Yang X, Wyatt R, Sodroski J
Department of Cancer Immunology & AIDS, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02115, USA.
J Virol. 2001 Feb;75(3):1165-71. doi: 10.1128/JVI.75.3.1165-1171.2001.
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.
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。