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Different In Vivo Effects of HIV-1 Immunodominant Epitope-Specific Cytotoxic T Lymphocytes on Selection of Escape Mutant Viruses▿ ‡

机译:HIV-1免疫抗原决定簇特异性细胞毒性T淋巴细胞对逃生突变病毒选择的不同体内作用

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摘要

HIV-1 escape mutants are well known to be selected by immune pressure via HIV-1-specific cytotoxic T lymphocytes (CTLs) and neutralizing antibodies. The ability of the CTLs to suppress HIV-1 replication is assumed to be associated with the selection of escape mutants from the CTLs. Therefore, we first investigated the correlation between the ability of HLA-A*1101-restricted CTLs recognizing immunodominant epitopes in vitro and the selection of escape mutants. The result showed that there was no correlation between the ability of these CTLs to suppress HIV-1 replication in vitro and the appearance of escape mutants. The CTLs that had a strong ability to suppress HIV-1 replication in vitro but failed to select escape mutants expressed a higher level of PD-1 in vivo, whereas those that had a strong ability to suppress HIV-1 replication in vitro and selected escape mutants expressed a low level of PD-1. Ex vivo analysis of these CTLs revealed that the latter CTLs had a significantly stronger ability to recognize the epitope than the former ones. These results suggest that escape mutations are selected by HIV-1-specific CTLs that have a stronger ability to recognize HIV-1 in vivo but not in vitro.
机译:众所周知,HIV-1逃逸突变体是通过HIV-1特异性细胞毒性T淋巴细胞(CTL)和中和抗体通过免疫压力选择的。假定CTL抑制HIV-1复制的能力与从CTL中选择逃避突变体有关。因此,我们首先研究了HLA-A * 1101限制性CTL在体外识别免疫优势表位的能力与逃避突变体选择之间的相关性。结果表明,这些CTL在体外抑制HIV-1复制的能力与逃避突变体的出现之间没有相关性。具有强大的体外抑制HIV-1复制能力但未能选择逃避突变体的CTL在体内表达更高水平的PD-1,而具有强大的体外抑制HIV-1复制能力和选择性逃避能力的CTL突变体表达低水平的PD-1。这些CTL的离体分析显示,后者的CTL识别抗原决定簇的能力明显强于前者。这些结果表明,逃避突变是由HIV-1特异的CTL选择的,这些CTL在体内而非体外具有更强的识别HIV-1的能力。

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