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"Charting the Course: Global Animal Stem Cell Therapy Market – openPR

Global Animal Stem Cell Therapy

In recent years, animal stem cell therapy has emerged as a promising avenue in veterinary medicine, offering novel solutions for treating various diseases and injuries in companion and livestock animals. Amidst evolving regulatory landscapes, technological advancements, and the lingering effects of the COVID-19 pandemic, understanding the dynamics of the global animal stem cell therapy market is paramount. This blog delves into the size, share, and impact of factors shaping the market from 2023 to 2031.

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The animal stem cell therapy market encompasses a range of products and services aimed at harnessing the regenerative potential of stem cells to treat conditions such as osteoarthritis, tendon injuries, and inflammatory bowel disease in animals. Key factors influencing market growth include resin type, application, technology, end-use industry, and regional trends.

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Resin type plays a crucial role in the development and manufacturing of stem cell therapy products for animals. Common materials used in cell culture and scaffold fabrication include synthetic polymers, hydrogels, and extracellular matrix components. Advances in biomaterials science continue to drive innovation, enhancing the efficacy and safety of stem cell-based treatments. Animal stem cell therapy finds applications across diverse veterinary specialties, including orthopedics, neurology, oncology, and wound healing. From autologous stem cell transplantation to allogeneic cell products, the market offers a spectrum of treatment modalities tailored to individual patient needs. Growing awareness of regenerative medicine principles and increasing pet ownership drive market demand.

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Technological advancements play a pivotal role in advancing animal stem cell therapy, facilitating cell isolation, expansion, differentiation, and delivery. Innovations such as automated cell culture systems, three-dimensional bioprinting, and gene editing technologies enhance the scalability and precision of stem cell-based treatments. Moreover, advancements in cryopreservation techniques ensure long-term storage and viability of stem cell products. The end-use industry encompasses veterinary clinics, research institutions, biotechnology companies, and pharmaceutical manufacturers. Collaborations between academia and industry drive translational research and commercialization of stem cell therapies. Moreover, partnerships between veterinary professionals and stem cell therapy providers enhance patient access and clinical outcomes.

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Geographic variations in the animal stem cell therapy market reflect differences in regulatory frameworks, healthcare infrastructure, and socioeconomic factors. While developed regions such as North America and Europe boast robust veterinary healthcare systems and regulatory pathways, emerging economies in Asia-Pacific and Latin America present untapped opportunities for market expansion. Moreover, the COVID-19 pandemic has influenced market dynamics, reshaping healthcare priorities and accelerating digital health solutions.

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"Charting the Course: Global Animal Stem Cell Therapy Market - openPR

Stem Cell Therapy Offers Hope for Paralyzed Dog’s Recovery – The Korea Bizwire

Dungdung running around after surgery when he temporarily recovered before his disc symptoms returned. (Image provided by KARA)

SEOUL, May 4 (Korea Bizwire) In a remarkable case highlighting the potential of stem cell treatments for animals, a dog named Dungdung who was paralyzed and unable to walk is regaining mobility after undergoing an innovative therapy in South Korea.

Dungdung was rescued in 2022 by the animal rights group KARA from a factory in Paju, where he had collapsed and could not move. Initially, after disk surgery and rehabilitation, the dog temporarily recovered the ability to walk.

However, within a year his condition relapsed, and he was diagnosed with paralysis of the hind legs, leaving him incontinent.

Seeking an alternative solution, KARA formed a partnership with the Medipet Animal Hospital, which specializes in treating severely ill and injured rescue animals through its animal regenerative medicine center.

Dungdung, who was immobilized when he was rescued. (Image: KARA)

Since March 2024, Dungdung has undergone two stem cell therapy sessions at Medipet, combined with water rehabilitation, cycling exercises, and laser treatments. The results have been astonishing.

The paralyzed legs regained nerve and muscle function, allowing Dungdung to slowly move them again, explained a regenerative medicine expert at Medipet. This shows stem cell therapy can open new possibilities for healing animals with severe, rare, and intractable conditions.

The expert expressed hope that this treatment could not only improve the health of suffering animals but provide a new lease on life for those who had lost hope.

The success of stem cell therapy marks significant progress in the animal welfare field, and we hope this technology can help save more animals, said Jeon Jin-kyung, head of KARA.

Dungdung was found at a factory in Paju.

The group will continue its rescue efforts for animals in distress while collaborating with Medipet on Dungdungs ongoing treatment.

We desperately hope that through intensive care, Dungdung will be able to walk again, said Kim Hyun-jung, director of KARAs animal hospital. Kim emphasized that stem cell therapy could substantially improve quality of life and alleviate symptoms for elderly animals, those who suffered abuse, or were injured in accidents.

She added it represents an important step in enhancing welfare for unadopted senior animals within the organization by working with outside expert institutions.

Updates on Dungdungs pioneering stem cell treatment are being provided on KARAs website and official social media channels.

Dungdung undergoing aquatic rehabilitation therapy.

Lina Jang (linajang@koreabizwire.com)

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Stem Cell Therapy Offers Hope for Paralyzed Dog's Recovery - The Korea Bizwire

Stem-cell-based embryo models used to study human twinning PET – BioNews

Embryo models generated from human stem cells have provided insights into how identical twins develop.

Blastoids are stem-cell-based embryo models (SCBEMs) that resemble embryos at the blastocyst stage (see BioNews 1020, 1088, 1091, 1124, 1204). Researchers at the MERLN Institute for Technology-Inspired Regenerative Medicine, at Maastricht University in the Netherlands, have studied the conditions under which single blastoids and 'twin' blastoids can form. Currently, little is understood about the mechanisms that lead to the formation of monozygotic twin embryos, which is something that occurs more frequently following IVF and that can be associated with pregnancy complications.

'Blastoids are stem-cell-derived in vitro models of the blastocyst stage of embryogenesis,' Dorian Luijkx, from the MERLN Institute and lead author of the study published in Advanced Materials, explained.

To generate blastoids, the researchers seeded stem cells into parallel microwells with transparent walls, which are flat plates with multiple wells used as small test tubes. Within each well, the stem cells clustered together to form structures which the researchers monitored and imaged as they grew. By adding a different combination of growth factors and chemicals to each well, the researchers were able to optimise the conditions for growing twin blastoids on a large scale.

The researchers found that seeding a higher number of stem cells per microwell increased the formation of twin blastoids. They also found that adding a high concentration of chemicals to promote stem cell differentiation into the trophectoderm, which is the outer layer of a blastocyst that goes on to form the placenta, increases the formation of twin blastoids. For this reason, the researchers suggest that rapid expansion of the trophectoderm may be a crucial event leading the inner cell mass to split and form twin blastoids. A similar process may be at work when twinning occurs during the development of embryos.

'We aim to delve deeper into the molecular and biophysical mechanisms that underlie the splitting of the inner cell mass, as these may give us clues as to how twinning rates in assisted reproductive technology can be reduced or completely avoided,' Dr Stefan Giselbrecht, one of the senior authors of the study, said.

To study embryo implantation, single and twin blastoids were moved to a microfluidic chip that contained a small sample of uterine tissue. The scientists noted that the twin blastoids adhered to the uterine tissue at a higher rate than the single blastoids, which Dr Giselbrecht added 'may suggest an advantage for a twin embryo in the implantation stage of development'.

Because blastoids and other SCBEMs are similar to but also different from human embryos, they can pose distinct ethical and regulatory challenges. Last year, the Health Council of the Netherlands recommended that some SCBEMs should be subject to the same regulation as human embryos, while other SCBEMs should not (see BioNews 1214).

In the UK, a project is underway to develop a recommended governance framework for research involving SCBEMs (see BioNews 1194). As part of this project, a public dialogue report has been published exploring what members of the public think and know about SCBEMs (see BioNews 1234). This report is due to be followed by the publication of a Code of Practice for UK research involving SCBEMs.

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Stem-cell-based embryo models used to study human twinning PET - BioNews

Stem cell-based embryo models: addressing the governance gap PET – BioNews

Stem-cell-based embryo models (SCBEMs) are, as the term suggests, similar to embryos in some respects but different from embryos in other respects. This is what makes SCBEMs so fascinating and useful in research, but this is also what makes them challenging to think about. Adding to the challenge is the existence of a large (and growing) variety of SCBEMs, which can differ considerably in their nature and extent of similarity to human embryos.

Perhaps unsurprisingly, the question of how best to categorise different SCBEMs and assess their most significant attributes is not fully settled. Arriving at a satisfactory answer to this question involves an interplay between scientific, ethical, regulatory and other considerations that is as subtle, in its way, as the interplay between biological phenomena that enables scientists to create SCBEMs in the first place.

All of this has led to some uncertainty regarding what rules should apply to research involving SCBEMs, and whether established rules are sufficient or whether new rules are called for. It became increasingly apparent to both of us, and to the organisations where we work respectively, the Progress Educational Trust (PET, the charity that publishes BioNews) and Cambridge Reproduction (an interdisciplinary initiative that brings together researchers across Cambridge) that there is a need for clearer guidance on the way SCBEMs can, and should, be used in UK research.

This need became particularly apparent at two workshops organised by Cambridge Reproduction in 2022, at which key figures from a wide variety of disciplines suggested that there should be some form of dedicated governance for SCBEM-related research in the UK. A major concern expressed at those workshops was that failure to establish dedicated governance would jeopardise research on (at least) two fronts it threatened to undermine public trust in research, and it was already undermining the confidence of researchers themselves, who wanted to know the boundaries within which they could pursue their work.

In order to address this pressing need for governance, PET and Cambridge Reproduction collaborated in 2023 to launch a project called Governance of Stem Cell-Based Embryo Models (G-SCBEM). For the past year, this project has been developing a Code of Practice for UK research involving SCBEMs (see BioNews 1194).

Work on the Code of Practice is drawing upon the insights of experts and practitioners from various areas of science, law and ethics, both within the UK and overseas. This sort of input is necessary, if the G-SCBEM Code of Practice is to be robust and credible, but it is not sufficient. A vital element that has to be included is the contribution of the general public.

The G-SCBEM Code of Practice will set out things that researchers ought to do and ought not to do so as to meet ethical standards, demonstrate responsibility and transparency, and take account of public hopes, concerns and sensitivities. If these stipulations are to be meaningful, then the Code of Practice must be informed by an accurate sense of how people understand the relevant ethical considerations, what people think is adequate in relation to demonstrating transparency, and what people's hopes, concerns and sensitivities actually are.

For all of these reasons and more, we were delighted to collaborate with social research agency Hopkins Van Mil and other colleagues (with support from Sciencewise and from the Biotechnology and Biological Sciences Research Council) on a recent public dialogue about SCBEMs. The content and findings of this public dialogue are presented in a new report.

Although the dialogue concerned SCBEMs, all of its public participants had previously participated in a 2023 public dialogue about human embryo research, which was conducted as part of the Human Developmental Biology Initiative (see BioNews 1213). This meant that participants had already had occasion to reflect in depth on the science and ethics of research involving human embryos. This left them well-placed to consider whether, and in what respects, research involving SCBEMs should be regarded differently.

Of course, public views are liable to evolve and the science is developing rapidly, so the G-SCBEM Code of Practice will be revised periodically to take account of the latest developments. But we are keen that the views of the wider public, as well as the views of the other stakeholders in our orbit, should inform the Code of Practice at the very outset. It is thanks to the public dialogue that we will be able to ensure that this is the case.

A growing number of projects, besides ours, are exploring ethical and policy dimensions of SCBEMs. In the UK, there has been a recent briefing on the subject by the Parliamentary Office of Science and Technology, and there is also a project underway from the Nuffield Council on Bioethics. Elsewhere, public perceptions of SCBEMs have recently been explored in the Netherlands, while the International Society for Stem Cell Research is building on its important earlier guidance in this area. We hope that the publication of this public dialogue report, and the imminent publication of the G-SCBEM Code of Practice, will help to establish a clearer context for all of these discussions.

Finally, we wish to conclude by expressing our heartfelt gratitude to the participants in the SCBEM public dialogue. As you will read in the public dialogue report, these participants were asked to consider some of the most cutting-edge achievements and conundrums in present-day research and policy, thinking through and weighing up both the related opportunities and the related risks. This was no easy task, but the insights that they offered in response were and are invaluable.

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Stem cell-based embryo models: addressing the governance gap PET - BioNews

Human stem-cell-based therapy for Parkinson’s disease proven safe PET – BioNews

A small clinical trial involving 12 patients with Parkinson's disease has reported no safety concerns with a newly developed human stem-cell-based therapy.

The therapy called TED A9 was delivered as a cell transplant injected directly into the brain of the participants as part of a Phase 1/2a clinical trial, which is principally concerned with assessing safety and dosing requirements.

The drug's developer, S.Biomedics, in Seoul, South Korea, claimed in a press release: 'According to Professor Jin-Woo Chang, [the principal investigator of the transplant conducted at Severance Hospital, Seoul,] none of the 12 Parkinson's disease participants had any side effects, complications, or unusual adverse reactions following the transplantation of TED-A9'.

The trial participants were aged between 50 and 75 years old, had been diagnosed with Parkinson's disease for more than five years, and had already motor complications such as freezing of gait or dyskinesia.

To ensure and monitor the safety of the treatment, an initial three patients were injected with a low dose (3.15 million cells) and monitored for three months, before another three patients were treated at high dose (6.3 million cells) and also monitored for three months.

No side effects, complications, or unusual adverse reactions were seen in either group during the three-month assessment period. Therefore, the clinical trial continued by adding three further patients to each of the low-dose and high-dose groups. Again, no safety concerns were seen.

Parkinson's symptoms are caused by the progressive loss of neurons that produce dopamine, a major chemical messenger in the brain. The TED-A9 therapy contains dopaminergic progenitor (precursor) cells, which had themselves been derived in the lab from embryonic stem cells.

The drug developers at S.Biomedics hope that the dopaminergic precursor cells in TED-A9 will treat Parkinson's disease by replacing the mature dopamine-producing nerve cells that are lost in patients.

Professor Dong-Wook Kim, a neurosurgeon and the principal developer of TED-A9, said: 'We have developed a fundamental therapeutic mechanism that directly replaces dopaminergic neurons lost in patients with Parkinson's disease. TED-A9 could represent a fundamental treatment that surpasses current therapies, which only temporarily alleviate the symptoms of Parkinson's disease,'.

The trial is expected to continue until February 2026, allowing safety of the therapy to be monitored for a total of five years. As part of the study, exploratory efficacy will also be examined for two years using clinical measures of motor symptoms and a patient questionnaire of daily life quality.

More Information is available at ClinicalTrials.gov.

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Human stem-cell-based therapy for Parkinson's disease proven safe PET - BioNews

Canine Stem Cell Therapy Market to Hit US$ 300.1 Million by 2034: Fact.MR Report – ForexTV.com

Canine Stem Cell Therapy Market to Hit US$ 300.1 Million by 2034: Fact.MR Report  ForexTV.com

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Canine Stem Cell Therapy Market to Hit US$ 300.1 Million by 2034: Fact.MR Report - ForexTV.com

The Future of Dog Health: Scientists Develop Unprecedented Painless Method To Reprogram Canine Stem Cells – SciTechDaily

Researchers at Osaka Metropolitan University have innovatively reprogrammed canine stem cells from urine to create induced pluripotent stem cells (iPSCs) without feeder cells. This breakthrough in non-invasive, pain-free stem cell generation paves the way for new advancements in veterinary regenerative medicine and genetic disease research, offering hope for treating previously incurable diseases in dogs. Credit: Shingo Hatoya, Osaka Metropolitan University

Dog owners may need to learn to appreciate their best friends urine. Researchers at Osaka Metropolitan University have developed a new method thats efficient, non-invasive, and painless for reprogramming stem cells from dogs urine. This breakthrough paves the way for advancements in veterinary regenerative treatments for our four-legged companions.

Induced pluripotent stem cells (iPSCs) have been widely employed in studies on human generative medicine. With the growing importance of advanced medical care for dogs and cats, there is an expectation that new therapies utilizing iPSCs will be developed for these companion animals, just as they have been for humans.

Unfortunately, canine somatic cells exhibit lower reprogramming efficiency compared to those of humans, limiting the types of canine cells available for generating iPSCs. IPSC induction often involves using feeder cells from a different species. However, considering the associated risks, minimizing xenogeneic components is often advisable, signifying the need to improve the efficiency of reprogramming various types of canine cells in dogs without using feeder cells.

A research team led by Professor Shingo Hatoya and Dr. Masaya Tsukamoto from the Graduate School of Veterinary Science at Osaka Metropolitan University has identified six reprogramming genes that can boost canine iPSC generation by about 120 times compared to conventional methods using fibroblasts. The iPSCs were created from urine-derived cells using a non-invasive, straightforward, and painless method.

Additionally, the researchers succeeded in generating canine iPSCs without feeder cells, a feat that had been impossible until now. The team aims to disseminate their findings in the global research community, contributing to advances in regenerative medicine and genetic disease research in veterinary medicine.

As a veterinarian, I have examined and treated many animals, explained Professor Hatoya. However, there are still many diseases that either cannot be cured or have not been fully understood. In the future, I am committed to continuing my research on differentiating canine iPSCs into various types of cells and applying them to treat sick dogs, hopefully bringing joy to many animals and their owners.

Reference: Generation of canine induced pluripotent stem cells under feeder-free conditions using Sendai virus vector encoding six canine reprogramming factors by Masaya Tsukamoto, Kazuto Kimura, Takumi Yoshida, Miyuu Tanaka, Mitsuru Kuwamura, Taro Ayabe, Genki Ishihara, Kei Watanabe, Mika Okada, Minoru Iijima, Mahito Nakanishi, Hidenori Akutsu, Kikuya Sugiura and Shingo Hatoya, 21 December 2023, Stem Cell Reports. DOI: 10.1016/j.stemcr.2023.11.010

The study was funded by the Japan Society for the Promotion of Science, the Japan Science and Technology Agency, Anicom Specialty Medical Institute, Inc, and Osaka Metropolitan University.

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The Future of Dog Health: Scientists Develop Unprecedented Painless Method To Reprogram Canine Stem Cells - SciTechDaily

Animal Stem Cell Therapy Market to Expand at a 5.2% CAGR through 2032, Reaching a Valuation of US$437.3 Million | Persistence Market Research -…

Animal Stem Cell Therapy Market to Expand at a 5.2% CAGR through 2032, Reaching a Valuation of US$437.3 Million | Persistence Market Research  ForexTV.com

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Animal Stem Cell Therapy Market to Expand at a 5.2% CAGR through 2032, Reaching a Valuation of US$437.3 Million | Persistence Market Research -...

Gallant Therapeutics Raises Over $15 Million in Series A Funding to Advance Pipeline of "Off-the-Shelf" Stem Cell … – Yahoo Finance

Gallant Therapeutics Raises Over $15 Million in Series A Funding to Advance Pipeline of "Off-the-Shelf" Stem Cell ...  Yahoo Finance

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Gallant Therapeutics Raises Over $15 Million in Series A Funding to Advance Pipeline of "Off-the-Shelf" Stem Cell ... - Yahoo Finance

Dogs can now get painless stem cell therapy – Earth.com

Dog owners might find a new reason to value their pets urine, thanks to groundbreaking research from Osaka Metropolitan University involving canine stem cell therapy.

A team of scientists has developed an innovative method to reprogram stem cells from canine urine, marking a significant step forward in veterinary regenerative treatments. This non-invasive and pain-free technique could revolutionize how we approach our furry friends healthcare.

In the realm of human medicine, iPSCs have been a cornerstone in regenerative studies. Recognizing the growing need for advanced medical treatments for pets, researchers anticipate similar breakthroughs for dogs and cats using iPSCs. However, a challenge has been the lower reprogramming efficiency in canine cells compared to human cells, limiting the potential applications in veterinary medicine.

Traditionally, iPSC induction often requires feeder cells from different species, which poses certain risks. The Osaka Metropolitan University research team, led by Professor Shingo Hatoya and Dr. Masaya Tsukamoto, tackled this issue head-on.

They identified six reprogramming genes that enhance canine iPSC generation by approximately 120 times using urine-derived cells compared to conventional fibroblast methods. This achievement is notable not only for its efficiency but also for eliminating the need for feeder cells.

The creation of iPSCs from urine is a significant milestone, offering a straightforward and humane method for cell collection. This advancement opens doors to new therapies in regenerative medicine and genetic disease research in veterinary science. The research team is eager to share their findings globally, hoping to enrich the field of veterinary medicine significantly.

Professor Hatoya, reflecting on his career and the limitations in treating various animal diseases, expressed his commitment to this research.

As a veterinarian, I have examined and treated many animals. However, there are still many diseases that either cannot be cured or have not been fully understood. In the future, I am committed to continue my research on differentiating canine iPSCs into various types of cells and applying them to treat sick dogs, hopefully bringing joy to many animals and their owners, Hatoya concluded.

This groundbreaking research not only exemplifies scientific innovation but also highlights the deep bond between humans and their canine companions, offering hope for more effective treatments in veterinary medicine.

As discussed above, stem cell therapy represents a significant leap in medical science, offering potential treatments for various diseases and injuries.

Stem cells are unique cells capable of transforming into various cell types in the body. They play a crucial role in the bodys healing process. There are two primary types of stem cells:

Stem cell therapy involves using stem cells to repair or replace damaged tissues or cells in the body. This process typically includes:

Stem cell therapy has a wide range of applications, including:

Stem cell therapy, particularly involving embryonic stem cells, faces ethical debates and regulatory hurdles. Concerns revolve around the moral implications of using embryonic cells and the need for stringent regulations to oversee stem cell research and therapy.

Advancements in stem cell research continue to unveil new potential therapies. Areas like iPSCs (induced pluripotent stem cells) are showing promise, as they can be generated directly from adult cells, circumventing ethical concerns associated with embryonic stem cells. The future of stem cell therapy holds promise for personalized medicine, where treatments are tailored to individual genetic profiles.

In summary, stem cell therapy is an exciting field of medicine with the potential to revolutionize treatment for various diseases and injuries. While it offers significant benefits, challenges and ethical concerns must be addressed to fully realize its potential. As research progresses, stem cell therapy may become a cornerstone in the treatment of many currently incurable diseases, heralding a new era in medical science.

The full study was published in the journal Stem Cell Reports.

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Dogs can now get painless stem cell therapy - Earth.com

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