Abstract
Annual Review of Immunology
Vol. 21:
139-176
(Volume publication date April 2003)
(doi:10.1146/annurev.immunol.21.120601.141107)
First Published online as a Review in Advance on October 28, 2002POSITIVE AND NEGATIVE SELECTION OF T CELLS Timothy K. Starr, Stephen C. Jameson, and Kristin A. HogquistCenter for Immunology and the Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota 55455; email: star0044@umn.edu james024@umn.edu hogqu001@umn.edu ▪ Abstract A functional immune system requires the selection of T lymphocytes expressing receptors that are major histocompatibility complex restricted but tolerant to self-antigens. This selection occurs predominantly in the thymus, where lymphocyte precursors first assemble a surface receptor. In this review we summarize the current state of the field regarding the natural ligands and molecular factors required for positive and negative selection and discuss a model for how these disparate outcomes can be signaled via the same receptor. We also discuss emerging data on the selection of regulatory T cells. Such cells require a high-affinity interaction with self-antigens, yet differentiate into regulatory cells instead of being eliminated. Most recent citing papers (via CrossRef)Positive selection optimizes the number and function of MHCII-restricted CD4+ T cell clones in the naive polyclonal repertoire Proceedings of the National Academy of Sciences 106(27):11241-11245 (2009) Rac GTPases play critical roles in early T-cell development Blood 113(17):3990-3998 (2009) Transcriptional complexes formed by NFAT dimers regulate the induction of T cell tolerance Journal of Experimental Medicine 206(4):867-876 (2009) Evolution of adaptive immunity Biology Bulletin 36(2):107-116 (2009) MicroRNAs: Control and Loss of Control in Human Physiology and Disease World Journal of Surgery 33(4):667-684 (2009)
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