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迈向艾滋病疫苗:非洲非人灵长类宿主自然感染猿猴免疫缺陷病毒的经验教训。

Toward an AIDS vaccine: lessons from natural simian immunodeficiency virus infections of African nonhuman primate hosts.

作者信息

Sodora Donald L, Allan Jonathan S, Apetrei Cristian, Brenchley Jason M, Douek Daniel C, Else James G, Estes Jacob D, Hahn Beatrice H, Hirsch Vanessa M, Kaur Amitinder, Kirchhoff Frank, Muller-Trutwin Michaela, Pandrea Ivona, Schmitz Jörn E, Silvestri Guido

机构信息

Seattle Biomedical Research Institute, Seattle, Washington, USA.

出版信息

Nat Med. 2009 Aug;15(8):861-5. doi: 10.1038/nm.2013.

Abstract

The design of an effective AIDS vaccine has eluded the efforts of the scientific community to the point that alternative approaches to classic vaccine formulations have to be considered. We propose here that HIV vaccine research could greatly benefit from the study of natural simian immunodeficiency virus (SIV) infections of African nonhuman primates. Natural SIV hosts (for example, sooty mangabeys, African green monkeys and mandrills) share many features of HIV infection of humans; however, they usually do not develop immunodeficiency. These natural, nonprogressive SIV infections represent an evolutionary adaptation that allows a peaceful coexistence of primate lentiviruses and the host immune system. This adaptation does not result in reduced viral replication but, rather, involves phenotypic changes to CD4(+) T cell subsets, limited immune activation and preserved mucosal immunity, all of which contribute to the avoidance of disease progression and, possibly, to the reduction of vertical SIV transmission. Here we summarize the current understanding of SIV infection of African nonhuman primates and discuss how unraveling these evolutionary adaptations may provide clues for new vaccine designs that might induce effective immune responses without the harmful consequences of excessive immune activation.

摘要

有效的艾滋病疫苗设计一直未能实现,以至于科学界不得不考虑经典疫苗配方之外的替代方法。我们在此提出,艾滋病毒疫苗研究可从对非洲非人灵长类动物自然感染猴免疫缺陷病毒(SIV)的研究中大大受益。天然SIV宿主(如乌黑白眉猴、非洲绿猴和山魈)具有人类感染艾滋病毒的许多特征;然而,它们通常不会发展为免疫缺陷。这些自然的、非进行性的SIV感染代表了一种进化适应,使灵长类慢病毒与宿主免疫系统能够和平共存。这种适应不会导致病毒复制减少,而是涉及CD4(+) T细胞亚群的表型变化、有限的免疫激活和保留的黏膜免疫,所有这些都有助于避免疾病进展,并可能减少SIV的垂直传播。在此,我们总结了目前对非洲非人灵长类动物感染SIV的认识,并讨论了揭示这些进化适应如何为新疫苗设计提供线索,这些新疫苗设计可能诱导有效的免疫反应,而不会产生过度免疫激活的有害后果。

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