Benkirane M, Blanc-Zouaoui D, Hirn M, Devaux C
Centre de Tri des Molécules anti-HIV, Institut National de la Santé et de la Recherche Médicale U249, Montpellier, France.
J Virol. 1994 Oct;68(10):6332-9. doi: 10.1128/JVI.68.10.6332-6339.1994.
We have studied the putative roles of human immunodeficiency virus (HIV)-associated and cell surface-expressed major histocompatibility complex class I (MHC-I) molecules in the course of the HIV life cycle by the combined use of MHC-I molecule-positive and MHC-I molecule-negative virus particles and MHC-I molecule-positive and MHC-I molecule-negative CD4+ human cells. We found (i) that several anti-MHC-I monoclonal antibodies neutralize cell infection by direct interaction with HIV-associated MHC-I antigens, (ii) that these HIV-associated MHC-I antigens are however dispensable for cell infection, and (iii) that the cell surface-expressed MHC-I molecules are unnecessary for productive infection of CD4+ human cells. These results clarify further the functions of MHC-I molecules during the HIV life cycle.
我们通过联合使用MHC-I分子阳性和MHC-I分子阴性病毒颗粒以及MHC-I分子阳性和MHC-I分子阴性CD4⁺人类细胞,研究了人类免疫缺陷病毒(HIV)相关的以及细胞表面表达的主要组织相容性复合体I类(MHC-I)分子在HIV生命周期中的假定作用。我们发现:(i)几种抗MHC-I单克隆抗体通过与HIV相关的MHC-I抗原直接相互作用来中和细胞感染;(ii)然而,这些HIV相关的MHC-I抗原对于细胞感染是可有可无的;(iii)细胞表面表达的MHC-I分子对于CD4⁺人类细胞的有效感染是不必要的。这些结果进一步阐明了MHC-I分子在HIV生命周期中的功能。