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	<title>organ transplant Archives - Amazing Health Advances</title>
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	<title>organ transplant Archives - Amazing Health Advances</title>
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		<title>Antibody Shows Promise for Preventing Organ Rejection After Transplantation</title>
		<link>https://amazinghealthadvances.net/antibody-promise-preventing-rejection-after-transplantation-8205/#utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=antibody-promise-preventing-rejection-after-transplantation-8205</link>
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		<dc:creator><![CDATA[The AHA! Team]]></dc:creator>
		<pubDate>Wed, 12 Jun 2024 04:30:14 +0000</pubDate>
				<category><![CDATA[Archive]]></category>
		<category><![CDATA[Health Advances]]></category>
		<category><![CDATA[antibody]]></category>
		<category><![CDATA[antibody therapies]]></category>
		<category><![CDATA[antibody treatment]]></category>
		<category><![CDATA[clinical trials]]></category>
		<category><![CDATA[Duke Health]]></category>
		<category><![CDATA[heart transplant]]></category>
		<category><![CDATA[monoclonal antibodies]]></category>
		<category><![CDATA[organ donor]]></category>
		<category><![CDATA[organ rejection]]></category>
		<category><![CDATA[organ transplant]]></category>
		<guid isPermaLink="false">https://amazinghealthadvances.net/?p=15925</guid>

					<description><![CDATA[<p>Duke Health &#8211; DURHAM, N.C. – A man-made antibody successfully prevented organ rejection when tested in primates that had undergone a kidney transplant, Duke Health researchers report. The finding clears the way for the new monoclonal antibody to move forward in human clinical trials. Results of the study appear online Aug. 30 in the journal Science Translational Medicine. “Current medications to prevent organ rejection are good overall, but they have a lot of side effects,” said lead author Imran J. Anwar, M.D., a surgical research fellow in Duke’s Department of Surgery. “These therapies suppress the immune system, putting patients at risk of infections and organ damage, and many cause non-immune complications such as diabetes and high blood pressure. “The push over the last decades has been to develop new, less toxic drugs,” Anwar said. “We are hopeful this antibody moves us closer to that goal.” Anwar and colleagues, including co-senior author Allan Kirk, M.D., Ph.D., chair of the Department of Surgery, focused on a monoclonal antibody identified as AT-1501. It was engineered to minimize the risk of blood clots, which had become problematic for an earlier version of this therapy. In studies using primates that had undergone kidney transplantation, AT-1501 prevented rejection without the need for additional immunosuppressive drugs or promoting blood clots, confirming its immunosuppressive potential. In animals that had undergone islet transplantation, AT-1501 alone did not lead to uniform rejection control, but it was effective in combination with existing immunosuppressive agents. The combination therapies in islet transplantation led to uniform islet graft survival without weight loss or infections that can typically arise. The islet transplants were performed by Norma Kenyon, Ph.D., co-senior author and professor at the University of Miami. “These data support AT-1501 as a safe and effective agent to promote both islet and kidney transplant survival and function and allow us to advance into clinical trials right away,” Kirk said. “This less toxic approach has been pursued for over 20 years, and I think we are finally at a turning point. This could be a great advance for people in need of organ transplants.” In addition to Kirk and Anwar, study authors include Dora M. Berman, Isabel DeLaura, Qimeng Gao, Melissa A. Willman, Allison Miller, Alan Gill, Cindy Gill, Steve Perrin, Camillo Ricordi, Philip Ruiz, Mingqing Song, Joseph M Ladowski, and Norma S. Kenyon. The study received funding support from the National Institutes of Health (U19-AI051731), the Diabetes Research Institute Foundation, and Anelixis Therapeutics, now Eledon Pharmaceuticals, which is developing AT-1501 for kidney and islet cell transplant. To read the original article click here.</p>
<p>The post <a href="https://amazinghealthadvances.net/antibody-promise-preventing-rejection-after-transplantation-8205/">Antibody Shows Promise for Preventing Organ Rejection After Transplantation</a> appeared first on <a href="https://amazinghealthadvances.net">Amazing Health Advances</a>.</p>
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		<title>Pig-To-Human Transplants Come A Step Closer With New Test</title>
		<link>https://amazinghealthadvances.net/pig-to-human-transplants-come-a-step-closer-with-new-test-7642/#utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=pig-to-human-transplants-come-a-step-closer-with-new-test-7642</link>
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		<dc:creator><![CDATA[AHA Publisher]]></dc:creator>
		<pubDate>Wed, 27 Oct 2021 07:00:18 +0000</pubDate>
				<category><![CDATA[Archive]]></category>
		<category><![CDATA[Health Advances]]></category>
		<category><![CDATA[human-pig transplant]]></category>
		<category><![CDATA[organ transplant]]></category>
		<category><![CDATA[pig's kidney]]></category>
		<category><![CDATA[transplant]]></category>
		<category><![CDATA[xenotransplantation]]></category>
		<guid isPermaLink="false">https://amazinghealthadvances.net/?p=13166</guid>

					<description><![CDATA[<p>Carla K Johnson via CBN News &#8211; Scientists temporarily attached a pig’s kidney to a human body and watched it begin to work, a small step in the decades-long quest to one day use animal organs for life-saving transplants. Pigs have been the most recent research focus to address the organ shortage, but among the hurdles: A sugar in pig cells, foreign to the human body, causes immediate organ rejection. The kidney for this experiment came from a gene-edited animal, engineered to eliminate that sugar and avoid an immune system attack. Surgeons attached the pig kidney to a pair of large blood vessels outside the body of a deceased recipient so they could observe it for two days. The kidney did what it was supposed to do — filter waste and produce urine — and didn&#8217;t trigger rejection. “It had absolutely normal function,” said Dr. Robert Montgomery, who led the surgical team last month at NYU Langone Health. “It didn’t have this immediate rejection that we have worried about.” This research is “a significant step,” said Dr. Andrew Adams of the University of Minnesota Medical School, who was not part of the work. It will reassure patients, researchers and regulators “that we’re moving in the right direction.” The dream of animal-to-human transplants — or xenotransplantation — goes back to the 17th century with stumbling attempts to use animal blood for transfusions. By the 20th century, surgeons were attempting transplants of organs from baboons into humans, notably Baby Fae, a dying infant, who lived 21 days with a baboon heart. With no lasting success and much public uproar, scientists turned from primates to pigs, tinkering with their genes to bridge the species gap. Pigs have advantages over monkeys and apes. They are produced for food, so using them for organs raises fewer ethical concerns. Pigs have large litters, short gestation periods and organs comparable to humans. Pig heart valves also have been used successfully for decades in humans. The blood thinner heparin is derived from pig intestines. Pig skin grafts are used on burns and Chinese surgeons have used pig corneas to restore sight. In the NYU case, researchers kept a deceased woman&#8217;s body going on a ventilator after her family agreed to the experiment. The woman had wished to donate her organs, but they weren’t suitable for traditional donation. The family felt “there was a possibility that some good could come from this gift,” Montgomery said. Montgomery himself received a transplant three years ago, a human heart from a donor with hepatitis C because he was willing to take any organ. “I was one of those people lying in an ICU waiting and not knowing whether an organ was going to come in time,” he said. Several biotech companies are in the running to develop suitable pig organs for transplant to help ease the human organ shortage. More than 90,000 people in the U.S. are in line for a kidney transplant. Every day, 12 die while waiting. The advance is a win for Revivicor, a subsidiary of United Therapeutics, the company that engineered the pig and its cousins, a herd of 100 raised in tightly controlled conditions at a facility in Iowa. The pigs lack a gene that produces alpha-gal, the sugar that provokes an immediate attack from the human immune system. In December, the Food and Drug Administration approved the gene alteration in the Revivicor pigs as safe for human food consumption and medicine. But the FDA said developers would need to submit more paperwork before pig organs could be transplanted into living humans. “This is an important step forward in realizing the promise of xenotransplantation, which will save thousands of lives each year in the not-too-distant future,” said United Therapeutics CEO Martine Rothblatt in a statement. Experts say tests on nonhuman primates and last month’s experiment with a human body pave the way for the first experimental pig kidney or heart transplants in living people in the next several years. Raising pigs to be organ donors feels wrong to some people, but it may grow more acceptable if concerns about animal welfare can be addressed, said Karen Maschke, a research scholar at the Hastings Center, who will help develop ethics and policy recommendations for the first clinical trials under a grant from the National Institutes of Health. “The other issue is going to be: Should we be doing this just because we can?” Maschke said. To read the original article click here. &#160;</p>
<p>The post <a href="https://amazinghealthadvances.net/pig-to-human-transplants-come-a-step-closer-with-new-test-7642/">Pig-To-Human Transplants Come A Step Closer With New Test</a> appeared first on <a href="https://amazinghealthadvances.net">Amazing Health Advances</a>.</p>
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		<title>Machine Keeps Human Livers Alive for One Week Outside of the Body</title>
		<link>https://amazinghealthadvances.net/machine-keeps-human-livers-alive-for-one-week-outside-of-the-body-6256/#utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=machine-keeps-human-livers-alive-for-one-week-outside-of-the-body-6256</link>
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		<dc:creator><![CDATA[AHA Publisher]]></dc:creator>
		<pubDate>Tue, 14 Jan 2020 08:00:17 +0000</pubDate>
				<category><![CDATA[Archive]]></category>
		<category><![CDATA[Health Advances]]></category>
		<category><![CDATA[Cancer]]></category>
		<category><![CDATA[liver]]></category>
		<category><![CDATA[liver disease]]></category>
		<category><![CDATA[organ transplant]]></category>
		<guid isPermaLink="false">http://amazinghealthadvances.net/?p=7473</guid>

					<description><![CDATA[<p>University of Zurich via Newswise &#8211; Researchers in Zurich have developed a machine that repairs injured human livers and keeps them alive outside the body for one week. Newswise — Researchers from the University Hospital Zurich, ETH Zurich, Wyss Zurich and the University of Zurich have developed a machine that repairs injured human livers and keeps them alive outside the body for one week. This breakthrough may increase the number of available organs for transplantation saving many lives of patients with severe liver diseases or cancer. Until now, livers could be stored safely outside the body for only a few hours. With the novel perfusion technology, livers &#8211; and even injured livers &#8211; can now be kept alive outside of the body for an entire week. This is a major breakthrough in transplantation medicine, which may increase the number of available organs for transplantation and save many lives of patients suffering from severe liver disease or a variety of cancers. Injured cadaveric livers, initially not suitable for use in transplantation, may regain full function while perfused in the new machine for several days. The basis for this technology is a complex perfusion system, mimicking most core body functions close to physiology. The corresponding study was published on January 13 in the scientific journal Nature Biotechnology. Offering What Other Machines Cannot &#8220;The success of this unique perfusion system &#8211; developed over a four-year period by a group of surgeons, biologists and engineers &#8211; paves the way for many new applications in transplantation and cancer medicine helping patients with no liver grafts available&#8221; explains Prof. Pierre-Alain Clavien, Chairman of the Department of Surgery and Transplantation at the University Hospital Zurich (USZ). When the project started in 2015, livers could only be kept on the machine for 12 hours. The seven-day successful perfusion of poor-quality livers now allows for a wide range of strategies, e.g. repair of preexisting injury, cleaning of fat deposits in the liver or even regeneration of partial livers. Liver4Life: A project from Wyss Zurich The Liver4Life project was developed under the umbrella of Wyss Zurich institute, which brought together the highly specialized technical know-how and biomedical knowledge of experts from the University Hospital Zurich (USZ), ETH Zurich and the University of Zurich (UZH). &#8220;The biggest challenge in the initial phase of our project was to find a common language that would allow communication between the clinicians and engineers,&#8221; explains Prof. Philipp Rudolf von Rohr, Professor of Process Engineering at ETH Zurich and co-leader with Professor Clavien of the study now published in Nature Biotechnology. Technology With Great Potential The inaugural study shows that six of ten perfused poor-quality human livers, declined for transplantation by all centers in Europe, recovered to full function within one week of perfusion on the machine. The next step will be to use these organs for transplantation. The proposed technology opens a large avenue for many applications offering a new life for many patients with end stage liver disease or cancer. To read the original article click here.</p>
<p>The post <a href="https://amazinghealthadvances.net/machine-keeps-human-livers-alive-for-one-week-outside-of-the-body-6256/">Machine Keeps Human Livers Alive for One Week Outside of the Body</a> appeared first on <a href="https://amazinghealthadvances.net">Amazing Health Advances</a>.</p>
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		<title>Living Skin Can Now Be 3D-Printed with Blood Vessels Included</title>
		<link>https://amazinghealthadvances.net/living-skin-can-now-be-3d-printed-with-blood-vessels-included-6113/#utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=living-skin-can-now-be-3d-printed-with-blood-vessels-included-6113</link>
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		<dc:creator><![CDATA[AHA Publisher]]></dc:creator>
		<pubDate>Mon, 04 Nov 2019 08:00:34 +0000</pubDate>
				<category><![CDATA[Archive]]></category>
		<category><![CDATA[Health Advances]]></category>
		<category><![CDATA[3D bioprinting]]></category>
		<category><![CDATA[3D Printing]]></category>
		<category><![CDATA[organ transplant]]></category>
		<category><![CDATA[skin grafts]]></category>
		<guid isPermaLink="false">http://amazinghealthadvances.net/?p=6990</guid>

					<description><![CDATA[<p>Rensselaer Polytechnic Institute via EurekAlert- Development is significant step toward skin grafts that can be integrated into patient&#8217;s skin. TROY, N.Y. &#8212; Researchers at Rensselaer Polytechnic Institute have developed a way to 3D print living skin, complete with blood vessels. The advancement, published online today in Tissue Engineering Part A, is a significant step toward creating grafts that are more like the skin our bodies produce naturally. &#8220;Right now, whatever is available as a clinical product is more like a fancy Band-Aid,&#8221; said Pankaj Karande, an associate professor of chemical and biological engineering and member of the Center for Biotechnology and Interdisciplinary Studies (CBIS), who led this research at Rensselaer. &#8220;It provides some accelerated wound healing, but eventually it just falls off; it never really integrates with the host cells.&#8221; A significant barrier to that integration has been the absence of a functioning vascular system in the skin grafts. Karande has been working on this challenge for several years, previously publishing one of the first papers showing that researchers could take two types of living human cells, make them into &#8220;bio-inks,&#8221; and print them into a skin-like structure. Since then, he and his team have been working with researchers from Yale School of Medicine to incorporate vasculature. In this paper, the researchers show that if they add key elements &#8212; including human endothelial cells, which line the inside of blood vessels, and human pericyte cells, which wrap around the endothelial cells &#8212; with animal collagen and other structural cells typically found in a skin graft, the cells start communicating and forming a biologically relevant vascular structure within the span of a few weeks. You can watch Karande explain this development here. &#8220;As engineers working to recreate biology, we&#8217;ve always appreciated and been aware of the fact that biology is far more complex than the simple systems we make in the lab,&#8221; Karande said. &#8220;We were pleasantly surprised to find that, once we start approaching that complexity, biology takes over and starts getting closer and closer to what exists in nature.&#8221; Once the Yale team grafted it onto a special type of mouse, the vessels from the skin printed by the Rensselaer team began to communicate and connect with the mouse&#8217;s own vessels. &#8220;That&#8217;s extremely important, because we know there is actually a transfer of blood and nutrients to the graft which is keeping the graft alive,&#8221; Karande said. In order to make this usable at a clinical level, researchers need to be able to edit the donor cells using something like the CRISPR technology, so that the vessels can integrate and be accepted by the patient&#8217;s body. &#8220;We are still not at that step, but we are one step closer,&#8221; Karande said. &#8220;This significant development highlights the vast potential of 3D bioprinting in precision medicine, where solutions can be tailored to specific situations and eventually to individuals,&#8221; said Deepak Vashishth, the director CBIS. &#8220;This is a perfect example of how engineers at Rensselaer are solving challenges related to human health.&#8221; Karande said more work will need to be done to address the challenges associated with burn patients, which include the loss of nerve and vascular endings. But the grafts his team has created bring researchers closer to helping people with more discrete issues, like diabetic or pressure ulcers. &#8220;For those patients, these would be perfect, because ulcers usually appear at distinct locations on the body and can be addressed with smaller pieces of skin,&#8221; Karande said. &#8220;Wound healing typically takes longer in diabetic patients, and this could also help to accelerate that process.&#8221; To read the original article click here.</p>
<p>The post <a href="https://amazinghealthadvances.net/living-skin-can-now-be-3d-printed-with-blood-vessels-included-6113/">Living Skin Can Now Be 3D-Printed with Blood Vessels Included</a> appeared first on <a href="https://amazinghealthadvances.net">Amazing Health Advances</a>.</p>
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