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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.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。
J Virol. 2010 Feb;84(3):1302-13. doi: 10.1128/JVI.01272-09. Epub 2009 Nov 11.
2
An affinity-enhanced neutralizing antibody against the membrane-proximal external region of human immunodeficiency virus type 1 gp41 recognizes an epitope between those of 2F5 and 4E10.一种针对人类免疫缺陷病毒1型gp41膜近端外部区域的亲和力增强型中和抗体识别的表位介于2F5和4E10的表位之间。
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Anti-human immunodeficiency virus type 1 (HIV-1) antibodies 2F5 and 4E10 require surprisingly few crucial residues in the membrane-proximal external region of glycoprotein gp41 to neutralize HIV-1.抗1型人类免疫缺陷病毒(HIV-1)抗体2F5和4E10在糖蛋白gp41的膜近端外部区域只需极少关键残基就能中和HIV-1。
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N-terminal residues of an HIV-1 gp41 membrane-proximal external region antigen influence broadly neutralizing 2F5-like antibodies.人类免疫缺陷病毒1型糖蛋白41膜近端外部区域抗原的N端残基影响广谱中和性2F5样抗体。
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Stable docking of neutralizing human immunodeficiency virus type 1 gp41 membrane-proximal external region monoclonal antibodies 2F5 and 4E10 is dependent on the membrane immersion depth of their epitope regions.人免疫缺陷病毒1型(HIV-1)gp41膜近端外部区域中和单克隆抗体2F5和4E10的稳定对接取决于其表位区域的膜浸入深度。
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Analysis of the human immunodeficiency virus type 1 gp41 membrane proximal external region arrayed on hepatitis B surface antigen particles.1型人类免疫缺陷病毒gp41膜近端外部区域排列在乙型肝炎表面抗原颗粒上的分析。
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ACS Chem Biol. 2025 Jul 18;20(7):1470-1480. doi: 10.1021/acschembio.5c00035. Epub 2025 Jun 20.
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Combining a rhesus cytomegalovirus/SIV vaccine with a neutralizing antibody to protect against SIV challenges in rhesus macaques.将恒河猴巨细胞病毒/猴免疫缺陷病毒疫苗与一种中和抗体联合使用,以保护恒河猴免受猴免疫缺陷病毒攻击。
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Mechanisms of sterilizing immunity provided by an HIV-1 neutralizing antibody against mucosal infection.一种HIV-1中和抗体提供的针对黏膜感染的杀菌免疫机制。
PLoS Pathog. 2024 Dec 26;20(12):e1012777. doi: 10.1371/journal.ppat.1012777. eCollection 2024 Dec.
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本文引用的文献

1
Broad and potent neutralizing antibodies from an African donor reveal a new HIV-1 vaccine target.一位非洲捐赠者体内广泛且强效的中和抗体揭示了一个新的HIV-1疫苗靶点。
Science. 2009 Oct 9;326(5950):285-9. doi: 10.1126/science.1178746. Epub 2009 Sep 3.
2
Broadly neutralizing human anti-HIV antibody 2G12 is effective in protection against mucosal SHIV challenge even at low serum neutralizing titers.广泛中和性人类抗HIV抗体2G12即使在血清中和效价较低时,也能有效保护机体免受黏膜猴-人免疫缺陷病毒攻击。
PLoS Pathog. 2009 May;5(5):e1000433. doi: 10.1371/journal.ppat.1000433. Epub 2009 May 15.
3
Effector memory T cell responses are associated with protection of rhesus monkeys from mucosal simian immunodeficiency virus challenge.效应记忆T细胞反应与恒河猴免受黏膜猿猴免疫缺陷病毒攻击的保护作用相关。
Nat Med. 2009 Mar;15(3):293-9. doi: 10.1038/nm.1935. Epub 2009 Feb 15.
4
Fc receptor but not complement binding is important in antibody protection against HIV.Fc受体而非补体结合在抗体抗HIV保护中起重要作用。
Nature. 2007 Sep 6;449(7158):101-4. doi: 10.1038/nature06106.
5
Adjunctive passive immunotherapy in human immunodeficiency virus type 1-infected individuals treated with antiviral therapy during acute and early infection.在急性和早期感染期间接受抗病毒治疗的1型人类免疫缺陷病毒感染个体中的辅助性被动免疫疗法。
J Virol. 2007 Oct;81(20):11016-31. doi: 10.1128/JVI.01340-07. Epub 2007 Aug 8.
6
Molecular typing of major histocompatibility complex class I alleles in the Indian rhesus macaque which restrict SIV CD8+ T cell epitopes.限制SIV CD8 + T细胞表位的印度恒河猴主要组织相容性复合体I类等位基因的分子分型。
Immunogenetics. 2007 Sep;59(9):693-703. doi: 10.1007/s00251-007-0233-7. Epub 2007 Jul 20.
7
In vivo and in vitro escape from neutralizing antibodies 2G12, 2F5, and 4E10.在体内和体外逃避中和抗体2G12、2F5和4E10。
J Virol. 2007 Aug;81(16):8793-808. doi: 10.1128/JVI.00598-07. Epub 2007 Jun 13.
8
Mamu-B*08-positive macaques control simian immunodeficiency virus replication.Mamu - B*08阳性猕猴可控制猿猴免疫缺陷病毒复制。
J Virol. 2007 Aug;81(16):8827-32. doi: 10.1128/JVI.00895-07. Epub 2007 May 30.
9
An affinity-enhanced neutralizing antibody against the membrane-proximal external region of human immunodeficiency virus type 1 gp41 recognizes an epitope between those of 2F5 and 4E10.一种针对人类免疫缺陷病毒1型gp41膜近端外部区域的亲和力增强型中和抗体识别的表位介于2F5和4E10的表位之间。
J Virol. 2007 Apr;81(8):4033-43. doi: 10.1128/JVI.02588-06. Epub 2007 Feb 7.
10
Subdominant CD8+ T-cell responses are involved in durable control of AIDS virus replication.亚优势CD8 + T细胞反应参与对艾滋病病毒复制的持久控制。
J Virol. 2007 Apr;81(7):3465-76. doi: 10.1128/JVI.02392-06. Epub 2007 Jan 24.

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.

DOI:10.1128/JVI.01272-09
PMID:19906907
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2812338/
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。