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Induction of a CD8+ Cytotoxic T Lymphocyte Response by Cross-priming Requires Cognate CD4+ T Cell Help

机译:交叉引发CD8 +细胞毒性T淋巴细胞反应的诱导需要相关的CD4 + T细胞帮助。

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摘要

Class I–restricted presentation is usually associated with cytoplasmic degradation of cellular proteins and is often considered inaccessible to exogenous antigens. Nonetheless, certain exogenous elements can gain entry into this so-called endogenous pathway by a mechanism termed cross-presentation. This is known to be effective for class I–restricted cytotoxic T lymphocyte (CTL) cross-priming directed against a variety of exogenous tumor, viral, and minor transplantation antigens. The related effect of cross-tolerance can also effectively eliminate responses to selected self components. In both cases, this presentation appears to require the active involvement of a bone marrow–derived antigen presenting cell (APC). Here, we show that CTL induction by cross-priming with cell-associated ovalbumin requires the active involvement of CD4+ helper T cells. Importantly, this CD4+ population is only effective when both the helper and CTL determinants are recognized on the same APC. Moreover, we would argue that the cognitive nature of this event suggests that the CD4+ T cell actively modifies the APC, converting it into an effective stimulator for the successful priming of the CTL precursor.
机译:I类受限的表现通常与细胞蛋白的细胞质降解有关,通常被认为是外源性抗原难以接近的。但是,某些外源性元素可以通过称为交叉展示的机制进入这一所谓的内源性途径。已知这对于针对多种外源性肿瘤,病毒和次要移植抗原的I类限制性细胞毒性T淋巴细胞(CTL)交叉引发是有效的。交叉容差的相关影响也可以有效消除对选定自身成分的响应。在这两种情况下,这种表现似乎都需要积极参与骨髓源性抗原呈递细胞(APC)的参与。在这里,我们显示通过交叉引发与细胞相关的卵清蛋白进行CTL诱导需要CD4 +辅助T细胞的主动参与。重要的是,只有在同一APC上同时识别了辅助和CTL决定簇时,该CD4 +种群才有效。此外,我们认为该事件的认知性质表明CD4 + T细胞会主动修饰APC,将其转变为有效引发CTL前体的有效刺激物。

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