[PDF][PDF] Induction of peripheral T cell tolerance in vivo requires CTLA-4 engagement

VL Perez, L Van Parijs, A Biuckians, XX Zheng… - Immunity, 1997 - cell.com
VL Perez, L Van Parijs, A Biuckians, XX Zheng, TB Strom, AK Abbas
Immunity, 1997cell.com
Studies of T cell anergy in vitro have led to the widely accepted view that anergy is induced
by T cell antigen recognition without costimulation. We show that the induction of T cell
anergy in vivo is due to an abortive T cell response that requires recognition of B7
molecules, since blocking B7 maintains T cells in an unactivated but functionally competent
state. Furthermore, the induction of anergy is prevented by blocking CTLA-4, the inhibitory T
cell receptor for B7 molecules. Thus, in vivo T cell anergy may be induced not because of a …
Abstract
Studies of T cell anergy in vitro have led to the widely accepted view that anergy is induced by T cell antigen recognition without costimulation. We show that the induction of T cell anergy in vivo is due to an abortive T cell response that requires recognition of B7 molecules, since blocking B7 maintains T cells in an unactivated but functionally competent state. Furthermore, the induction of anergy is prevented by blocking CTLA-4, the inhibitory T cell receptor for B7 molecules. Thus, in vivo T cell anergy may be induced not because of a lack of costimulation, but as a result of specific recognition of B7 molecules by CTLA-4. In contrast, blocking CD28 on T cells prevents priming but not the induction of tolerance. Therefore, the outcome of antigen recognition by T cells is determined by the interaction of CD28 or CTLA-4 on the T cells with B7 molecules.
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