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HIV-1 感染产生的靶向 V2 的类疫苗抗体鉴定出具有广泛 ADCC 活性的额外 K169 结合轻链基序。

V2-Directed Vaccine-like Antibodies from HIV-1 Infection Identify an Additional K169-Binding Light Chain Motif with Broad ADCC Activity.

机构信息

National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg 2131, South Africa; Faculty of Health Sciences, University of the Witwatersrand, Johannesburg 2000, South Africa.

National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg 2131, South Africa.

出版信息

Cell Rep. 2018 Dec 11;25(11):3123-3135.e6. doi: 10.1016/j.celrep.2018.11.058.

Abstract

Antibodies that bind residue K169 in the V2 region of the HIV-1 envelope correlated with reduced risk of infection in the RV144 vaccine trial but were restricted to two ED-motif-encoding light chain genes. Here, we identify an HIV-infected donor with high-titer V2 peptide-binding antibodies and isolate two antibody lineages (CAP228-16H/19F and CAP228-3D) that mediate potent antibody-dependent cell-mediated cytotoxicity (ADCC). Both lineages use the IGHV5-51 heavy chain germline gene, similar to the RV144 antibody CH58, but one lineage (CAP228-16H/19F) uses a light chain without the ED motif. A cocrystal structure of CAP228-16H bound to a V2 peptide identified a IGLV3-21 gene-encoded DDxD motif that is used to bind K169, with a mechanism that allows CAP228-16H to recognize more globally relevant V2 immunotypes. Overall, these data further our understanding of the development of cross-reactive, V2-binding, antiviral antibodies and effectively expand the human light chain repertoire able to respond to RV144-like immunogens.

摘要

在 HIV-1 包膜的 V2 区结合残基 K169 的抗体与 RV144 疫苗试验中降低感染风险相关,但仅限于两种 ED 基序编码的轻链基因。在这里,我们鉴定了一位 HIV 感染供体,其具有高滴度的 V2 肽结合抗体,并分离出两种抗体谱系(CAP228-16H/19F 和 CAP228-3D),它们介导有效的抗体依赖性细胞介导的细胞毒性(ADCC)。这两种谱系都使用 IGHV5-51 重链胚系基因,类似于 RV144 抗体 CH58,但其中一种谱系(CAP228-16H/19F)使用不具有 ED 基序的轻链。与 CAP228-16H 结合的 V2 肽的共晶结构确定了一个 IGLV3-21 基因编码的 DDxD 基序,用于结合 K169,其机制允许 CAP228-16H 识别更具全球相关性的 V2 免疫型。总体而言,这些数据进一步加深了我们对交叉反应性、V2 结合性抗病毒抗体的发展的理解,并有效地扩展了能够对 RV144 样免疫原产生反应的人类轻链库。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa62/6342559/c6ac2faa3f55/nihms-1517193-f0002.jpg

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