首页> 外文期刊>Microbiology and Immunology >Protective immune responses induced by a non-pathogenic simian/humanimmunodeficiency virus (SHIV) against a challenge of a pathogenic SHIV inmonkeys
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Protective immune responses induced by a non-pathogenic simian/humanimmunodeficiency virus (SHIV) against a challenge of a pathogenic SHIV inmonkeys

机译:非致病性猿猴/人类免疫缺陷病毒(SHIV)诱导的针对病原性SHIV猴攻击的保护性免疫应答

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摘要

A simian/human immunodeficiency virus (SHIV)-NM3n containing the human nef, but not the monkey nef, and vpr genes of SIV was inoculated into two cynomolgus monkeys, resulting in systemic infection with a minimum level of transient virus load. In order to study the nature of immune responses associated with the prevention of a pathogenic SHIV, the SHIV-NM3n-inoculated monkeys and three naive monkeys were intravenously challenged with a pathogenic SHIV containing the envelope gene of HIV-1 89.6. After the heterologous virus challenge, all of the SHIV-NM3n-inoculated animals completely avoided the loss of CD4(+) T lymphocytes in PBMC as well as lymphoid tissues compared to pathogenic SHIV-injected control animals. The inhibition of CD4(+) cell depletion was associated with maintaining the proliferative response of helper T-cells against SIV p27 in the previously nonpathogenic virus-inoculated animals following the pathogenic virus challenge. Furthermore, the decline of CD28(+) cells, the increase in CD95(+) cells, and the enhancement of in vitro apoptosis in PBMC were inhibited in the non-pathogenic virus-inoculated animals. These results suggest that nonpathogenic SHIV-NM3n infection induces the protection of monkeys from heterologous pathogenic viruses that may be associated with blocking the change in immune responses and the cell loss induced by a pathogenic virus.
机译:将包含人nef(但不包括猴nef)和SIV的vpr基因的猿猴/人免疫缺陷病毒(SHIV)-NM3n接种到两只食蟹猴中,以最小的瞬时病毒负荷水平进行全身感染。为了研究与预防病原性SHIV相关的免疫反应的性质,将接种了SHIV-NM3n的猴子和三只幼稚的猴子静脉内攻击含有HIV-1 89.6包膜基因的病原性SHIV。异源病毒攻击后,与注射病原性SHIV的对照动物相比,所有SHIV-NM3n接种的动物都完全避免了PBMC和淋巴样组织中CD4(+)T淋巴细胞的丢失。 CD4(+)细胞耗竭的抑制与病原病毒攻击后,在先前非致病性病毒接种动物中维持辅助性T细胞针对SIV p27的增殖反应有关。此外,CD28(+)细胞的下降,CD95(+)细胞的增加和PBMC中体外凋亡的增强在非致病病毒接种的动物中受到抑制。这些结果表明,非致病性SHIV-NM3n感染可诱导猴子免受异源病原性病毒的侵害,这可能与阻断免疫应答的变化和由病原性病毒引起的细胞损失有关。

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