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Monthly Archives: July 2022
Kringle Pharma : Research Collaboration with Kyoto University in Biomaterial-assisted Regenerative Medicine using HGF – Marketscreener.com
Posted: July 3, 2022 at 2:35 am
Press release 1 July 2022
Research Collaboration with Kyoto University in Biomaterial-assisted
Regenerative Medicine using HGF
Kringle Pharma, Inc. (Head office located in Osaka, Japan; President & CEO, Kiichi Adachi; "KRINGLE"), a late clinical-stage biopharmaceutical company, today announces signing of collaborative research agreement with Kyoto University (Located in Kyoto, Japan) focused on applied research combining HGF with biomaterials to create novel regenerative medicine products.
Professor Yasuhiko Tabata, Laboratory of Biomaterials, Institute for Life and Medical Sciences, Kyoto University, is a renowned leading scientist in the field of regenerative medicine utilizing biomaterials. Professor Tabata and KRINGLE jointly initiate applied research on regenerative medicine based on the biomaterial technologies and KRINGLE's recombinant human HGF (development code: KP-100). The goal of this collaboration is to develop biomaterial-assisted regenerative medicine using HGF for the treatment of incurable diseases.
Regenerative medicine is a treatment method that promotes the functional regeneration of tissues and organs by administering cells and other materials prepared outside the body to the damaged tissues or organs. In recent years, research on stem cell transplantation therapy using iPS cells and other stem cells has been attracting attention. The importance of biomaterials in regenerative medicine has been recognized, and intensive research is being conducted not only on their function as a scaffold for transplanted cells, but also on the combined use of drug delivery systems (DDS) technology and drugs to efficiently reach target cells, improve stability in vivo, and control drug release.
HGF is an endogenous biological protein responsible for the regeneration and repair of tissues and organs. Previous studies revealed that HGF administration resulted in functional recovery in animal models for various diseases. KRINGLE has been developing KP-100 for incurable diseases such as acute spinal cord injury, ALS, vocal fold scar and acute kidney injury. Through this collaboration, KRINGLE aims to maximize the therapeutic potential of HGF, expanding target indications over the existing pipelines, eventually providing novel therapies for patients suffering from incurable diseases.
About Hepatocyte Growth Factor (HGF)
HGF was originally discovered as an endogenous mitogen for mature hepatocytes. Subsequent studies demonstrated that HGF exerts multiple biological functions based on its mitogenic, motogenic, anti-apoptotic, morphogenic, anti-fibrotic and angiogenic activities, and facilitates regeneration and protection of a wide variety of organs including not only liver, but also kidneys, heart, lungs, nerve tissues and skin.
About Biomaterials
Biomaterials are materials that are used in the body by itself or in combination with biological components including cells, proteins, nucleic acids or bacteria. Biomaterial technologies (e.g., scaffold to promote the formation of biological tissues, DDS technology to enhance the biological activity of proteins and genes that have cell differentiation and proliferation effects, etc.) can be utilized to enhance the regenerative and repair
capabilities of biological tissues.
Source: Yasuhiko Tabata, "Regenerative medicine in terms of DDS technology - Regenerative therapy and regenerative research," (2015)
About Kringle Pharma, Inc. https://www.kringle-pharma.com/en/
Kringle Pharma is a late clinical-stage biopharmaceutical company established in December 2001 to develop novel biologics based on HGF. Currently, Kringle's clinical programs with recombinant human HGF are: 1) Phase 3 ongoing in acute spinal cord injury, 2) investigator-initiated Phase 2 ongoing in ALS, 3) Phase 2/3 in preparation in vocal fold scar, and 4) Phase 1a and 1b completed in acute kidney injury. Kringle's mission is to contribute to societal and global healthcare through the continued research, development and commercialization of HGF drug for patients suffering from incurable diseases.
For more information, please contact
Daichika Hayata
Director, Pharmaceutical Development
Kringle Pharma, Inc.
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Kringle Pharma : Research Collaboration with Kyoto University in Biomaterial-assisted Regenerative Medicine using HGF - Marketscreener.com
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Vascudyne Receives BioBusiness Award from Regenerative Medicine Minnesota for Treatment of Nerve Injury – – Benzinga
Posted: July 3, 2022 at 2:35 am
St. Paul, M.N.
--News Direct--
Vascudyne, Inc., a biotechnology trailblazer in regenerative medicine, announced today that it was awarded a grant from Regenerative Medicine Minnesota for a project titled "Development of a Peripheral Nerve Wrap Using Regenerative Engineering Tissue Tube".
The one-year, $100,000 grant will commence in June 2022 and utilize Vascudyne's TRUE Tissue technology that is unique and 100% natural. The TRUE Tissue allogeneic biomaterial is completely biological, non-immunogenic and regenerates by the host. Nothing synthetic or artificial is ever used in the manufacturing process, in contrast to other regenerative medicine soft tissue biomaterials made from synthetic polymer-based scaffolds that slowly degrade in the body and may lead to adverse immune response.
Chronic nerve compression is one of the most common peripheral nerve injuries with carpal tunnel syndrome being the most common type of nerve compression affecting 3-6% of the general population. Tissues isolated from the patient are used in surgery but have shortcomings such as donor site morbidity, limited availability, and risk of surgical complications.
"We are excited to expand our TRUE Tissue platform technology to other soft tissue applications such as nerve repair," said Rick Murphy, Vascudyne's Chief Operating Officer. "The exquisite regenerative properties of our 100% biological biomaterial combined with its non-immunogenic properties and off-the-shelf availability are a perfect fit for addressing the challenging nerve injury applications. Demonstrating these benefits in a preclinical nerve injury model will greatly advance the field of peripheral nerve injury and offer a promising alternative to current treatments that often lack complete and functional nerve repair."
Vascudyne has prioritized commercialization of its cardiovascular products and recently announced the first clinical results of its regenerative vascular conduit for hemodialysis access. "While we are initially focusing on cardiovascular applications for our TRUE Tissue technology, we continue research and development efforts in other soft tissue applications such as nerve injury repair," stated Dr. Zeeshan Syedain, Vascudyne's Chief Scientific Officer. "This grant from the Regenerative Medicine Minnesota will help accelerate our preclinical animal study timeline and demonstrate safety and efficacy of the TRUE Tissue technology as a peripheral nerve wrap."
Vascudyne licensed its proprietary TRUE Tissue technology developed by world renowned tissue engineering leader Robert Tranquillo, PhD, Distinguished McKnight University Professor, and his colleagues from the University of Minnesota in 2017.
TRUE Tissue products are not available for commercial sale.
About Vascudyne
Headquartered in the heart of Medical Alley in Minnesota, Vascudyne is on a mission to improve patient care with regenerative biomaterials that are inspired by nature. Vascudyne, a privately held company founded in 2014, uses the TRUE Tissue technology to develop TRUE to Nature biomaterials for soft tissue repair and replacement. For more information, please visit https://www.vascudyne.com/.
About TRUE Tissue Technology
TRUE Tissue is developed from cells isolated from donor tissue and is 100% biological. There are no synthetic materials or chemical fixation used, and implanted tissues are completely cell-derived and acellular. The TRUE Tissue technology can be readily shaped into tubes, sheets, and other geometries making it suitable for many soft tissue applications, is mechanically comparable to native tissues, and is a ready to use, off-the-shelf allograft.
Forward Looking Statements
This announcement contains forward-looking statements. Such statements may include, without limitation, statements identified by words such as "projects," "may," "will," "could," "would," "should," "believes," "expects," "anticipates," "estimates," "intends," "plans," "potential" or similar expressions. These statements relate to future events or Vascudyne's clinical development programs, reflect management's current beliefs and expectations and involve known and unknown risks, uncertainties and other factors that may cause Vascudyne's actual results, performance or achievements to be materially different. Vascudyne undertakes no obligation to publicly update any forward-looking statements, whether as a result of new information, future presentations or otherwise, except as required by applicable law.
Vascudyne, Inc.
Sandy Williams, Marketing Director
+1 952-412-5975
View source version on newsdirect.com: https://newsdirect.com/news/vascudyne-receives-biobusiness-award-from-regenerative-medicine-minnesota-for-treatment-of-nerve-injury-723124309
2022 News Direct Corp.
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CDL’s new global Advanced Therapies stream brings together industry leader CCRM, four top universities on two continents – GlobeNewswire
Posted: July 3, 2022 at 2:35 am
Toronto, Ontario, Canada, June 30, 2022 (GLOBE NEWSWIRE) -- Creative Destruction Lab (CDL) is launching a new Advanced Therapies stream for pre-seed and seed-stage ventures at the forefront of biotech. To bring this program to life, CDL has partnered with CCRM, a leader in accelerating the development and commercialization of regenerative medicine-based technologies.
Advanced Therapies will be launched at four world-class CDL locations the University of British Columbia, the University of Oxford, the University of Toronto, and the University of Wisconsin-Madison creating an international network that will foster the next generation of biotech companies.
Health tech is fundamentally changing treatment strategies the targeting of general symptoms in broad populations is being replaced by highly targeted therapies, and potential cures, in more refined patient subgroups. This sea change is a result of advancements in both molecular techniques and the analysis of biological data. CDL alumni ventures are among those companies at the forefront.
Advanced Therapies is for founders leveraging cell and gene therapies, biologics, antibody-drug conjugates, and other biological products to innovate solutions to biological, medical, and health-care issues.
CDLs Advanced Therapeutics stream combines a proven model for success and a founder-friendly mindset with a core group of biotech mentors who know what it takes to bring these therapies to patients. Adding CCRMs capabilities and expertise is like rocket fuel to accelerate the trajectory of these cutting-edge companies, said Dawn Bell, a CDL Health mentor and Global Development Head, Strategic Partnerships at Novartis.
This new stream will bring together entrepreneurs, investors, and scientists with expertise building massively scalable companies. Selected participants will work with these mentors to sharpen objectives, prioritize time and resources, raise capital, and build networks with experts working on the frontiers of research.
The growing number of startup founders working in advanced therapies, including CDL alumni such as Notch Therapeutics, have proven that Advanced Therapies is a necessary addition to CDLs programming. CDL is partnering with CCRM for the launch of this new stream.
Health tech is rapidly evolving to better serve people around the world. CDL, in partnership with CCRM, is eager to support cutting-edge research and founders who are looking to advance therapeutics and innovate the healthcare landscape, said Sonia Sennik, Executive Director at CDL.
CCRM, a global public-private partnership located in Toronto, Canada, has a deep network of researchers, investors, leading companies, and entrepreneurs that have been supporting the establishment of early-stage companies for a decade.
I always envisioned that CDL and CCRM would join forces to enhance early-stage company creation and company scaling in the area of advanced therapies, said Michael May, President and CEO, CCRM.
CCRM has a unique global position in this space. And I believe CDL is developing a best-in-class process of its own so it just seemed like a perfect marriage of skills, interests, and track record to partner in one of the hottest areas in biotech.
In addition to harnessing the global networks of CDL and CCRM, Advanced Therapies will leverage the academic and scientific communities of four leading institutions in North America and Europe. Each brings its own deep expertise and standout network in the field:
Join a CDL Health webinar to learn more. Companies and founders interested in applying to the Advanced Therapies stream can contact health@creativedestructionlab.com for more information. Applications will be accepted online until August 31, 2022.
About Creative Destruction Lab
Creative Destruction Lab (CDL) is a nonprofit organization that delivers an objectives-based program for massively scalable, seed-stage, science- and technology-based companies. Its nine-month program allows founders to learn from experienced entrepreneurs, increasing their likelihood of success. Founded in 2012 by Professor Ajay Agrawal at the University of Torontos Rotman School of Management, the program has expanded to 12 sites across six countries. Participating ventures have created $20 billion (CAD) in equity value.
About Centre for Commercialization of Regenerative Medicine
CCRM is a global, public-private partnership headquartered in Canada. It receives funding from the Government of Canada, the Province of Ontario, and leading academic and industry partners. CCRM supports the development of regenerative medicines and associated enabling technologies, with a specific focus on cell and gene therapy. A network of researchers, leading companies, strategic investors and entrepreneurs, CCRM accelerates the translation of scientific discovery into new companies and marketable products for patients, with specialized teams, funding and infrastructure. CCRM is hosted at its Toronto site by the University of Toronto and is the commercialization partner of Medicine by Design. Visit us at ccrm.ca.
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CDL's new global Advanced Therapies stream brings together industry leader CCRM, four top universities on two continents - GlobeNewswire
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3D Bioprinting Market: Rise in Prevalence of Regenerative Therapies to Drive the Global Market – BioSpace
Posted: July 3, 2022 at 2:35 am
Wilmington, Delaware, United States: Additive manufacturing or 3D printing is witnessing innovations left, right and center. In various industries such as education, manufacturing, engineering, and medical, the use is extensive. It is pertinent to note here that it is the printing of biomaterials such as cells, components etc. in three dimension and that while it is a new area, it has made notable advancement in the past few years.
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It is important to note here that basis the kind of material, approach of bioprinting changes. It also changes according to cell types, cell growth factors, and other complexities relating to living tissues. This happens because there is a need for process to be sensitive to differences in these cells.
The domain of 3D bioprinting comes into play in a number of disciplines. Some of these include cell biology, physics, biomaterial sciences, and engineering. And, this process can also be use by experts in these fields and researchers so a wide variety of tissue can be developed. Designing and sizing of bones, vascular grafts, multi-layered skin, cartilaginous structure, tracheal splints, and cardiac tissue. As 3D bioprinting is used widely in this field, market for the same will chart significant growth.
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Thus, it does not come as a surprise that as per a comprehensive market report brought out by Transparency Market Research (TMR), the global 3D bioprinting market is on a high growth trajectory over the forecast period of 2017 and 2025. The repost carries incisive insights on market dynamics and unravels trends and drivers that are shaping the landscape of the market over the coming years. Besides, it gives a peek into regional growth potential share, and opportunities, etc.
3D Bioprinting Market Key Trends and Drivers
Demand or high throughput models of tissue, used extensively in drug research and discovery processes, is all set to propel growth in the global bioprinting market. And, since pharmaceutical and biotechnology market are coextensive with 3D bioprinting, development in the former leads to growth in the latter. Here, it is worth noting that advanced drug screening is also adding to the growth curve of the global 3D bioprinting market in a positive manner.
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Additionally, extensive use in regenerative therapies which includes transplantation and generation will also underpin notable growth in the market. And, the advancements in regenerative medicine is also supporting this growth curve over the forecast period.
3D Bioprinting Market Key Players
The global 3D bioprinting market is fragmented and key players in the landscape include TeVido BioDevices, Rainbow Biosciences, 3D Systems, Inc., regenHU, EnvisionTEC GmbH, Stratasys Ltd., nScrypt, Inc., Regenovo Biotechnology Co., GeSiM, and Aspect Biosystems Ltd. These are profiled in the report and provide insight into strategies deployed by each to maintain a prominent hold over the global 3D bioprinting market.
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3D Bioprinting Market Regional Analysis
The regional analysis of the report is segmented into North America, Europe, Asia Pacific, Latin America, and Middle East and Africa. Europe and North America will account for a prominent share of the global bioprinting market. There is a high demand for 3D printing in advanced clinical applications in the region. It is important to talk here of the upscaling of research and development in biotechnology and pharmaceutical industry in a number of North American and European countries.
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Meet the newest grantees of the Cohen Translational Engineering Fund – The Hub at Johns Hopkins
Posted: July 3, 2022 at 2:35 am
ByDanny Jacobs
Two faculty teams with members affiliated with the Johns Hopkins Whiting School of Engineering have received grants for their research through the Cohen Translational Engineering Fund.
The fund, made possible by a generous commitment from Sherry and Neil Cohen '83, serves as a catalyst for translating cutting-edge research into practice by providing faculty with critical early funding. The grant is designed to help researchers move their work out of the laboratory and toward commercializationthe process includes developing patents, obtaining materials and supplies, and building prototypes.
"We are pleased to continue helping Whiting School of Engineering faculty advance their cutting-edge research," says Neil Cohen, who is also the founder of venture capital firm Emerald Development Managers. "Previous grantees are already realizing promising developments in their work, and we look forward to seeing this year's grantees further strengthen the pipeline of innovation and entrepreneurship coming out of the Whiting School of Engineering and Johns Hopkins."
Grantees receive a maximum of $100,000 for a nine-month project. Since its inception eight years ago, the Cohen Fund has awarded more than $1.3 million for 28 projects. Among the past recipients are LifeSprout, a regenerative medicine company; Ready Robotics, creator of operating software for industrial automation; Galen Robotics, which is developing steady-hand surgical robots; and Vectech, which is developing a surveillance system of cloud-connected smart mosquito traps.
A panel of experienced researchers, engineers, startup entrepreneurs, and business executives reviewed presentations from the five faculty finalists for this year's award in March.
"This year's recipients reflect the wide breadth of research done at the Whiting School and the key role that many Whiting faculty members play in cross-school collaborations," says Brian Stansky, senior director of FastForward. "Once again, the generous funding provided by Sherry and Neil Cohen will help multiple faculty members meaningfully move their academic research toward commercialization. We look forward to working with both recipient teams over the course of these projects and beyond."
The grantees are detailed below.
Principal investigator: Mark Foster, associate professor, Department of Electrical and Computer Engineering
The pitch: Monitoring 3D laser printing in real time to save manufacturers time and money
Laser powder bed fusion, or LPBF, is a 3D-printing process that uses high-powered lasers to rapidly melt and solidify metal powder into 3D objects such as heat sinks (which move heat away from a hot device) and jet fuel nozzles. The process, known as additive manufacturing, often leads to microscopic, random defects in the object, costing manufacturers time and money to replace parts.
Image caption: Mark Foster
Foster, working with Milad Alemohammad, a postdoctoral fellow, and Steven Storck, a senior materials scientist at the Johns Hopkins University Applied Physics Laboratory, has created novel, high-speed spectroscopic sensors that can be integrated into LPBF printing machines and provide real-time data so operators can correct defective layers as the object is being made.
The team developed the sensor at the request of collaborators at JHU APL's additive manufacturing center. They have received $250,000 in seed funding sponsored by the Army Research Laboratory and enabled by the MEDE+ AI-M program at the Hopkins Extreme Materials Institute, and they have taken part in the National Science Foundation's I-Corps program through Johns Hopkins Technology Ventures.
The team plans to use the funding to continue to refine its sensors as well as develop a user dashboard.
Principal investigators: Danielle Gottlieb Sen, director of pediatric cardiac surgery at Johns Hopkins Medicine and Youseph Yazdi, assistant professor of biomedical engineering and executive director of the Center for Bioengineering Innovation and Design
The pitch: Detecting a potentially deadly disease in infants and premature babies before symptoms appear
Image caption: Danielle Gottlieb Sen
Necrotizing enterocolitis, or NEC, is an often-fatal intestinal disease that disproportionately affects infants with congenital heart disease as well as premature babies. Treatment of NEC is most effective when started early, but currently, a diagnosis is confirmed only after symptoms appear, at which point substantial damage may already have occurred. Treatment can involve extended hospital stays or surgeries, and NEC can cause lifelong complications.
Image caption: Youseph Yazdi
Gottlieb Sen and Yazdi, working with Ellen Roche, on faculty at the Institute for Medical Engineering & Science at the Massachusetts Institute of Technology, are developing a noninvasive device that goes on a baby's belly to monitor intestinal ischemia, inadequate blood flow that is a known biomarker of the onset of NEC. The device, which will connect to bedside monitors, uses near-infrared spectroscopy, or NIRS, sensors to continuously record, store, and transmit data.
The team is building NIRS sensors that account for differences in pediatric patient size, and they are mapping pediatric intestine and vascular beds to ensure monitoring specificity. Their work could serve as a platform to develop accurate NIRS sensors for others tissues and diseases.
The team plans to use the funding to build the device as well as obtain results to start the process of receiving device approval from the U.S. Food and Drug Administration.
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Doctors Clinic welcomes new patients who are ready to improve their quality of life – Digital Journal
Posted: July 3, 2022 at 2:35 am
Patients struggling with weight loss can look no further than the Doctors Clinic, and specifically the practice of Gerald Parker, DO.
For patients who have tried dieting but failed to lose weight and keep it off, its time to try something different. At Doctors Clinic in Amarillo, Texas, Gerald Parker, DO has been helping patients of all ages lose weight for over 39 years with personalized medical weight loss programs. If youre ready to commit to your health and finally get rid of your extra pounds, contact Doctors Clinic or make an appointment online today.
What do medical weight loss programs include?
Doctors Clinic has a unique approach to weight loss. The providers dont rely on fads or gimmicks they help you change your relationship with food so you can follow a sensible, delicious, and sustainable diet and incorporate safe, moderate exercise into your daily routine.
Health assessment
Your doctor provides an exam and testing to identify how much weight you need to lose and whether you have any conditions that will affect your weight loss journey. They also track your blood pressure and glucose and cholesterol levels so you can see more improvements than just the number on the scale.
Meal planning
Your doctor helps you create a nutritious meal plan using real food that you buy at the grocery store. They can help you adjust your diet to get through plateaus or add variation if you need it. They also teach you about macros, nutrients, and other details to consider when choosing food.
Motivation
Making changes is challenging, but Doctors Clinic is in your corner every day. You have regular appointments to check your progress and adjust your program as necessary. You have small goals to keep you motivated as you work toward your ideal weight. Trust the medical weight loss program your doctor believes in your success.
Dr. Parker has been a guest speaker at national physician meetings including those for physicians specializing in weight loss. His nearly four decades of providing expert guidance and personalized care to patients put him at the forefront of medical professionals with the acumen to ensure every patient meets their goal.
Doctors Clinic offers cutting-edge regenerative and integrative medicine therapies to address each patients individual needs. A holistic, patient-focused approach helps patients address issues ranging from allergies and pain to weight management, while also enhancing their overall health and well-being.
Doctors Clinic welcomes new patients who are ready to improve their quality of life with personalized care and work with a true wellness partner. Appointments are available by calling the practice or using the online scheduling tool.
About Doctors Clinic:
Doctors Clinic, in Amarillo, Texas, is a state-of-the-art practice providing comprehensive health services for adult patients and specializing in regenerative medicine. Gerald Parker, DO is an experienced and compassionate provider who is committed to helping patients look and feel their best. The practice is happy to help patients on their wellness journey, whether theyre looking to enhance their health or if they need support to recover from injuries or diseases quickly and safely.
Media ContactCompany Name: Doctors ClinicContact Person: Gerald ParkerEmail: Send EmailPhone: (806) 355-8263Country: United StatesWebsite: Doctorsclinicamarillo.com
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Stem Cell Transplant Reverses Sickle Cell Disease in Adults
Posted: July 3, 2022 at 2:34 am
At a Glance
Sickle cell disease is an inherited blood disorder that affects more than 90,000 Americans, mostly of African descent. The condition arises from a genetic defect that alters the structure of hemoglobin, the oxygen-carrying protein found in red blood cells. The modified hemoglobin causes normally round red blood cells to become stiff, sticky, and sickle-shaped. The deformed cells can block blood flow, causing severe pain, organ damage, and stroke.
There is no widely available cure for sickle cell disease. Some children with the disease have been successfully treated with blood stem cell, or bone marrow, transplants. This approach, though, was thought to be too toxic for use in adults. High doses of chemotherapy are used to destroy all of a childs bone marrow, which is then replaced with marrow from a donor. Stem cell recipients typically need to take immunosuppressants for months to a few years. These medications can cause serious side effects.
In earlier studies, transplant recipients were found to have a mix of their own and the donors cells in their blood. Despite the mix, sickle cell disease was reversed. Based in part on these findings in children, as well as other preliminary work, a team at NIHs Clinical Center in Bethesda, Maryland, set out to test a modified transplant procedure in adults with sickle cell disease. The clinical trial was conducted by researchers from NIHs National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) and National Heart, Lung, and Blood Institute (NHLBI). Results appeared online on July 1, 2014, in the Journal of the American Medical Association.
Thirty patients, ages 16 to 65, with severe sickle cell disease enrolled in the study between 2004 and 2013. The patients first underwent a less toxic regimen to kill off some of their marrow cells. They then underwent a stem cell transplant, receiving cells donated by a healthy brother or sister.
The team found that the stem cell transplant reversed the disease in 26 of 30 patients (87%). The patients had normal hemoglobin, fewer hospitalizations, and lower use of narcotics to treat pain from the disease. The patients didnt experience graft-versus-host diseasein which donor cells attack the recipientafter a median follow up of 3.4 years. Fifteen patients successfully stopped immunosuppression medications a year after the transplant. The treatment was unsuccessful in 4 patients, and some complications, such as infections, occurred.
Side effects caused by immunosuppressants can endanger patients already weakened by years of organ damage from sickle cell disease, says senior author Dr. John Tisdale. Not having to permanently rely on this medication, along with use of the relatively less-toxic partial stem cell transplant, means that even older patients and those with severe sickle cell disease may be able to reverse their condition.
The researchers continue to follow the patients to track the success of the approach. People with sickle cell disease interested in joining NIH blood stem-cell transplant studies may call 1-800-411-1222 or visit the NIH clinical trials registry at https://clinicaltrials.gov for more information.
Funding:NIHs National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) and National Heart, Lung, and Blood Institute (NHLBI).
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Tisch Multiple Sclerosis Research Center of New York Study Featured in BioSpace – Business Wire
Posted: July 3, 2022 at 2:33 am
NEW YORK--(BUSINESS WIRE)--The Tisch Multiple Sclerosis Research Center of New York, the worlds largest independent research center focusing on MS, is proud to announce that its FDA-approved stem cell treatment study was featured in an article in BioSpace.
Preliminary analysis of the study results found that stem cell treatments substantially improved muscle strength and disability scores, particularly among patients with lower levels of disability. Interviewing Dr. Saud A. Sadiq, the Director and Chief Research Scientist of the Tisch MSRCNY, as well as Senior Research Scientist Dr. Violaine Harris, the article features the progress and key results of the stem cell treatment study, as well as the broader history and goals of the center.
We are excited to share more about our stem cell treatment research, which is a key study in service of our centers overarching goal of finding the cause of and the cure for MS, said Dr. Sadiq. Furthermore, the study has enormous potential not only for the treatment of MS patients, but also promising potential implications for those with other neurodegenerative diseases. Were delighted to share our analysis with the broader public and scientific community, and look forward to sharing further updates on this groundbreaking research as it progresses.
The full BioSpace article can be accessed here.
About the Tisch MS Research Center of New York
The mission of the Tisch Multiple Sclerosis Research Center of New York is to conduct groundbreaking medical research to ensure unparalleled care and positive outcomes for MS patients. Its integrated relationship with the International Multiple Sclerosis Management Practice (IMSMP) accelerates the pace at which research discoveries translate from lab bench to bedside. The Center aims to identify the cause of MS, understand disease mechanisms, optimize therapies, and repair the damage caused by MS while offering patients access to the best and most advanced treatments possible.
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Amendment added to PA budget bill would make Pitt, other universities stop fetal tissue research – WPXI Pittsburgh
Posted: July 3, 2022 at 2:33 am
Amendment added to Pennsylvania budget bill would make Pitt, other universities stop fetal tissue research
An amendment just added to the state budget bill would make the University of Pittsburgh promise that they would stop fetal tissue research.
Some politicians and doctors are differing on the topic.
On the heels of Roe v. Wade being overturned, State Representative Jerry Knowles is calling for several universities to stop doing fetal cell research.
Pitt is one of those universities, plus Temple, Lincoln and Penn State.
Pitt is expected to receive $155 million in the next year from grant money, and is known for their fetal cell research and work.
Rep. Knowles told Channel 11, I respect doctors. I dont claim to be a doctor, or a scientist. I dont think you need to be a doctor or a scientist to determine what is unethical, what is evil, and what is barbaric.
Its something local infectious disease physician Dr. Amesh Adalja disagrees with.
We have already seen benefits from stem cell research, and research that derives from fetus cells. Even some of the covid vaccines were developed. This is a life saving technology.
Pitt spokesperson Chuck Finder sent us a statement:
The University of Pittsburgh devotes every dollar of the general support appropriation it receives from the state to help support a tuition discount for Pennsylvania students and families. Were optimistic the legislature will preserve this investment in our students.
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Free Fecal Water Syndrome in Horses and What To Do About It The Horse – TheHorse.com
Posted: July 3, 2022 at 2:33 am
Unlike diarrhea in horses, free fecal water (FFW) syndrome is not life-threatening and involves free water being passed before, after, or with normal fecal balls. But because horses bodies need to conserve water, losing excess fluid in their manureeven if it is apparently benignindicates a gastrointestinal (GI) disturbance is making it difficult for the horse to manage or resorb water.
Horses move monumental volumes of water through their gastrointestinal tracts on a daily basis, said Burt Staniar, PhD, associate professor of equine science in Pennsylvania State College of Agricultural Sciences Department of Animal Science, during his virtual presentation at the 2022 EquiSUMMIT.
In terms of intake, horses need approximately 30 liters (1 liter is a bit more than 1/4 gallon) of water a day. A surprising amount of this can come from forage. Staniar said an average 500-kilogram (1,100-pound) horse consuming fresh forage from pasture containing 80% water might take in more than 22 liters of water daily.
This is simply from the forage. Even hay has 10-15% water, said Staniar.
An average horses GI tract contains an estimated 73 liters of water at any given point, which moves continuously between the circulatory and GI systems. For example, the horse secretes about 40 liters of water in saliva per day, and bile and pancreatic secretions add an additional 55 liters of water per day to the small intestine. In the hindgut (the cecum and large colon, or large intestine), however, water is resorbed, not secreted: 15 liters by the cecum and large colon each and an additional 6 liters by the small colon.
Overall, about 100 liters or 25 gallons of water are secreted into and absorbed from the gastrointestinal tract by a horse at rest, said Staniar. Water movements and conservation during exercise become even more critical due to waters essential roles in maintaining health and athletic performance.
He added, A healthy GI tract is integral for supporting these water movements. It is absolutely critical to have intact tight junctions, which are the protein links that hold the colonic cells together lining the walls of the hindgut.
When those tight junctions break down or do not function correctly, which can happen in response to any type of stress, changes in gut permeability could ensue, which negatively affect the horses ability to absorb water.
While risk factors and causes of FFW syndrome are unclear, stress could be involved. Staniar said study results suggest affected horses are lower in the herds social hierarchy, which could be a source of stress that ultimately alters tight-junction function.
Without knowing the exact cause but appreciating that abnormal water resorption is an underlying contributing factor, Staniar recommended evaluating the type of fiber being offered to horses and other nutrients that might enhance GI function.
Fiber is found in fresh and dry forages, including pelleted feeds.
Recognizing that different types of forage have unique chemical and physical properties, we can use a variety of forages to maximize GI health, he advised.
Consider, for example, the different properties of the various forages: long-stem grass hay, alfalfa, beet pulp, whole oats, soybean hulls, and wheat middlings. These, said Staniar, contain different amounts and types of fiber and moisture and can be used in various combinations to enhance gastric function.
For example, the fiber in beet pulp might be more digestible than the fiber in long-stem grass hay, but the fiber in the hay might cause the horse to chew more than the fiber in the beet pulp, the latter example leading to greater saliva production, Staniar noted. Owners need to be open to trying different types and combinations of fiber.
In addition, he explained that dietary fiber facilitates microbial fermentation in the hindgut, with the byproducts providing energy to the horse and supporting the integrity of the intestinal wall.
This concept supports the idea that pre- and probiotics, as well as butyric acid (which feed those hindgut microorganisms), will help maintain tight junctions and can be used in a multiprong approach to managing FFW, said Staniar.
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Free Fecal Water Syndrome in Horses and What To Do About It The Horse - TheHorse.com
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