Development and characterization of a panel of anti-idiotype antibodies to 1C10 that cross-neutralize HIV-1 subtype B viruses
نویسندگان
چکیده
The V3 loop of the human immunodeficiency virus type 1 (HIV-1) envelope protein (Env) is one conserved immunogenic regions targeted by neutralizing antibodies (nAb). Two different binding modes anti-V3 abs have been reported in studies using two mimotopes: ladle-type and cradle-type. We previously isolated a nAb, 1C10, that potently broadly neutralized clade B viruses. Despite its potent neutralization activity, 1C10 possesses no unique features amino acid sequence. hypothesized potency derived from antigen-binding characteristics, which are not consequence nAbs. To analyze epitope-paratope interactions between loop, we produced five anti-idiotypic (anti-Id abs) mice immunized with nAb. idiotopes anti-Id Abs on heavy chain were estimated alanine scanning, germline reversion mutagenesis, sibling clone. Next-generation sequencing combined homology modeling revealed contact R315 at tip D53 CDRH2 Phe/Asp CDRH3. These acids enriched anti-Id-ab-reactive cell receptors encoded IGHV3-30 gene. also found 20% HIV-infected individuals had specific to abs, as well both mimotopes, did respond linear peptide. Our findings showed induced recognized key formation essential for steric nAb loop. coexistence ab reactivity mimotopes HIV-positive individuals.
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ژورنال
عنوان ژورنال: Frontiers in virology
سال: 2022
ISSN: ['2673-818X']
DOI: https://doi.org/10.3389/fviro.2022.932187