Idiotopes of antibodies against HIV‐1 CD4‐induced epitope shared with those against microorganisms

Author:

Biswas Shashwata1,Kuwata Takeo1ORCID,Yamauchi Soichiro2,Okazaki Kyo2,Kaku Yu1,Hasan Md Zahid1ORCID,Morioka Hiroshi2,Matsushita Shuzo1ORCID

Affiliation:

1. Division of Clinical Retrovirology, Joint Research Center for Human Retrovirus Infection Kumamoto University Kumamoto Japan

2. Department of Analytical and Biophysical Chemistry, Faculty of Medical and Pharmaceutical Sciences Kumamoto University Kumamoto Japan

Abstract

AbstractInduction of antibodies (Abs) against the conformational CD4‐induced (CD4i) epitope is frequent in HIV‐1 infection. However, the mechanism of development of anti‐CD4i Abs is unclear. We used anti‐idiotypic (aID) monoclonal Abs (mAbs) of anti‐CD4i mAbs to isolate anti‐CD4i mAbs from infected subjects and track the causative antigens. One anti‐aID mAb sorted from infected subjects by aID mAbs had the characteristics of anti‐CD4i Abs, including IGHV1‐69 usage and ability to bind to HIV‐1 Env enhanced by sCD4. Critical amino acid sequences for the binding of six anti‐aID mAbs, with shared idiotope to anti‐CD4i mAbs, were analysed by phage display. The identified amino acid sequences showed similarity to proteins from human microbiota and infectious agents. Peptides synthesized from Caudoviricetes sp and Vibrio vulnificus based on the identified sequences were reactive to most anti‐aID and some anti‐CD4i mAbs. These results suggest that anti‐CD4i Abs may evolve from B cells primed by microorganisms.

Funder

Japan Agency for Medical Research and Development

Publisher

Wiley

Subject

Immunology,Immunology and Allergy

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