Xenotransplantation is generally considered the most likely near-term solution to the major limitation imposed on the field of transplantation today by the severe shortage of cadaver donor organs. For a variety of reasons, the pig now appears to be the donor species of choice, and miniature swine, developed in this laboratory, have several advantages as potential xenograft donors. Because the immune response to such discordant transplantation is exceedingly strong the success of clinical xenografting is likely to depend, at least in part, on finding ways of inducing specific hyporesponsiveness, or tolerance, rather than relying entirely on non-specific immunosuppression. In this Program Project grant we will utilize a large animal pig to primate model to study and overcome the major pediments to such discordant xenotransplantation, and will emphasize the induction of tolerance as a major part of the approach. We will concentrate on four major areas, each constituting the basis of a component grant of the program: 1) avoiding the return of natural antibodies or the effects thereof; 2) producing durable tolerance at the T Cell level; 3) avoiding coagulopathy following xenogeneic transplantation; and 4) understanding and managing the potential infectious disease problems associated with xenotransplantation. All of these projects are highly interactive, and utilize numerous shared resources, many of which will be made available through the large animal core. The work will be carried out in a unique environment, which provides interactions with scientists working in basic and cellular immunology and working on relevant small animal models in the same research center, as well as with clinicians committed to taking new therapies to clinical applications.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
1P01AI045897-01A1
Application #
6292662
Study Section
Special Emphasis Panel (ZAI1-NBS-I (S2))
Program Officer
Rose, Stephen M
Project Start
2000-09-15
Project End
2005-08-31
Budget Start
2000-09-15
Budget End
2001-08-31
Support Year
1
Fiscal Year
2000
Total Cost
$1,481,206
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02199
Sykes, Megan (2018) IXA Honorary Member Lecture, 2017: The long and winding road to tolerance. Xenotransplantation 25:e12419
Proto, Jonathan D; Doran, Amanda C; Subramanian, Manikandan et al. (2018) Hypercholesterolemia induces T cell expansion in humanized immune mice. J Clin Invest 128:2370-2375
Chen, Mo; Wang, Yuantao; Wang, Hui et al. (2018) Elimination of donor CD47 protects against vascularized allograft rejection in mice. Xenotransplantation :e12459
Watanabe, Hironosuke; Sahara, Hisashi; Nomura, Shunichiro et al. (2018) GalT-KO pig lungs are highly susceptible to acute vascular rejection in baboons, which may be mitigated by transgenic expression of hCD47 on porcine blood vessels. Xenotransplantation 25:e12391
Sachs, David H (2018) Transplantation tolerance through mixed chimerism: From allo to xeno. Xenotransplantation 25:e12420
Fishman, Jay A; Sachs, David H; Yamada, Kazuhiko et al. (2018) Absence of interaction between porcine endogenous retrovirus and porcine cytomegalovirus in pig-to-baboon renal xenotransplantation in vivo. Xenotransplantation 25:e12395
Mastroianni, Melissa; Ng, Zhi Yang; Goyal, Ritu et al. (2018) Topical Delivery of Immunosuppression to Prolong Xenogeneic and Allogeneic Split-Thickness Skin Graft Survival. J Burn Care Res 39:363-373
Tanabe, T; Watanabe, H; Shah, J A et al. (2017) Role of Intrinsic (Graft) Versus Extrinsic (Host) Factors in the Growth of Transplanted Organs Following Allogeneic and Xenogeneic Transplantation. Am J Transplant 17:1778-1790
Yamada, Kazuhiko; Sykes, Megan; Sachs, David H (2017) Tolerance in xenotransplantation. Curr Opin Organ Transplant 22:522-528
Holzer, Paul W; Leonard, David A; Shanmugarajah, Kumaran et al. (2017) A Comparative Examination of the Clinical Outcome and Histological Appearance of Cryopreserved and Fresh Split-Thickness Skin Grafts. J Burn Care Res 38:e55-e61

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