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抗独特型抗体引发抗 HIV-1 特异性 B 细胞反应。

Anti-idiotypic antibodies elicit anti-HIV-1-specific B cell responses.

机构信息

Laboratory of Molecular Immunology, The Rockefeller University, New York, NY.

Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA.

出版信息

J Exp Med. 2019 Oct 7;216(10):2316-2330. doi: 10.1084/jem.20190446. Epub 2019 Jul 25.

Abstract

Human anti-HIV-1 broadly neutralizing antibodies (bNAbs) protect against infection in animal models. However, bNAbs have not been elicited by vaccination in diverse wild-type animals or humans, in part because B cells expressing the precursors of these antibodies do not recognize most HIV-1 envelopes (Envs). Immunogens have been designed that activate these B cell precursors in vivo, but they also activate competing off-target responses. Here we report on a complementary approach to expand specific B cells using an anti-idiotypic antibody, iv8, that selects for naive human B cells expressing immunoglobulin light chains with 5-amino acid complementarity determining region 3s, a key feature of anti-CD4 binding site (CD4bs)-specific VRC01-class antibodies. In mice, iv8 induced target cells to expand and mature in the context of a polyclonal immune system and produced serologic responses targeting the CD4bs on Env. In summary, the results demonstrate that an anti-idiotypic antibody can specifically recognize and expand rare B cells that express VRC01-class antibodies against HIV-1.

摘要

人类抗 HIV-1 广泛中和抗体(bNAbs)可在动物模型中预防感染。然而,在不同的野生型动物或人类中,bNAbs 并未通过疫苗接种产生,部分原因是表达这些抗体前体的 B 细胞不能识别大多数 HIV-1 包膜(Env)。已经设计了免疫原,可在体内激活这些 B 细胞前体,但它们也会激活竞争性的非靶向反应。在这里,我们报告了一种使用抗独特型抗体 iv8 来扩增特定 B 细胞的互补方法,iv8 选择表达具有 5 个氨基酸互补决定区 3 的免疫球蛋白轻链的幼稚人类 B 细胞,这是抗 CD4 结合位点(CD4bs)特异性 VRC01 类抗体的一个关键特征。在小鼠中,iv8 在多克隆免疫系统的背景下诱导靶细胞扩增和成熟,并产生针对 Env 上 CD4bs 的血清学反应。总之,这些结果表明,抗独特型抗体可以特异性识别和扩增表达针对 HIV-1 的 VRC01 类抗体的稀有 B 细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/466e/6780999/b8219abe4438/JEM_20190446_GA.jpg

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