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Short communication: broader T cell responses directed against human immunodeficiency virus type 1 in infected Chinese individuals through blood-borne transmission in comparison with mucosal transmission.

机译:简短交流:与中国人通过粘膜传播相比,中国人通过血液传播传播的针对1型人类免疫缺陷病毒的T细胞反应更为广泛。

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摘要

Cellular immune responses play a critical role in the control of human immunodeficiency virus type 1 (HIV-1), but less is known about the impact of transmission routes on immune defenses against HIV-1. Here, we report that subjects infected with HIV-1 through contaminated blood showed stronger HIV-specific T cell responses than those infected through mucosa, both in breadth (6.9±2.5 vs. 2.3±0.5, p=0.0293) and in magnitude [1270.0±544.9 vs. 409.5±121.3 SFU per million peripheral blood mononuclear cells (PBMCs), p=0.0223], by using a matrix of 404 overlapping peptides spanning all expressed HIV-1 proteins in an interferon (IFN)-γ enzyme-linked immunospot (ELISpot) assay. Our observation indicates that different mechanisms might be involved in the priming/generating of anti-HIV-specific T cell responses through different transmission routes.
机译:细胞免疫应答在控制人类1型免疫缺陷病毒(HIV-1)中起着至关重要的作用,但是关于传播途径对HIV-1免疫防御的影响知之甚少。在这里,我们报道了通过污染的血液感染HIV-1的受试者在宽度(6.9±2.5对2.3±0.5,p = 0.0293)和大小上均表现出比通过粘膜感染的HIV特异的T细胞应答更强[1270.0通过使用干扰素(IFN)-γ酶联免疫斑点中跨越所有表达的HIV-1蛋白的404个重叠肽矩阵,将每百万个外周血单核细胞(PBMC)的±544.9 vs. 409.5±121.3 SFU,p = 0.0223] (ELISpot)分析。我们的观察表明,通过不同的传播途径引发/产生抗HIV特异性T细胞应答可能涉及不同的机制。

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