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Living at high altitude leads to longer life by changing metabolism – Earth.com

An estimated two million people worldwide reside above 4,500 meters (14,764 feet) in elevation, comparable to the heights of Mount Rainier, Mount Whitney, and numerous peaks in Colorado and Alaska. Intriguingly, these individuals have been observed to have lower rates of metabolic diseases, such as diabetes, coronary artery disease, hypercholesterolemia, and obesity. Researchers supported by the U.S. National Science Foundation at Gladstone Institutes have recently made strides in understanding this phenomenon.

The scientists discovered that chronic exposure to low oxygen levels, as experienced at high altitudes, altered the way mice metabolized sugars and fats. The study, published in the journal Cell Metabolism, offers insights into the metabolic differences in people living at high altitudes and suggests potential new treatments for metabolic diseases.

When an organism is exposed to chronically low levels of oxygen, different organs reshuffle their fuel sources and their energy-producing pathways, explained Isha Jain, senior author of the study. We hope these findings will help us identify metabolic switches that might be beneficial for metabolism even outside of low-oxygen environments.

At sea level, where a third of the global population resides, oxygen accounts for approximately 21% of the air we breathe. However, at elevations above 4,500 meters, oxygen makes up a mere 11% of the air. Despite these lower oxygen levels, known as hypoxia, people can adapt and thrive in these conditions.

Previous research on hypoxias impact has often been limited to isolated cells or cancerous tumors, which are commonly oxygen-deficient. Jains group aimed to investigate the long-term effects of hypoxia on organs throughout the body. They collaborated with colleagues at Gladstone and the University of California, San Francisco, to house adult mice in pressure chambers containing 21%, 11%, or 8% oxygen levels all of which are survivable by humans and mice.

Over three weeks, the researchers monitored the mices behavior, temperature, carbon dioxide levels, blood glucose levels, and used positron emission tomography (PET) scans to study nutrient consumption by different organs. In the initial days of hypoxia, mice in 11% or 8% oxygen environments exhibited reduced mobility and periods of complete stillness.

However, by the end of the third week, their movement patterns normalized. Likewise, their blood carbon dioxide levels, which typically decrease when mice or humans breathe faster to compensate for low oxygen, initially dropped but returned to normal levels by the end of the study.

The animals metabolism, on the other hand, appeared to be more permanently affected by hypoxia. Mice in hypoxic cages experienced decreases in blood glucose levels and body weight, with neither returning to pre-hypoxic levels.

These metabolic changes parallel those observed in humans living at high altitudes and are associated with a reduced risk of diseases, including cardiovascular disease. This understanding of hypoxias contribution could pave the way for developing new drugs that replicate these beneficial effects, offering hope for those suffering from metabolic diseases.

There is a growing body of research focused on understanding the biological processes of aging and developing strategies to extend human lifespan. Some of the prominent areas of research include:

These research areas, along with many others, represent the ongoing efforts to unravel the complex biology of aging and develop interventions that can promote healthy aging and extend human lifespan.

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Living at high altitude leads to longer life by changing metabolism - Earth.com

The Explorers: A Passion for Science Leads to New Territory – University of California San Diego

Unusual Breadth

This quest soon led them to seek out real-world problems that could have a bigger impact on peoples lives than basic science. They moved to the West Coast, where they pursued a mix of research and development jobs in biotechincluding at Amgen and Invitrogen (acquired by Thermo Fisher)and at universities including UC Berkeley (Molokanova), UC San Diego and Stanford University (Savtchenko).

These experiences working at intersection of physics and biology coupled with decades of work across multiple scenarios in academics and industry gave the couple a unique perspective on many of the biggest problems in neuroscience and drug discovery, as well as the business processes that helped or hindered progress.

So, as they discussed whether to start their own companies, they didnt have to deliberate for long.

It was pretty clear to me that the science was coming along nicely, and that our contribution [as entrepreneurs] would be serious, meaningful, said Savtchenko.

One major challenge the pair had observed in the biotech industry involved initial testing of potential drug compoundsresults that informed whether compounds would be pursued or discarded from consideration for further development as medicines.

Savtchenko noted that biotech and pharmaceutical companies spend billions of dollars on screening drug compounds for safety and activityin vitro(in cell culture), yet the environment in plastic cell culture dishes drastically differs from the human body, especially for nerve cells (a.k.a. neurons) and heart cells (a.k.a. cardiomyocytes).

The biggest difference between neurons in the brain and neurons in a cell culture dish is whether they receive external input or not, Savtchenko explained. From the very first moment of our existence, it is normal and, in fact, necessary for our brains to be constantly bombarded by various signals (e.g., stimuli from sight, hearing, feeling, tasting)the results determine our development, define our individual personalities and, often, affect our health.

He continued, To discover drugs that can fix aberrations in brain activity and heal a patient, it is imperative to test the drug effects on functionally active, input-receiving, dynamic response-producing neurons. Otherwise, clinical studies in human patients might produce drastically different outcomes than priorin vitrostudiesresulting in failed projects, loss of multibillion dollar investments, and disappointment for millions of patients.

The development of medication that could affect the heart faces similar challenges. Testing for drug cardiotoxicity is often performed in highly artificial conditionsin an electrically insulated culture dish of human stem-cell derived cardiomyocytes, spontaneously contracting at a single frequency. In real-life, adult heart rates can vary almost two-fold over the course of a day in response to changing conditions.

Highlighting the importance of such testing, in recent decades several blockbuster drugs have been removed from the market because they were linked to irregular heartbeat, accounting for 30% of all post-approval withdrawals.

Savtchenko and Molokanova wanted to find a way to safely and reliably stimulate cells in a dish while testing their response in the presence of drug compounds so that the results of these screening studies would better predict the drugs affect in humans. Reaching this goal would mean that fewer drugs would fail at the last stages of drug discovery process, resulting in safer, more efficient, and less expensive drugs.

After her industry experience working with different materials, including semiconductor quantum dots, to stimulate cells in culture, Molokanova hit on the idea to harness the unique properties of a new two-dimensional carbon allotrope, graphene.

Graphene had been discovered by Andre GeimandKonstantin Novoselov (coincidentally fellow alumni of Savtchenkos alma mater, MIPT), who were awarded the 2010 Nobel Prize in Physics for this finding. In the Nobel announcement, the Royal Swedish Academy of Sciencesdescribedgraphene as a thin flake of ordinary carbon, just one atom thick [with] exceptional properties that originate from the remarkable world of quantum physics.

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The Explorers: A Passion for Science Leads to New Territory - University of California San Diego

Asia Pacific Stem Cell Therapy Market Size, Demand, Share, Revenue, Key Players, Growth, and Forecast 2023 to – openPR

Astute Analytica's recently published report on the Asia Pacific Stem Cell Therapy Market offers the latest data and determines growth prospects and challenges. A tool for evaluating the potential for new goods and services is the constraints and opportunity analysis. This aids businesses in locating and forecasting market opportunities.

Request Of this Sample Report Here- https://www.astuteanalytica.com/request-sample/asia-pacific-stem-cell-therapy-market

The study also contains a compilation of qualitative and quantitative evaluations made by subject-matter experts in their fields as well as representatives from various industries found all along the supply chain.

The Asia Pacific stem cell therapy market is poised for substantial growth in the coming years, with a projected compound annual growth rate (CAGR) of 10.29% between 2023 and 2031. This growth is expected to drive the market value up to US$ 3,420.05 Mn by 2031, following a successful revenue performance of US$ 1,453.61 Mn in 2022.

The paper discusses further findings that researchers made based on the comprehensive data and also offers information on the state of the market. The paper discusses kinds and applications based on various nations and important locations. The market's most active companies are described in detail with regard to attributes like corporate portfolio, business strategy, financial overview, recent developments, and industry share.

Leading Companies

AlloSourceAnterogen Co. Ltd.Arce TherapeuticsAstellas Pharma IncBiogend TherapeuticsBiorestorative Therapies Inc.Brainstorm Cell Limited.Cellular Biomedicine GroupCORESTEMFujifilm Holding CorporationHolostem Terapie Avanzate SrlJCR Pharmaceuticals Co. Ltd.Kangstem BiotechMEDIPOST Co. Ltd.Mesoblast LtdPersonalized Stem CellsPELL Biotech Co., Ltd.Pluristem Inc.RTI SurgicalSartorius AGSewon CellontechSmith+NephewSTEMPEUTICS RESEARCH PVT LTD.Takeda Pharmaceutical Company LimitedVericel CorpOther Prominent PlayersMore Full Report Here- https://www.astuteanalytica.com/industry-report/asia-pacific-stem-cell-therapy-market

We continuously monitor the direct impact COVID-19 (Update Omicron mutations study) has on the market, in addition to the indirect influence of related industries. The report will contain the observations.

The geographical regions are divided into several major categories for production, consumption, revenue (in US dollars), and market share in this analysis. We'll discuss the predicted growth of the market in this region between 2021 and 2031.

Segmentation Overview

The Asia Pacific stem cell therapy market is segmented based on therapy type, product, cell source, technology, application and end user.

By Therapy Type segmented, the Asia Pacific stem cell therapy market is sub-segmented into:

Autologous Stem Cell TherapyAllogeneic Stem Cell TherapyBy Product segment, the Asia Pacific stem cell therapy market is sub-segmented into:

Adult Stem Cells (ASCs)Human Embryonic Stem Cells (HESCs)Induced Pluripotent Stem Cells (iPSCs)Very Small Embryonic Like Stem CellsBy Cell source segment, the Asia Pacific stem cell therapy market is sub-segmented into:

Adipose tissue derived MSCsBone marrow derived MSCsPlacental/umbilical cord derived MSCsOther Cell SourcesBy technology segment, the Asia Pacific stem cell therapy market is sub-segmented into:

Cell AcquisitionCell ProductionCryopreservationExpansion and Sub-CultureBy application segment, the Asia Pacific stem cell therapy market is sub-segmented into:

Musculoskeletal DisordersWounds and InjuriesAcute Graft-Versus-Host Disease (AGVHD)SurgeriesGastrointestinal DiseasesCardiovascular DiseasesInflammatory & Autoimmune DiseasesNeurological DisordersOthersBy end user segment, the Asia Pacific stem cell therapy market is sub-segmented into:

HospitalsResearch institutesSurgical institutesOthersBy country, the Asia Pacific stem cell therapy market is sub-segmented into:

ChinaIndiaJapanAustralia & New ZealandASEANTaiwanSouth KoreaRest of Asia Pacific

Access Sample Report Here- https://www.astuteanalytica.com/request-sample/asia-pacific-stem-cell-therapy-market

About Astute Analytica:

Astute Analytica is a global analytics and advisory company that has built a solid reputation in a short period, thanks to the tangible outcomes we have delivered to our clients. We pride ourselves in generating unparalleled, in-depth, and uncannily accurate estimates and projections for our very demanding clients spread across different verticals. We have a long list of satisfied and repeat clients from a wide spectrum including technology, healthcare, chemicals, semiconductors, FMCG, and many more. These happy customers come to us from all across the globe.

They are able to make well-calibrated decisions and leverage highly lucrative opportunities while surmounting the fierce challenges all because we analyze for them the complex business environment, segment-wise existing and emerging possibilities, technology formations, growth estimates, and even the strategic choices available. In short, a complete package. All this is possible because we have a highly qualified, competent, and experienced team of professionals comprising business analysts, economists, consultants, and technology experts. In our list of priorities, you-our patron-come at the top. You can be sure of the best cost-effective, value-added package from us, should you decide to engage with us.

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Asia Pacific Stem Cell Therapy Market Size, Demand, Share, Revenue, Key Players, Growth, and Forecast 2023 to - openPR

With A CAGR of 4.9%, Research Antibodies Market Size Worth USD 2.17 Billion By 2030 | Emergen Research – EIN News

Research Antibodies Market Trends An increase in research and development (R&D) activities related to the fields of neurobiology

Emergen Research

The global research antibodies market is projected to be worth USD 5,325.8 Million by 2027, according to a current analysis by Emergen Research. The market for research antibodies is witnessing a high demand due to its growing application in neurobiology, infectious diseases, oncology, stem cells, and immunology, among others. Increased investments in research in the field of stem cells is also a crucial growth factor of the Research Antibodies market.

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Research Antibodies Market, By Antibody Type (Monoclonal and Polyclonal), By Antibody Type (Primary Antibodies and Secondary Antibodies), By Application, By Technology, By End-use, and By Region Forecast to 2030. An increase in research and development (R&D) activities related to the fields of neurobiology, oncology and stem cell research, the increasing incidence of cancer and infectious diseases, and the growing demand from the biopharmaceutical industry for these antibiotics are the main drivers of the market. increase the revenue. Research antibodies are antibodies that can bind to specific molecules, which are used as basic detection tools needed in scientific research and are also important tools for studying protein function in cell.

Key Players Included in this report are:

Lonza Group, Becton, Dickinson, and Company, Agilent Technologies, Abcam PLC, PerkinElmer Inc., Bio-Rad Laboratories, Merck Millipore, F. Hoffmann-La Roche AG, Thermo Fisher Scientific, Cell Signaling Technology Inc.

What can be explored with the Research Antibodies Market Study?

Gain Market Understanding

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Some Key Highlights from the Report

The research antibodies market has been divided into hospitals, dental offices, and other end-uses. Over the projected period, it is anticipated that the dental clinics segment will contribute the most to total revenue. They meet a variety of client needs and offer the necessary knowledge, along with a vast array of technologically cutting-edge tools and supplies, to perform any orthodontic procedure. Better patient reimbursement dental policies are available at dental clinics. Furthermore, the significant market share of dental clinics is caused by an increase in orthodontists' private practises. Some major companies in the global research antibodies market report include Merck KGaA, Johnson & Johnson Services, Inc., Eli Lilly and Company., Bio-Rad Laboratories, Inc., Cell Signalling Technology, Inc., PerkinElmer Inc., ROCKLAND IMMUNOCHEMICALS, INC., Novartis AG, BD, and Abcam plc. Market Segmentation Analysis

Players can concentrate on high-growth regions and, if necessary, modify their business plan according to the research report. The Research Antibodies Market is divided into a variety of categories, uses, and geographical areas. Players gain from the report's regional segmentation research since it offers pertinent data and insights into important geographic marketplaces.

Antibody Type Outlook (Revenue, USD Million; 2017-2027) Monoclonal Polyclonal Product Outlook (Revenue, USD Million; 2017-2027) Primary Antibodies Secondary Antibodies COVID-19 Impact Analysis

The post-COVID-19 phase has undergone substantial change, and Research Antibodies Market research highlights the opportunities and difficulties that still exist. This study report thoroughly examines the effects of the COVID-19 pandemic on the global economy and post-pandemic market behaviour.

Ask for Customization

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Regional Outlook

We carefully examined each division, regional classification, national study, and subject-specific data set during the market research. This Research Antibodies Market research report's goal is to look at growth patterns, promising futures, important obstacles, and expected results. Information on significant market participants, strategic alliances, plans, new product launches, and joint ventures are all included in the research.

Research Methodology

Emergen Research follows a cohesive methodology to reduce the residual errors to a minimum level by refining the scope, validating through primary insights, and nurturing the in-house database on a regular basis. A dynamic model is formulated to capture the regular fluctuations in the market and thereby, being updated with any shifts in the market dynamics.

PRIMARY RESEARCH MODEL

Post conglomeration of the data obtained through secondary research; a validation process is initiated to verify the numbers or figures. This process is usually performed by having a detailed discussion with the industry experts. Discussions with the subject matter experts were conducted to obtain quantitative and qualitative information and validate our market research findings.

Key Reasons to Purchase Research Antibodies Market Report

The reader will be in a position to comprehend and react to marketing strategies like using strengths and conducting a SWOT analysis.

The research looks into the dynamics of the target market and how the conflict between Russia and Ukraine has affected it.

Look Over transcripts provided by Emergen Research

Artificial Neural Network Market

https://usahealthnewswire.blogspot.com/2023/04/artificial-neural-network-market-global.html

Nebulizers Market

https://usahealthnewswire.blogspot.com/2023/04/nebulizers-market-size-share-price.html

Routing Market

https://usahealthnewswire.blogspot.com/2023/04/routing-market-global-industry-size.html

Industrial Robotics Market

https://usahealthnewswire.blogspot.com/2023/04/industrial-robotics-market-global.html

Thank you for reading our report. Please get in touch with us if you have any query regarding the report or its customization. Our team will ensure the report is best suited to your needs.

About Us:

Emergen Research is a market research and consulting company that provides syndicated research reports, customized research reports, and consulting services. Our solutions purely focus on your purpose to locate, target, and analyse consumer behavior shifts across demographics, across industries, and help clients make smarter business decisions. We offer market intelligence studies ensuring relevant and fact-based research across multiple industries, including Healthcare, Touch Points, Chemicals, Types, and Energy. We consistently update our research offerings to ensure our clients are aware of the latest trends existent in the market. Emergen Research has a strong base of experienced analysts from varied areas of expertise. Our industry experience and ability to develop a concrete solution to any research problems provides our clients with the ability to secure an edge over their respective competitors.

Eric LeeEmergen Research+91 90210 91709sales@emergenresearch.comVisit us on social media:FacebookTwitterLinkedIn

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With A CAGR of 4.9%, Research Antibodies Market Size Worth USD 2.17 Billion By 2030 | Emergen Research - EIN News

EW GROUP SHINES AT 12TH A4M SYMPOSIUM 2023 & – InvestorsObserver

BANGKOK , April 11, 2023 /PRNewswire/ -- European Wellness Biomedical Group (EW Group) made a successful showing at an exclusive event, the 12 th A4M Symposium 2023, which was held in Centara, Bangkok , 16 th -19 th February 2023 .

The two-day A4M Symposium, commenced with a welcome ceremony featuring Dr. Manus Potaporn (Deputy Director General of Medical Services Department, Thailand ) as a Guest of Honour, hosted by Prof. Dr. Mike Chan (A4M Thailand President), Dr. Jakkriss Bumisawasdi (A4M Thailand Honorary President), and Dr. Robert Goldman (A4M Founder).

On February 19 , European Wellness Academie (EWA), a non-profitable educational arm of EW Group, brought an exclusive workshop, "All-On Bioregen Optimization," to explore the world of anti-aging and regenerative medicine, featured some of the world's leading anti-aging experts.

Prof. Dr. Mike Chan , presented his two topics, "The Application of Regenerative Precursor Stem Cells, Peptides & Exosomes in Precision Medicine" and "Phyto-Myco-based Nano Organo Peptides: A New Trend in Precision Medicine."

"Precision Medicine in Age Reversal," which brought together the anti-aging and wellness industries on a single platform to achieve Precision Medicine's goals, which are patient-centred, may divide patients into subgroups based on their illness vulnerability, prognosis, or response to a specific treatment. It is devised and administered after comprehensive diagnostics utilizing Panomic Analysis and System Biology to analyse the patient's state at a molecular level and apply targeted therapies to address illness progression.

Anti-aging medicine aims to improve human ageing and maximize physical and mental well-being. Scientific data and medical journals supported the model's focus on Advanced Clinical Preventive and Regenerative Medicine.

The involvement of the healthcare and wellness industries will have a significant influence on the anti-aging sector for many years to come. Yet, by fact these sectors worked together to improve the quality of life for individuals and will contribute to defining the very future of modern medicine.

European Wellness Biomedical Group

An award-winning European group, most renowned for its pioneering development in organ-specific precursor (progenitor) stem cell therapeutics, biological and synthetic peptides, biological regenerative medicine, immunotherapies, and nutraceutical and cosmeceuticals.

EW Group's multinational business divisions include research and developments, bio-manufacturing, biomedical academies, hospital and wellness centres and nutraceutical product distribution across 80 countries worldwide. EW Group also owns and operates a growing network of internationally accredited Hospital and Medical Centres specializing in Regenerative Bio-Medicine and luxury Wellness Centres globally. EW Group is headquartered in Germany and Malaysia ( Asia Pacific ) with research vested in Germany , Switzerland , Czech Republic and United Kingdom .

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Media Contact: Ferellica Anne Martin +6088 448 989 (Ext: 337) media@european-wellness.com

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EW GROUP SHINES AT 12TH A4M SYMPOSIUM 2023 & - InvestorsObserver

Jasper Therapeutics Appoints David Hinds as Senior Vice President … – GlobeNewswire

REDWOOD CITY, Calif., April 10, 2023 (GLOBE NEWSWIRE) -- Jasper Therapeutics, Inc. (Nasdaq: JSPR) (Jasper), a biotechnology company focused on development of briquilimab, a novel antibody therapy targeting c-Kit (CD117) to address diseases such as chronic spontaneous urticaria, lower to intermediate risk myelodysplastic syndromes (MDS) as well as novel stem cell transplant conditioning regimes, today announced the appointment of David Hinds, as the Companys Senior Vice President, Development Operations.

We are pleased to welcome David to our team. His outstanding track record in setting strategic directions for clinical research and operations will allow us to effectively advance our development programs for briquilimab, said Ronald Martell, President and Chief Executive Officer of Jasper. As we navigate through a critical phase in our advancement of this promising asset, Davids leadership will be instrumental in rapidly progressing briquilimab in chronic spontaneous urticaria and initiating chronic lower-risk MDS study, all while maintaining momentum in the SCID, Fanconi Anemia, and sickle cell disease transplant studies recruitment.

Mr. Hinds brings more than 25 years of experience in operations and clinical program development across multiple therapeutic areas, all phases of development, and all regions of the world. Throughout his career, Mr. Hinds held a number of leadership roles, most recently as Vice President and General Partner at ICON plc, the worlds leading clinical research organization. Previously he served as Vice President, Clinical Operations at PellePharm and Tioma Therapeutics. He also led the clinical development and operations strategy at Alios Biopharma, Takeda, Clinipace, Exelixis, Kai Pharmaceuticals, Genentech, Genitope Corporation, and Intermune. He directly contributed to the success of global products including Rituxan, Adcetris, Velcade, Truvada, Orbactiv, Pirfenidone, and Celebrex. Mr. Hinds earned a Masters of Business Administration from Moore School of Business, University of South Carolina, and a Bachelor of Science in Biology at The Citadel The Military College of South Carolina.

I am thrilled to join the Jasper team at such an exciting time as the Company expands the development of briquilimab into chronic mast cell diseases and advances its novel conditioning approach for stem cell transplant, said Mr. Hinds. I look forward to contributing to the Jasper team by leveraging all the hard work that has been accomplished to date and executing on near-term clinical milestones.

About Jasper

Jasper is a clinical-stage biotechnology company developing briquilimab, a monoclonal antibody targeting c-Kit (CD117) as a therapeutic for chronic mast and stem cell diseases such as chronic urticaria and lower to intermediate risk myelodysplastic syndromes (MDS) and as a conditioning agent for stem cell transplants for rare diseases such as sickle cell disease (SCD), Fanconi anemia (FA) and severe combined immunodeficiency (SCID). To date, briquilimab has a demonstrated efficacy and safety profile in over 130 dosed subjects and healthy volunteers, with clinical outcomes as a conditioning agent in SCID, acute myeloid leukemia (AML), MDS, FA, and SCD. In addition, briquilimab is being advanced as a transformational non-genotoxic conditioning agent for gene therapy. For more information, please visit us atwww.jaspertherapeutics.com.

Forward-Looking Statements

Certain statements included in this press release that are not historical facts are forward-looking statements for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements are sometimes accompanied by words such as believe, may, will, estimate, continue, anticipate, intend, expect, should, would, plan, predict, potential, seem, seek, future, outlook and similar expressions that predict or indicate future events or trends or that are not statements of historical matters. These forward-looking statements include, but are not limited to, statements regarding briquilimabs potential, including with respect to its potential to address diseases such as chronic spontaneous urticaria, lower to intermediate risk myelodysplastic syndromes as well as novel stem cell transplant conditioning regimes, its potential to address a variety of patient populations by targeting c-Kit expressed on stem cells and mast cells and its efficacy and safety profile, pathways to market, the expansion of briquilimab development, Jaspers expectations regarding the timing of clinical trials and recruitment for clinical trials and Jaspers expectations regarding its cash and cash equivalents and planned operating and capital expenditures. These statements are based on various assumptions, whether or not identified in this press release, and on the current expectations of Jasper and are not predictions of actual performance. These forward-looking statements are provided for illustrative purposes only and are not intended to serve as, and must not be relied on by an investor as, a guarantee, an assurance, a prediction or a definitive statement of fact or probability. Many actual events and circumstances are beyond the control of Jasper. These forward-looking statements are subject to a number of risks and uncertainties, including general economic, political and business conditions; the risk that the potential product candidates that Jasper develops may not progress through clinical development or receive required regulatory approvals within expected timelines or at all; the risk that clinical trials may not confirm any safety, potency or other product characteristics described or assumed in this press release; the risk that Jasper will be unable to successfully market or gain market acceptance of its product candidates; the risk that prior study results may not be replicated; the risk that Jaspers product candidates may not be beneficial to patients or successfully commercialized; patients willingness to try new therapies and the willingness of physicians to prescribe these therapies; the effects of competition on Jaspers business; the risk that third parties on which Jasper depends for laboratory, clinical development, manufacturing and other critical services will fail to perform satisfactorily; the risk that Jaspers business, operations, clinical development plans and timelines, and supply chain could be adversely affected by the effects of health epidemics, including the ongoing COVID-19 pandemic; the risk that Jasper will be unable to obtain and maintain sufficient intellectual property protection for its investigational products or will infringe the intellectual property protection of others; and other risks and uncertainties indicated from time to time in Jaspers filings with the SEC, including its Annual Report on Form 10-K for the year ended December 31, 2022. If any of these risks materialize or Jaspers assumptions prove incorrect, actual results could differ materially from the results implied by these forward-looking statements. While Jasper may elect to update these forward-looking statements at some point in the future, Jasper specifically disclaims any obligation to do so. These forward-looking statements should not be relied upon as representing Jaspers assessments of any date subsequent to the date of this press release. Accordingly, undue reliance should not be placed upon the forward-looking statements.

Contacts:

John Mullaly (investors)LifeSci Advisors617-429-3548jmullaly@lifesciadvisors.com

Jeet Mahal (investors)Jasper Therapeutics650-549-1403jmahal@jaspertherapeutics.com

Lauren Barbiero (media)Real Chemistry646-564-2156lbarbiero@realchemistry.com

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Jasper Therapeutics Appoints David Hinds as Senior Vice President ... - GlobeNewswire

Arthritis: The Latest on Joint Replacement, Repair, and New … – Healthline

For the millions of Americans who live with arthritis (inflammation of the joints that can affect one or multiple joints), the condition can significantly impact ones quality of life.

For those who have osteoarthritis, the degenerative disease is caused by the regular mechanical wear-and-tear on the joints over time. Those who have rheumatoid arthritis find the autoimmune disease causing pain and inflammation throughout their body, with their own immune systems attacking the tissue lining in their joints.

Arthritis can affect ones ability to get around easily, perform common everyday tasks, and simply live in comfort without inflammation and pain.

About 24% of all adults in the United States have arthritis, which is a leading cause of work disability, leading to a total annual cost of wages lost and escalating medical bills totaling $303.5 billion, according to the Centers for Disease Control and Prevention (CDC).

Many may have to turn to joint repair and replacement procedures as a way to treat their arthritis. Its so common that about 790,000 total knee replacements and 450,000 hip replacements are performed each year in the U.S., a number that will only keep growing as the nations population ages, reports the American College of Rheumatology.

To address this need, a range of technological innovations and advancements in treatment have emerged in recent years to create more long-lasting, effective treatments to repair joints affected by arthritis.

Healthline spoke with experts about the latest advancements from growing new cartilage cells to using injectables to spur more efficient healing in joint repair for arthritis, and whats next as we look to the future of the field.

When asked to assess the overall state of the field of joint repair and replacement, Dr. Susan Goodman, an attending rheumatologist at the Hospital for Special Surgery in New York, said she believes we are looking at a future with no need for joint replacements.

But to get to that point, she told Healthline that there are several significant hurdles ahead.

For a condition such as rheumatoid arthritis [RA], the problem of joint damage develops from the unchecked inflammation that erodes cartilage. For patients with RA, it is critical to control the inflammatory disease so that the new or engineered cartilage doesnt get damaged in the same way, Goodman said. For the time being, since artificial/engineered tissue has only been used in small areas of the damaged joint, it would not be a solution for patients with inflammatory arthritis who have abnormalities in their entire joint.

When it comes to joints like the knee, which are very susceptible to mechanical forces of weight and impact, a condition like obesity will also lead to damage in the engineered joint.

Dr. Kristofer Jones, a board-certified, fellowship-trained orthopedic surgeon who specializes in sports-related musculoskeletal injuries of the knee, shoulder, and elbow, told Healthline that we are ahead of where we were 10 to 15 years ago and a lot of new research has come out along with a lot of new products that look at alternative ways to resurface new cartilage, with either a patients own cells or using allograft tissue, or transplanted tissue between patients.

The research shows these new tissue types are certainly durable and provide patients with long-lasting pain relief, but the issue is the progression of joint degeneration in other areas of the knee, Jones added.

He said its not uncommon to have performed a cartilage transplant procedure to address one part of the knee and then two or three years later see the same patient experience degeneration in other areas, with new symptoms.

We are good right now at resurfacing small-to-medium size lesions with the durable tissue, but we havent quite figured out how to turn off the button that has started in some of these patients where you are looking at progressive joint degeneration in other areas, Jones explained.

From his perspective, Dr. Sid Padia, a specialist in vascular and interventional radiology at UCLA Medical Center, told Healthline that, in general, there really has been no significant impact or change in the standard of care for patients with joint disease.

Theres been no seismic shift reorienting how we view the treatment of people with joint disease, but there have been several promising and new therapies that have shown potential benefits in the treatment of various joint diseases. That being said, much of these potential new therapies currently being studied have not come to fruition with respect to long term clinical benefit, he said.

Many of the new minimally invasive therapies have shown in studies or have shown short term benefit and thats because these studies have not assessed long-term outcomes and have not compared it [the given procedure] to a control group, so its hard for the medical community to really accept these new treatment options, Padia added. So, I think there is a tremendous opportunity for a breakthrough treatment simply because in many of these patients, the treatment options are still quite limited.

Jones said one of the current advancements that stands out the most to him is the use of biologic injectables, or orthobiologics.

These are injectable substances used by orthopaedic surgeons to help your injuries heal more quickly. They can be used for tendons, ligaments, and broken bones, for example, and are derived from substances that naturally occur in your body, according to the American Academy of Orthopaedic Surgeons.

Jones cited injectable therapies like those using platelet-rich plasma (PRP), where the plasma is injected right into a tissue, and bone marrow aspirate concentrate, which uses bone marrow cells, as two examples.

PRP, bone marrow aspirate concentrate, amniotic suspension allograft injections these are all things that we are studying to determine how we can best utilize them to treat patients who have knee pain from arthritis, he said.

Jones explained that many of these injectable therapies that are being developed are to augment surgical procedures to move the healing process along and also better create more favorable cell homeostasis so further joint degeneration doesnt happen.

He said we can expect to see a lot more of these kinds of injections available in the coming years to treat symptomatic knee pain. Jones cited a Phase III trial for which he is the principal investigator at UCLA.

At UCLA we have this Phase III FDA trial that is looking at one of these products, the trial ended and we are currently crunching the numbers to look at the data to see if there are no adverse patient events, he said.

At UCLA, Padia has been working on an alternative to knee replacement that could offer pain relief to those individuals who might not be candidates for surgery.

You might not qualify for knee surgery due to a medical complication that puts you at high risk or if you are at advanced age, for instance. Younger people might also delay surgery due to the fact theyll ultimately need another knee replacement surgery or procedure within the next 20 years.

The procedure is called genicular artery embolization. Its a minimally invasive procedure during which particles that are smaller than grains of sand are injected by way of a small catheter into enlarged knee arteries. This only takes two hours to perform and you can head home the same day and return to regular physical activities later that day.

Weve published our results, done randomized trials that show genicular artery embolization in the knee can lead to reduction in pain and weve adapted this procedure for people with tennis elbow, which is something fairly common in people who play racket sports, Padia explained. Given the increase in the use of pickleball, we are starting to see a lot more people with tennis elbow.

He added that treating something like tennis elbow is fairly limited and surgical correction is rarely done. As a result, steroid injections are often the mainstay treatment for this condition, offering a short-term benefit.

People are often left with no other option than to quit their physical activity, so weve developed this procedure for tennis elbow and its had a very promising effect in people, he said.

A 2022 study in the journal Advanced Functional Materials highlights research out of Duke University that shed light on what was described as the first synthetic gel-based substitute for cartilage.

The researchers behind this gel say it can be pulled and pressed with more force and weight than naturally occurring cartilage. This substance is also three times more resistant to the regular wear and tear that often fuels osteoarthritis and joint pain.

A company called Sparta Biomedical is developing this hydrogel product and testing them on sheep, with human clinical trials expected to start this year, according to a press release.

To put in perspective how powerful this material is, natural cartilage can handle 5,800 to 8,500 pounds per inch of tugging and squishing before hitting its breaking point. The hydrogel is reportedly 26% stronger than natural cartilage in suspension and 66% stronger in compression, reads the release.

When asked what is exciting to him in the field outside of surgery right now, Jones pointed to synthetic forms of cartilage that are as durable if not more durable than the real thing.

We are a little further away from seeing that being used clinically, the issue is trying to figure out how to get those different synthetic tissue types to adhere to bone and be durable for the long term, Jones explained. That may be something that down the line is a possible alternative to traditional joint replacement. The whole point of all of this is to preserve your joint and the natural feel for it.

In late 2022, research from The Forsyth Institute was published in the journal Science Advances, pointing to a potential mechanism for generating new cartilage cells.

The goal of this study was to figure out how to regenerate cartilage. We wanted to determine how to control cell fate, to cause the somatic cell to become cartilage instead of bone, Dr. Takamitsu Maruyama of Forsyth said in a release.

The research contributes to a growing body of research that suggests future of joint repair to treat arthritis might be at the cellular level.

I think the greatest potential [for the future] are the use of stem cells, Padia said. The use of stem cells is, number one, a relatively straightforward minimally invasive procedure. It does have the potential to have significant impact on people with joint diseases. The key is there needs to be an appropriate and accurate way to select the ideal patients who benefit from a stem cell treatment, there needs to be comparative studies ideally with a placebo studies conducted with adequate amount of time for long-term results.

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Arthritis: The Latest on Joint Replacement, Repair, and New ... - Healthline

2023 Stem Cell Therapy Market Key Trends: Dynamics Shaping the … – Digital Journal

PRESS RELEASE

Published April 11, 2023

Stem Cell Therapy Market Report 2023 | 125 Pages Latest Research | provides all-inclusive update on growth segments, recent developments of top players [Ernst & Young, Aon Consulting, McKinsey & Company, Accenture, PriceWaterhouseCoopers (PwC), Affiliated Computer Services, KPMG Consulting] with their revenue and CAGR status. It also covers various marketing strategies of top manufacturers.

"Final Report will add the analysis of the impact of COVID-19 on this industry."

Global Stem Cell Therapy Market Report 2023-2028 is a comprehensive analysis of the latest trends and opportunities in the industry. The report presents a detailed assessment of the market size, growth factors, and demand status, as well as the challenges and risks faced by businesses across all geographic regions. It also features the latest technological advancements, SWOT, and PESTLE analysis, providing a holistic overview of the industry's competitive landscape and regional segments. This insightful report covers key players profiling with their company profiles, supply-demand scope, and global trending technologies.

Additionally, Stem Cell Therapy market (125 Pages) report is a valuable addition to any company's future strategies and path forward, as it offers a deep understanding of the industry revenue and competitive landscape. With its precise information and thoughtful analysis, the report provides businesses with the necessary tools to make informed decisions and stay ahead of the competition.

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The global Stem Cell Therapy market size was valued at USD 12932.56 million in 2022 and is expected to expand at a CAGR of 8.2% during the forecast period, reaching USD 20753.25 million by 2028.Stem-cell therapy is the use of stem cells to treat or prevent a disease or condition.Bone marrow transplant is the most widely used stem-cell therapy, but some therapies derived from umbilical cord blood are also in use. Research is underway to develop various sources for stem cells, and to apply stem-cell treatments for neurodegenerative diseases and conditions, diabetes, heart disease, and other conditions.With the ability of scientists to isolate and culture embryonic stem cells, and with scientists' growing ability to create stem cells using somatic cell nuclear transfer and techniques to create induced pluripotent stem cells, controversy has crept in, both related to abortion politics and to human cloning. Additionally, efforts to market treatments based on transplant of stored umbilical cord blood have been controversial.

Key Players covered in the global Stem Cell Therapy Market are:

The report focuses on the Stem Cell Therapy market size, segment size (mainly covering product type, application, and geography), competitor landscape, recent status, and development trends. Furthermore, the report provides detailed cost analysis, supply chain. Technological innovation and advancement will further optimize the performance of the product, making it more widely used in downstream applications. Moreover, Consumer behavior analysis and market dynamics (drivers, restraints, opportunities) provides crucial information for knowing the Stem Cell Therapy market.

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Most important types of Stem Cell Therapy products covered in this report are:

Most widely used downstream fields of Stem Cell Therapy market covered in this report are:

Key Takeaways from the Global Stem Cell Therapy Market Report:

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Following Chapter Covered in the Stem Cell Therapy Market Research:

Chapter 1 mainly defines the market scope and introduces the macro overview of the industry, with an executive summary of different market segments ((by type, application, region, etc.), including the definition, market size, and trend of each market segment.

Chapter 2 provides a qualitative analysis of the current status and future trends of the market. Industry Entry Barriers, market drivers, market challenges, emerging markets, consumer preference analysis, together with the impact of the COVID-19 outbreak will all be thoroughly explained.

Chapter 3 analyzes the current competitive situation of the market by providing data regarding the players, including their sales volume and revenue with corresponding market shares, price and gross margin. In addition, information about market concentration ratio, mergers, acquisitions, and expansion plans will also be covered.

Chapter 4 focuses on the regional market, presenting detailed data (i.e., sales volume, revenue, price, gross margin) of the most representative regions and countries in the world.

Chapter 5 provides the analysis of various market segments according to product types, covering sales volume, revenue along with market share and growth rate, plus the price analysis of each type.

Chapter 6 shows the breakdown data of different applications, including the consumption and revenue with market share and growth rate, with the aim of helping the readers to take a close-up look at the downstream market.Chapter 7 provides a combination of quantitative and qualitative analyses of the market size and development trends in the next five years. The forecast information of the whole, as well as the breakdown market, offers the readers a chance to look into the future of the industry.

Chapter 8 is the analysis of the whole market industrial chain, covering key raw materials suppliers and price analysis, manufacturing cost structure analysis, alternative product analysis, also providing information on major distributors, downstream buyers, and the impact of COVID-19 pandemic.

Chapter 9 shares a list of the key players in the market, together with their basic information, product profiles, market performance (i.e., sales volume, price, revenue, gross margin), recent development, SWOT analysis, etc.

Chapter 10 is the conclusion of the report which helps the readers to sum up the main findings and points.

Chapter 11 introduces the market research methods and data sources.

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The report delivers a comprehensive study of all the segments and shares information regarding the leading regions in the market. This report also states import/export consumption, supply and demand Figures, cost, industry share, policy, price, revenue, and gross margins.

Client Focus:

Yes. As the COVID-19 and the Russia-Ukraine war are profoundly affecting the global supply chain relationship and raw material price system, we have definitely taken them into consideration throughout the research

With the aim of clearly revealing the competitive situation of the industry, we concretely analyze not only the leading enterprises that have a voice on a global scale, but also the regional small and medium-sized companies that play key roles and have plenty of potential growth.

Both Primary and Secondary data sources are being used while compiling the report.

Primary sources include extensive interviews of key opinion leaders and industry experts (such as experienced front-line staff, directors, CEOs, and marketing executives), downstream distributors, as well as end-users.

Secondary sources include the research of the annual and financial reports of the top companies, public files, new journals, etc. We also cooperate with some third-party databases.

Yes. Customized requirements of multi-dimensional, deep-level and high-quality can help our customers precisely grasp market opportunities, effortlessly confront market challenges, properly formulate market strategies and act promptly, thus to win them sufficient time and space for market competition.

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Detailed TOC of Stem Cell Therapy Market Forecast Report 2023-2028:

1 Stem Cell Therapy Market Overview

1.1 Product Overview and Scope of Stem Cell Therapy Market

1.2 Stem Cell Therapy Market Segment by Type

1.2.1 Global Stem Cell Therapy Market Sales Volume and CAGR (%) Comparison by Type (2018-2028)

1.3 Global Stem Cell Therapy Market Segment by Application

1.3.1 Stem Cell Therapy Market Consumption (Sales Volume) Comparison by Application (2018-2028)

1.4 Global Stem Cell Therapy Market, Region Wise (2018-2028)

1.5 Global Market Size of Stem Cell Therapy (2018-2028)

1.5.1 Global Stem Cell Therapy Market Revenue Status and Outlook (2018-2028)

1.5.2 Global Stem Cell Therapy Market Sales Volume Status and Outlook (2018-2028)

1.6 Global Macroeconomic Analysis

1.7 The impact of the Russia-Ukraine war on the Stem Cell Therapy Market

2 Industry Outlook

2.1 Stem Cell Therapy Industry Technology Status and Trends

2.2 Industry Entry Barriers

2.2.1 Analysis of Financial Barriers

2.2.2 Analysis of Technical Barriers

2.2.3 Analysis of Talent Barriers

2.2.4 Analysis of Brand Barrier

2.3 Stem Cell Therapy Market Drivers Analysis

2.4 Stem Cell Therapy Market Challenges Analysis

2.5 Emerging Market Trends

2.6 Consumer Preference Analysis

2.7 Stem Cell Therapy Industry Development Trends under COVID-19 Outbreak

2.7.1 Global COVID-19 Status Overview

2.7.2 Influence of COVID-19 Outbreak on Stem Cell Therapy Industry Development

3 Global Stem Cell Therapy Market Landscape by Player

3.1 Global Stem Cell Therapy Sales Volume and Share by Player (2018-2023)

3.2 Global Stem Cell Therapy Revenue and Market Share by Player (2018-2023)

3.3 Global Stem Cell Therapy Average Price by Player (2018-2023)

3.4 Global Stem Cell Therapy Gross Margin by Player (2018-2023)

3.5 Stem Cell Therapy Market Competitive Situation and Trends

3.5.1 Stem Cell Therapy Market Concentration Rate

3.5.2 Stem Cell Therapy Market Share of Top 3 and Top 6 Players

3.5.3 Mergers and Acquisitions, Expansion

4 Global Stem Cell Therapy Sales Volume and Revenue Region Wise (2018-2023)

4.1 Global Stem Cell Therapy Sales Volume and Market Share, Region Wise (2018-2023)

4.2 Global Stem Cell Therapy Revenue and Market Share, Region Wise (2018-2023)

4.3 Global Stem Cell Therapy Sales Volume, Revenue, Price and Gross Margin (2018-2023)

4.4 United States Stem Cell Therapy Sales Volume, Revenue, Price and Gross Margin (2018-2023)

4.4.1 United States Stem Cell Therapy Market Under COVID-19

4.5 Europe Stem Cell Therapy Sales Volume, Revenue, Price and Gross Margin (2018-2023)

4.5.1 Europe Stem Cell Therapy Market Under COVID-19

4.6 China Stem Cell Therapy Sales Volume, Revenue, Price and Gross Margin (2018-2023)

4.6.1 China Stem Cell Therapy Market Under COVID-19

4.7 Japan Stem Cell Therapy Sales Volume, Revenue, Price and Gross Margin (2018-2023)

4.7.1 Japan Stem Cell Therapy Market Under COVID-19

4.8 India Stem Cell Therapy Sales Volume, Revenue, Price and Gross Margin (2018-2023)

4.8.1 India Stem Cell Therapy Market Under COVID-19

4.9 Southeast Asia Stem Cell Therapy Sales Volume, Revenue, Price and Gross Margin (2018-2023)

4.9.1 Southeast Asia Stem Cell Therapy Market Under COVID-19

4.10 Latin America Stem Cell Therapy Sales Volume, Revenue, Price and Gross Margin (2018-2023)

4.10.1 Latin America Stem Cell Therapy Market Under COVID-19

4.11 Middle East and Africa Stem Cell Therapy Sales Volume, Revenue, Price and Gross Margin (2018-2023)

4.11.1 Middle East and Africa Stem Cell Therapy Market Under COVID-19

5 Global Stem Cell Therapy Sales Volume, Revenue, Price Trend by Type

5.1 Global Stem Cell Therapy Sales Volume and Market Share by Type (2018-2023)

5.2 Global Stem Cell Therapy Revenue and Market Share by Type (2018-2023)

5.3 Global Stem Cell Therapy Price by Type (2018-2023)

5.4 Global Stem Cell Therapy Sales Volume, Revenue and Growth Rate by Type (2018-2023)

6 Global Stem Cell Therapy Market Analysis by Application

6.1 Global Stem Cell Therapy Consumption and Market Share by Application (2018-2023)

6.2 Global Stem Cell Therapy Consumption Revenue and Market Share by Application (2018-2023)

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2023 Stem Cell Therapy Market Key Trends: Dynamics Shaping the ... - Digital Journal

Research identifies new target that may prevent blood cancer – VUMC Reporter

Alexander Bick, MD, PhD

by Bill Snyder

An international coalition of biomedical researchers co-led by Alexander Bick, MD, PhD, at Vanderbilt University Medical Center has determined a new way to measure the growth rate of precancerous clones of blood stem cells that one day could help doctors lower their patients risk of blood cancer.

The technique, called PACER, led to the identification of a gene that, when activated, drives clonal expansion. The findings, published April 12 in the journal Nature, suggest that drugs targeting this gene, TCL1A, may be able to suppress clonal growth and associated cancers.

We think that TCL1A is a new important drug target for preventing blood cancer, said Bick, the studys co-corresponding author with Stanford Universitys Siddhartha Jaiswal, MD, PhD.

More than 10% of older adults develop somatic (non-inherited) mutations in blood stem cells that can trigger explosive, clonal expansions of abnormal cells, increasing the risk for blood cancer and cardiovascular disease.

Since arriving at VUMC in 2020, Bick, assistant professor of Medicine in the Division of Genetic Medicine and director of the Vanderbilt Genomics and Therapeutics Clinic, has contributed to more than 30 scientific papers that are revealing the mysteries of clonal growth (hematopoiesis).

With age, dividing cells in the body acquire mutations. Most of these mutations are innocuous passenger mutations. But sometimes, a mutation occurs that drives the development of a clone and ultimately causes cancer.

Prior to this study, scientists would measure clonal growth rate by comparing blood samples taken decades apart. Bick and his colleagues figured out a way to determine the growth rate from a single timepoint, by counting the number of passenger mutations.

You can think of passenger mutations like rings on a tree, Bick said. The more rings a tree has, the older it is. If we know how old the clone is (how long ago it was born) and how big it is (what percentage of blood it takes up), we can estimate the growth rate.

The PACER technique for determining the passenger-approximated clonal expansion rate was applied to more than 5,000 individuals who had acquired specific, cancer-associated driver mutations in their blood stem cells, called clonal hematopoiesis of indeterminate potential or CHIP, but who did not have blood cancer.

Using a genome-wide association study, the investigators then looked for genetic variations that were associated with different clonal growth rates. To their surprise, they discovered that TCL1A, a gene which had not previously been implicated in blood stem cell biology, was a major driver of clonal expansion when activated.

The researchers also found that a commonly inherited variant of the TCL1A promoter, the DNA region which normally initiates transcription (and thus activation) of the gene, was associated with a slower clonal expansion rate and a markedly reduced prevalence of several driver mutations in CHIP, the second step in the development of blood cancer.

Experimental studies demonstrated that the variant suppresses gene activation.

Some people have a mutation that prevents TCL1A from being turned on, which protects them from both faster clone growth and from blood cancer, Bick said. Thats what makes the gene so interesting as a potential drug target.

The research is continuing with the hope of identifying additional important pathways relevant to precancerous growth in other tissues as well as blood, he added.

Researchers from more than 50 institutions across the United States, as well as Germany, Sweden and the Netherlands participated in the study. Other VUMC co-authors were Taralyn Mack, Benjamin Shoemaker, MD, MSCI, and Dan Roden, MD.

The research at VUMC is supported by National Institutes of Health grant OD029586, a Burroughs Wellcome Fund Career Award for Medical Scientists, the E.P. Evans Foundation & RUNX1 Research Program, a Pew-Stewart Scholar for Cancer Research Award, the VUMC Brock Family Endowment, and a Young Ambassador Award from the Vanderbilt-Ingram Cancer Center.

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Research identifies new target that may prevent blood cancer - VUMC Reporter

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