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Immunogenicity of virus-like particles containing modified human immunodeficiency virus envelope proteins

机译:含有修饰的人免疫缺陷病毒包膜蛋白的病毒样颗粒的免疫原性

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摘要

Extensive glycosylation and variable loops of the HIV envelope protein (Env) are reported to shield some neutralizing epitopes. Here, we investigated the immunogenicity of mutated HIV Envs presented in virus-like particles (VLPs). We immunized mice with simian human immunodeficiency virus (SHIV) VLPs containing mutant HIV Env with reduced glycosylation (3G), variable loop-deleted mutations (dV1V2), or combinations of both types of mutations (3G-dV2−1G), and evaluated immune responses. Immune sera from mice that received VLPs with modified HIV Envs (3G or dV1V2) showed higher neutralizing activities against the homologous HIV 89.6 virus as well as heterologous viruses when compared with wild type SHIV VLP-immunized mice. Lymphocytes from immunized mice produced HIV Env-specific cytokines, with the 3G-dV2−1G mutant producing high levels of cytokines. Interestingly, both dendritic cells and B cells were found to interact with VLPs suggesting that VLPs are effective immunogens. Therefore, this study suggests that VLPs containing modified HIV Env have the potential to be developed as candidate vaccines capable of inducing cellular and humoral immune responses including neutralizing activities.
机译:据报道,广泛的糖基化和HIV包膜蛋白(Env)的可变环可屏蔽某些中和表位。在这里,我们调查了病毒样颗粒(VLP)中呈现的突变HIV Env的免疫原性。我们用猿猴人免疫缺陷病毒(SHIV)VLP免疫小鼠,该病毒含有糖基化减少(3G),可变环缺失突变(dV1V2)或两种类型的突变组合(3G-dV2-1G)的突变HIV Env,并进行了免疫评估回应。与野生型SHIV VLP免疫小鼠相比,接受带有修饰的HIV Envs(3G或dV1V2)的VLP的小鼠的免疫血清显示出对同源HIV 89.6病毒以及异源病毒更高的中和活性。免疫小鼠的淋巴细胞产生HIV Env特异性细胞因子,而3G-dV2-1G突变体产生高水平的细胞因子。有趣的是,发现树突状细胞和B细胞都与VLP相互作用,表明VLP是有效的免疫原。因此,这项研究表明,含有修饰的HIV Env的VLP有可能被开发为候选疫苗,能够诱导细胞和体液免疫反应,包括中和活性。

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