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Influence of correlated antigen presentation on T-cell negative selection in the thymus

机译:相关抗原呈递对胸腺T细胞阴性选择的影响

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摘要

The thymus is the primary organ for the generation of naive T cells, a key component of the immune system. Tolerance of T cells to self is achieved primarily in the thymic medulla, where immature T cells (thymocytes) sample self-peptides presented by medullary thymic epithelial cells (mTECs). A sufficiently strong interaction activates the thymocytes leading to negative selection. A key question of current interest is whether there is any structure in the manner in which mTECs present peptides: can any mTEC present any peptide at any time, or are there particular patterns of correlated peptide presentation? We investigate this question using a mathematical model of negative selection. We find that correlated patterns of peptide presentation may be advantageous in negatively selecting low-degeneracy thymocytes (that is, those thymocytes which respond to relatively few peptides). We also quantify the probability that an auto-reactive thymocyte exits the thymus before it encounters a cognate antigen. The results suggest that heterogeneity of gene co-expression in mTECs has an effect on the probability of escape of autoreactive thymocytes.
机译:胸腺是幼稚T细胞(免疫系统的关键组成部分)产生的主要器官。 T细胞对自身的耐受性主要是在胸腺髓质中实现的,在胸腺髓质中,未成熟的T细胞(胸腺细胞)会采样由胸腺髓质上皮细胞(mTEC)呈现的自身肽。足够强的相互作用激活胸腺细胞,导致阴性选择。当前关注的一个关键问题是mTECs呈递肽的方式是否存在任何结构:任何mTEC能否在任何时间呈递任何肽,或者是否存在相关肽呈递的特定模式?我们使用否定选择的数学模型调查此问题。我们发现,肽呈递的相关模式可能有利于负面选择低变性胸腺细胞(即那些对相对较少的肽有反应的胸腺细胞)。我们还量化了自身反应性胸腺细胞在遇到同源抗原之前离开胸腺的可能性。结果表明,mTECs基因共表达的异质性对自身反应性胸腺细胞逃逸的可能性有影响。

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