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急性感染恒河猴中猿猴免疫缺陷病毒特异性CD8 +淋巴细胞反应

Simian immunodeficiency virus-specific CD8+ lymphocyte response in acutely infected rhesus monkeys.

作者信息

Yasutomi Y, Reimann K A, Lord C I, Miller M D, Letvin N L

机构信息

Harvard Medical School, New England Regional Primate Research Center, Southborough, Massachusetts 01772-9102.

出版信息

J Virol. 1993 Mar;67(3):1707-11. doi: 10.1128/JVI.67.3.1707-1711.1993.

Abstract

To assess the possible role of cytotoxic T lymphocytes (CTLs) in containing the spread of human immunodeficiency virus in acutely infected individuals, the temporal evolution of the virus-specific CD8+ lymphocyte response was defined in simian immunodeficiency virus of macaques (SIVmac)-infected rhesus monkeys. A brief period of SIVmac plasma antigenemia was seen 9 to 16 days following intravenous infection with SIVmac, ending as the absolute number of CD8+ peripheral blood lymphocytes (PBLs) increased. In a prospective assessment of the ability of CD8+ lymphocytes of these monkeys to suppress SIVmac replication in autologous PBLs, inhibitory activity was detected as early as 4 days, with a more pronounced effect 12 to 16 days following infection. SIVmac Gag- and Nef-specific CD8+ effector cell activities were demonstrable in PBLs of animals by 2 weeks following virus inoculation. In fact, SIVmac-specific CTL precursors were documented in the PBLs of rhesus monkeys 4 to 6 days after SIVmac infection. These studies indicate that AIDS virus-specific CD8+ CTLs are present in PBLs within days of infection and may play an important role in containing the early spread of virus.

摘要

为评估细胞毒性T淋巴细胞(CTL)在抑制人类免疫缺陷病毒在急性感染个体中传播方面的潜在作用,在感染猕猴猿免疫缺陷病毒(SIVmac)的恒河猴中确定了病毒特异性CD8 +淋巴细胞反应的时间演变。静脉注射SIVmac后9至16天出现短暂的SIVmac血浆抗原血症期,随着CD8 +外周血淋巴细胞(PBL)绝对数量的增加而结束。在对这些猴子的CD8 +淋巴细胞抑制自体PBL中SIVmac复制能力的前瞻性评估中,早在4天就检测到抑制活性,感染后12至16天效果更明显。接种病毒后2周,在动物的PBL中可证明SIVmac Gag和Nef特异性CD8 +效应细胞活性。事实上,在SIVmac感染后4至6天,在恒河猴的PBL中记录到SIVmac特异性CTL前体。这些研究表明,艾滋病病毒特异性CD8 + CTL在感染后数天内存在于PBL中,并可能在抑制病毒的早期传播中发挥重要作用。

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