Siggs Owen Marc, Makaroff Lydia Elizabeth, Liston Adrian
John Curtin School of Medical Research and School of Biochemistry and Molecular Biology, The Australian National University, Canberra 2601, Australia.
Curr Opin Immunol. 2006 Apr;18(2):175-83. doi: 10.1016/j.coi.2006.01.001. Epub 2006 Feb 3.
The generation of T cell receptor (TCR) sequence diversity is the strength of adaptive immunity, yet is also the Achilles' heel. To purge highly self-reactive T cells from the immune system, generation of diversity has coevolved with a mechanism of negative selection. Recent studies have revealed new insights addressing the why and how of negative selection by examining situations in which negative selection has failed in human and animals models of autoimmunity. Both thymocyte extrinsic and intrinsic mechanisms are required to restrict the TCR repertoire to a non-autoreactive set. Negative selection also ensures that T cells emerge with receptors that are focussed on the peptide moiety of MHC-peptide complexes.
T细胞受体(TCR)序列多样性的产生是适应性免疫的优势,但也是其致命弱点。为了从免疫系统中清除高度自身反应性的T细胞,多样性的产生与阴性选择机制共同进化。最近的研究通过研究在人类和动物自身免疫模型中阴性选择失败的情况,揭示了关于阴性选择的原因和方式的新见解。胸腺细胞外在和内在机制都需要将TCR库限制为非自身反应性集合。阴性选择还确保T细胞以聚焦于MHC-肽复合物肽部分的受体出现。