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广谱中和单克隆抗体 2F5 和 4E10 针对人类免疫缺陷病毒 1 型 gp41 膜近端外部区域,可预防猴免疫缺陷病毒 SHIVBa-L 的粘膜攻击。

Broadly neutralizing monoclonal antibodies 2F5 and 4E10 directed against the human immunodeficiency virus type 1 gp41 membrane-proximal external region protect against mucosal challenge by simian-human immunodeficiency virus SHIVBa-L.

机构信息

Department of Immunology and Microbial Science and the International AIDS Vaccine Initiative Neutralizing Antibody Center, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, CA 92037, USA.

出版信息

J Virol. 2010 Feb;84(3):1302-13. doi: 10.1128/JVI.01272-09. Epub 2009 Nov 11.

Abstract

The membrane-proximal external region (MPER) of HIV-1, located at the C terminus of the gp41 ectodomain, is conserved and crucial for viral fusion. Three broadly neutralizing monoclonal antibodies (bnMAbs), 2F5, 4E10, and Z13e1, are directed against linear epitopes mapped to the MPER, making this conserved region an important potential vaccine target. However, no MPER antibodies have been definitively shown to provide protection against HIV challenge. Here, we show that both MAbs 2F5 and 4E10 can provide complete protection against mucosal simian-human immunodeficiency virus (SHIV) challenge in macaques. MAb 2F5 or 4E10 was administered intravenously at 50 mg/kg to groups of six male Indian rhesus macaques 1 day prior to and again 1 day following intrarectal challenge with SHIV(Ba-L). In both groups, five out of six animals showed complete protection and sterilizing immunity, while for one animal in each group a low level of viral replication following challenge could not be ruled out. The study confirms the protective potential of 2F5 and 4E10 and supports emphasis on HIV immunogen design based on the MPER region of gp41.

摘要

HIV-1 的膜近端外部区域(MPER)位于 gp41 外域的 C 末端,高度保守,对于病毒融合至关重要。三种广泛中和的单克隆抗体(bnMAbs),2F5、4E10 和 Z13e1,针对线性表位映射到 MPER,使这个保守区域成为一个重要的潜在疫苗靶点。然而,没有 MPER 抗体被明确证明能提供针对 HIV 挑战的保护。在这里,我们表明,两种单抗 2F5 和 4E10 都可以为猕猴提供针对粘膜性猿猴 - 人免疫缺陷病毒(SHIV)挑战的完全保护。在静脉内以 50mg/kg 的剂量给 6 只雄性印度猕猴中的每组 50mg/kg,在直肠内用 SHIV(Ba-L)攻击前一天和攻击后一天再次给药。在两组中,五分之六的动物完全受到保护和绝育免疫,而对于每组中的一只动物,在挑战后不能排除低水平的病毒复制。这项研究证实了 2F5 和 4E10 的保护潜力,并支持强调基于 gp41 的 MPER 区域的 HIV 免疫原设计。

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