Immune Reactions Found Behind Human Rejection of Transplanted Pig Kidneys
Targeting Immune Responses May Save Future Organ Transplants
The findings set the stage for more successful clinical trials in the near future.
More than 800,000 Americans have late-stage kidney disease yet only 3% receive a transplant each year, according to the U.S. Centers for Disease Control and Prevention. To boost the supply of available organs, experts are exploring the use of genetically modified pig kidneys. The genetic changes are meant to keep the human immune system from recognizing the animal organ as foreign, and attacking it to cause rejection. However, recipients' immune reactions can still lead to organ damage and failure after the surgery.
To better understand the immune mechanisms behind xenotransplant rejection, a new investigation, led by NYU Langone Health researchers, explored the transplantation of a genetically engineered pig kidney into a brain-dead recipient with a beating heart and on a ventilator, whose family donated his body to science. For 61 days after the surgery, the team was able to collect samples of tissue, blood, and body fluid at a pace that is impossible to safely maintain in primates or living patients. As a result, they had a rare opportunity to trace the network of interactions that occur among immune cells when a pig organ is being tolerated by a human and when it undergoes a rejection episode.
In the first of two reports publishing online
Once the researchers uncovered this set of reactions, they for the first time successfully reversed the rejection using a combination of drugs approved by the Food and Drug Administration to temper both the antibody and T cell activity. There was no evidence of permanent damage or reduced kidney function after the intervention.
"Our results better prepare us for anticipating and addressing harmful immune reactions during pig-organ transplantation in living humans," said study lead author
The findings also confirmed that a pig kidney can effectively serve as a replacement for a human kidney, says Montgomery, who is also the chair of the Department of Surgery and director of the NYU Langone Transplant Institute.
The second report in Nature outlines immune activity in greater detail, says Montgomery, who is a co-author. The research team conducted a multi-omics analysis, which integrates information about gene function, gene expression (activity level), and proteins, as well as other data, to gain a holistic understanding of complex mechanisms at work in the immune system.
Measuring about 5,100 expressed human and pig genes in the pig xenograft, the authors identified every type of immune cell in the tissue, tracked immune behavior over the two-month period, and observed the organ rejection in day-by-day snapshots.
The analysis revealed three major immune responses against the pig kidney: on postoperative day (POD) 21, driven by a part of the human recipient's immune system that responds generally to intruders (innate) rather than to a specific target; on POD 33, driven by a specific population of human white blood cells that engulf invaders (macrophages); and on POD 45, driven mostly by the human T cell response. Montgomery says that by measuring levels of various blood biomarkers the researchers were able to spot these attacks up to five days before they were clinically visible in the tissue.
"Our multi-omics analysis uncovers various biomarkers that shows promise as an early-warning system for pig organ rejection," said study co-lead author
"The specific immune reactions revealed in our investigation provide clear pig and human targets for therapies to improve the success of xenotransplantation to address the dire shortage of available organs," said study senior author
According to Keating, now that the researchers understand which antibodies and T cells are damaging the transplanted pig kidney, they next plan to investigate what molecules the immune response is targeting through the different layers of DNA, RNA, and protein datasets generated.
Keating says future studies in other human decedents and in live patients are needed to confirm the findings.
The gene edited pig organ was provided by Revivicor, a subsidiary of United Therapeutics. Funding for the studies was provided by National Institutes of Health grants U19AI191396, P30CA016087, R01AI144522, S10RR027050, and S10OD020056. Additional study funding was provided by Yosemite, United Therapeutics, Imam Abdulrahman bin Faisal University, the Vaisala Fund, the Aarne Koskelon Foundation, the Antti and Tyyne Soininen Foundation, and the Finnish Cultural Foundation.
Montgomery consults with and holds roles with ProCure On-Demand; the Spanish Society of Transplantation; the Transplant Society; LiveOnNY; the National Kidney Foundation; Sanofi-Aventis
Other NYU Langone researchers involved in the clinical study are
Other NYU Langone researchers involved in the mutli-omics study are
About NYU Langone Health
NYU Langone Health is a fully integrated health system that consistently achieves the best patient outcomes through a rigorous focus on quality that has resulted in some of the lowest mortality rates in the nation. Vizient, Inc. has ranked NYU Langone No. 1 out of 118 comprehensive academic medical centers across the nation for four years in a row, and U.S. News & World Report recently ranked four of its clinical specialties number one in the nation. NYU Langone offers a comprehensive range of medical services with one high standard of care across seven inpatient locations, its Perlmutter Cancer Center, and more than 320 outpatient locations in the
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SOURCE NYU Grossman School of Medicine and NYU Langone Health
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