Novel Therapeutic Approach for Inhibition of HIV-1 Using Cell-Penetrating Peptide and Bacterial Toxins.

Journal of AIDS & clinical research Pub Date : 2017-10-01 Epub Date: 2017-10-23 DOI:10.4172/2155-6113.1000737
Steven Samuels, Zainab Alwan, Marceline Egnin, Jessie Jaynes, Terry D Connell, Gregory C Bernard, Toufic Nashar
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引用次数: 2

Abstract

Despite advancements in our understanding of HIV-1 pathogenesis, critical virus components for immunity, vaccines trials, and drugs development, challenges remain in the fight against HIV-1. Of great importance is the inhibitory function of microbicidal cell penetrating peptides and bacterial toxins that interfere with production and neutralize infection of HIV-1 particles. We demonstrate that the neutralizing activity of a cationic 18 amino acids peptide, is similar to a broadly neutralizing human antibody, and inhibits production of two HIV-1 strains in human cell lines. Pretreatment of cells with bacterial toxins or toxoids derived from enterotoxigenic E. coli, boost subsequent activity of the peptide against HIV-1, to inhibit simultaneously production and infection. The synthetic peptide crosses the cell membrane into the cytoplasm and nucleus. In vitro analysis of a possible target for this peptide revealed specific binding to recombinant HIV-1 gag p24. This is the first demonstration of a synergy between bacterial toxins and a cell-penetrating peptide against HIV-1.

Abstract Image

Abstract Image

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利用细胞穿透肽和细菌毒素抑制HIV-1的新治疗方法。
尽管我们对HIV-1的发病机制、免疫的关键病毒成分、疫苗试验和药物开发的理解取得了进展,但与HIV-1的斗争仍然存在挑战。重要的是杀微生物细胞穿透肽和细菌毒素的抑制功能,这些肽和细菌毒素干扰HIV-1颗粒的产生和中和感染。我们证明了阳离子18个氨基酸肽的中和活性,类似于广泛中和的人类抗体,并抑制人类细胞系中两种HIV-1菌株的产生。用产肠毒素大肠杆菌的细菌毒素或类毒素预处理细胞,可以提高随后抗HIV-1肽的活性,同时抑制生产和感染。合成肽穿过细胞膜进入细胞质和细胞核。在体外分析该肽可能的靶标显示特异性结合重组HIV-1 gag p24。这是首次证明细菌毒素和细胞穿透肽之间的协同作用对抗HIV-1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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