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. Author manuscript; available in PMC: 2013 Sep 26.
Published in final edited form as: Am J Transplant. 2012 Aug 17;12(10):2575–2587. doi: 10.1111/j.1600-6143.2012.04224.x

Figure 3. PD-1: PD-L1 signaling in allograft tolerance.

Figure 3

This figure illustrates some of the potential interactions of this pathway in lymphoid organs and in a cardiac allograft. (A), Tolerogenic DCs interact with naïve T cells and may induce either alloantigen-specific Tregs (iTregs) or decreased activation of effector T cell (T eff), depending on the presence (or absence) of TGF-β. (B), After activation by DCs in secondary lymphoid organs, alloantigen-specific effector T cells migrate to the graft where initial interaction with PD-L1 in the endothelium might inhibit T effector responses. Additional T eff cells that infiltrate the graft may be suppressed by iTregs or local cells expressing PD-L1 (APCs or non-hematopoieitic cells). Whether PD1/PDL1 on iTregs play a significant role in the direct suppression of T eff remains to be determined. Other potential costimulatory interactions are not depicted in this figure for simplicity.