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可溶性稳定包膜糖蛋白三聚体对原发性人类免疫缺陷病毒中和抗体的诱导作用增强。

Improved elicitation of neutralizing antibodies against primary human immunodeficiency viruses by soluble stabilized envelope glycoprotein trimers.

作者信息

Yang X, Wyatt R, Sodroski J

机构信息

Department of Cancer Immunology & AIDS, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

J Virol. 2001 Feb;75(3):1165-71. doi: 10.1128/JVI.75.3.1165-1171.2001.

Abstract

Human immunodeficiency virus (HIV-1) envelope glycoprotein subunits, such as the gp120 exterior glycoprotein, typically elicit antibodies that neutralize T-cell-line-adapted (TCLA), but not primary, clinical isolates of HIV-1. Here we compare the immunogenicity of gp120 and soluble stabilized trimers, which were designed to resemble the functional envelope glycoprotein oligomers of primary and TCLA HIV-1 strains. For both primary and TCLA virus proteins, soluble stabilized trimers generated neutralizing antibody responses more efficiently than gp120 did. Trimers derived from a primary isolate elicited antibodies that neutralized primary and TCLA HIV-1 strains. By contrast, trimers derived from a TCLA isolate generated antibodies that neutralized only the homologous TCLA virus. Thus, soluble stabilized envelope glycoprotein trimers derived from primary HIV-1 isolates represent defined immunogens capable of eliciting neutralizing antibodies that are active against clinically relevant HIV-1 strains.

摘要

人类免疫缺陷病毒1型(HIV-1)包膜糖蛋白亚基,如gp120外膜糖蛋白,通常能引发中和T细胞系适应型(TCLA)HIV-1的抗体,但不能中和HIV-1的原代临床分离株。在此,我们比较了gp120和可溶性稳定三聚体的免疫原性,这些三聚体旨在模拟原代和TCLA HIV-1毒株的功能性包膜糖蛋白寡聚体。对于原代和TCLA病毒蛋白,可溶性稳定三聚体比gp120更有效地产生中和抗体反应。源自原代分离株的三聚体引发的抗体能中和原代和TCLA HIV-1毒株。相比之下,源自TCLA分离株的三聚体产生的抗体仅能中和同源TCLA病毒。因此,源自HIV-1原代分离株的可溶性稳定包膜糖蛋白三聚体代表了明确的免疫原,能够引发对临床相关HIV-1毒株具有活性的中和抗体。

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