THE CD154-CD40 COSTIMULATORY PATHWAY IN TRANSPLANTATION
- 1 January 2002
- journal article
- review article
- Published by Wolters Kluwer Health in Transplantation
- Vol. 73 (Supplement) , S36-S39
- https://doi.org/10.1097/00007890-200201151-00012
Abstract
The CD154-CD40 pathway is one of the critical costimulatory pathways that are required for full activation of T cells during alloimmune responses. Blockade of this pathway with anti-CD154 antibodies has been reported to prolong allograft survival in experimental transplantation models and to induce tolerance in some instances. However, anti-CD154 monotherapy cannot induce tolerance in “stringent” models such as skin and islet transplantation and is not sufficient to prevent chronic graft vasculopathy in vascularized organ transplantation. Therefore, combined therapies of anti-CD154 antibodies plus donor-specific transfusion, bone marrow infusion, or B7 blockade by CTLA4-Ig have been tried, and synergistic effects for tolerance induction have been reported. Furthermore, the efficacy of CD154 blockade in primate models has been confirmed for islet and kidney transplantation. The mechanisms of CD154 blockade in vivo include CTLA4-dependent anergy or regulation, T-cell apoptosis, and induction of regulatory cells. Finally, anti-CD154 antibody therapy has been reported to result in unexpected thromboembolic complications in both primates and humans, although the etiology of these conditions remains unclear. In addition, not all antibodies cause this side effect. Clinical trials with humanized anti-CD154 monoclonal antibodies are underway in severe autoimmune diseases, but its development in transplantation is unclear at this time.Keywords
This publication has 45 references indexed in Scilit:
- The role of CD154-CD40 versus CD28-B7 costimulatory pathways in regulating allogeneic Th1 and Th2 responses in vivoJournal of Clinical Investigation, 2000
- RETRACTED: The Fas/Fas Ligand Pathway and Bcl-2 Regulate T Cell Responses to Model Self and Foreign AntigensImmunity, 1998
- Long-term acceptance of skin and cardiac allografts after blocking CD40 and CD28 pathwaysNature, 1996
- The Roles of Costimulation and Fas in T Cell Apoptosis and Peripheral ToleranceImmunity, 1996
- CD40-gp39 INTERACTIONS PLAY A CRITICAL ROLE DURING ALLOGRAFT REJECTIONTransplantation, 1996
- CD28 costimulation can promote T cell survival by enhancing the expression of Bcl-xLImmunity, 1995
- Fas(CD95)/FasL interactions required for programmed cell death after T-cell activationNature, 1995
- bcl-x, a bcl-2-related gene that functions as a dominant regulator of apoptotic cell deathCell, 1993
- lnterleukin-2 programs mouse αβ T lymphocytes for apoptosisNature, 1991
- Cyclosporin A inhibits activation-induced cell death in T-cell hybridomas and thymocytesNature, 1989