Parello Caitlin S, Huseby Eric S
Department of Pathology, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Department of Pathology, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Trends Immunol. 2015 Jun;36(6):337-43. doi: 10.1016/j.it.2015.04.004. Epub 2015 May 12.
Adaptive immunity is predicated on the ability of the T cell repertoire to have pre-existing specificity for the universe of potential pathogens. Recent findings suggest that T cell receptor (TCR)-self-major histocompatibility protein (pMHC) interactions limit autoimmune responses while enhancing T cell response to foreign antigens. We review these findings here, placing them in context of the current understanding of how TCR-self-pMHC interactions regulate T cell activation thresholds, and suggest that TCR-self-pMHC interactions increase the efficiency of the T cell repertoire by giving a competitive advantage to peptide cross-reactive T cells. We propose that self-reactivity and peptide cross-reactivity are controlled by particular CDR3 sequence motifs, which would allow thymic selection to contribute to solving the feat of broad pathogen specificity by exporting T cells that are pre-screened by positive and negative selection for the ability to be 'moderately' peptide cross-reactive.
适应性免疫基于T细胞库对潜在病原体总体具有预先存在的特异性的能力。最近的研究结果表明,T细胞受体(TCR)与自身主要组织相容性蛋白(pMHC)的相互作用在限制自身免疫反应的同时增强了T细胞对外来抗原的反应。我们在此回顾这些研究结果,将它们置于当前对TCR与自身pMHC相互作用如何调节T细胞激活阈值的理解背景下,并表明TCR与自身pMHC的相互作用通过赋予肽交叉反应性T细胞竞争优势来提高T细胞库的效率。我们提出,自身反应性和肽交叉反应性由特定的互补决定区3(CDR3)序列基序控制,这将使胸腺选择通过输出经阳性和阴性选择预先筛选出具有“适度”肽交叉反应能力的T细胞,从而有助于解决广泛病原体特异性这一难题。