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North America ultra-low temperature freezer market is anticipated to reach US$ 313.19 million in 2027 from US$ 220.25 million in 2019 – GlobeNewswire

August 24, 2020 13:05 ET | Source: ReportLinker

New York, Aug. 24, 2020 (GLOBE NEWSWIRE) -- Reportlinker.com announces the release of the report "North America Ultra-Low Temperature Freezer Market to 2027 Regional Analysis and Forecasts by Type ; End User ; and, Country" - https://www.reportlinker.com/p05953821/?utm_source=GNW High costs associated with ultra-low temperature freezers, is likely to restrain the growth of the market in the coming years.

However, developments in the healthcare market are expected to have a positive impact on the growth of the North American ultra-low temperature freezer market in the coming years. Ultra-low temperature freezers are designed for storage of biological materials such as virus, bacteria, eukaryotic cells, blood, and semen. These freezers are used in blood banks, hospitals, epidemic prevention services, research institutes, and biomedical engineering facilities, among others. Blood and blood components perform numerous vital functions in the human body.Consequently, severe blood loss could result in life-threatening conditions such as hypovolemic/hemorrhagic shock, which require immediate blood transfusion to prevent organ failure and death.

Blood transfusion is also used as supportive therapy for surgery, chemotherapy, and stem cell and organ transplantation, as well as in the treatment of acute and chronic diseases caused by deficiencies or defects in plasma proteins or cellular blood components, to avoid complications such as life-threatening hemorrhage or improve quality of life by reducing anemia-related symptoms. As per the data provided by the WHO, anemia affects ~25% of the population, which accounts for 1.6 billion people worldwide; toddlers and children of preschool age have the highest prevalence of anemia at 47.4% of their population group. Moreover, the number of people with hemophilia in the US is estimated to be ~20,000 individuals. The worldwide incidence of hemophilia is not well known but estimated among more than 400,000 people as per the National Hemophilia Foundation. According to the American National Red Cross 2018 data findings, about 7,000 units of platelets and 10,000 units of plasma are required daily in the US, and about 21 million blood components are transfused each year in the US. The Singapore Red Cross Society needs ~120,000 units of blood every year to meet the transfusion needs of patients, which is equivalent to ~400 units of blood per day. The increasing demand for access to safe blood and blood components for transfusion has led to the manufacturing or development of various types of blood bank freezers, which has increased the adoption of ULT freezers for secure storage along with strict guidelines of the WHO for the storage of blood samples. Moreover, the country is witnessing the increasing number of COVID-19 cases.For instance, in the US, the number of cases has been increased to 614,246 with 26,064 reported deaths.

Additionally, Mexico and Canada cases are also growing.The US and Canada have witnessed a sudden rise in the number of cases in just few days, which has compelled the governments to shut down all the business in order to prevent the spread of the COVID-19.

However, Mexico is likely to be least affected due to less research and development activities in the biomedical industry. In terms of type, the upright ULT freezers segment accounted for the largest share of the North American ultra-low temperature freezer market in 2019 and is estimated to mark the highest CAGR in the market during the forecast period, owing to the factors such as easier to organize because of having shelves. Also, the convenience of use of upright freezers has led to its dominance during 2019 and is expected to witness similar trend over the coming years. Centers For Disease Control And Prevention (CDC), Food and Drug Administration (FDA), Biomedical Research Centers (BRCs), Society of Infectious and Tropical Diseases (SIMIT), and International Stem Cell Corporation (ISCO) are among the significant primary and secondary sources for ultra-low temperature freezer included in the report. Read the full report: https://www.reportlinker.com/p05953821/?utm_source=GNW

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North America ultra-low temperature freezer market is anticipated to reach US$ 313.19 million in 2027 from US$ 220.25 million in 2019 - GlobeNewswire

Incysus Therapeutics Announces Name Change to IN8bio, Inc. – GlobeNewswire

August 24, 2020 07:00 ET | Source: IN8bio, Inc.

NEW YORK, Aug. 24, 2020 (GLOBE NEWSWIRE) -- Incysus Therapeutics, Inc., a clinical-stage biopharmaceutical company focused on delivering innovative gamma-delta () T cell immunotherapies for the treatment of cancer, today announced that it has changed its name to IN8bio, Inc. (IN8bio or the Company). The Companys new name reflects its novel approach to cell therapy, focused on the development of gamma-delta T cells for anti-cancer therapies. These powerful immune cells possess properties of both innate and adaptive immune cells and can serve as a functional bridge between the two systems to impact tumor killing.

IN8bio was founded to develop novel immunotherapies to treat cancer. Our new name, IN8bio, reflects that focus, commented William Ho, President, Chief Executive Officer and co-founder of IN8bio. As we continue to treat patients in our ongoing clinical programs, we are focused on delivering the next generation of innovative cancer therapies.

IN8bio is using autologous, allogeneic and genetically modified gamma-delta T cells to address the high unmet need in both solid and liquid tumors. IN8bio entered the clinic in 2020 with two Phase 1 clinical trials which are currently enrolling patients. In February 2020, IN8bio initiated enrollment in a Phase 1 clinical trial of gamma-delta T cell immunotherapy in leukemia patients undergoing allogeneic stem cell transplantation. That trial, the first clinical trial of an expanded and activated allogeneic gamma-delta T cell immunotherapy, is being conducted with its partners at the University of Kansas Cancer Center. Additionally, in February 2020, IN8bio initiated enrollment in a Phase 1 clinical trial of patients with newly diagnosed glioblastoma, which is a difficult to treat brain tumor that progresses rapidly. This trial is being conducted at the ONeal Comprehensive Cancer Center at the University of Alabama at Birmingham. IN8bios proprietary Drug Resistant Immunotherapy (DRI), which is being used in the glioblastoma trial, is the first genetically engineered gamma-delta T cell therapy to be administered to patients.

About IN8bio IN8bio is focused on delivering novel immunotherapies for the treatment of cancer. By using allogeneic and genetically modified gamma-delta () T cells, IN8bios technology addresses certain challenges that immunotherapies face targeting cold, low mutation cancers. IN8bios immuno-oncology programs include activated and gene-modified adoptive cellular therapies that are designed to protect cells from chemotherapy and may allow novel combinations of drugs to disrupt the tumor microenvironment and increase immunogenicity. IN8bios first clinical program is targeted to address leukemia in patients who are undergoing hematopoietic stem cell transplant (HSCT) and its second program is targeted to the treatment of newly diagnosed glioblastoma in combination with chemotherapy. For more information about the Company and its programs, visit http://www.IN8bio.com.

Forward Looking Statements Certain statements herein concerning the Companys future expectations, plans and prospects, including without limitation, the Companys current expectations regarding its business strategy, product candidates, and clinical development process and timing, constitute forward-looking statements. The use of words such as may, might, will, should, expect, plan, anticipate, believe, estimate, project, intend, future, potential, or continue, the negative of these and other similar expressions are intended to identify such forward looking statements. Such statements, based as they are on the current expectations of management, inherently involve numerous risks and uncertainties, known and unknown, many of which are beyond the Companys control. Consequently, actual future results may differ materially from the anticipated results expressed in such statements. In the case of forward-looking statements regarding investigational product candidates and continuing further development efforts, specific risks which could cause actual results to differ materially from the Companys current expectations include: scientific, regulatory and technical developments; failure to demonstrate safety, tolerability and efficacy; final and quality controlled verification of data and the related analyses; expense and uncertainty of obtaining regulatory approval, including from the U.S. Food and Drug Administration; and the Companys reliance on third parties, including licensors and clinical research organizations. Do not place undue reliance on any forward-looking statements included herein, which speak only as of the date hereof and which the Company is under no obligation to update or revise as a result of any event, circumstances or otherwise, unless required by applicable law.

Contact: IN8bio, Inc. William Ho, President & CEO who@IN8bio.com +1 646.600.6GDT info@IN8bio.com http://www.IN8bio.com

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Incysus Therapeutics Announces Name Change to IN8bio, Inc. - GlobeNewswire

Joint Pain Injections Market Size By Product Analysis, By Application, By End-Users, By Regional Outlook, By Top Companies and Forecast to 2027 -…

Sanofi S.A

Joint Pain Injections Market Segment Analysis-

The research report includes specific segments by Type and Application. Each type provides information about the production during the forecast period of 2015 to 2027. The application segment also provides consumption during the forecast period of 2015 to 2027. Understanding the segments helps in identifying the importance of different factors that aid market growth.

Joint Pain Injections Market, By Application

Shoulder & Elbow Knee & Ankle Spinal Joints Hip Joint Others

Joint Pain Injections Market, By Type

Steroid Joint Injections Hyaluronic Acid Injections Platelet-rich Plasma (PRP) Injections Placental Tissue Matrix (PTM) Injections Others

Joint Pain Injections Market, By Distribution Channel

Hospital Pharmacies Online Pharmacies Retail Pharmacies

The study analyses the following key business aspects:

Analysis of Strategies of Leading Players: Market players can use this analysis to gain a competitive advantage over their competitors in the Joint Pain Injections market.

Study on Key Market Trends: This section of the report offers a deeper analysis of the latest and future trends of the Joint Pain Injections market.

Market Forecasts:Buyers of the report will have access to accurate and validated estimates of the total market size in terms of value and volume. The report also provides consumption, production, sales, and other forecasts for the Joint Pain Injections market.

Regional Growth Analysis:All major regions and countries have been covered in the report. The regional analysis will help market players to tap into unexplored regional markets, prepare specific strategies for target regions, and compare the growth of all regional markets.

Segmental Analysis:The report provides accurate and reliable forecasts of the market share of important segments of the Joint Pain Injections market. Market participants can use this analysis to make strategic investments in key growth pockets of the Joint Pain Injections market.

Business Opportunities in Following Regions and Countries:

North America (United States, Canada, and Mexico)

Europe (Germany, UK, France, Italy, Russia, Spain, and Benelux)

Asia Pacific (China, Japan, India, Southeast Asia, and Australia)

Latin America (Brazil, Argentina, and Colombia)

How will the report assist your business to grow?

The document offers statistical data about the value (US $) and size (units) for the Joint Pain Injections industry between 2020 to 2027.

The report also traces the leading market rivals that will create and influence the Joint Pain Injections business to a greater extent.

Extensive understanding of the fundamental trends impacting each sector, although greatest threat, latest technologies, and opportunities that could build the global Joint Pain Injections market both supply and offer.

The report helps the customer to determine the substantial results of major market players or rulers of the Joint Pain Injections sector.

Reason to Buy this Report:

Save and reduce time carrying out entry-level research by identifying the growth, size, leading players, and segments in the global Joint Pain Injections Market. Highlights key business priorities in order to assist companies to realign their business strategies. The key findings and recommendations highlight crucial progressive industry trends in Joint Pain Injections Market, thereby allowing players to develop effective long term strategies.

Thank you for reading our report. The report is available for customization based on chapters or regions. Please get in touch with us to know more about customization options, and our team will ensure you get the report tailored according to your requirements.

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Our 250 Analysts and SMEs offer a high level of expertise in data collection and governance use industrial techniques to collect and analyze data on more than 15,000 high impact and niche markets. Our analysts are trained to combine modern data collection techniques, superior research methodology, expertise, and years of collective experience to produce informative and accurate research.

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Joint Pain Injections Market Size By Product Analysis, By Application, By End-Users, By Regional Outlook, By Top Companies and Forecast to 2027 -...

When your hair falls off and leaves scars – The Star, Kenya

The texture was different. In fact, my remaining hair seemed to look like the hair of our Muslim sisters. It was soft and light, something that was quite different from my natural hair, she said.

But she said even with the texture change, her hair began falling off and only a little was left at the back of her head.

There were patches on my head which turned into wounds. When I slept at night, I could wake up and find my hair on the pillow. This left me worried. When I combed my hair, the hair fell off, she said.

Onyinge then decided to braid her hair to see if the falling off would be tamed.

This did not work. I then decided to do weaves or wear wigs as I sought for a solution, she said.

An adults head has 100,000150,000 hair follicles, and each follicle can grow about 20 individual hairs. On average, every normal individual loses 75 to 100 hairs a day.

In 2016, Onyinge could not walk with her hair, whether it was braided or not.

Painful wounds began forming in the patches that were now scars. The hair was now not growing anymore. This is the time I decided to go and see a specialist, who recommended some lotions that I was to apply on my head, she said.

The pain on the wounds reduced but the hair continued to fall off.

LOST HOPE

The specialist told Onyinge that whatever condition it was, it must have been inherited.

I went to the specialist to repair my hair but then he asked me if anybody in my family had the same problem. This is the time I had to tell him about my father and my sister, she said.

It was at this point that she was given a lotion to apply on her hair, which did not guarantee that her hair would grow.

The doctor first drew blood from my system and extracted plasma, which was used to inject my scalp. I had 15 injections on my scalp just as a way to treat my hair loss, she said.

Trichologist Hillary Onyango says that the plasma used for the injection should be able to stimulate the growth of the hair follicles.

Though she had to part with around Sh15,000 per session, Onyinge said the hair continued to fall off.

Then a few days ago, a friend told me he knew a good doctor who could help me with the condition. I decided to give it a shot. When I arrived, I realised the clinic was being run by a man and his wife, all from Indian origin, she said.

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When your hair falls off and leaves scars - The Star, Kenya

Ron Evans steals a trick from I/O, and points the way to a transformational diabetes therapy – Endpoints News

Salk Institute scientist and serial biotech entrepreneur Ron Evans showed new mouse work yesterday that could point to a long-sought holy grail for diabetes treatment.

The study, published in Nature,involved a new approach for islet cell transplant, a diabetes therapy where dysfunctional insulin-producing cells on the pancreas are replaced with functional ones. The treatment has been around for a while and new ones are in development, but theyve been hampered by the fact that patients will reject the cells unless they go on immuno-suppressive drugs.

But, working with iPSC stem cells and tricks from immunotherapy, Evans and his team developed what they called immune-evasive clusters of cells essentially mini pancreases. Placed into mice, these cells secreted proper amounts of insulin without coming under fire from immune cells, pointing the way toward a similar approach in humans.

Most type 1 diabetics are children and teenagers, Evans said in a statement. We hope that regenerative medicine in combination with immune shielding can make a real difference in the field by replacing damaged cells with lab-generated human islet-like cell clusters that produce normal amounts of insulin on demand.

Evans, who most recently co-founded and sold to Astellas the exercise-in-a-pill biotech Mitobridge, and his co-authors are hardly alone in this race. ViaCyte has received major backing from both private donors and the Juvenile Diabetes Research Foundation for their own stem cell-derived islet cell transplant. Flagship also launched Sigilon earlier this year with $80.3 million in Series B funding. With technology from Robert Langer, the company is developing polymers that can encase cells for transplant. A diabetes program is in the IND-enabling phase with Eli Lilly.

Four years ago, Evans and his team figured out how to make functional pancreatic beta cells for the first time, using a series of molecular switches to get them to not only produce insulin but do so in response to glucose, as normal cells do. But that still left questions about how to go from individual cells into pancreas-like clusters, and how to get those cells to avoid the immune system when transplanted.

To cluster the cells, Evans lab figured out that a protein involved in embryonic development called WNT4 could trigger the same molecular mechanisms that created the functional beta cells. Adding that protein led to the creation of 3-D clusters of cells similar to what would be seen in a humans. They called them human islet-like organoids, or HILOs.

To make those organoids, Evans and Eiji Yoshihara, a scientist in his lab, stole a trick from another field: immuno-oncology. Using short pulses of a protein called interferon gamma, Yoshihara got the cells to express PD-L1.

The PD-L1 had the opposite effect of the PD-L1 inhibitors used in cancer. Rather than making sure T cells saw a tumor, they made sure T cells didnt see the islet cells.

This is the first study to show that you can protect HILOs from the immune system without genetic manipulation, Michael Downes, an author on the paper, said. If we are able to develop this as a therapy, patients will not need to take immune-suppressing drugs.

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Ron Evans steals a trick from I/O, and points the way to a transformational diabetes therapy - Endpoints News

Research Roundup: Lasting Immunity to COVID-19 and More – BioSpace

Every week there are numerous scientific studies published. Heres a look at some of the more interesting ones.

Multiple Studies Suggest Lasting Immunity to COVID-19 After Infection

Although probably not enough time has passed to know definitively, several studies are now suggesting that even mild cases of COVID-19 stimulate lasting immune responses, not only in disease-fighting antibodies, but in B- and T-cells.

Things are really working as theyre supposed to, Deepta Bhattacharya, an immunologist at the University of Arizona, and an author of one of the studies, told The New York Times.

Its difficult, probably impossible, to predict how long those immune responses will last, but many of the researchers believe the results are promising for long-term protection.

This is exactly what you would hope for, Marion Pepper, an immunologist at the University of Washington and an author of a study currently being reviewed by the journal Nature. All the pieces are there to have a totally protective immune response.

Pepper notes that the protective effects cant be completely evaluated until there is proof that people exposed to the virus a second time can fight it off. But the data suggests the immune system is indeed able to fight resistance a second time. Some of this qualification comes from unconfirmed reports of people being reinfected by the virus.

Antibody responses are typically relatively short-lived, disappearing from the blood weeks or months after being produced. Generally, the majority of the B-cells that produce antibodies die off, too. But the body keeps some longer-lived B-cells that are able to manufacture virus-fighting antibodies should the immune system be triggered by re-exposure to the virus. Some stay in the bloodstream while others wait in the bone marrow where they manufacture small numbers of antibodies that can sometimes be observed years, even decades later. Several studies, some by Bhattacharya and Pepper, have identified antibodies at low levels in the blood months after people recovered from COVID-19.

The antibodies decline, but they settle in what looks like a stable nadir, Bhattacharya said. These have been observed about three months after symptoms show up. The response looks perfectly durable.

Additional studies, including one published in the journal Cell, have isolated T-cells from recovered patients that can attack SARS-CoV-2. In laboratory studies, the T-cells produced signals to fight the virus and cloned themselves in large numbers to fight the potential infection.

This is very promising, said Smita Iyer, an immunologist at the University of California, Davis, who was not involved in the new studies, but has researched immune responses to the novel coronavirus in rhesus macaques. This calls for some optimism about herd immunity, and potentially a vaccine.

It's still has not been definitely determined if milder cases of COVID-19 will lead to long-term or even medium-term immunity. There have been some studies that suggest it does not and some newer studies suggesting it does. Iyer notes that the recent paper indicates, You can still get durable immunity without suffering the consequences of infection.

This idea is reinforced by Eun-Hyung Lee, an immunologist at Emory University who was not involved in these studies. He told The New York Times, Yes, you do develop immunity to this virus, and good immunity to this virus. Thats the message we want to get out there.

Why Seasonal Flu Vaccines Only Last a Year

As most everyone knows, flu vaccines only last about a year. Some of this is related to viral mutations. But in fact, the actual immunity itself caused by the vaccine does not appear to last longer than a year, even though the flu vaccine increases the number of antibody-producing cells specific for the flu in the bone marrow. Researchers out of Emory Vaccine Center found that for most newly-generated plasma cell lineages, between 70 and 99% of the cells were gone after one year, but that the levels of antibody-secreting cells in blood correlated with long-term response in the bone marrow.

Gut Bacteria Can Help Immuno-Oncology Therapies

Researchers with the University of Calgary identified gut bacteria that help our immune system fight cancerous tumors. This also helped provide more information about why immunotherapy works in some cases, but not others. By combining immunotherapy with specific microbial therapy, they believe they can help the immune system and immunotherapy be more effective in treating three types of cancer: melanoma, bladder and colorectal cancers. They found that specific bacteria were essential for immunotherapy to work in colorectal cancer tumors in germ-free mice. The bacteria produced a small molecule called inosine that interacts directly with T-cells and together with immunotherapy.

An Online Calculator to Predict Stroke Risk

Scientists at the University of Virginia Health System developed an online tool that measures the severity of a patients metabolic syndrome, a mix of conditions that includes high blood pressure, abnormal cholesterol levels and excess body fat. With it, they can then predict the patients risk for ischemic stroke. The study discovered that stroke risk increased consistently with metabolic syndrome severity even in patients that did not have diabetes. The tool is available for free at https://metscalc.org/.

A Link Between Autism and Cholesterol

Researchers at Harvard Medical School, Massachusetts Institute of Technology (MIT) and Northwestern University identified a subtype of autism that is the result of a cluster of genes that regulate cholesterol metabolism and brain development. They believe this information can help design precision-targeted therapies for this specific type of autism and improve screening efforts for earlier diagnosis of autism. They analyzed the DNA from brain samples that they then confirmed with the medical records of autistic individuals. They found that children with autism and their parents had significant alterations in lipid blood. However, there is much more to be understood, emphasizing the complexity of autism, which is affected by a variety of genetic and environmental factors.

Researchers Grow First Functioning Mini Human Heart Model

Investigators with Michigan State University grew the first miniature human heart model in the laboratory that is complete with all primary heart cell types and a functioning structure of chambers and vascular tissue. They utilized induced pluripotent stem cells which were obtained from consenting adults and created a functional mini heart in a few weeks. The primary value was in giving them an unprecedented view into how a fetal heart develops.

In the lab, we are currently using heart organoids to model congenital heart diseasethe most common birth defect in humans affecting nearly 1% of the newborn population, said Aitor Aguirre, senior author and assistant professor of biomedical engineering at MSUs Institute for Quantitative Health Science and Engineering. With our heart organoids, we can study the origin of congenital heart disease and find ways to stop it.

Another area of focus is that improving on the final organoid will help with future research. Current heart organoids are not identical yet to human hearts and so are flawed in their use as research models.

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Research Roundup: Lasting Immunity to COVID-19 and More - BioSpace

The global market for Peripheral Blood Mononuclear Cells (PBMC) is projected to grow at a CAGR of around 9% during 2020 – 2025 – GlobeNewswire

August 21, 2020 13:04 ET | Source: ReportLinker

New York, Aug. 21, 2020 (GLOBE NEWSWIRE) -- Reportlinker.com announces the release of the report "Global Peripheral Blood Mononuclear Cells Market, By Product, By Application, By Technique, By Source, By Region, Competition, Forecast & Opportunities, 2025" - https://www.reportlinker.com/p05953172/?utm_source=GNW

The global market for Peripheral Blood Mononuclear Cells (PBMC) is projected to grow at a CAGR of around 9% during 2020 - 2025.The PBMC are crucial to carry out the biology and pathology related studies as well as in clinical research.

Besides, PBMCs are also utilized in research related to fatal diseases, immunology, vaccine development, etc. However, high cost of PBMCs related studies might act as a challenge for the adoption of technology, especially in developing economies. The global peripheral blood mononuclear cells market is segmented based on product, application, technique, source, and region.The product segment is further divided into cryopreserved or frozen PBMC, cultured or fresh PBMC and peripheral blood mononuclear cell isolation & viability kits.

As of 2019, the cryopreserved PBMC or the frozen PBMC segment held the highest market share as they can be used for longer durations of time if stored carefully at lower temperatures.In terms of regional analysis, North America accounted for the largest market share in the year 2019, on the back of a number of pre-existing peripheral blood mononuclear cells-based companies in the region.

The economy of the region is also rich enough, which makes it easier to carry out the complex and costly R&D procedures. Major players operating in the global peripheral blood mononuclear cells market include Astarte Biologics, Inc., ATZLabs, BioIVT, BioLegend, Inc., BioVision, Bio-Rad, Cell Applications, Inc., Celgene, Creative Bioarray, Dapcel, Inc, HemaCare, iXCells Biotechnologies, Miltenyi Biotec, Merck, Novo Nordisk, Precision Medicine, Qiagen NV, STEMCELL Technologies Inc., Thermo Fisher Scientific, ZenBio, Inc., etc.

Years considered for this report:

Historical Years: 2015 - 2018 Base Year: 2019 Estimated Year: 2020 Forecast Period: 2021 - 2025

Objective of the Study:

To analyze and forecast the market size of global peripheral blood mononuclear cells market. To classify and forecast global peripheral blood mononuclear cells market based on product, application, technique, source, and region. To identify drivers and challenges for global peripheral blood mononuclear cells market. To examine competitive developments such as expansions, new product launches, mergers & acquisitions, etc., in global peripheral blood mononuclear cells market. To conduct pricing analysis for global peripheral blood mononuclear cells market. To identify and analyze the profile of leading players operating in global peripheral blood mononuclear cells market. The analyst performed both primary as well as exhaustive secondary research for this study.Initially, the analyst sourced a list of leading market players across the globe.

Subsequently, the analyst conducted primary research surveys with the identified companies.While interviewing, the respondents were also enquired about their competitors.

Through this technique, the analyst could include the research organizations and companies which could not be identified due to the limitations of secondary research. The analyst examined the research organizations and companies, and presence of all major players across the globe. The analyst calculated the market size of global peripheral blood mononuclear cells market using a bottom-up approach, wherein data for various end-user segments was recorded and forecast for the future years. The analyst sourced these values from the industry experts and company representatives and externally validated through analyzing historical data of these product types and applications for getting an appropriate, overall market size.

Various secondary sources such as company websites, news articles, press releases, company annual reports, investor presentations and financial reports were also studied by the analyst.

Key Target Audience:

Biotechnology and pharma companies and other stakeholders Government bodies such as regulating authorities and policy makers Organizations, forums and alliances related to peripheral blood mononuclear cells Market research and consulting firms The study is useful in providing answers to several critical questions that are important for the industry stakeholders such as research organizations & companies and partners, end users, etc., besides allowing them in strategizing investments and capitalizing on market opportunities.

Report Scope:

In this report, global peripheral blood mononuclear cells market has been segmented into following categories, in addition to the industry trends which have also been detailed below: Market, By Product: o Cryopreserved or Frozen PBMC o Cultured or Fresh PBMC o Peripheral Blood Mononuclear Cell Isolation & Viability Kits Market, By Application: o Immunology o Infectious disease o Hematology o Others Market, By Technique: o Density gradient centrifugation process o Leukapheresis Market, By Source: o Human o Animals Market, By Region: o Asia-Pacific - China - India - Japan - South Korea - Singapore - Australia o Europe - France - Germany - United Kingdom - Italy o North America - United States - Mexico - Canada o South America - Brazil - Argentina - Colombia o Middle east & Africa - South Africa - Saudi Arabia - UAE

Competitive Landscape

Company Profiles: Detailed analysis of the major companies present in global peripheral blood mononuclear cells market.

Available Customizations:

With the given market data, we offers customizations according to a companys specific needs. The following customization options are available for the report:

Company Information

Detailed analysis and profiling of additional market players (up to five). Read the full report: https://www.reportlinker.com/p05953172/?utm_source=GNW

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The global market for Peripheral Blood Mononuclear Cells (PBMC) is projected to grow at a CAGR of around 9% during 2020 - 2025 - GlobeNewswire

Stem Cell Therapy Market Segmentation, Assessment and Growth Opportunities by Forecast 2025 – Scientect

Global Stem Cell Therapy Market: Overview

Also called regenerative medicine, stem cell therapy encourages the reparative response of damaged, diseased, or dysfunctional tissue via the use of stem cells and their derivatives. Replacing the practice of organ transplantations, stem cell therapies have eliminated the dependence on availability of donors. Bone marrow transplant is perhaps the most commonly employed stem cell therapy.

Osteoarthritis, cerebral palsy, heart failure, multiple sclerosis and even hearing loss could be treated using stem cell therapies. Doctors have successfully performed stem cell transplants that significantly aid patients fight cancers such as leukemia and other blood-related diseases.

Know the Growth Opportunities in Emerging Markets

Global Stem Cell Therapy Market: Key Trends

The key factors influencing the growth of the global stem cell therapy market are increasing funds in the development of new stem lines, the advent of advanced genomic procedures used in stem cell analysis, and greater emphasis on human embryonic stem cells. As the traditional organ transplantations are associated with limitations such as infection, rejection, and immunosuppression along with high reliance on organ donors, the demand for stem cell therapy is likely to soar. The growing deployment of stem cells in the treatment of wounds and damaged skin, scarring, and grafts is another prominent catalyst of the market.

On the contrary, inadequate infrastructural facilities coupled with ethical issues related to embryonic stem cells might impede the growth of the market. However, the ongoing research for the manipulation of stem cells from cord blood cells, bone marrow, and skin for the treatment of ailments including cardiovascular and diabetes will open up new doors for the advancement of the market.

Global Stem Cell Therapy Market: Market Potential

A number of new studies, research projects, and development of novel therapies have come forth in the global market for stem cell therapy. Several of these treatments are in the pipeline, while many others have received approvals by regulatory bodies.

In March 2017, Belgian biotech company TiGenix announced that its cardiac stem cell therapy, AlloCSC-01 has successfully reached its phase I/II with positive results. Subsequently, it has been approved by the U.S. FDA. If this therapy is well- received by the market, nearly 1.9 million AMI patients could be treated through this stem cell therapy.

Another significant development is the granting of a patent to Israel-based Kadimastem Ltd. for its novel stem-cell based technology to be used in the treatment of multiple sclerosis (MS) and other similar conditions of the nervous system. The companys technology used for producing supporting cells in the central nervous system, taken from human stem cells such as myelin-producing cells is also covered in the patent.

The regional analysis covers:

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Global Stem Cell Therapy Market: Regional Outlook

The global market for stem cell therapy can be segmented into Asia Pacific, North America, Latin America, Europe, and the Middle East and Africa. North America emerged as the leading regional market, triggered by the rising incidence of chronic health conditions and government support. Europe also displays significant growth potential, as the benefits of this therapy are increasingly acknowledged.

Asia Pacific is slated for maximum growth, thanks to the massive patient pool, bulk of investments in stem cell therapy projects, and the increasing recognition of growth opportunities in countries such as China, Japan, and India by the leading market players.

Global Stem Cell Therapy Market: Competitive Analysis

Several firms are adopting strategies such as mergers and acquisitions, collaborations, and partnerships, apart from product development with a view to attain a strong foothold in the global market for stem cell therapy.

Some of the major companies operating in the global market for stem cell therapy are RTI Surgical, Inc., MEDIPOST Co., Ltd., Osiris Therapeutics, Inc., NuVasive, Inc., Pharmicell Co., Ltd., Anterogen Co., Ltd., JCR Pharmaceuticals Co., Ltd., and Holostem Terapie Avanzate S.r.l.

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Stem Cell Therapy Market Segmentation, Assessment and Growth Opportunities by Forecast 2025 - Scientect

Congress must save lives and reauthorize cell transplant funding | Opinion – NorthJersey.com

Ronald Roth, Special to the USA TODAY NETWORK Published 4:02 a.m. ET Aug. 19, 2020

In May of this year, religious Jews celebrated Pesach Sheni. Pesach Sheni literally means Second Passover and marks the day in ancient times when someone who was unable to participate in Passover was given a second chance to observe the holiday.

The concept of second chances is a powerful one, not just in the Jewish faith, but in our society as a whole. Some times a second chance is more than just an opportunity for spiritual or personal redemption some times a second chance is literally a second chance at life itself.

I know this first-hand, because thanks to a bone marrow transplant, I was given a second chance at life.

In May 2015, I was diagnosed with a myelofibrosis, a rare form of blood cancer. For three years, I travelled back and forth to Mount Sinai Hospital for blood tests and medications that treated my illness. For those first three years I was fortunate to have few symptoms of my disease and I was able to continue my very busy schedule as rabbi of Fair Lawn Jewish Center/Congregation Bnai Israel.

Patrick Gustoso registers for the National Marrow Donor Program on March 28, 2017, at the Nutley Health Department. Organizers hope to find a match for resident Anne Rotonda.(Photo: Owen Proctor/NorthJersey.com)

In the spring of 2018, my medical fortunes changed dramatically as the disease began a more rapid progression. Since my diagnosis, I had known that a bone marrow transplant would be my only chance at a cure and in August 2018, I received that bone marrow transplant and a second chance at life.

After my transplant, I became an ambassador advocate for National Marrow Donor Program/Be The Match. I committed myself to using this second chance to help others who are in need of access to life-saving cellular therapy. I am not alone in this, all across the country men and women, doctors and patients, survivors and co-survivors, donors and recipients are working tirelessly to make sure live-saving materials are delivered to those in need.

We cant do it alone, we need help help from our elected officials in Washington.

The CW Bill Young Cell Transplantation program provides access to live-saving bone marrow, peripheral blood stem cell and cord blood transplants for patients living with one of more than 70 blood cancers or disorders for which a transplant is the only curative option.

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Since its inception, the CW Bill Young Cell Transplantation Program has always enjoyed broad bipartisan support in both chambers of Congress. The program has been reauthorized by Congress every five years. It is up for re-authorization again this year and Congress should act swiftly to ensure the program remains able to fulfill its critical live-saving function.

Over the past 30 years, the National Marrow Donor Program (NMDP)/Be The Match has been entrusted by Congress to operate this critical program. During that time, more than 100,000 life-saving and life-extending transplants have been facilitated through the national registry.Many of these transplants took place here in New Jersey.

The Program is up for reauthorization again this summer and it is absolutely imperative that both chambers act swiftly to ensure that the program is reauthorized and that the critical life-saving work continues.The mission of the national registry to match patients and donors and ensure the timely transportation of lifesaving cellular products through the United States and around the world has been made even more challenging by COVID-19.Despite the pandemic, NMDP/Be The Match completed more transplants in June than in any single month in the programs history.This was only made possible by having the status of a federally authorized program that is recognized by other Federal, state, and local agencies and foreign governments.Should the programs authorization lapse at the end of September, there is concern that the program may not be able to operate as efficiently during the continuing public health emergency.

By reauthorizing the CW Bill Young Cell Transplantation Program, Congress can help give second chances to tens of thousands of men and women in need all across the country and here in New Jersey.

Rabbi Ronald Roth lives in Fair Lawn.

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Congress must save lives and reauthorize cell transplant funding | Opinion - NorthJersey.com

How Far Have We Come In Treating COVID-19? – The Dispatch

Six months and counting into our coronavirus era, weve gotten much better at quantifying the fight against the disease. How well a country or state or county is faring is broken down into charts and scatterplots: Cases per capita and tests run per capita, hospital capacity and PPE availability, test positivity rate and test turnaround rate and case fatality rate.

Given that blizzard of data, its strange that one question remains so difficult to examine: How much better are we actually getting at fighting the disease?

Weve certainly gotten better at fighting the diseases spread. Everyone knows the drill by now: Masks, social distancing, washing your hands. Whats less obvious is how far weve progressed in the task of healing the very sick. Doctors and hospitals have tried to defeat the virus with a cornucopia of drugs and treatments. But in part because that effort has been so improvisational and eclectic, tracking its effectiveness over time remains a serious challenge.

The central fact of the current stage of the pandemic is this: Although new cases soared throughout July and August far above what we saw in April and May, daily COVID deaths have not climbed back to their late-April heights. That rate may continue to rise even with new cases descending againdeaths are, after all, a lagging indicatorbut the discrepancy is too sharp to ignore.

But this discrepancy itself does not necessarily indicate improved outcomes in COVID treatment, because other differences between the pandemics spring manifestation and its summer one affect the data too. The first wave of the pandemic was clustered primarily in New York and New Jersey, states that failed terribly at keeping the virus, which is most dangerous to the elderly, out of nursing homes. Further, our national testing operation was then in such a sorry state that it's hard to tell how much viral spread we missed the first time around.

I think most of the reduction in fatality rate across the country is accounted for by protecting vulnerable populations and by overtesting, Dr. Howard Forman, a Yale radiologist and health policy professor, told The Dispatch. So by testing more people who are healthier, we make ourselves look better.

This certainly isnt to say there hasnt been improvement in treating the virus. Clinicians will tell you in no uncertain terms theyve seen genuine progress. Gone is the desperate chaos of the early months, with their frantic smorgasbord of ad-hoc treatments and what-have-you-got-to-lose therapeutics; now doctors share a sort of anti-COVID folklore, wedding what solid clinical data exists with treatments that their compatriots around the country have found effective from hard experience.

Theres kind of two parts to the decision-making, said Dr. Megan Ranney, an emergency physician and professor at Brown University. Part one, and the part that we are all most comfortable with, is relying on peer-reviewed evidence. She rattled off a few examples: The antiviral drug remdesivir, which has been shown to reduce COVIDs recovery time; the anti-inflammatory dexamethasone, which can help soothe a berserk immune response to the virus; placing patients who are struggling to breathe on their stomachs rather than their backs.

The other side is the anecdote, the case series, the shared experiences of groups of physicians, she said. This was particularly prominent early in the pandemic when we really had nothing, and no guidance whatsoever. We saw Facebook and WhatsApp groups spring up, as well as email listservs, to try to allow real-time sharing of best practices and to allow people to compare what worked in one setting to what worked in another.

This loose-cannon treatment style helped doctors begin to catch up to a horribly powerful virus under incredibly bad circumstances, but it had its drawbacks too. Several doctors we spoke to brought up the example of hydroxychloroquine, a drug that showed some early promise in treating COVID patients but was ultimately shown in controlled clinical trials to be unhelpful in treating very sick patients. Ordinarily, that would be the end of the road for a given treatmentbut in this case, there were already a number of small case studies and doctors personal testimonies floating around with positive assessments of the drug and endorsements from President Donald Trump created a political constituency for its success. Such case studies and anecdotes are inherently less reliable than large-scale clinical trials, but their existence helped fan the flames of the bizarre conspiracy theories that cropped up around the drug.

And it isnt true that doctors are comfortable now, exactly. It can be hard to remember that were still in the very early days of the fight against a brand-new disease. Staying up to date on all the research coming out is a constant struggle of its own. Just this week, for instance, the FDA unexpectedly decided not to issue an emergency authorization for convalescent plasma, a promising treatment involving transfusions of antibody-rich blood serum donated by those who have already had COVID-19, suggesting the data was not yet strong enough to support it.

I still feel likemaybe not that Im working in the dark, but that maybe Im working with one eye closed, said Dr. Akino Yamashita, who has spent the year treating COVID patients in New Jersey and New York. Every day, its Oh, theres this new study, theres this new article. But does [one study] really change what I do when I see the next patient with this disease? Probably not.

Of the convalescent plasma story, she added: Certainly this goes along with the theme that although there are more treatment options available now, this is a constantly changing story.

Nor does the constant churn of new research focus only on better understanding the effects of the treatments already in circulation. Possible new treatments are working their way through the early stages of clinical trials all the time. Antibody treatments, both artificially manufactured and derived from animals, and stem cell therapies featuring cells known as MSCs (which stands, somewhat confusingly, for either medicinal signaling cells or mesenchymal stem cells)these are a few of the bleeding-edge projects that could potentially follow hydroxychloroquine and remdesivir into the public consciousness in the months to come.

Of course, this multiplication of possible treatments brings another set of challenges entirely.

The standard of treatment for a severe COVID-19 illness is changing, Dr. David Ingbar, a professor of medicine and pulmonary care expert at the University of Minnesota, told The Dispatch. Dr. Ingbar is currently heading up an early clinical trial into treating COVID with MSCs.

Now we believe dexamethasone works in certain populations at certain levels of illness, he said. We know that remdesivir has some benefit in terms of shortening the disease and maybe improving mortality. There are suggestions that, if given early, convalescent plasma might be beneficial. What we dont know very much about is, how do all of these treatments interact? Is it better to get one from column A, B, C, D, and E? Or are only certain combinations beneficial? So its a complicated field, and I think we all as clinicians want to help our patients as much as possible. But there is potential to do harm as well as good with all these treatments.

Presented like this, all this can seem like a dreary deluge of obstacles and complications. So its worth stating unequivocally: All of this is a pretty good problem to have. It may be a while before we can say for sure how far back our medical researchers and clinicians have beaten the virus already. But that fight gets a little less favorable to the virus, and a little more favorable to the humans, every day.

People forget that the longer you can wait to get COVIDhopefully well get a vaccine quickly, so well be able to protect us all from getting infectedbut if you get infected today, your chance of living through that infection is better than if you got infected in February or March, Dr. Ranney said. And I expect that to continue to improve. Its not a linear process. Its two steps forward, one step back in terms of that knowledge generation. So there are going to continue to be things that change, there are going to continue to be things that we think help and maybe dont. Thats normal in medicine. But overall, the trajectory is absolutely a positive and encouraging trajectory in terms of our ability to effectively treat and save lives of patients who are sick with COVID.

Photograph by Go Nakamura/Getty Images.

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How Far Have We Come In Treating COVID-19? - The Dispatch