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一种1型人类免疫缺陷病毒(HIV-1)B亚型衍生疫苗无法预防黑猩猩被HIV-1 E亚型毒株感染。

Failure of a human immunodeficiency virus type 1 (HIV-1) subtype B-derived vaccine to prevent infection of chimpanzees by an HIV-1 subtype E strain.

作者信息

Girard M, Yue L, Barré-Sinoussi F, van der Ryst E, Meignier B, Muchmore E, Fultz P N

机构信息

Institut Pasteur, Paris, France.

出版信息

J Virol. 1996 Nov;70(11):8229-33. doi: 10.1128/JVI.70.11.8229-8233.1996.

Abstract

Generation of an effective vaccine against human immunodeficiency virus type 1 (HIV-1) must overcome problems associated with extensive genetic diversity. Although we previously reported vaccine-induced protection of chimpanzees against infection with an HIV-1 strain different from the one used to make the immunogens, both the HIV-1 vaccine and challenge strains were classified within subtype B. To determine whether the HIV-1-specific immunity elicited might also prevent infection by a strain of HIV-1 from a different clade, the same chimpanzees were given booster inoculations with the rgp160-MN/LAI (recombinant hybrid gp160 molecule) and V3-MN immunogens and then were challenged by intravenous inoculation of a comparable dose of a subtype E HIV-1 from the Central African Republic. Both animals became infected with the subtype E virus, indicating that intraclade vaccine-mediated protection does not predict interclade protection, at least in the context of intravenous challenge and the HIV-1 strains used. This study has important implications for planned phase III efficacy trials of similar vaccine preparations in Thailand where HIV-1 subtype B and E strains cocirculate.

摘要

开发一种针对人类免疫缺陷病毒1型(HIV-1)的有效疫苗必须克服与广泛基因多样性相关的问题。尽管我们之前报道过疫苗诱导的黑猩猩对与用于制备免疫原的HIV-1毒株不同的毒株感染具有保护作用,但HIV-1疫苗毒株和攻击毒株均属于B亚型。为了确定所引发的HIV-1特异性免疫是否也能预防来自不同进化枝的HIV-1毒株的感染,对相同的黑猩猩用rgp160-MN/LAI(重组杂交gp160分子)和V3-MN免疫原进行加强接种,然后通过静脉注射来自中非共和国的相当剂量的E亚型HIV-1进行攻击。两只动物均感染了E亚型病毒,这表明至少在静脉内攻击和所使用的HIV-1毒株的背景下,进化枝内疫苗介导的保护不能预测进化枝间的保护作用。这项研究对于泰国计划进行的类似疫苗制剂的III期疗效试验具有重要意义,在泰国HIV-1 B亚型和E亚型毒株共同流行。

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