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Monthly Archives: February 2014
Laminine Testimonial – Stroke – Video
Posted: February 20, 2014 at 8:45 pm
Laminine Testimonial - Stroke
Laminine is availabe in the Philippines!!! "The Closest Alternative To Stem Cell Therapy..." "The miracle formula from a 9-day-old fertilized hen eggs" For M...
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Mountain Ridge Animal Hospital and Pain Management Center of Lafayette, Colorado Helps Local Shepherd Manage the Pain …
Posted: February 20, 2014 at 8:45 pm
Poway, California (PRWEB) February 20, 2014
Four-and-a-half year old Dakota, a German Shepherd from Colorado, is managing the pain from osteoarthritis with the help of stem cell therapy thanks to Mountain Ridge Animal Hospital and Pain Management Center of Lafayette. Dakotas positive results showed almost immediately, and just a few months post stem cell therapy using Vet-Stem, Inc. services, he is doing activities that he has not done for years.
Dakota was diagnosed with hip dysplasia at just three years old, and in less than two years time his owners felt his quality of life had significantly started to deteriorate. Robert Landry, DVM at Mountain Ridge Animal Hospital and Pain Management Center has been doing regenerative cell therapy with Vet-Stem for six years, treating various types of orthopedic issues and arthritis in small animals, and determined Dakota was a good candidate for the procedure.
Dr. Landry began Dakotas procedure on a Tuesday in October by collecting a small sample of fat called the falciform fat pad, which was sent overnight to Vet-Stems lab in San Diego, California. Received the next morning, the lab processed Dakotas fat and created injectable doses of his own stem cells to be overnighted back to Dr. Landry. Thursday Dakota received his hip injections and recovery began.
Dakotas results were almost immediate, Dakotas owners expressed, He moves around with ease now and can even go up and down the stairs. Last week he jumped into the back of my SUV, which he hasn't done in years. Before the stem cell therapy Dakota never wagged his tail, and now he doesnt stop! His quality of life is so much better and he seems truly happier.
Dr. Landry and the team at Mountain Ridge Animal Hospital and Pain Management Center specialize in companion animal health care, striving to provide the highest quality in Veterinary health care and customer service. Some of their specialties are pain management, surgery, and regenerative medicine. By understanding and valuing the special role that pets play in a family Dr. Landry and team are genuine advocates for each pet's health and care.
About Vet-Stem, Inc. Vet-Stem, Inc. was formed in 2002 to bring regenerative medicine to the veterinary profession. The privately held company is working to develop therapies in veterinary medicine that apply regenerative technologies while utilizing the natural healing properties inherent in all animals. As the first company in the United States to provide an adipose-derived stem cell service to veterinarians for their patients, Vet-Stem, Inc. pioneered the use of regenerative stem cells in veterinary medicine. The company holds exclusive licenses to over 50 patents including world-wide veterinary rights for use of adipose derived stem cells. In the last decade over 10,000 animals have been treated using Vet-Stem, Inc.s services, and Vet-Stem is actively investigating stem cell therapy for immune-mediated and inflammatory disease, as well as organ disease and failure. For more on Vet-Stem, Inc. and Veterinary Regenerative Medicine, visit http://www.vet-stem.com or call 858-748-2004.
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Mountain Ridge Animal Hospital and Pain Management Center of Lafayette, Colorado Helps Local Shepherd Manage the Pain ...
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Biology 07-6 Cell Differentiation and Stem Cells – Video
Posted: February 20, 2014 at 9:44 am
Biology 07-6 Cell Differentiation and Stem Cells
This video explains the process of cell differentiation, the role of gene expression in this process, as well as the potential medical applications of stem c...
By: HollowayScience
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Biology 07-6 Cell Differentiation and Stem Cells - Video
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Stem Cell Treatment at "EmCell" – Video
Posted: February 20, 2014 at 9:44 am
Stem Cell Treatment at "EmCell"
http://www.emcell.com/ Stem cell therapy is the rapidly developing area of modern medicine. Unique properties of fetal stem cells, the core of EmCell treatme...
By: Stem Cell Therapy Center "EMCELL"
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Stem Cell Treatment at "EmCell" - Video
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Joseph Glorioso, Ph.D., receives Pioneer Award
Posted: February 19, 2014 at 5:50 pm
PUBLIC RELEASE DATE:
19-Feb-2014
Contact: Vicki Cohn vcohn@liebertpub.com 914-740-2100 x2156 Mary Ann Liebert, Inc./Genetic Engineering News
New Rochelle, NY, February 19, 2014Joseph C. Glorioso, III, PhD (University of Pittsburgh School of Medicine, PA) devoted much of his research career to developing herpes viruses as efficient vectors for delivering therapeutic genes into cells. In recognition of his leadership and accomplishments, he has received a Pioneer Award from Human Gene Therapy, a peer-reviewed journal from Mary Ann Liebert, Inc., publishers. Human Gene Therapy is commemorating its 25th anniversary by bestowing this honor on the leading 12 Pioneers in the field of cell and gene therapy selected by a blue ribbon panel* and publishing a Pioneer Perspective by each of the award recipients. The Perspective by Dr. Glorioso is available on the Human Gene Therapy website.
As he recounts in his essay "Herpes Simplex Viral Vectors: Late Bloomers with Big Potential," it took 30 years to create broadly applicable HSV vector designs and a useful gene delivery platform. Since herpes simplex virus has a natural affinity for the nervous system, Dr. Glorioso believes that "gene delivery to the brain represents the most important frontier for HSV-mediated gene therapy and provides a unique opportunity to study complex processes such as learning and memory and to treat complex genetic and acquired diseases, including brain degeneration, epilepsy, and cancer."
In addition, says Dr. Glorioso, some herpes viral delivery systems are proving useful for gene transfer in the emerging field of cellular reprogramming to produce stem cells for tissue regeneration.
"Joe began his work in gene therapy early in the development of the field focusing on the very challenging objective of targeting the central nervous system. His work with HSV vectors represents an incredibly elegant blending of basic virology and translational science," says James M. Wilson, MD, PhD, Editor-in-Chief of Human Gene Therapy, and Director of the Gene Therapy Program, Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia.
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*The blue ribbon panel of leaders in cell and gene therapy, led by Chair Mary Collins, PhD, MRC Centre for Medical Molecular Virology, University College London selected the Pioneer Award recipients. The Award Selection Committee selected scientists that had devoted much of their careers to cell and gene therapy research and had made a seminal contribution to the field--defined as a basic science or clinical advance that greatly influenced progress in translational research.
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Regenerating orthopedic tissues within the human body
Posted: February 19, 2014 at 5:50 pm
By combining a synthetic scaffolding material with gene delivery techniques, researchers at Duke University are getting closer to being able to generate replacement cartilage where it's needed in the body.
Performing tissue repair with stem cells typically requires applying copious amounts of growth factor proteins -- a task that is very expensive and becomes challenging once the developing material is implanted within a body. In a new study, however, Duke researchers found a way around this limitation by genetically altering the stem cells to make the necessary growth factors all on their own.
They incorporated viruses used to deliver gene therapy to the stem cells into a synthetic material that serves as a template for tissue growth. The resulting material is like a computer; the scaffold provides the hardware and the virus provides the software that programs the stem cells to produce the desired tissue.
The study appears online the week of Feb. 17 in the Proceedings of the National Academy of Sciences.
Farshid Guilak, director of orthopaedic research at Duke University Medical Center, has spent years developing biodegradable synthetic scaffolding that mimics the mechanical properties of cartilage. One challenge he and all biomedical researchers face is getting stem cells to form cartilage within and around the scaffolding, especially after it is implanted into a living being.
The traditional approach has been to introduce growth factor proteins, which signal the stem cells to differentiate into cartilage. Once the process is under way, the growing cartilage can be implanted where needed.
"But a major limitation in engineering tissue replacements has been the difficulty in delivering growth factors to the stem cells once they are implanted in the body," said Guilak, who is also a professor in Duke's Department of Biomedical Engineering. "There's a limited amount of growth factor that you can put into the scaffolding, and once it's released, it's all gone. We need a method for long-term delivery of growth factors, and that's where the gene therapy comes in."
For ideas on how to solve this problem, Guilak turned to his colleague Charles Gersbach, an assistant professor of biomedical engineering and an expert in gene therapy. Gersbach proposed introducing new genes into the stem cells so that they produce the necessary growth factors themselves.
But the conventional methods for gene therapy are complex and difficult to translate into a strategy that would be feasible as a commercial product.
This type of gene therapy generally requires gathering stem cells, modifying them with a virus that transfers the new genes, culturing the resulting genetically altered stem cells until they reach a critical mass, applying them to the synthetic cartilage scaffolding and, finally, implanting it into the body.
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Regenerating orthopedic tissues within the human body
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Stem Cell Treatment at "EmCell" – Video
Posted: February 19, 2014 at 5:47 pm
Stem Cell Treatment at "EmCell"
http://www.emcell.com/ Stem cell therapy is the rapidly developing area of modern medicine. Unique properties of fetal stem cells, the core of EmCell treatme...
By: Stem Cell Therapy Center "EMCELL"
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Stem Cell Treatment at "EmCell" - Video
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Laminine Testimonial – Chronic Kidney Disease – Video
Posted: February 19, 2014 at 5:47 pm
Laminine Testimonial - Chronic Kidney Disease
Laminine is availabe in the Philippines!!! "The Closest Alternative To Stem Cell Therapy..." "The miracle formula from a 9-day-old fertilized hen eggs" For M...
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Laminine Testimonial - Chronic Kidney Disease - Video
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Gene Therapy Might Grow Replacement Tissue Inside the Body
Posted: February 19, 2014 at 1:44 pm
Duke researchers use gene therapy to direct stem cells into becoming new cartilage on a synthetic scaffold even after implantation into a living body
By Ken Kingery
By combining a synthetic scaffolding material with gene delivery techniques, researchers at Duke University are getting closer to being able to generate replacement cartilage where it's needed in the body.
Performing tissue repair with stem cells typically requires applying copious amounts of growth factor proteinsa task that is very expensive and becomes challenging once the developing material is implanted within a body. In a new study, however, Duke researchers found a way around this limitation by genetically altering the stem cells to make the necessary growth factors all on their own.
They incorporated viruses used to deliver gene therapy to the stem cells into a synthetic material that serves as a template for tissue growth. The resulting material is like a computer; the scaffold provides the hardware and the virus provides the software that programs the stem cells to produce the desired tissue.
The study appears online the week of Feb. 17 in the Proceedings of the National Academy of Sciences.
An artistic rendering of human stem cells on the polymer scaffolds. Photo courtesy of Charles Gersbach and Farshid Guilak, Duke University
The traditional approach has been to introduce growth factor proteins, which signal the stem cells to differentiate into cartilage. Once the process is under way, the growing cartilage can be implanted where needed.
But a major limitation in engineering tissue replacements has been the difficulty in delivering growth factors to the stem cells once they are implanted in the body, said Guilak, who is also a professor in Dukes Department of Biomedical Engineering. Theres a limited amount of growth factor that you can put into the scaffolding, and once its released, its all gone. We need a method for long-term delivery of growth factors, and thats where the gene therapy comes in.
A microscopic view using electron microscopy of human stem cells and viral gene carriers adhering to the fibers of a polymer scaffold. Photo courtesy of Charles Gersbach and Farshid Guilak, Duke University
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Gene Therapy Might Grow Replacement Tissue Inside the Body
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Deep TCR sequencing reveals extensive renewal of the T cell repertoire following autologous stem cell transplant in MS
Posted: February 19, 2014 at 1:43 pm
A new study describes the complexity of the new T cell repertoire following immune-depleting therapy to treat multiple sclerosis, improving our understanding of immune tolerance and clinical outcomes.
In the Immune Tolerance Network's (ITN) HALT-MS study, 24 patients with relapsing, remitting multiple sclerosis received high-dose immunosuppression followed by a transplant of their own stem cells, called an autologous stem cell transplant, to potentially reprogram the immune system so that it stops attacking the brain and spinal cord. Data published in the Journal of Clinical Investigation quantified and characterized T cell populations following this aggressive regimen to understand how the reconstituting immune system is related to patient outcomes.
ITN investigators used a high-throughput, deep-sequencing technology (Adaptive Biotechnologies, ImmunoSEQTM Platform) to analyze the T cell receptor (TCR) sequences in CD4+ and CD8+ cells to compare the repertoire at baseline pre-transplant, two months post-transplant and 12 months post-transplant.
Using this approach, alongside conventional flow cytometry, the investigators found that CD4+ and CD8+ lymphocytes exhibit different reconstitution patterns following transplantation. The scientists observed that the dominant CD8+ T cell clones present at baseline were expanded at 12 months post-transplant, suggesting these clones were not effectively eradicated during treatment. In contrast, the dominant CD4+ T cell clones present at baseline were undetectable at 12 months, and the reconstituted CD4+ T cell repertoire was predominantly composed of new clones.
The results also suggest the possibility that differences in repertoire diversity early in the reconstitution process might be associated with clinical outcomes. Nineteen patients who responded to treatment had a more diverse repertoire two months following transplant compared to four patients who did not respond. Despite the low number of non-responders, these comparisons approached statistical significance and point to the possibility that complexity in the T cell compartment may be important for establishing immune tolerance.
This is one of the first studies to quantitatively compare the baseline T cell repertoire with the reconstituted repertoire following autologous stem cell transplant, and provides a previously unseen in-depth analysis of how the immune system reconstitutes itself following immune-depleting therapy.
About The Immune Tolerance Network
The Immune Tolerance Network (ITN) is a research consortium sponsored by the National Institute of Allergy and Infectious Diseases, part of the National Institutes of Health. The ITN develops and conducts clinical and mechanistic studies of immune tolerance therapies designed to prevent disease-causing immune responses, without compromising the natural protective properties of the immune system. Visit http://www.immunetolerance.org for more information.
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The above story is based on materials provided by Immune Tolerance Network. Note: Materials may be edited for content and length.
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