Inbred miniature swine provide a unique preclinical model for the study of transplantation immunity and tolerance. Over the past two decades, we have utilized this model to study a robust form of tolerance of MHC class I-mismatched renal allografts that is routinely achieved following a short course of calcineurin inhibitors. This proposal represents the fifth consecutive renewal of this RO1, the last renewal of which was as a Merit Award (G37). During the last project period, we have made significant progress in understanding the role of regulatory T cells (Treg) in the induction and maintenance of tolerance as well as in the adoptive transfer of tolerance in this model. We have demonstrated a requirement for both the donor kidney graft and the functioning thymus to maintain the balance between alloreactivity and down-regulation of immune reactivity to the graft, needed for persistence of tolerance. We have also demonstrated that the cells required for adoptive transfer of tolerance to a re-transplanted kidney are present within the kidney itself but that transfer of tolerance sufficient for acceptance of a naive, donor-matched kidney requires additional peripheral cells from the tolerant donor. In the next project period, we intend to investigate the nature of the signals that emanate from the kidney and lead to intra-thymic generation of Tregs and the nature of the cells within the kidney and in the periphery that are responsible for the adoptive transfer of tolerance to a naive recipient. Specifically, we will: 1) Examine the nature of the peripheral and intra-thymic processes responsible for the balance between alloagressive and regulatory T cell responses to donor antigens of a renal allograft; and 2) Determine the nature of the intra-graft and peripheral regulatory cells required for adoptive transfer of tolerance to a second donor kidney, following re-transplantation of kidneys from long-term tolerant (LTT) animals. The broader goal of these studies remains to develop an understanding of the mechanisms by which allograft tolerance is induced and maintained in this large-animal model, in order to permit development of appropriate protocols for induction of tolerance to organ allografts in the clinic.

Public Health Relevance

This grant utilizes inbred miniature swine as a unique preclinical, large-animal model for the study of transplantation immunity and tolerance. In this project period, we intend to study the immunologic signals that lead to tolerance and the mechanism by which this tolerance can be transferred to another animal. The broader goal of these studies is to develop appropriate protocols for induction of tolerance to organ allografts in the clinic.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
High Priority, Short Term Project Award (R56)
Project #
2R56AI031046-26
Application #
9398190
Study Section
Special Emphasis Panel (ZRG1-IMM-C (02))
Program Officer
Nabavi, Nasrin N
Project Start
1991-04-01
Project End
2018-01-31
Budget Start
2017-02-08
Budget End
2018-01-31
Support Year
26
Fiscal Year
2017
Total Cost
$732,600
Indirect Cost
$251,574
Name
Columbia University (N.Y.)
Department
Surgery
Type
Schools of Medicine
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Michel, S G; Madariaga, M L L; LaMuraglia 2nd, G M et al. (2018) The effects of brain death and ischemia on tolerance induction are organ-specific. Am J Transplant 18:1262-1269
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
Vallabhajosyula, Prashanth; Hirakata, Atsushi; Weiss, Matthew et al. (2017) Effect of the Diabetic State on Islet Engraftment and Function in a Large Animal Model of Islet-Kidney Transplantation. Cell Transplant 26:1755-1762