gradient is established once again, only this time in the opposite direction that occurred in the lungs. At the cellular level, the exchange of oxygen and carbon dioxide commences across the cellular/capillary membrane until an equilibrium of each gas is established. Blood flow continues through the venules, veins, vena cava, heart, and back into the lungs with a hemoglobin oxygen pressure of 40 mmHg and a carbon dioxide pressure of 45 mmHg. Rinse and repeat, every minute, of every day, for life.

Unfortunately, external and internal respiration can also be negatively influenced and inhibited by various disease processes. At the time of this article, the most notable respiratory pathology is caused by COVID-19, the coronavirus. View the YouTube video from the Cleveland Clinics Dr. Sanjay Mukhopadhyay (found in the reference listings) to get a first-hand view of what COVID-19 does to the alveolar-capillary membrane.

Additionally, here are some other common respiration pathologies:

Hopefully, now you understand the difference between ventilation and respiration. Even though these are independent physiological processes, they are also mutually dependent to ensure the survival of the human body. So, the next time someone misuses one of these terms set them straight with a smile. Tell em Chris told you.

Chris Ebright is an EMS education specialist with ProMedica Air and Mobile in Toledo, Ohio, managing all aspects of internal continuing EMS education as well as for numerous EMS systems in northwest Ohio and southeast Michigan. He has been a nationally registered paramedic for 25 years, providing primary EMS response, land and air critical care transportation. Chris has educated hundreds of first responders, EMTs, paramedics, and nurses for 24 years with his trademark whiteboard artistry sessions, including natives from the Cayman Islands and Australia. Chris passion for education is also currently featured as a monthly article contributor, published on the Limmer Education website. He has been a featured presenter at numerous local, state and national EMS conferences over the past 13 years, and enjoys traveling annually throughout the United States meeting EMS professionals from all walks of life. Chris is a self-proclaimed sports, movie and rollercoaster junkie and holds Bachelor of Education degree from the University of Toledo in Toledo, Ohio. He can be contacted via email at c.ebrightnremtp@gmail.com or through his website http://www.christopherebright.com.

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What is the difference between ventilation and respiration? - EMS1.com

Cytovia Therapeutics partners with Inserm to develop selective CD38 NK therapeutics and offer new treatment options for Multiple Myeloma patients |…

Details Category: DNA RNA and Cells Published on Thursday, 08 October 2020 15:15 Hits: 194

NEW YORK, NY, USA and PARIS, France I October 08, 2020 I Cytovia Therapeutics ("Cytovia"), an emerging biopharmaceutical company, announces today that it has entered a research and licensing agreement with Inserm to develop NK engager bi-specific antibodies and iPSC CAR NK cell therapy targeting CD38, a key marker of multiple myeloma. The licensing agreement has been negotiated and signed by Inserm Transfert, the private subsidiary of Inserm, on behalf of Inserm (the French National Institute of Health and Medical Research) and its academic partners. Cytovia is licensing Inserm's CD38 antibody and Chimeric Antigen Receptor (CAR) patent and applying its proprietary NK engager bispecific antibody and iPSC CAR NK technology platforms. The research agreement will include evaluation of the therapeutic candidates at Hpital Saint-Louis Research Institute (Inserm Unit 976) under the leadership of Professors Armand Bensussan and Jean-Christophe Bories.

Dr Daniel Teper, Cytovia's Chairman and CEO commented: "We are delighted to partner with one of the top centers of excellence in the world for research and treatment in hematology. CD38 is a validated target and Natural Killer cells have significant cytotoxicity to Myeloma cells. We are looking forward to bringing promising new options to address the unmet needs of patients with Multiple Myeloma and aim for a cure."

Professor Armand Bensussan, Director of The Immuno-Oncology Research Institute at Hpital Saint-Louis added: "We have demonstrated the selectivity of our novel CD38 antibody in killing myeloma cells but not normal cells such as NK, T, and B cells. The activation of NK cells through NKp46 may enhance the efficacy of the bispecific antibody in patients not responsive to CD38 monoclonal antibody therapy. CD38 CAR NK is a promising approach forrelapsed/refractory patients and an alternative to CAR T therapies."

About Multiple Myeloma Multiple Myeloma is a currently incurable cancer, affecting a type of white blood cell known as plasma cells. It leads to an accumulation of tumor cells in the bone marrow, rapidly outnumbering healthy blood cells. Instead of producing beneficial antibodies, cancerous cells release abnormal proteins causing several complications. While symptoms are not always present, the majority of patients are diagnosed due to symptoms such as bone pain or fracture, low red blood cell counts, fatigue, high calcium levels, kidney problems, and infections. According to the World Cancer Research Fund, Multiple Myeloma is the second most common blood cancer, with nearly 160,000 new annual cases worldwide, including close to 50,000 in Europe. 32,000 in the US, and 30,000 in Eastern Asia. Over 95% of cases are diagnosed late, with a 5-year survival rate of 51%. Initial treatment comprises of a combination of different therapies, including biological and targeted therapies, corticosteroids, and chemotherapy, with the option for bone marrow transplants for eligible patients. Immunotherapy and cell therapy are the most promising new treatment option for Multiple Myeloma, with the potential for long term cancer remission.

About CAR NK cells Chimeric Antigen Receptors (CAR) are fusion proteins that combine an extracellular antigen recognition domain with an intracellular co-stimulatory signaling domain. Natural Killer (NK) cells are modified genetically to allow insertion of a CAR. CAR-NK cell therapy has demonstrated initial clinical relevance without the limitations of CAR-T, such as Cytokine Release Syndrome, neurotoxicity or Graft vs Host Disease (GVHD). Induced Pluripotent Stem Cells (iPSC) - derived CAR-NKs are naturally allogeneic, available off-the-shelf and may be able to be administered on an outpatient basis. Recent innovative developments with the iPSC, an innovative technology, allow large quantities of homogeneous genetically modified CAR NK cells to be produced from a master cell bank, and thus hold promise to expand access to cell therapy for many patients.

About Cytovia Cytovia Therapeutics Inc is an emerging biotechnology company that aims to accelerate patient access to transformational immunotherapies, addressing several of the most challenging unmet medical needs in cancer and severe acute infectious diseases. Cytovia focuses on Natural Killer (NK) cell biology and is leveraging multiple advanced patented technologies, including an induced pluripotent stem cell (iPSC) platform for CAR (Chimeric Antigen Receptors) NK cell therapy, next-generation precision gene-editing to enhance targeting of NK cells, and NK engager multi-functional antibodies. Our initial product portfolio focuses on both hematological malignancies such as multiple myeloma and solid tumors including hepatocellular carcinoma and glioblastoma. The company partners with the University of California San Francisco (UCSF), the New York Stem Cell Foundation (NYSCF), the Hebrew University of Jerusalem, and CytoImmune Therapeutics. Learn more at http://www.cytoviatx.com

About Inserm Founded in 1964, the French National Institute of Health and Medical Research (Inserm) is a public science and technology institute, jointly supervised by the French Ministry of National Education, Higher Education and Research, and the Ministry of Social Affairs, Health and Womens Rights. Inserm is the only French public research institute to focus entirely on human health and position itself on the pathway from the research laboratory to the patients bedside. The mission of its scientists is to study all diseases, from the most common to the rarest. With an initial 2020 budget of 927.28 million, Inserm supports nearly 350 laboratories throughout France, with a team of nearly 14,000 researchers, engineers, technicians, and post-doctoral students. http://www.inserm.fr

SOURCE: Cytovia Therapeutics

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Cytovia Therapeutics partners with Inserm to develop selective CD38 NK therapeutics and offer new treatment options for Multiple Myeloma patients |...

Dolly the Sheep: ’90s Media Sensation – Mental Floss

It was Saturday, February 22, 1997, and Scottish researchers Ian Wilmut and Keith Campbell were expecting a final moment of calm before the results of their unprecedented scientific experiment were announced to the world.

The team had kept the breakthrough under wraps for seven months while they waited for their paper to be published in the prestigious journal Nature. Confidential press releases had gone out to journalists with the strict instruction not to leak the news before February 27.

But that night, the team was tipped off that journalist Robin McKie was going to break the story the very next day in the British newspaper The Observer.

Wilmut and Campbell raced to the lab at the Roslin Institute on Sunday morning as McKie's story hit the media like a thunderbolt. International news outlets had already started swarming at the institute for access to Wilmut and Campbell's creation: Dolly the sheep, the world's first mammal successfully cloned from a single adult cell. Shielded from the general public, she stuck her nose through the fence and munched calmly on the hay in her pen, unperturbed by the horde of news photographers. Dolly, a woolly, bleating scientific miracle, looked much like other sheep, but with a remarkable genetic difference.

By the end of that Sunday, February 23, nearly every major newspaper in the world carried headlines about Dolly the sheep.

Born on July 5, 1996, Dolly was cloned by Wilmut and Campbell's team at the Roslin Institute, a part of the University of Edinburgh, and Scottish biotechnology company PPL Therapeutics. The scientists cloned Dolly by inserting DNA from a single sheep mammary gland cell into an egg of another sheep, and then implanting it into a surrogate mother sheep. Dolly thus had three mothersone that provided the DNA from the cell, the second that provided the egg, and the third that carried the cloned embryo to term. Technically, though, Dolly was an exact genetic replica of only the sheep from which the cell was taken.

Following the announcement, the Roslin Institute received 3000 phone calls from around the world. Dolly's birth was heralded as one of the most important scientific advances of the decade.

But Dolly wasn't science's first attempt at cloning. Researchers had been exploring the intricacies of cloning for almost a century. In 1902, German embryologists Hans Spemann and Hilda Mangold, his student, successfully grew two salamanders from a single embryo split with a noose made up of a strand of hair. Since then, cloning experiments continued to become more sophisticated and nuanced. Several laboratory animal clones, including frogs and cows, were created before Dolly. But all of them had been cloned from embryos. Dolly was the first mammal to be cloned from a specialized adult cell.

Embryonic stem cells, which form right after fertilization, can turn into any kind of cell in the body. After they modify into specific types of cells, like neurons or blood cells, they're call specialized cells. Since the cell that gave rise to Dolly was already specialized for its role as a mammary gland cell, most scientists thought it would be impossible to clone anything from it but other mammary gland cells. Dolly proved them wrong.

Many scientists in the '90s were flabbergasted. Dollys advent showed that specialized cells could be used to create an exact replica of the animal they came from. It means all science fiction is true, biology professor Lee Silver of Princeton University told The New York Times in 1997.

The Washington Post reported that "Dolly, depending on which commentator you read, is the biggest story of the year, the decade, even the century. Wilmut has seen himself compared with Galileo, with Copernicus, with Einstein, and at least once with Dr. Frankenstein."

Scientists, lawmakers, and the public quickly imagined a future shaped by unethical human cloning. President Bill Clinton called for review of the bioethics of cloning and proposed legislation that would ban cloning meant ''for the purposes of creating a child (it didn't pass). The World Health Organization concluded that human cloning was "ethically unacceptable and contrary to human integrity and morality" [PDF]. A Vatican newspaper editorial urged governments to bar human cloning, saying every human has "the right to be born in a human way and not in a laboratory."

Meanwhile, some scientists remained unconvinced about the authenticity of Wilmut and Campbells experiment. Norton Zinder, a molecular genetics professor at Rockefeller University, called the study published in Nature "a bad paper" because Dolly's genetic ancestry was not conclusive without testing her mitochondriaDNA that is passed down through mothers. That would have confirmed whether Dolly was the daughter of the sheep that gave birth to her. In The New York Times, Zinder called the Scottish pair's work ''just lousy science, incomplete science." But NIH director Harold Varmus toldthe Times that he had no doubt that Dolly was a clone of an adult sheep.

Because she was cloned from a mammary gland cell, Dolly was nameddad joke alertafter buxom country music superstar Dolly Parton. (Parton didnt mind the attribution.) Like her namesake, Dolly the sheep was a bona fide celebrity: She posed for magazines, including People; became the subject of books, journal articles, and editorials; had an opera written about her; starred in commercials; and served as a metaphor in an electoral campaign.

And that wasn't all: New York Times reporter Gina Kolata, one of the first journalists to give readers an in-depth look at Dolly, wroteClone: The Road to Dolly, and the Path Ahead and contrasted the animal's creation with the archetypes in Frankenstein and The Island of Dr. Moreau. American composer Steve Reich was so affected by Dolly's story that he featured it in Three Tales, a video-opera exploring the dangers of technology.

The sheep also became an inadvertent political player when the Scottish National Party used her image on posters to suggest that candidates of other parties were all clones of one another. Appliance manufacturer Zanussi used her likeness for a poster with her name and the provocative caption "The Misappliance of Science" (the poster was later withdrawn after scientists complained). In fact, so widespread was the (mis)use of her name that her makers eventually trademarked it to stop the practice.

Following Dolly, many larger mammals were cloned, including horses and bulls. Roslin Biomed, set up by the Roslin Institute to focus on cloning technology, was later sold to the U.S.-based Geron Corporation, which combined cloning technology with stem cell research. But despite her popularityand widespread fearDolly's birth didn't lead to an explosion in cloning: Human cloning was deemed too dangerous and unethical, while animal cloning was only minimally useful for agricultural purposes. The sheep'sreal legacy is considered to be the advancement in stem cell research.

Dollys existence showed it was possible to change one cells gene expression by swapping its nucleus for another. Stem cell biologist Shinya Yamanaka told Scientific American that Dollys cloning motivated him to successfully develop stem cells from adult cells. He later won a Nobel Prize for his results, called induced pluripotent stem cells (iPS) because they're artificially created and can have a variety of uses. They reduced the need for embryonic stem cells in research, and today, iPS cells form the basis for most stem cell research and therapies, including regenerative medicine.

Dolly had sixoffspring, and led a productive, sociable life with many human fans coming to visit her. In 2003, a veterinary examination showed that Dolly had a progressive lung disease, and she was put down. But four clonescreated from the same cell line in 2007 faced no such health issues and aged normally.

Dolly is still a spectacle, though, nearly 25 years after her creation: Her body was taxidermied and puton display at the National Museum of Scotland in Edinburgh.

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Dolly the Sheep: '90s Media Sensation - Mental Floss

Regeneron, Pfizer and BioNTech Accused of Infringing Allele Patent in Connection with COVID-19 Technologies – IPWatchdog.com

Only through use of mNeonGreen were [Pfizer and BioNTech] able to develop and test the BNT162 vaccine candidate at lightspeed, making them first to market [and] earning them an immediate $400 million in grants and over $4 billion in sales of the vaccine to- date. Allele Complaint

Allele Biotechnology and Pharmaceuticals, Inc. (Allele) has accused Regeneron Pharmaceuticals, Inc. (Regeneron); Pfizer, Inc. (Pfizer); and BioNTech SE and BioNTech US, Inc. (collectively BioNTech) for allegedly infringing U.S. Patent No. 10,221,221 (the 221 patent), which is directed to an artificial flourescent, i.e. mNeonGreen, used for testing COVID-19 assays against vaccine candidates. Allele argues that Regeneron, Pfizer and BioNTech have been infringing the 221 patent by taking mNeonGreen for their own unauthorized commercial testing and development.

Regeneron has been in the news lately for famously providing the antibody cocktail given to President Donald Trump shortly after he tested positive for COVID-19 last week. The cocktail is name in the complaint as one of the allegedly infringing technologies.

The 221 patent, titled Monomeric Yellow-Green Fluorescent Protein from Cephalochordate, was assigned to Allele and directed to high performance monomeric yellow-green fluorescent proteins. Although mNeonGreen was Alleles breakthrough in fluorescent protein technology, Allele has many other achievements, including advances in RNA interference, Fluorescent Proteins, Induced Pluripotent Stem Cells (iPSCs), Genome Editing, and camelid derived Single Domain Antibodies. Most recently, Allele has also been actively engaged in combating COVID-19, initiating impactful diagnostic and therapeutic platforms premised on speed, accuracy, and sensitivity. Alleles mNeonGreen technology has been licensed to hundreds of organizations and universities. As asserted by Allele, mNeonGreen facilitates quick, targeted, and precise receptor research, including for potential therapeutics to treat COVID-19.

Allele filed a Complaint against Regeneron in the U.S. District Court for the Southern District of New York alleging that Regeneron has been using Alleles patented mNeonGreen technology. Allele cited multiple published articles and papers written by Regeneron representatives. The Complaint noted that Regeneron did not have a license to use Alleles mNeonGreen technology, despite Alleles consistent showing that it is willing to license its mNeonGreen technology on reasonable terms in order to help facilitate the use of that protein by third parties in their efforts to develop new and essential technologies. Also, according to the Complaint, Allele sought to discuss licensing arrangements with Regeneron after learning of the infringement of the 221 patent, but Regeneron ignored Alleles attempts.

The Complaint asserted that Regeneron directly infringed the mNeonGreen technology claimed in the 221 patent and, by way of its publications, press releases, and other papers, caused others to directly infringe the mNeonGreen technology claimed in the 221 patent. Thus, Allele asked the court, in part, for: (1) a finding that the 221 patent is valid and enforceable, (2) a judgment that Regeneron had infringed, actively induced infringement of, and/or contributed to the infringement of one or more claims of the 221 patent, (3) a judgment that Regenerons infringement was willful, and (4) an award of damages or other monetary relief to adequately compensate Allele for Regenerons infringement of the 221 patent, and such damages be trebled under 35 U.S.C. 284 and awarded to Allele, with pre-judgment and post-judgment interest as allowed by law.

The Complaint against Pfizer and BioNTech (collectively, Defendants) was filed in the U.S. District Court for the Southern District of California and alleges that the Defendants infringed Alleles 221 patent using mNeonGreen throughout their COVID-19 vaccine trials. Pfizer was engaged with BioNTech in the development of their BNT162 MRNA-based vaccine candidate. Allele asserted that [o]nly through use of mNeonGreen were Defendants able to develop and test the BNT162 vaccine candidate at lightspeed making them first to market, earning them an immediate $400 million in grants and over $4 billion in sales of the vaccine to- date [which]was simply the downstream benefit that Defendants enjoyed (and presumably the world will enjoy from the vaccine) from their choice to use Alleles mNeonGreen.

According to the Complaint, BioNTech adopted Alleles mNeonGreen technology in its COVID-19 vaccine trial and literally infringed claims 1, 2, 4 and 5 of the 221 patent. Allele asserted that it has not granted the Defendants authorization, license, or permission to practice the inventions claimed in the 221 Patent. Allele also asserted that Defendants infringement was willful because the defendants had actual knowledge of the 221 Patent and the obvious risk of infringement by continued use of mNeonGreen throughout their development of their COVID-19 vaccine candidate in the United States. Thus, Allele requested, in part, that the court (1) find that the 221 Patent has been infringed by the Defendants in violation of 35 U.S.C. 271, (2) find that the Defendants infringement of the 221 Patent was been willful, (3) award adequate damages to compensate Allele for the Defendants infringement, and (4) an award of treble damages for the period of any willful infringement by the Defendants pursuant to 35 U.S.C. 284.

Image Source: Deposit Photos Author: Rewat Image ID: 358544690

Rebecca Tapscott is an intellectual property attorney who has joined IPWatchdog as our Staff Writer. She received her Bachelor of Science degree in chemistry from the University of Central Florida and received her Juris Doctorate in 2002 from the George Mason School of Law in Arlington, VA.

Prior to joining IPWatchdog, Rebecca has worked as a senior associate attorney for the Bilicki Law Firm and Diederiks & Whitelaw, PLC. Her practice has involved intellectual property litigation, the preparation and prosecution of patent applications in the chemical, mechanical arts, and electrical arts, strategic alliance and development agreements, and trademark prosecution and opposition matters. In addition, she is admitted to the Virginia State Bar and is a registered patent attorney with the United States Patent and Trademark Office. She is also a member of the American Bar Association and the American Intellectual Property Law Association.

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Regeneron, Pfizer and BioNTech Accused of Infringing Allele Patent in Connection with COVID-19 Technologies - IPWatchdog.com

Proposition 14: With Handful of Cures, Calif. Stem Cell Agency Has Mixed Record. Will Voters Pony Up Another $5.5 Billion? – KQED

A Yes vote authorizes the state to sell $5.5 billion in general obligation bonds primarily for stem cell research and the development of new medical treatments in California. A No vote would mean the state's stem cell research agency will probably shut down by 2023.

In the ramp-up to the 2004 election, a California TV viewer may have come across the popular actor Michael J. Fox urging her to vote Yes on a state proposition. His voice slurred faintly by Parkinsons disease, he still sounded wry, boyish and familiar.

My most important role lately is as an advocate for patients and for finding new cures for diseases, said Fox, eyes level with the camera. Californias Stem Cell Research Initiative 71 will support research to find cures for diseases that affect millions of people, including cancer, diabetes, Alzheimer's and Parkinson's.

Within that 30-second spot, Fox, diagnosed at age 29 with a neurodegenerative disorder that typically does not strike until after 60, used the word "cures" three times.

Proposition 71, which passed with 59% of the vote, authorized the sale of $3 billion in bonds to create an agency that funded stem cell research. The successful campaign grew out of a time, in the early 2000s, when the promise of stem cell and regenerative medicine excited both scientists and the public.

Whether the project has lived up to that promise is a matter of opinion. How voters view the record of the agency may go a long way in their decision whether or not to replenish the fund, which is fast running out of money, with an additional $5.5 billion, to be raised with new bonds authorized by Proposition 14, now on the ballot.

President Bush A Demon to Attack

Scientists since the1800s have known about stem cells, which are not yet dedicated to any particular anatomical function and have the potential to become nerve cells, blood cells, skin cells or any other type. They are found in blastocysts, which are human embryos four to five days after fertilization, and in a few areas, such as bone marrow and gonads, in adults.

In the late 1990s, researchers developed ways to steer the development of these cells, and the possibilities for improving medicine seemed endless. If malfunctioning cells were at the root of a particular disease, could new healthy cells tailored to the job fix what was wrong? Scientists and many members of the public were eager to find out.

Anti-abortion groups, however, a key constituency of President George W. Bush, opposed the research, and in 2001 he limited federal funding to a few existing lines of embryonic stem cells, severely curtailing research.

Some in the state of California wanted to get around Bushs restrictions, and Proposition 71 was born.

"(T)hey had this demon they could attack in the campaign the Bush administration," said David Jensen, author of "California's Great Stem Cell Experiment," who also writes the blog California Stem Cell Report. "They could say, 'This is a great opportunity, and the only way we're going to get it done is to do it here in California.'"

The measure created the California Institute for Regenerative Medicine. The stem cell research agency is unique in the U.S.

"No other state has done this kind of level of funding and focus on this kind of thing, said Jensen. It's a really cutting-edge area of science."

A Few Successes

The pace of innovation has been slower than many hoped. As it turned out, grand discoveries were not around the corner, and to date there is no widespread stem cell treatment approved for the public. To date, CIRM has funded more than 64 trials directly and aided in 31 more. Not all have or will result in treatments.

But despite the lack of a marquee cure like one for Alzheimers or Parkinsons, the agency has seen some notable triumphs.

"Probably one of the most spectacular successes they have certainly so far," said Jensen, "is clinical trials that have saved the lives of what they say are 40 children."

Those children were born with severe combined immunodeficiency (SCID), commonly known as "bubble baby syndrome," a rare, generally fatal condition in which a child is born without a working immune system. An FDA-approved gene therapy that grew out of CIRM-funded research can now cure the disease by taking a patients own blood stem cells and modifying them to correct the SCID mutation. The altered cells generate new, healthy blood cells and repair the immune system.

The FDA has also approved two drugs for rare blood cancers that were developed with CIRM funds.

Sandra Dillon, a graphic designer in San Diego, credits one of the drugs with saving her life. She was diagnosed when she was just 28, in 2006. Her doctors told her they would try to manage her symptoms, but that she was going to get progressively sicker.

"Even just the idea of a cure or getting better wasn't even on the table back then," said Dillon, who is featured in ads for the Yes on 14 campaign.

"I remember just praying and begging into the universe, please, someone just look at my disease, please someone help, who is going to look at this thing.

By 2010, Dillon was extremely ill. She connected with a doctor at UC San Diego who received early-stage funding from CIRM and told her she could take part in clinical trials.

"For the first time, there was this moment of, 'Oh, my gosh! There are researchers doing something. And it could help me and I can get access to it.' It was amazing."

The drug received FDA approval in 2019, and today Dillons cancer has retreated to the point where she can live a normal life.

"I love that I am not tethered to a hospital anymore. I can go out on long backpacking trips and hiking and surfing," she said. "I am a completely different person with this drug. And I have a whole future ahead of me."

The original funding raised by Proposition 71 is running out. Proposition 14 would authorize the sale of a new bond to refill the agency piggy bank. Gov. Gavin Newsom, the UC Board of Regents, and scores of patient advocacy groups also support the measure.

Many newspaper editorial boards, however, oppose the proposition, including the San Francisco Chronicle, Mercury News and Los Angeles Times.

Right now the state still owes about $1 billion toward the debt created by Proposition 71. If Proposition 14 passes, the yearly price tag to pay off the new bond would be about $260 million per year for about 30 years.

One of the selling points of the original proposition was the potential for the state to earn big money in royalties from the treatments it helped develop, says Jeff Sheehy, an HIV patient advocate and the only CIRM board member to oppose Proposition 14.

"The promises were made that this would pay for itself. We would be able to pay back the bonds with the money we would get from royalties, etc., etc.

That has not worked out as envisioned: CIRM estimates it has received less than $500,000 in royalties. Early this year, Forty Seven, a company whose therapies were heavily funded by CIRM, sold to Gilead for $4.9 billion. While millions went to various researchers, neither CIRM nor the state of California received anything.

One of the flaws in the original measure is that we [the agency] cannot hold stock in the products that we develop," says Sheehy. "And that's because the California Constitution says that the state of California cannot, as a government entity, hold equity.

Proposition 14 makes it impossible for the state to use profits from its investment on, say, schools or other funding priorities. Instead, any royalties earned must be fed back into programs to make CIRM-funded treatments more affordable.

"What it does is it basically takes all of our returns that we get from this and gives it back to the pharmaceutical and biotech companies," said Sheehy. "It becomes just a blatant giveaway to these companies when we should be requiring access and requiring fair pricing."

Sheehy says he supports medical research, but doesn't like the state going into more debt to pay for it. The greater the state's obligations in bond money, which has to be paid back with interest, the less there is in the general fund, and Sheehy says the state has more pressing needs than stem cell research things like housing, education and transportation.

"The biggest and perhaps the most compelling reason why I feel so strongly that this is not a good idea is that we simply cannot afford it, he said. "If we think this is so important," asks Sheehy, "why don't we just don't pay for [this research] out of the general fund? It would be cheaper.

Opponents of Proposition 14 also point to longstanding complaints of conflicts of interest among the agency board. Most of the $3 billion distributed by the agency has gone to institutions with connections to board members. Critics say the structural conflicts of interest between the board and agency are not addressed in the new measure. Proposition 14 would balloon an already huge board of 29 members to 35.

Funding needs for stem cell research also are not as acute as they were back in 2004. The federal National Institutes of Health now funds some basic stem cell research, spending about $2 billion a year, with $321 million of that going toward human embryonic stem cell research. And private ventures, like nonprofits started by tech billionaires, are pouring more money into biotech.

The problem with assuming that, says Melissa King, executive director of Americans for Cures, the stem cell advocacy group behind the Yes on 14 campaign, is that CIRM fills a neglected funding need.

The NIH does not fund clinical trials at nearly the rate that CIRM can and has been, King said.

She says that's important because of what she calls the "Valley of Death," where promising early-stage research frequently fails to translate into promising treatments that can be tested in clinical-stage research. (What works well in a test tube often does not work well in an organism.) This weeding-out process is costly but necessary. And its where CIRM focused a lot of its effort.

The first- and maybe even second-phase clinical trials, its very difficult to get those funded, King said. It is too much of a risk for business to take on on its own. Venture [capital] isnt going there. Angel [funding] isnt going there.

What voters have to ask themselves, says writer Jensen, is whether stem cell funding is "a high priority for the state of California? Different people make different judgments about that."

CIRM supporters say if Prop. 14 doesn't pass, critical research will stall. Others say federal and private funding will step in and fill the gap.

Absent new funding, the institute expects it will wind down operations leading to a complete sundown in 2023.

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Proposition 14: With Handful of Cures, Calif. Stem Cell Agency Has Mixed Record. Will Voters Pony Up Another $5.5 Billion? - KQED

Woman who lost her partner to cancer last year set to run 10K in his memory – Warrington Guardian

A 29-YEAR-old who tragically lost her partner to cancer last year will be running 10K to raise vital funds for a blood cancer charity in his memory.

Hannah Kenyon, a teaching assistant from Culcheth, is taking part in the Tatton Park 10K this weekend, in tribute to her boyfriend, Jonny Williams, who died from Non-Hodgkins Lymphoma in February last year.

She will be raising money for Anthony Nolan, a charity which finds matching donors for people with blood cancer.

Speaking about her relationship with Jonny, Hannah said: "Jonny and I met at school, I always liked him but we didnt get together until we were in college.

"In March 2018, after having been together been for nine years, we bought our own home which we wanted to renovate and really make our own."

In July of that year, Jonny, who was an electrician, noticed lumps on his neck and started suffering from extreme abdominal pain.

After several trips to hospital, he was eventually diagnosed with stage four Non-Hodgkins Lymphoma.

Hannah recalled: "It was such a shock and Jonny had to start chemotherapy literally straight away.

"However, it wasnt working the way doctors had hoped and his cancer continued to progress.

"This was when a stem cell transplant was first mentioned - the goal was for chemotherapy to get Jonny into remission so he could then have a stem cell transplant, which would hopefully cure him."

With only one half brother and two half sisters, there was no chance of finding Jonny a match within his own family.

Anthony Nolan jumped into action and searched their register of potential stem cell donors for a special stranger who could save his life.

"We were told that Jonny had three potential donors," Hannah said.

"The day we found out, no words needed to be spoken to know how extremely lucky we felt, as I know there are people out there who desperately need a donor but dont have one."

After just a few months, Jonny and Hannah received the devastating news that Jonnys cancer had progressed, which meant that he was unable to have a transplant.

He died less than one week later.

Hannah explained: "It was and still is completely devastating, and at times it still feels like a blur.

"Jonny was such a positive person, Ive never known anyone so positive, and he tried to live as normal a life as possible during his illness.

"He wanted no fuss and always had hope and optimism for the future.

"Even though Jonny was unable to have a transplant, it is just unreal that three strangers were willing to help him.

"I know what its like to hear the news that someone out there is a match and is willing to save a life, which is why I just wont stop shouting about Anthony Nolan."

After Jonny's death, Hannah continued to renovate the house they had bought together.

She also started running and will now be putting on her trainers this weekend in aid of Anthony Nolan, alongside her friend, Sam.

"I know that Jonny would be buzzing about me doing this, he always was my number one fan," Hannah said.

"Sunday, I am sure, will be a really emotional day, but Ive got a playlist of Jonnys favourite songs that Im going to listen to whilst Im running that will keep me going."

You can sponsor Hannah at justgiving.com/fundraising/10kforjonny.

To find out more about Anthony Nolan, visit anthonynolan.org/events.

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Woman who lost her partner to cancer last year set to run 10K in his memory - Warrington Guardian