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CTL Responses of High Functional Avidity and Broad Variant Cross-Reactivity Are Associated with HIV Control

机译:高功能亲和力和广泛的交叉反应性的CTL反应与HIV控制相关。

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Cytotoxic T lymphocyte (CTL) responses targeting specific HIV proteins, in particular Gag, have been associated with relative control of viral replication in vivo. However, Gag-specific CTL can also be detected in individuals who do not control the virus and it remains thus unclear how Gag-specific CTL may mediate the beneficial effects in some individuals but not in others. Here, we used a 10mer peptide set spanning HIV Gag-p24 to determine immunogen-specific T-cell responses and to assess functional properties including functional avidity and cross-reactivity in 25 HIV-1 controllers and 25 non-controllers without protective HLA class I alleles. Our data challenge the common belief that Gag-specific T cell responses dominate the virus-specific immunity exclusively in HIV-1 controllers as both groups mounted responses of comparable breadths and magnitudes against the p24 sequence. However, responses in controllers reacted to lower antigen concentrations and recognized more epitope variants than responses in non-controllers. These cross-sectional data, largely independent of particular HLA genetics and generated using direct ex-vivo samples thus identify T cell responses of high functional avidity and with broad variant reactivity as potential functional immune correlates of relative HIV control.
机译:靶向特定HIV蛋白(特别是Gag)的细胞毒性T淋巴细胞(CTL)反应与体内病毒复制的相对控制有关。但是,也可以在不控制病毒的个体中检测到Gag特异的CTL,因此尚不清楚Gag特异的CTL如何介导某些个体的有益作用,而在其他个体中却没有。在这里,我们使用了一个跨过HIV Gag-p24的10mer肽组来确定免疫原特异性T细胞应答,并评估了25个没有I类保护性HLA的控制者和25个非控制者的功能特性,包括功能亲和力和交叉反应性等位基因。我们的数据挑战了一个普遍的信念,即Gag特异性T细胞应答仅在HIV-1控制器中支配病毒特异性免疫,因为两组对p24序列都具有相当广度和强度的应答。但是,与非对照相比,对照中的反应对较低的抗原浓度有反应,并识别出更多的表位变异。这些横截面数据很大程度上独立于特定的HLA遗传学,并使用直接的离体样本生成,因此将T细胞反应识别为具有高功能亲和力且具有广泛的变异反应性,这是相对HIV控制的潜在功能性免疫相关因素。

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