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Families pay thousands to store childrens stem cells, but the cells are rarely useful – The Dallas Express

Posted: July 21, 2024 at 2:35 am

Banking umbilical cord blood has been heavily pushed on parents by doctors and hospitals for decades.

The process is far from inexpensive.

The initial collection and processing fees can range from $1,200 for cord blood only and can go up to $2,895 for the top package: cord blood, tissue and placenta stem cells, Robert Hariri, founder and CEO of Celularity, a human cellular therapeutic company that owns private cord blood bank LifebankUSA, told Forbes. Annual storage fees can run another $150 to $400 per year.

Companies use fearmongering to convince new parents that banking cord blood could potentially save a life.

However, according to a new investigative report from The New York Times, potentially life-saving stem cells from the umbilical cord and placenta rarely get used. Worse yet, when the cord blood is needed, it often proves to be too little or contaminated. Heres the start of the story:

Millions of pregnant women get the pitch through their OB-GYN: Put a bit of your newborns umbilical cord on ice, as a biological insurance policy. If your child one day faces cancer, diabetes or even autism, the precious stem cells in the cord blood could become a tailor-made cure.

Many families are happy to pay for the assurance of a healthy future. More than two million umbilical cord samples sit in a handful of suburban warehouses across the country. Its a lucrative business, with companies charging several thousand dollars upfront plus hundreds more every year thereafter. The industry has grown rapidly, bolstered by investments from medical device companies, hospital partnerships and endorsements from celebrities like Drew Barrymore and Chrissy Teigen.

But the leading banks have consistently misled customers and doctors about the technologys promise, an investigation by The New York Times found. Doctors rarely use cord blood anymore, thanks to advances that have made it easier to transplant adult stem cells. And the few parents who try to withdraw cord blood samples often find that they are unusable either because their volume is too low or they have been contaminated with microbes.

When the first cord blood banks opened three decades ago, doctors were optimistic about turning the stem cells, otherwise discarded as medical waste, into a powerful new treatment for patients with leukemia and other blood disorders. Private banks promised peace of mind for anxious parents-to-be, knowing the cells would be ready and waiting if their child ever got sick.

That potential has not materialized. Just 19 stem-cell transplants using a childs own cord blood have been reported since 2010, according to the Center for International Blood and Marrow Transplant Research. Newer research has led many doctors to abandon cord blood in favor of adult stem cells.

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Families pay thousands to store childrens stem cells, but the cells are rarely useful - The Dallas Express

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The dubious consent question at the heart of the Human Genome Project : Short Wave – NPR

Posted: July 21, 2024 at 2:35 am

Launched in 1990, a major goal of the Human Genome Project was to sequence the human genome as fully as possible. In 2003, project scientists unveiled a genome sequence that accounted for over 90% of the human genome as complete as possible for the technology of the time. Darryl Leja, NHGRI/Flickr hide caption

Launched in 1990, a major goal of the Human Genome Project was to sequence the human genome as fully as possible. In 2003, project scientists unveiled a genome sequence that accounted for over 90% of the human genome as complete as possible for the technology of the time.

The Human Genome Project was a massive undertaking that took more than a decade and billions of dollars to complete. For it, scientists collected DNA samples from anonymous volunteers who were told the final project would be a mosaic of DNA. Instead, over two-thirds of the DNA comes from one person: RP11. No one ever told him. Science journalist Ashley Smart talks to host Emily Kwong about his recent investigation into the decision to make RP11 the major donor and why unearthing this history matters to genetics today.

Read Ashley's full article in Undark Magazine here.

Curious about other biology stories? Email us at shortwave@npr.org.

Listen to Short Wave on Spotify and Apple Podcasts.

Listen to every episode of Short Wave sponsor-free and support our work at NPR by signing up for Short Wave+ at plus.npr.org/shortwave.

Today's episode was produced by Berly McCoy and edited by Rebecca Ramirez. They both checked the facts. Kwesi Lee was the audio engineer.

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The dubious consent question at the heart of the Human Genome Project : Short Wave - NPR

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Cell Therapy Market to Attain a USD 190.91 Billion Valuation in 2031, Rising Investments in Stem Cell Research Spearhead Market Expansion | SkyQuest…

Posted: July 21, 2024 at 2:35 am

WESTFORD, Mass., July 19, 2024 /PRNewswire/ -- According toSkyQuest, the global Cell Therapy Marketsize was valued at USD 3.9 Billion in 2022 and is poised to grow from USD 6.7 Billion in 2023 to USD 190.91 Billion by 2031, growing at a CAGR of 52% during the forecast period (2024-2031).

The use of different types of cells in unique ways to treat diseases and disorders is known as cell therapy. Advancements in cell research and the growing acceptance of cell therapies for the treatment of multiple chronic indications are forecasted to augment market growth in the future. Growing demand for regenerative medicine is also estimated to open new avenues of opportunities for cell therapy providers in the long run. The global cell therapy market is segmented into cell types, therapy types, therapeutic areas, end user, and regions.

Download a detailed overview:

https://www.skyquestt.com/sample-request/cell-therapy-market

Cell Therapy Market Overview:

Report Coverage

Details

Market Revenue in 2023

$ 6.7 billion

Estimated Value by 2031

$ 190.91 billion

Growth Rate

Poised to grow at a CAGR of 52%

Forecast Period

20242031

Forecast Units

Value (USD Billion)

Report Coverage

Revenue Forecast, Competitive Landscape, Growth Factors, and Trends

Segments Covered

Therapy Type, Technology, Therapeutic Area, End User, and Region

Geographies Covered

North America, Europe, Asia Pacific, Middle East & Africa, Latin America

Report Highlights

High investments in cell therapy research and development

Key Market Opportunities

Increasing incidence of musculoskeletal disorders and high use of cell therapies to treat the same

Key Market Drivers

Growing use of cell therapies to treat cancer indications

Segments covered in Cell Therapy Market are as follows:

Request Free Customization of this report:

https://www.skyquestt.com/speak-with-analyst/cell-therapy-market

High Demand for Novel Cancer Treatments to Help Oncology Segment Maintain Prominence

Cases of cancer are increasing rapidly on a global level and subsequently the demand for novel treatments for the same as well. Investments in oncology research are also increasing and reaching new heights. Cell therapies have been showing great promise in treating multiple types of cancers. Cell therapy companies are continually focusing on getting new approvals for their offerings related to different cancer indications thereby helping this segment maintain a high market share.

On the other hand, the demand for cell therapies for the treatment of musculoskeletal disorders is estimated to surge at an impressive pace. Rising cases of musculoskeletal tissue degeneration and the growing demand for repair or replacement of damaged musculoskeletal tissues will also create a new business scope for cell therapy providers.

High Use of CAR-T Therapies Helps Autologous Therapies Account for Dominant Share

Autologous cell therapies are preferred for their lower risk of life-threatening complications as compared to other types of therapies. There are also no specific requirements to match the donor and receivers in an autologous cell therapy. A higher possibility of treatment success and reduced risk of transplant rejection are also key factors that help this segment hold a high market share. CAR-T therapies are being extensively used to treat a wide array of indications and they are classified under the autologous segment.

View report summary and Table of Contents (TOC):

https://www.skyquestt.com/report/cell-therapy-market

Stem Cells are Estimated to be Used Extensively for Multiple Cell Therapy Types

Stem cells can be guided or manipulated to perform certain biological functions, which is why they are mostly used in cell therapies. Growing investments in stem cell research, the high availability of stem cells, and the proven efficacy of stem cells in the development of novel cell therapies are all factors that help this segment generate new opportunities for cell therapy providers.

High demand for advanced treatments and therapeutics around the world is forecasted to create opportunities for new as well-established cell therapy providers.

Related Report:

3D Bioprinting Market

Cell-Based Assays Market

3D Cell Culture Market

Stem Cell Manufacturing Market

Stem Cell Therapy Market

About Us:

SkyQuest is an IP focused Research and Investment Bank and Accelerator of Technology and assets. We provide access to technologies, markets and finance across sectors viz. Life Sciences, CleanTech, AgriTech, NanoTech and Information & Communication Technology.

We work closely with innovators, inventors, innovation seekers, entrepreneurs, companies and investors alike in leveraging external sources of R&D. Moreover, we help them in optimizing the economic potential of their intellectual assets. Our experiences with innovation management and commercialization has expanded our reach across North America, Europe, ASEAN and Asia Pacific.

Contact:Mr. Jagraj Singh SkyQuest Technology 1 Apache Way, Westford, Massachusetts 01886 USA (+1) 351-333-4748 Email: sales@skyquestt.com Visit Our Website:https://www.skyquestt.com/

Logo : https://mma.prnewswire.com/media/2446095/SkyQuest_Logo.jpg

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Cell Therapy Market to Attain a USD 190.91 Billion Valuation in 2031, Rising Investments in Stem Cell Research Spearhead Market Expansion | SkyQuest...

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Transhuman Hackers Using Tech Implants To Hack Others – The Project

Posted: July 21, 2024 at 2:35 am

From paying for things with the wave of your hand to video cameras in place of eyes.

This is the wonderful world of transhumans; people who modify their bodies using technology to enhance their abilities to superhuman levels.

The transhumanist movement ultimately believes humans can eradicate ageing and death by merging with machines and augmenting our bodies and minds.

Worldwide, there are reportedly more than 50,000 people with these implants, which some say are the way of the future.

But not everyone is using their powers for good, with some even weaponising their implants to hack others.

Real-life transhuman Len Noe calls himself an ethical hacker, and he has 10 implants so far.

Len can now bypass security protocols, let himself into buildings and hack into your phone in 30 seconds.

But after a rough upbringing on the streets in Detroit, mixing with bikie gangs, Len is now using his hacking skills for good and helping us understand the dawn of a new digitally enhanced day.

Len Hoe told The Project that his journey to transhumanism started with tattoos and standardaugmentation.

A lot of the greatest medical benefits that we've actually having in the modern age, it originally started by people experimenting on themselves, Len said.

So self-experimentation has been around forever. I guess the question I would ask, why not?

Len said having the technology alone wasnt enough, you also had to have knowledge on how to use it.

If Len wanted to hypothetically skim a security card to enter a building, he explained It's not just I walk up and your badge information comes to me, he explained.

I need to have the skills to get that information. I have to have tools to copy it off your card, and then I also have to have the intent to do something malicious with it.

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Transhuman Hackers Using Tech Implants To Hack Others - The Project

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What Parents Should Know About Cord Blood Banking – The New York Times

Posted: July 21, 2024 at 2:35 am

Pregnant women are bombarded with advertisements on social media, in childbirth classes, even in their doctors offices urging them to bank the blood in their babys umbilical cord and gain peace of mind.

Private banks claim that the stem cells inside the blood are a powerful tool to have on hand in case a child one day becomes seriously ill. They charge several thousand dollars upfront for storage plus hundreds more every year thereafter.

But an investigation by The New York Times found that leading banks have consistently misled parents about the technologys promise. The few parents who try to withdraw samples often find that they are unusable either because their volume is too low or they have been contaminated with microbes.

Heres what parents should know about cord blood banking.

In the 1990s, transplant doctors saw cord blood as a promising new source of stem cells for patients with sickle cell anemia and leukemia who could not find suitable matches from their families or bone marrow donor registries.

The major cord blood banks Cord Blood Registry, ViaCord and Cryo-Cell told The Times that the cells they store had saved childrens lives and that no one knew what scientists may one day discover.

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What Parents Should Know About Cord Blood Banking - The New York Times

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Assessment of Cytomegalovirus DNA doubling time and virus-specific T-cell responses in the management of CMV infection in allogeneic hematopoietic…

Posted: July 21, 2024 at 2:35 am

Marty FM, Ljungman P, Chemaly RF, Maertens J, Dadwal SS, Duarte R, et al. Letermovir prophylaxis for cytomegalovirus in hematopoietic-cell transplantation. N Engl J Med. 2017;377:243344.

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Vyas A, Raval AD, Kamat S, LaPlante K, Tang Y, Chemaly RF. Real-world outcomes associated with letermovir use for cytomegalovirus primary prophylaxis in allogeneic hematopoietic cell transplant recipients: a systematic review and meta-analysis of observational studies. Open Forum Infect Dis. 2022;10:ofac687.

Article PubMed PubMed Central Google Scholar

Cassaniti I, Colombo AA, Bernasconi P, Malagola M, Russo D, Iori AP, et al. Positive HCMV DNAemia in stem cell recipients undergoing letermovir prophylaxis is expression of abortive infection. Am J Transplant. 2021;21:162228.

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Solano C, Gimnez E, Albert E, Piana JL, Navarro D. Immunovirology of cytomegalovirus infection in allogeneic stem cell transplant recipients undergoing prophylaxis with letermovir: a narrative review. J Med Virol. 2023;95:e29005.

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Gimnez E, Guerreiro M, Torres I, Aguilar C, Albert E, Hernndez-Boluda JC, et al. Features of cytomegalovirus DNAemia and virus-specific T-cell responses in allogeneic hematopoietic stem-cell transplant recipients during prophylaxis with letermovir. Transpl Infect Dis. 2023;25:e1402.

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Solano C, Gimnez E, Piana JL, Vinuesa V, Poujois S, Zaragoza S, et al. Preemptive antiviral therapy for CMV infection in allogeneic stem cell transplant recipients guided by the viral doubling time in the blood. Bone Marrow Transplant. 2016;51:71822.

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Huntley D, Talaya A, Gimnez E, Martnez A, Hernndez-Boluda JC, Hernani R, et al. Features of cytomegalovirus DNAemia Blips in allogeneic hematopoietic stem cell transplant recipients: implications for optimization of preemptive antiviral therapy strategies. Biol Blood Marrow Transplant. 2020;26:9727.

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Zamora D, Duke ER, Xie H, Edmison BC, Akoto B, Kiener R, et al. Cytomegalovirusspecific Tcell reconstitution following letermovir prophylaxis after hematopoietic cell transplantation. Blood. 2021;138:3443.

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Gabanti E, Borsani O, Colombo AA, Zavaglio F, Binaschi L, Caldera D, et al. Human cytomegalovirusspecific Tcell reconstitution and lateonset cytomegalovirus infection in hematopoietic stem cell transplantation recipients following letermovir prophylaxis. Transplant Cell Therapy. 2022;28:211.e1211.e9.

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Lauruschkat CD, Muchsin I, Rein A, Erhard F, Grathwohl D, Dlken L, et al. CD4+T cells are the major predictor of HCMV control in allogeneic stem cell transplant recipients on letermovir prophylaxis. Front Immunol. 2023;14:1148841.

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Zavaglio F, Vitello D, Bergami F, Arena F, Borsani O, Colombo AA, et al. Human Cytomegalovirus (HCMV)-specific T-cell response after letermovir prophylaxis is predictive for subsequent HCMV reactivation in haematopoietic stem cell transplant recipients. J Clin Virol. 2023;165:105519.

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Lauruschkat CD, Muchsin I, Rein AF, Erhard F, Grathwohl D, Dlken L, et al. Impaired T and memory-like NK-cell reconstitution is linked to late-onset HCMV reactivation after letermovir cessation. Blood Adv. 2024;8:296779.

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Assessment of Cytomegalovirus DNA doubling time and virus-specific T-cell responses in the management of CMV infection in allogeneic hematopoietic...

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3D Artificial Cornea from Stem Cells: Chula Researchers Advance Canine Corneal Wound Treatment – Times Higher Education

Posted: July 21, 2024 at 2:34 am

Chulalongkorn Universitys Faculty of Veterinary Science and the Faculty of Engineering have worked together to research and develop a three-dimensional artificial cornea from stem cells that offers a way to treat deep corneal wounds in dogs. The innovation helps to solve the problem of treatment methods that rely on tissue replacement which is hard to find and very expensive. It makes it possible for dogs to be able to see clearly and comfortably once again.

Does your dog have any of these symptoms? The inability to fully open its eyes, squinting or blinking frequently, shedding lots of tears, sometimes the tears are thick, and the mucus appears greenish. The sclera is unusually red and not clear like before. The cornea becomes cloudy and there are blood vessels in it.

If your answer is yes then your pet might be suffering from a corneal ulcer which, if left untreated could eventually cause blindness.

Nowadays, the number of dogs receiving treatment for corneal ulcers has increased tremendously.The small animal hospital at the Faculty of Veterinary Medicine, Chulalongkorn Universityalone is already treating dogs with corneal ulcers daily.

Veterinarian Dr. Chutirat Torssahakul,the Department of Internal Medicine, Faculty of Veterinary Medicine

We find quite a number of lesions like this in dogs. Corneal ulcers occur as a result of many reasons, such as dogs scratching their own eyes because they have allergies causing itching around the eyes followed by scratching until the lesions form. Fights with other dogs, being scratched by a cat, or accidentally bumps into objectsVeterinarian Dr. Chutirat Torssahakul of the Department of Internal Medicine,Faculty of Veterinary Medicine, Chulalongkorn Universityaddressed the problems that became the starting point for the research and innovation development. Three-dimensional artificial cornea from stem cells enables your beloved pet to have perfect vision once again. The current treatment being used is to have grafts made from replacement tissue derived from porcine bladder or canine placentas which are rare and relatively expensive. There is also the possibility of causing post-surgery reaction and inflammation. Therefore, we thought that if we could produce our own innovative artificial cornea using natural materials that are easily found and reduce the chance of causing inflammation this might be a better option. Dr. Chutirat explained.

Three-dimensional artificial cornea from stem cells a brighter alternative

As a result of the effort and intention to solve eye problems for dogs, the Faculty of Veterinary Sciences research team throughthe Veterinary Stem Cell and Bioengineering Innovation Center (VSCBIC)has therefore embarked on additional studies on stem cells and is working with the Biomedical Engineering Research Center of the Faculty of Engineering, Chulalongkorn University recognizing its expertise in tissue engineering to help make adhesive materials for growing stem cells.

Image showing a 3D corneal patch made from silk fibroin and gelatin

According to Veterinary Professor Dr. Chutirat Artificial corneal tissue is obtained by cultivating real dog corneal stem cells on a natural material structure made from silk fibroin mixed with gelatin. The material can be cheaply and easily found in Thailand. It is strong and durable, clear and transparent, and adheres well to cells making them three-dimensional which is comparable to real corneal tissue.

This innovation can be used to treat corneal perforations in dogs as well as large corneal wounds where the tissue cannot be stitched or even deep wounds in which a large amount of corneal tissue has been lost. In cases of dogs with mild or moderate levels of corneal ulcer problems, currently, 2 methods for treatment are still in use.

But in cases where the wound in the cornea is so large that tissue must be used to replace the missing part, we usually use a graft which could be the dogs own conjunctiva. The other option is to use replacement tissue such as tissues derived from human or canine placentas. These are costly and difficult to find so we have invented a new way to treat them and that is the three-dimensional artificial cornea made from stem cells.

4 outstanding features of the 3D artificial cornea innovation

At present, the 3D artificial cornea from stem cells innovation is still in the laboratory testing stage to study whether the 3D artificial cornea can actually be used as a cornea replacement, and to determine how it interacts with the animals body. According to Veterinary Professor Dr. Chutirat in many countries research on such innovations is also currently underway at the laboratory level.

The research we have done has produced satisfactory results. It is expected that this innovation will be applied to dogs in the next few years. Moreover, we have plans to apply this knowledge to cats as well from cell collection, locating cells, separating cells, and arranging cells Dr. Chutirat concluded.

Those who are interested can further read the research paper on the subject at https://pubmed.ncbi.nlm.nih.gov/35120168/

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3D Artificial Cornea from Stem Cells: Chula Researchers Advance Canine Corneal Wound Treatment - Times Higher Education

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Cord Blood Banks Sold Families on False Hope – myheraldreview.com

Posted: July 21, 2024 at 2:34 am

Millions of pregnant women get the pitch through their OB-GYN: Put a bit of your newborns umbilical cord on ice, as a biological insurance policy. If your child one day faces cancer, diabetes or even autism, the precious stem cells in the cord blood could become a tailor-made cure.

Many families are happy to pay for the assurance of a healthy future. More than 2 million umbilical cord samples sit in a handful of suburban warehouses across the country. Its a lucrative business, with companies charging several thousand dollars upfront plus hundreds more every year thereafter. The industry has grown rapidly, bolstered by investments from medical device companies, hospital partnerships and endorsements from celebrities such as Drew Barrymore and Chrissy Teigen.

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Cord Blood Registry, in Tucson, Ariz., on June 26, 2024. The company stores more than one million samples, double the number it had in 2014. (Rebecca Noble/The New York Times)

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Renee Johnson in Scottsdale, Ariz., on July 7, 2024. Johnson banked her sons cord blood with ViaCord in 2014 and learned years later the cells were infected with E. coli. (Rebecca Noble/The New York Times)

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Anna Lazos at her home in Egg Harbor Township, N.J., on June 27, 2024. After spending thousands of dollars on cord blood storage, Lazos asked to withdraw a sample to enroll her son in an autism clinical trial. The company told her that the cells were contaminated with E. coli. (Hannah Yoon/The New York Times)

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Jenna Edwards with her son at home in Parkland, Fla., on June 24, 2024. When Edwards tried in 2017 to withdraw her sons cord blood cells for a clinical trial to treat his cerebral palsy, she learned that the company had found bacteria in the sample, but still charged her for the next two years. (Eva Marie Uzcategui/The New York Times)

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Cord Blood Banks Sold Families on False Hope - myheraldreview.com

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A Seventh Person Has Most Likely Been Cured of HIV Following Stem Cell Transplant – Them

Posted: July 21, 2024 at 2:34 am

A German man is reportedly the seventh person in history to be cured of HIV, according to researchers who will present the information at the 2024 International AIDS Conference in Munich, Germany.

Multiple tests given to the German man were unable to detect any copies of the virus in his body following a stem cell transplant for acute myeloid leukemia that occurred in 2015, according to a report in NBC News. The man stopped taking antiretroviral medication for his HIV in 2018 and remains in remission, or a state of having no virus present in the body.

The man has chosen to remain anonymous, but did issue a statement about his medical condition. A healthy person has many wishes, he said, a sick person only one.

The longer we see these HIV remissions without any HIV therapy, the more confidence we can get that were probably seeing a case where we really have eradicated all competent HIV, Dr. Christian Gaebler, a physician and scientist at the Charit-Universittsmedizin Berlin, told NBC News.

While any cure news is always welcomed both in the HIV community and to those outside it, the German mans case is emblematic of a trend that is proving hard to replicate for the 39 million people living with HIV worldwide. In each of the seven cases, according to NBC News, the cure came as the result of stem cell treatments for people living with HIV who had developed blood cancer. Such stem cell transplants are toxic and can be fatal, as NBC News, making it unethical as a treatment for the overwhelming majority of people with HIV.

When HIV enters a persons body, it functionally turns a persons immune cells into factories that make more and more copies of the virus. However, existing alongside these copies of the virus that actively attack a persons immune system is the latent HIV reservoir, a group of immune cells that have been overtaken by HIV but are not currently reproducing new copies of the virus. These dormant cells can awaken at any time, and targeting these cells is a major problem for HIV cure researchers. Often, these reservoirs are located in hard-to-reach areas, including the lymph nodes, the gut, and the brain, according to The Body, an HIV/AIDS news and information site.

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A Seventh Person Has Most Likely Been Cured of HIV Following Stem Cell Transplant - Them

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Cell BioEngines Secures an Additional $2 Million in Funding – GlobeNewswire

Posted: July 21, 2024 at 2:34 am

NEW YORK, July 20, 2024 (GLOBE NEWSWIRE) -- Cell BioEngines, Inc., a New York, USA-based company researching stem cells in order to develop new cell therapies unlocked $1.75 million additional funds from SOSV and the Partnership Fund through the new therapeutics seed track, available for therapeutics start-ups. In addition, Cell BioEngines raised $0.25 million from Empire State Developments NY Ventures, the states venture capital arm through the Pre-Seed and Seed Matching Fund Program.

This reflects strong growth and investor confidence in our innovative approach to advancing cell therapies, particularly timely as we expand within New York State, said Dr. Ajay Vishwakarma, Founder and CEO.

The funds will support our first multicenter clinical trial, aimed at hematological cancer patients unable to find a donor and seeking an alternative to HLA-haploidentical blood stem cell transplants. CBE-101 represents a novel approach with expanded cord blood-derived hematopoietic cell therapy, aligned with Cell BioEngines' vision to deliver 'off-the-shelf' cell-based therapies to patients, he added.

About Cell BioEngines

Cell BioEngines, Inc., founded in Dec 2022, is a clinical-stage biotech company focused on developing allogeneic 'off-the-shelf' stem cell-derived therapies as drugs for human disease treatment. The company leverages its proprietary platform technology using universal 'non-gene-modified' donor blood stem cells obtained from umbilical cord to produce clinical grade cells at scale.

For more information about Cell BioEngines, and to learn more the latest Company developments, please visit http://www.cellbioengines.com

Contact

Mark Joubert., J.D. Chief Legal Officer Cell BioEngines, Inc info@cellbioengines.com

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Cell BioEngines Secures an Additional $2 Million in Funding - GlobeNewswire

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