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

机译:迈向艾滋病疫苗:非洲非人类灵长类动物宿主的天然猿猴免疫缺陷病毒感染的经验教训。

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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.
机译:有效的艾滋病疫苗的设计使科学界无法作出努力,以至于必须考虑替代经典疫苗制剂的替代方法。我们在这里建议,HIV疫苗的研究可以极大地受益于非洲非人类灵长类动物的天然猿猴免疫缺陷病毒(SIV)感染的研究。天然SIV宿主(例如煤烟黑man,非洲绿猴和山d)具有人类感染HIV的许多特征。但是,它们通常不会发展为免疫缺陷。这些自然的,非进行性的SIV感染代表了进化适应,使灵长类慢病毒与宿主免疫系统和平共处。这种适应并不导致病毒复制减少,而是涉及CD4(+)T细胞亚型的表型改变,有限的免疫激活和保留的粘膜免疫力,所有这些都有助于避免疾病的进展,并可能有助于减少垂直SIV传输。在这里,我们总结了对非洲非人类灵长类动物SIV感染的当前理解,并讨论了如何阐明这些进化适应性可能为新疫苗设计提供线索,这些疫苗设计可以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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