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

抗独特型抗体可诱导抗HIV-1特异性B细胞反应

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作者:Pia Dosenovic ,Anna-Klara Pettersson ,Abigail Wall ,Eddy S Thientosapol ,Junli Feng ,Connor Weidle ,Komal Bhullar ,Ervin E Kara ,Harald Hartweger ,Joy A Pai ,Matthew D Gray ,K Rachael Parks ,Justin J Taylor ,Marie Pancera ,Leonidas Stamatatos ,Michel C Nussenzweig ,Andrew T McGuire

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.

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