Cytokine regulation of chronic cardiac allograft rejection: evidence against a role for Th1 in the disease process

• Published in: Transplantation Vol. 67; no. 12; p. 1548
• Main Authors: Piccotti, J R, Li, K, Chan, S Y, Eichwald, E J, Bishop, D K
• Format: Journal Article
• Language: English
• Published: United States 27.06.1999
• Subjects: Adjuvants, Immunologic - physiology; Adoptive Transfer; Animals; Antibodies, Monoclonal - pharmacology; CD4 Antigens - immunology; Cell Division - physiology; Chronic Disease; Cytokines - physiology; Graft Rejection - immunology; Graft Rejection - physiopathology; Graft Survival - immunology; Heart Transplantation - immunology; Interferon-gamma - metabolism; Mice; Mice, Inbred BALB C; Mice, Inbred C57BL; Mice, SCID; Spleen - cytology; T-Lymphocytes, Cytotoxic - immunology; T-Lymphocytes, Helper-Inducer - immunology; Th1 Cells - physiology
• ISSN: 0041-1337
• DOI: 10.1097/00007890-199906270-00008

Transient depletion of CD4+ T cells in cardiac allograft recipients prolongs allograft survival; however, grafts exhibit signs of chronic rejection characterized by collagen deposition and neointima development. Although it is believed that Th1 cells promote acute graft rejection, the role of these cells in chronic rejection remains unclear. Hence, our study evaluated whether Th1 cells are associated with the development of chronic cardiac allograft rejection. Splenocytes obtained from C57BL/6 recipients bearing BALB/c hearts with signs of chronic rejection were adoptively transferred into C57BL/6 SCID cardiac allograft recipients. As a measure of Th1 function, interferon-y production was determined after restimulation of recipient splenocytes with donor alloantigens. Transfer of splenocytes in SCID allograft recipients resulted in accelerated chronic rejection in the majority of mice. Characterization of these cells before transfer revealed hyporesponsive Th1 function. However, donor-specific proliferative responses and precursor interleukin-2 producing helper and cytotoxic T lymphocyte frequencies were comparable to that of naive splenocytes. Further, splenocytes obtained from SCID recipients with advanced signs of chronic rejection remained deficient in Th1 function, suggesting that Th1 are not involved in this disease process. This possibility was further supported by the development of chronic rejection in IL-12 knockout recipients. Finally, when splenocytes used for adoptive transfer retained Th1 function, transfer of these cells into SCID recipients resulted in acute allograft rejection. We have established a model in which the mediators of chronic rejection may be further explored. In this system, the absence rather than the presence of donor-reactive Th1 is associated with chronic rejection. These data indicate that Th1-independent effector mechanisms are responsible for chronic rejection in this model.