Hair Transplant Market – Rise in the Incidences of Alopecia to Bolster Demand in the Market – BioSpace

The global hair transplant market is forecasted to be driven by the growing number of people suffering from hair loss or hair thinning problem. An emerging pattern of baldness amongst both women and men has augmented the demand for hair transplant surgery in the last few years.

Transplantation of hair refers to a surgical procedure comprising removal of hair follicles from the donor site and then planting it in the balding area of the head. Rising incidences of various causative factors like stress, hormonal imbalance, stress, and augmented fixation about ones physical appearance is likely to boost the global hair transplant market.

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The global hair transplant market has been segmented based on market, method, product, therapy, gender, service provider, and region. The main objective of providing such a comprehensive report is to provide a deep insight into the market.

Global Hair Transplant Market: Notable Developments

The global hair transplant market is witness to many developments in the field in the last few years. These market developments indicate a trend in the global hair transplant market. One such development of the market is mentioned below:

Some of the key market players of the global hair transplant market are

Global Hair Transplant Market: Growth Drivers

Rise in the Incidences of Alopecia to Bolster Demand in the Market

Hair transplant has come up as a popular way or solution for hair thinning and balding problems. It has garnered commercial interest as well. According to the findings of California-based National Alopecia Areata Foundation, nearly 6.8 millionpeoplein the US and around 147 million people worldwide already suffer from alopeciaareata or will suffer from the same at some point of time in their lives. The global hair transplant market is likely to grow rapidly on the back of the rising incidences of alopecia. The medical term for hair thinning or balding is called alopecia.

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In addition to stress, other factors that cause these problems are deterioration in the quality of water, genetics, illness, side effects of certain medications, and aging. As the number of people suffering from alopecia rises, the scope for the global hair transplant market is likely to widen over the tenure of assessment. In addition, growing fixation over physical appearance is another factor that is estimated to encourage the growth of global hair transplant market in forthcoming years.

Global Hair Transplant Market: Regional Outlook

The global hair transplant market is split into the leading regions of North America, Europe, Asia Pacific, Middle East and Africa, and Latin America. Considering geographical segmentation, it is estimated North America is likely dominate the market in the years to come. Increased media and celebrity influence together with augmented awareness about ones physical appearance is likely to encourage growth of the market over the tenure of assessment.

North America hair transplant market is also driven by the high income of the people in the region, which makes hair transplant an affordable solution for hair thinning and balding.

The global hair transplant market is segmented as:

By Market

By Method

By Product

By Therapy

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Hair Transplant Market - Rise in the Incidences of Alopecia to Bolster Demand in the Market - BioSpace

Global Stem Cells Market Disclosing Latest Technology Advancement, Global Share, Rising Application Opportunities by Types and Trends 2027 – Scientect

A comprehensive research report namelyGlobal Stem Cells Market which discloses an all-encompassing breakdown of the global industry by delivering detailed information about Forthcoming Trends. The Stem Cells Market report delivers an exhaustive analysis of global market size, segmentation market growth, market share, competitive Landscape also an in-depth study of the market enlightening key forecast to 2027, recent developments, opportunities analysis, strategic market growth analysis, and technological innovations.

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Major Companies Profiled in This Stem Cells Market Report:

Neuralstem, Inc. Stempeutics Research Pvt. Ltd. Reneuron Group Plc Mesoblast Neostem Oncology, Llc Pluristem Therapeutics Inc. Stemcells, Inc. Gamida Cell Ltd. Anterogen Co., Ltd. Orthocyte Corporation Pharmicell Co., Ltd. Apceth GmbHCompany KG Ocata Therapeutics, Inc. U.S. Stem Cell, Inc. (Bioheart) Medipost Co., Ltd. Biotime, Inc. Cell Cure Neurosciences Ltd.

Stem Cells Market report Segmentation: North America, Europe, Asia Pacific, Latin America, and the Middle East and Africa. This report similarly reduces the current, past, and upcoming market business strategies, estimation analysis having a place with the forecast conditions.

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This all-inclusive study covers an overview of various aspects of the industry including outlook, current Stem Cells Market trends, and advance during the forecast period. Along with this, an in-depth analysis of each section of the report is also provided in the report that consists of the strategies adopted by the key players, challenges, and threats as well as advancements in the industry.

Stem Cells Market Segmentation by Type:

Adult Stem Cell Human Embryonic Stem Cell Induced Pluripotent Stem Cell Rat Neural Stem Cell Other

Based on End Users/Application, the Stem Cells Market has been segmented into:

Drug Discovery and Development Stem Cells Regenerative Medicine

Years Considered to Estimate the Stem Cells Market Size:

History Year: 2015-2019

Base Year: 2019

Estimated Year: 2020

Forecast Year: 2020-2027

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Report Answers Following Questions:

Major Point of TOC:

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Global Stem Cells Market Disclosing Latest Technology Advancement, Global Share, Rising Application Opportunities by Types and Trends 2027 - Scientect

3D Cell Cultures Industry Report 2020-2025: Impact of COVID-19 on the World of Cell Culture – PRNewswire

DUBLIN, Aug. 19, 2020 /PRNewswire/ -- The "3D Cell Cultures: Technologies and Global Markets" report has been added to ResearchAndMarkets.com's offering.

The report includes:

Whether the discussion is about stem cells, tissue engineering, or microphysiological systems, their vital role in drug discovery, toxicology, and other areas leading to new product development, 3D cell culture is becoming the environment that will increasingly define the basis for future advances.

To mix metaphors, 3D cell culture is also cross-roads through which just about everything else passes on its way to building knowledgebases or introducing new products. This study is needed to bring together and make sense out of the broad body of information encompassed by 3D cell culture.

Three-dimensional cell culture has been used by researchers for many years now, with early adoption and now key roles in cancer and stem cells. Organ-on-a-chip technology, also known as microphysiological systems, is leading to dramatic breakthroughs. Also, stem cell research coupled with synthetic biology is opening new areas. This study is needed to provide a perspective on these advances.

Furthermore, classical toxicology testing programs have been in place for many decades, and over the past 20 years, animal welfare and scientific activities have spurred the development of in vitro testing methods. In silico methods are advancing in novel ways that need to be analyzed and considered in terms of their impacts on cell culture.

This report investigates the recent key technical advances in 3D cell culture equipment, raw materials, assay kits, analytical methods, and clinical research organization (CRO) services. It should also be pointed out that this report takes a somewhat different position on 2D cell culture. It has been criticized for its inadequacies and the misleading information it can produce. However, a review of industry practices makes it clear that it still has its place and will contribute to future advances in unexpected ways.

The company section looks at many of the suppliers who provide equipment, assays, cells, reagents, and services used in 3D cell culture. This study sought to understand business models and market maturity dynamics in greater depth as well as providing more quantitative analysis of their operations.

Key Topics Covered

Chapter 1 Introduction

Chapter 2 Summary

Chapter 3 Highlights and Issues

Chapter 4 Tissue and Cell Culture: Technology and Product Background

Chapter 5 Assays, Imaging and Analysis

Chapter 6 Regulation and Standardization

Chapter 7 3D Models for Cancer

Chapter 8 Landscape for Toxicology and Drug Safety Testing

Chapter 9 Stem Cell Landscape

Chapter 10 Regenerative Medicine: Organ Transplants and Skin Substitutes

Chapter 11 Company Profiles

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3D Cell Cultures Industry Report 2020-2025: Impact of COVID-19 on the World of Cell Culture - PRNewswire

Combating COVID-19 with Cell-Free Expression – The Scientist

Imagine the ability to rewire, reshape, and use parts of a living system to build something new. It is not science fiction, nor is it Frankensteins monster. It is synthetic biology, a relatively nascent field that is making a profound impact on society and healthcare. As the world continues to grapple with the ongoing effects of the COVID-19 pandemic, researchers are turning to synthetic biology, and in particular, to cell-free expression systems to develop new rapid diagnostic tools, vaccines, and treatments.

Its a way to program information. We all do that every day in our cell phones; we program information in zeros and ones. Synthetic biology takes that to a totally new dimension. Rather than just being able to control information, I now get to control information that builds atoms, said Michael Jewett, a professor of chemical and biological engineering at Northwestern University.

Synthetic biologists such as Jewett combine engineering principles, computer programming, and molecular biology to design and build synthetic gene circuits and other molecular components that rewire living cells for a variety of new applications, including biological sensors and diagnostic tests.

Going Cell-Free

Rewiring a living system is tricky. Cells are already biologically programmed to achieve their own functional goals, not the goals of the researcher. To circumvent this problem, synthetic biologists remove the cell wall and extract the cells molecular machinery, including the core factors needed for transcription and translation. This cell-free expression system can then be coerced to produce and even detect proteins of interest.

It's like if you took a car, you lift up the hood, pull out the engine, and you repurpose it for something else. We're repurposing the molecular machinery to do some objective function, said Jewett. Working outside a cellular system prevents the cell from responding and changing its gene expression profile, ensuring a reproducible and stable molecular expression system.

The complexities itself are much lower than that of the living cells, and it's easier to control the different features in that you can dictate, at least at the outset, what [compounds] are there and how much is there, said James Collins a professor of biological engineering at the Massachusetts Institute of Technology.

Scientists have used cell-free expression systems for two decades as a basic research tool to make discoveries about the living world. In fact, scientists used cell-free systems to uncover the genetic code in the 1960s. However, many of these early systems were small-scale, did not last very long, and could not make complex proteins. Within the last 20 years, researchers have addressed each of these problems, transforming cell-free expression systems from a basic tool into a useable technology platform.

The systems now, instead of lasting five minutes, last 15 to 20 hours in batch reactions. They can make really complex proteins all the way up to full-length antibodies, which are used in medicine. They can carry out pretty complex integrated circuitry that can basically detect, sense, and respond to something just like a cell, said Jewett.

Researchers also developed better ways to support cell-free expression systems by supplying the system with glucose as a source of energy and other biological compounds such as amino acids needed to produce proteins. Scientists even solved the problem of scalability. If you imagine running a PCR reaction, which is typically two or five microliters, in a 1000-liter scale, that's what we're doing economically, which is crazy. In fact, many people kind of deemed that impossible 10 years ago, but it's happening, said Jewett.

Cell-free expression systems can be rapidly pre-assembled and stored in a laboratory freezer, or freeze-dried in a powdered form. This eliminates the need for researchers to regrow cells. The problems then reduce to automated liquid handling, said Jewett. Automated liquid handling robots enable researchers to run more samples at a time for rapid library screening or analyzing genetic parts and gene circuits.

Making cell-free expression systems is an art that, much like any other laboratory technique, takes skill, practice, and time. Some researchers make their own cell-free expression systems, but others purchase commercial ready-to-use master mixes. These mixes, such as the myTXTL Cell-Free Expression System from Arbor Biosciences, come pre-loaded with all the molecular components for a given reaction so that the researcher only has to add their DNA sample for reliable and robust high-yield protein expression.

The homebrew has some really nice efforts by Michael Jewett and his team to get them highly functional, but when we make our own, we're not as good and so it often doesnt have the functionality level that we need, said Collins. My team has used Arbor Biosciences; they have very good products. In the cell-free world, they're one of the go-to [companies]. Like homebrewed systems, purchased premixed cell-free systems can also be paired with automated liquid handling for high-throughput and efficient library screening or analysis.

Pivoting

These advances made it possible for synthetic biologists to develop practical technologies that mitigate disease and impact society. When the COVID-19 pandemic struck, synthetic biologists pivoted the cell-free expression technology that they were using for other diseases to develop new diagnostics, materials, and treatments specifically for COVID-19.

Keith Pardee, a synthetic biologist at the University of Toronto was working on a three-year project to send Zika virus diagnostic testing kits to low- and middle-income countries. When the COVID-19 outbreak happened, we thought this is obviously a natural thing for us to do. So, we basically are taking that platform for Zika and applying it to SARS-CoV-2, said Pardee.

Pardee extracts enzymes needed for transcription and translation from Escherichia coli to create a cell-free expression system that senses parts of the SARS-CoV-2 genome and triggers a molecular switch to produce a reporter protein. It also eliminates the need to purify RNA from the sample and can replace RT-PCR for more rapid diagnostic testing. Because we didnt have that black box of working with a cell, we were able to get sensors very quickly, maybe within two days of having the synthetic DNA arrive in the lab, we had sensors working, said Pardee.

Pardee will send COVID-19 diagnostic kits in two waves to the same countries that he was planning to send the Zika kits, only now he has added Toronto, Canada to the list. The first wave will supply 1000 test kits a day for two weeks. The second wave will contain a lab-in-a-box, that could convert a common microbiology lab into a diagnostic testing lab to maintain a sustained testing capacity.

Similarly, James Collins was developing a suite of clothing-based sensors for healthcare workers, first responders, and military personnel to detect the presence of viruses or compounds. The idea would be like a lab coat of the future, said Collins. He conceived the idea during the Ebola outbreak of 2014. Collins and his team freeze-dried cell-free expression systems and locked them onto a piece of paper, and later into fabric. They then showed that the system could be rehydrated and transcription and translation activated by adding liquid.

We were revising this publication when the pandemic hit, and realized that we could embody the same technology into facemasks by having an insert that can be added. If a person is infected, they'll give out particles in water vaporthat is coughing, sneezing, talkingand that itself could activate these freeze-dried components, said Collins. If a person were infected, the mask would produce a fluorescent signal that could be detected using a handheld fluorometer.

Collinss previous discoveries in synthetic biology also contributed to the technology behind the Moderna vaccine for COVID-19, which is in the late-stages of development. Ten years ago, with George Daly and Derek Rossi, Collins developed a stable synthetic mRNA system to express proteins directly in cells. They used the technology to efficiently reprogram induced pluripotent stem cells, but mentioned in the paper that the technology could be used for RNA-based vaccine development.

I've been so motivated by so many scientists, by how much we're all redirecting; we're pivoting, said Jewett. Four months ago, Jewetts research focused primarily on developing water-based diagnostics for identifying toxins. Using the same cell-free expression approaches, Jewett is now developing CRISPR-based diagnostics for rapid COVID-19 detection and working on antiviral frontline approaches to stop COVID-19 infection.

Using cell-free expression systems, Jewetts team identifies proteins that could cloak the COVID-19 spike protein and prevent its connection to cell receptors. Identifying good clones using classic mammalian cell-culture can take 12 -18 months. We need two months. We need four weeks. We need to have technologies that can meet the pace of this pandemic, said Jewett. Instead of growing cells, Jewett and his team thaw pre-built, frozen cell-free expression stocks, add DNA, and identify good candidates within a day.

If other laboratories are interested in pivoting but are unable to pre-assemble frozen stocks or lack the technical experience needed, they can reach out to commercial providers, such as Arbor Biosciences for reliable cell-free expression systems. Arbor Biosciences is adept at developing robust cell-free systems that can be immediately implemented in COVID-19 research or in other disease-based research for rapid, efficient, and dependable discovery.

In this era of emergent and reemerging pandemic outbreaks, what we need is speed. Cell-free systems really offer this exciting component, and the technology is well suited to address that need, said Jewett. Cell-free expression systems alone will not solve the COVID-19 pandemic, but it can complement existing technologies. Research is just developing. We, like many others, have been conceiving ideas and schemes and now's the time, said Jewett. We have to make an impact with whatever we can.

Meet the Sponsor

Arbor Biosciences is a development and manufacturing company founded by scientists to serve our peers in molecular biology applications.

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Combating COVID-19 with Cell-Free Expression - The Scientist

Study sheds light on why retinal ganglion cells are vulnerable to glaucoma – Jill Lopez

Millions of sufferers of glaucoma might someday benefit from a study released today inSTEM CELLSin which a "disease in a dish" stem cell model was used to examine the mechanism in glaucoma that causes retinal ganglion cells (RGCs) to degenerate, resulting in loss of vision. The knowledge the study provides could result in new therapeutic approaches for this leading cause of blindness worldwide.

RGCs are a group of nerve cells located in the retina that send images to the brain and enable you to see. Glaucoma attacks these cells and, once they die, they are not replaced. However, why and how glaucoma causes the RGCs to degenerate is something of a mystery.

Stem cell modeling of the disease may shed light on this. Over the past decade, significant progress has been made using induced pluripotent stem cell (iPSC) technology to mimic glaucoma. This includes the generation of human RGCs from iPSCs, which led to the development of a disease model for primary open angle glaucoma (POAG) -- the most common form of glaucoma -- as well as an optic nerve model that demonstrated the supportive role of mTOR signaling in the regeneration of hRGC axons following chemical axotomy.

"However, both these models can be improved by characterizing the developmental trajectories of control and disease-specific RGCs," said Iqbal Ahmad, Ph.D., of the University of Nebraska Medical Center. He and his UNMC colleagues, Pooja Teotia, Ph.D., and Meng Niu, Ph.D., conducted the study reported on inSTEM CELLS.

Dr. Ahmad continued, "This characterization includes the generation of hRGCs through normal developmental time and stages containing a complement of different subtypes, against which the developmental aspects of RGC abnormality in a disease model can be evaluated. Information about different RGC subtypes is not only important from a functional viewpoint, but also for understanding the underlying mechanism of glaucomatous degeneration, given the emerging evidence that the susceptibility and resistance of RGCs are subtype dependent."

In developing their model, the researchers used a single cell transcriptome analysis of human RGCs generated from normal (controls) and SIX6 risk allele iPS cells. (Previous studies have identified a significant association between POAG and SIX6, a gene that plays a role in ocular development.)

They observed that the developmental trajectories, beginning from neural stem cells to RGCs, were similar between SIX6 risk allele and control RGCs.

"However," Dr. Ahmad said, "we observed that the differentiation of SIX6 risk allele RGCs was stalled at the retinal progenitor cell stage, keeping them immature and deficient in subtype composition, compared to the controls. This was likely due to dysregulated mTOR and Notch signaling pathways that play an important role in RGC development. Furthermore," he added, "SIX6 risk allele RGCs, as compared to controls, expressed fewer genes corresponding to RGC subtypes that are preferentially resistant to degeneration.

"The immature phenotype of SIX6 risk allele RGCs with under-represented degeneration-resistant subtypes, may make them vulnerable to glaucomatous degeneration," he concluded.

"This study demonstrates the power of single cell sequencing methods for providing new insights into POAG pathology at the cellular and molecular level, which is necessary for formulation of new therapeutic approaches", said Dr. Jan Nolta, Editor-in-Chief ofSTEM CELLS. "This is truly remarkable and something that we could have not imagined was feasible thirteen years ago until the concept of patient specific iPSC disease modelling was invented. This is an excellent step forward and a phenomenon we will see becoming a daily reality in disease phenotyping and drug discovery."

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Study sheds light on why retinal ganglion cells are vulnerable to glaucoma - Jill Lopez

Israel and UAE team up on stem cell therapy research for COVID-19 – UPI News

David Adom wears protective clothing while working in a coronavirus drive through tent in Jerusalem. On Monday, Israel and United Arab Emirates stem cell companies announced collaboration on research on COVID-19 treatments. Photo by Debbie Hill/UPI | License Photo

Aug. 17 (UPI) -- Israel and United Arab Emirates stem cell therapy companies signed an agreement Monday to collaborate on researching potential treatment for COVID-19.

The accord between Israel's Pluristem Therapeutics and UAE's Abu Dhabi Stem Cells Center aims to capitalize on each company's expertise to develop therapies and regenerative medicines for the treatment of severe diseases including COVID-19, according to a joint statement.

Both companies have been treating COVID-19 patients with stem cells.

Pluristem has been treating COVID-19 patients with a placenta-based stem cell therapy. The U.S. Food and Drug Administration cleared the Israel stem cell therapy company in May for a Phase II study of the treatment for severe COVID-19 cases. Preliminary results released in May from compassionate-use programs in Israel and the United States were promising, showing that 75 percent of participants no longer needed mechanical ventilation within 28 days.

The Abu Dhabi Stem Cells Center has started a therapy that returns blood-based stem cells back into the patient's lungs as a fine mist through a nebulizer.

"We are extremely proud to partner with our colleagues at the ADSCC by sharing knowledge and expertise that we believe will advance healthcare within and across our borders," Pluristem CEO and President Yaky Yanay said in the statement.

The ADSCC's General Manager Dr. Yendry Ventura also commented on the deal in the statement.

"Pluristem is a major player in the cell therapy field with years of experience, a unique platform and robust clinical pipeline," Ventura said. "We are excited to join forces and to promote the research and development of cell therapies for the best of the patients and the human society as a whole."

The deal is the second cross-border agreement since President Donald Trump brokered a deal to normalize ties between Israel and the UAE. It follows a cross-border deal on Sunday between UAE-based APEX National Investment and Israel's TeraGroup to conduct research on the coronavirus.

World News // 21 minutes ago

South Korea official proposes changes to U.S. working group

Aug. 18 (UPI) -- South Korea's newly appointed unification chief proposed "readjustments" to a bilateral working-level group with the United States, during a meeting with the top U.S. envoy in Seoul.

World News // 3 hours ago

6.6-magnitude earthquake strikes Philippines; 1 dead

Aug. 18 (UPI) -- A 6.6-magnitude earthquake struck central Philippines Tuesday, killing at least one person, officials said.

World News // 14 hours ago

Toronto police agree to $12.5M settlement for mass arrests at G-20

Aug. 17 (UPI) -- Ten years after mass-arrests in Toronto at the 2010 G-20 economic summit, the Toronto Police Services Board will pay a $12.5 million settlement to members of a class-action lawsuit of 1,100 people who were detained.

World News // 19 hours ago

Spanish Royal Household confirms former king Juan Carlos I is in UAE

Aug. 17 (UPI) -- Spain's Royal Household confirmed Monday that emeritus king, Juan Carlos I, is in United Arab Emirates after uncertainty since he went into exile two weeks ago amid financial scandals.

World News // 19 hours ago

China has new weapon to target airfields, state media says

Aug. 17 (UPI) -- Beijing's military has developed a hybrid weapon capable of destroying an entire airfield with one hit, according to Chinese state media on Monday.

World News // 20 hours ago

South Korea police to handle spy cases, report says

Aug. 17 (UPI) -- Seoul's National Police Agency will take control over all investigations into anti-state espionage previously conducted by the National Intelligence Service.

World News // 22 hours ago

BTS music label worth $2.5B ahead of IPO, report says

Aug. 17 (UPI) -- The South Korean label that manages boy band BTS is expected to make an initial public offering after passing a preliminary screening, according to a South Korean press report.

World News // 22 hours ago

Ryanair cuts capacity for next 2 months due to restrictions

Aug. 17 (UPI) -- Irish carrier Ryanair announced Monday it will reduce flight capacity by 20% in September and October, due to European travel restrictions.

World News // 23 hours ago

North Korea quiet as U.S., South Korea exercises to resume

Aug. 17 (UPI) -- North Korea is keeping silent ahead of U.S.-South Korea military exercises this week.

World News // 23 hours ago

German regulators investigate Amazon pricing policies

Aug. 17 (UPI) -- Antitrust regulators in Germany are investigating complaints that Amazon is unfairly leveraging its dominant position in the e-commerce market to affect pricing during the coronavirus pandemic.

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Israel and UAE team up on stem cell therapy research for COVID-19 - UPI News

Immatics Announces European Clinical Expansion of its Adoptive Cell Therapy Programs – GlobeNewswire

August 18, 2020 07:00 ET | Source: https://immatics.com/

multilang-release

Tuebingen, Germany and Houston, Texas, Aug. 18, 2020 (GLOBE NEWSWIRE) --

Tuebingen, Germany and Houston, Texas, August 18, 2020 Immatics N.V. (NASDAQ: IMTX, Immatics), a clinical-stage biopharmaceutical company active in the discovery and development of T cell redirecting cancer immunotherapies, announced today the treatment of the first patient in the IMA202-101 trial in Europe following the Clinical Trial Application (CTA, the equivalent of an IND approval by FDA) approval by Paul-Ehrlich-Institute (PEI), the regulatory body for cell and gene therapies in Germany. In addition, Immatics has been granted regulatory approval by PEI to initiate another phase I clinical trial in Germany to evaluate safety, tolerability and initial signs of clinical efficacy of IMA203.

The clinical trials of the IMA200 series will investigate up to three novel cancer immunotherapies, which include IMA202 (NCT03441100) and IMA203 (NCT03686124). IMA202 and IMA203 are designed to target unique peptides derived from either melanoma-associated antigen 1 (MAGEA1) or preferentially expressed antigen in melanoma (PRAME), respectively. Both are built on Immatics proprietary ACTengine approach in which the patients own T cells are genetically engineered to express an exogenous T cell receptor (TCR) directed against true cancer targets. By introducing this novel cancer specific TCR, the goal is to redirect and selectively activate the patients T cells to fight the tumor. The studies will investigate the safety and tolerability of Immatics Adoptive Cell Therapies (ACT) in patients with target-positive solid cancers and seek initial signals of anti-tumor activity. Moreover, persistence of the infused engineered T cells will be monitored in the patients blood as T cell persistence is considered a major pre-requisite to obtain an anti-tumor response. The aim is to develop innovative personalized immunotherapies targeting a patients tumor selectively and effectively.

The initial group of clinical trial sites in Germany includes the University Hospital Carl Gustav Carus in Dresden, the University Hospital Bonn and the University Hospital of Wrzburg. Previous patients in the IMA200 series were initially enrolled at The University of Texas MD Anderson Cancer Center in Houston, Texas, and more recently at the Columbia University Irving Medical Center in New York and the UPMC Hillman Cancer Center in Pittsburgh, Pennsylvania.

Cedrik Britten, MD, Chief Medical Officer of Immatics commented: As part of our strategy to increase the geographical foot-print for our clinical sites, we are currently expanding them in the US and in Europe. We are delighted to have gained a new regulatory approval from PEI and to have treated the first patient in Germany. This expansion elevates our clinical organization to a global level and adds operational flexibility that has become even more important in light of the global COVID-19 pandemic. We look forward to continuing to collaborate with leading clinicians to advance our mission of delivering the power of T cells to cancer patients on both sides of the Atlantic.

Dr. Martin Wermke, Coordinating Investigator and Head of the Early Clinical Trial Unit of the National Center for Tumor Diseases Dresden (NCT/UCC) at the University Hospital Carl Gustav Carus in Dresden, Germany, commented: Having been involved since the early stages of this clinical research, I am excited to witness the next phase of development of this fascinating pipeline of immunotherapies. I am confident that Immatics innovative T cell therapies hold the potential to alter the future therapeutic landscape of solid and hematologic malignancies.

Additional information about the clinical studies is available at http://www.immatics.com/clinical-programs/ and http://www.clinicaltrials.gov.

About Immatics Adoptive Cell Therapies Adoptive Cell Therapy (ACT) is a therapeutic approach that uses natural or engineered T cells to fight cancer. Immatics has developed three innovative, proprietary approaches to produce Adoptive Cell Therapies: ACTengine, off-the-shelf ACTallo and the multi-target pilot trial ACTolog.

About ACTengine Immatics clinical product class ACTengine is a personalized approach for patients with advanced solid cancers. Patients own T cells are genetically modified to express a novel proprietary TCR cognate to one of Immatics cancer targets identified by its proprietary XPRESIDENT target discovery platform.

About the ACTengine clinical trials (IMA201, IMA202 and IMA203)

Patient receiving an investigational therapy based on Immatics ACTengine approach.

Notes to Editors

About Immatics Immatics combines the discovery of true targets for cancer immunotherapies with the development of the right T cell receptors with the goal of enabling a robust and specific T cell response against these targets. This deep know-how is the foundation for our pipeline of Adoptive Cell Therapies and TCR Bispecifics as well as our partnerships with global leaders in the pharmaceutical industry. We are committed to delivering the power of T cells and to unlocking new avenues for patients in their fight against cancer.

Immatics pipeline consists of two distinct therapeutic modalities of Adoptive Cell Therapies and TCR Bispecifics. Adoptive Cell Therapy programs are developed in collaboration through Immatics US with The University of Texas MD Anderson Cancer Center and co-funded by the Cancer Prevention and Research Institute of Texas (CPRIT). The ACT T cell products are manufactured at the Evelyn H. Griffin Stem Cell Therapeutics Research Laboratory in collaboration with UTHealth.

For regular updates about Immatics, visit http://www.immatics.com. You can also follow us on Twitter and LinkedIn.

Forward-Looking Statements: Certain statements in this press release may be considered forward-looking statements. Forward-looking statements generally relate to future events or Immatics future financial or operating performance. For example, statements concerning the timing of product candidates and Immatics focus on partnerships to advance its strategy are forward-looking statements. In some cases, you can identify forward-looking statements by terminology such as may, should, expect, intend, will, estimate, anticipate, believe, predict, potential or continue, or the negatives of these terms or variations of them or similar terminology. Such forward-looking statements are subject to risks, uncertainties, and other factors which could cause actual results to differ materially from those expressed or implied by such forward looking statements. These forward-looking statements are based upon estimates and assumptions that, while considered reasonable by Immatics and its management, are inherently uncertain. New risks and uncertainties may emerge from time to time, and it is not possible to predict all risks and uncertainties. Factors that may cause actual results to differ materially from current expectations include, but are not limited to, various factors beyond management's control including general economic conditions and other risks, uncertainties and factors set forth in filings with the Securities and Exchange Commission (SEC). Nothing in this presentation should be regarded as a representation by any person that the forward-looking statements set forth herein will be achieved or that any of the contemplated results of such forward-looking statements will be achieved. You should not place undue reliance on forward-looking statements, which speak only as of the date they are made. Immatics undertakes no duty to update these forward-looking statements.

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Immatics Announces European Clinical Expansion of its Adoptive Cell Therapy Programs - GlobeNewswire

Canine Stem Cell Therapy Market to Witness Stunning Growth to Generate Massive Revenue During Forecast 2020 2026 | VETSTEM BIOPHARMA, Cell Therapy…

Canine Stem Cell Therapy Market research is an intelligence report with meticulous efforts undertaken to study the right and valuable information. The data which has been looked upon is done considering both, the existing top players and the upcoming competitors. Business strategies of the key players and the new entering market industries are studied in detail. Well explained SWOT analysis, revenue share and contact information are shared in this report analysis.

The global Canine Stem Cell Therapy Market size is expected to Expand at Significant CAGR of +4% during forecast period (2020-2026).

The non-invasive stem cell obtaining procedure, augmented possibility of accomplishing high quality cells, and lower price of therapy coupled with high success rate of positive outcomes have collectively made allogeneic stem cell therapy a preference for veterinary physicians. Moreover, allogeneic stem cell therapy is 100% safe, which further supports its demand on a global level.

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Note In order to provide more accurate market forecast, all our reports will be updated before delivery by considering the impact of COVID-19.

Top Key Vendors of this Market are:

VETSTEM BIOPHARMA, Cell Therapy Sciences, Regeneus, Aratana Therapeutics, Medivet Biologics, Okyanos

Various factors are responsible for the markets growth trajectory, which are studied at length in the report. In addition, the report lists down the restraints that are posing threat to the global Canine Stem Cell Therapy market. It also gauges the bargaining power of suppliers and buyers, threat from new entrants and product substitute, and the degree of competition prevailing in the market. The influence of the latest government guidelines is also analyzed in detail in the report. It studies the Canine Stem Cell Therapy markets trajectory between forecast periods.

The report provides insights on the following pointers:

Market Penetration:Comprehensive information on the product portfolios of the top players in the Canine Stem Cell Therapy market.

Product Development/Innovation:Detailed insights on the upcoming technologies, R&D activities, and product launches in the market.

Competitive Assessment: In-depth assessment of the market strategies, geographic and business segments of the leading players in the market.

Market Development:Comprehensive information about emerging markets. This report analyzes the market for various segments across geographies.

Market Diversification:Exhaustive information about new products, untapped geographies, recent developments, and investments in the Canine Stem Cell Therapy market.

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The report summarized the high revenue that has been generated across locations like, North America, Japan, Europe, Asia, and India along with the facts and figures of Canine Stem Cell Therapy market. It focuses on the major points, which are necessary to make positive impacts on the market policies, international transactions, speculation, and supply demand in the global market.

Global Canine Stem Cell Therapy Market Segmentation:

Market Segmentation by Type:

Allogeneic Stem Cells Autologous Stem cells

Market Segmentation by Application:

Veterinary Hospitals Veterinary Clinics Veterinary Research Institutes

Table of Contents

Global Canine Stem Cell Therapy Market Research Report 2020 2026

Chapter 1 Canine Stem Cell Therapy Market Overview

Chapter 2 Global Economic Impact on Industry

Chapter 3 Global Market Competition by Manufacturers

Chapter 4 Global Production, Revenue (Value) by Region

Chapter 5 Global Supply (Production), Consumption, Export, Import by Regions

Chapter 6 Global Production, Revenue (Value), Price Trend by Type

Chapter 7 Global Market Analysis by Application

Chapter 8 Manufacturing Cost Analysis

Chapter 9 Industrial Chain, Sourcing Strategy and Downstream Buyers

Chapter 10 Marketing Strategy Analysis, Distributors/Traders

Chapter 11 Market Effect Factors Analysis

Chapter 12 Global Canine Stem Cell Therapy Market Forecast

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Canine Stem Cell Therapy Market to Witness Stunning Growth to Generate Massive Revenue During Forecast 2020 2026 | VETSTEM BIOPHARMA, Cell Therapy...

NK Cell Therapy and Stem Cell Therapy Industry Market Structure Analysis for the Period 2026 – The News Brok

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NK Cell Therapy and Stem Cell Therapy Industry Market Structure Analysis for the Period 2026 - The News Brok

Why Young and Female Patients Don’t Respond as Well to Cancer Immunotherapy – UC San Diego Health

Cancer immunotherapy empowering a patients own immune system to clear away tumors on its own holds great promise for some patients. But for other patients, immunotherapy just doesnt work.

Researchers at University of California San Diego School of Medicine have found evidence that helps explain why patients who are young and/or female have especially low response rates to some types of cancer immunotherapy.

Their findings suggest that since the typically robust immune systems of young and female patients are better at getting rid of tumor cells, the cells left behind are not as readily visible to the immune system to begin with, rendering some types of immunotherapy ineffective.

Due to a process known as immuno-editing, younger and female patients with cancer have cancer-causing genetic mutations that are least visible to the immune system according to a new Nature Communications study by Hannah Carter, PhD, and team at UC San Diego School of Medicine.

The study is published August 17, 2020, in Nature Communications.

Now that we know why some patients dont respond as well to immunotherapy, we can begin developing more informed approaches to treatment decisions for instance, developing predictive algorithms to determine a persons likely response before initiating immunotherapies that may have a high probability of not working or working poorly for them, said senior author Hannah Carter, PhD, associate professor of medicine at UC San Diego School of Medicine.

Cancerous or infected cells wave molecular flags that tell the immune system to clear them away before the problem gets out of control. The flag poles molecules of the Major Histocompatibility Complexes (MHC) are displayed at the surface of most cells in the body. MHCs hold up antigen flags bits of just about everything from inside the cells and display them to immune cell surveyors that are constantly checking for damaged or infected cells. Since tumor cells carry a lot of mutations, they show up frequently among these flags, allowing the immune system to detect and eliminate them.

But some tumor cells evade the immune system by also throwing up a stop sign molecule that keeps the immune system from recognizing the MHC flags. And heres where immune checkpoint inhibitors come in: This type of cancer immunotherapy uses antibodies to make the tumor cell once again visible to the patients immune system.

So why would a persons age or sex influence how well immune checkpoint inhibitors work?

Sex and age differences have long been observed when it comes to immune response. For example, females have twice the antibody response to flu vaccines and are far more susceptible to autoimmune diseases. Similarly, human immune systems tend to weaken as we age. But if females and younger people have stronger immune responses in most cases, you might expect cancer immunotherapy to work better for them, not worse.

To get to the bottom of this conundrum, Carters team looked at genomic information for nearly 10,000 patients with cancer available from the National Institutes of Healths The Cancer Genome Atlas, and another 342 patients with other tumor types available from the International Cancer Genome Consortium database and published studies. They found no age or sex-related differences in MHC function.

What they did find was that, compared to older and male patients with cancer, younger and female patients tend to accumulate more cancer-causing genetic mutations of the sort that MHCs cant present to the immune system as efficiently. Carter said this is likely because robust immune systems of the young and female are better at getting rid of cells displaying well-presented mutant self-antigens, leaving behind tumor cells that rely more heavily on the poorly presented mutations. This selective pressure is known as immuno-editing.

So if a tumor cell doesnt present highly visible, mutated self antigens to begin with, checkpoint inhibitor drugs cant help reveal them to the immune system, she said.

This shows an important thing, that the interplay between the cancer genome and the adaptive arm of the immune system is not a static one, said co-author Maurizio Zanetti, MD, professor of medicine at UC San Diego School of Medicine and head of the Laboratory of Immunology at UC San Diego Moores Cancer Center. Two simple but important variables, age and sex, influence this interplay. The study also emphasizes the master role of the MHC in dictating the outcome of this interplay, reaffirming its central role in the evolution of disease, cancer included, at the level of the individual and population.

Carter cautions that their findings for younger patients dont necessarily apply to children since, genetically speaking, pediatric tumors are very different from adult tumors. In addition, she noted that, like most genomics databases, those used in this study contain data primarily from people of Caucasian descent, and more diversity is needed to confirm that the findings can be generalized to all populations.

Cancer isnt just one disease, and so the way we treat it cant be one-size-fits-all, she said. All checkpoint inhibitors can do is remove the generic block that tumors put up to hide from the immune system. The more we learn about how interactions between tumors and immune systems might vary, the better positioned we are to tailor treatments to each persons situation.

Co-authors of the study also include: Andrea Castro, Rachel Marty Pyke, Xinlian Zhang, Wesley Kurt Thompson, Ludmil B. Alexandrov, Maurizio Zanetti, UC San Diego; and Chi-Ping Day, National Institutes of Health.

The study was funded, in part, by the National Institutes of Health (grants T15LM011271, DP5-OD017937, RO1CA220009, P41GM103504, 5R01CA155010-02, 5R01HL103532-03, 2P50CA101942-11A1, R50RCA211482A, R35CA197633, P01CA168585, 5P50CA168536, GM08042, 1RO1CA155010-02, 5R01HL103532-03, R21CA216772-01A1, T32HL007627, P50CA165962, P01CA163205, K08CA188615), National Science Foundation (graduate fellowship 2015205295), Mark Foundation for Cancer Research (grant 18-022-ELA), CIFAR Fellowship, Blavatnik Family Foundation, Broad Institute SPARC Program, BroadIgnite, BroadNext10, Francis and Adele Kittredge Family Immuno-Oncology and Melanoma Research Fund, Faircloth Family Research Fund, DFCI Center for Cancer Immunotherapy, Leukemia and Lymphoma Society, American Association for Cancer Research, Geoffrey Beene Cancer Research Center, Society for Memorial Sloan Kettering Cancer Center, Lung Cancer Research Foundation, Frederick Adler Chair Fund, One Ball Matt Memorial Golf Tournament, Queen Wilhelmina Cancer Research Award, STARR Foundation, Ludwig Trust, Stand Up To Cancer-Cancer Research Institute Cancer Immunology Translational Cancer Research Grant, Stand Up To Cancer-American Cancer Society Lung Cancer Dream Team Translational Research Grant (grant SU2C-AACR-DT17-15), Ben and Catherine Ivy Foundation, Zuckerman STEM Leadership Program, Benoziyo Endowment Fund for the Advancement of Science, DFCI Center for Cancer Immunotherapy Research fellowship, Howard Hughes Medical Institute and American Cancer Society (grant PF-17-042-01LIB).

Disclosure: Co-author Rachel Marty Pyke is an employee and holds stock in Personalis.

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Why Young and Female Patients Don't Respond as Well to Cancer Immunotherapy - UC San Diego Health