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University of California at San Francisco Diabetes Center, San Francisco, CA 94143-0540
SUMMARY
Egen and Allison have reported that cytotoxic T lymphocyte antigen-4 (CTLA-4), an immune-responseinhibiting protein, accumulates in a two-step process at immune synapses (the sites of physical contact between T cells and antigen-presenting cells). Depending upon the strength of the signal through the T cell receptor (TCR), CTLA-4 may reside at a cytoplasmic location near the synapse (in instances of weaker stimulation) or localize to the synapse itself (under strong TCR signaling conditions). Chikuma and Bluestone discuss these findings and how CTLA-4 might inhibit T cell activation, either by increasing the threshold for activation, or by dampening existing immune responses. These findings also have important ramifications for autoimmunity and the breadth of T cell proliferation (diverse vs. narrow clonal expansion) in immune responses.
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