National Institutes of Health/National Institute Of Allergy and Infectious Diseases (NIH/NIAID)
米国
引用
ジャーナル: Sci Immunol / 年: 2026 タイトル: Rapidly acquired HIV-1 neutralization breadth in a rhesus V2 apex knockin mouse model after a single bolus immunization. 著者: Amrit Raj Ghosh / Rumi Habib / Nitesh Mishra / Ryan S Roark / Madhav Akauliya / Ali A Albowaidey / Joel D Allen / Khaled Amereh / Gabriel Avillion / Maria Bottermann / Bo Liang / Namit ...著者: Amrit Raj Ghosh / Rumi Habib / Nitesh Mishra / Ryan S Roark / Madhav Akauliya / Ali A Albowaidey / Joel D Allen / Khaled Amereh / Gabriel Avillion / Maria Bottermann / Bo Liang / Namit Chaudhary / Sean Callaghan / Jonathan Dye / Xuduo Li / Jordan R Ellis-Pugh / Rohan Roy Chowdhury / Nicole E James / Xiaotie Liu / Laura Maiorino / Paula M Villavicencio / Rebecca Nedellec / Prabhgun Oberoi / Kirsten J Sowers / Younghoon Park / Thavaleak Prum / Linette Rodriguez / Maria Ssozi / Jonathan L Torres / Agnes A Walsh / John E Warner / Stephanie R Weldon / Liling Xu / Kevin Wiehe / Max Crispin / Andrew B Ward / Usha Nair / Beatrice H Hahn / Dennis R Burton / Lawrence Shapiro / Peter D Kwong / Darrell J Irvine / Raiees Andrabi / George M Shaw / Facundo D Batista / 要旨: Current immunization strategies to elicit broadly neutralizing antibodies (bnAbs) against HIV-1 generally propose complex, multiboost regimens. In rhesus macaques, simian-human immunodeficiency virus ...Current immunization strategies to elicit broadly neutralizing antibodies (bnAbs) against HIV-1 generally propose complex, multiboost regimens. In rhesus macaques, simian-human immunodeficiency virus (SHIV) infection rapidly drives the development of some bnAb classes sharing structural similarities with those in humans. Here, we generated a knockin (KI) mouse model with B cells bearing the unmutated common ancestor of a V2 apex-targeted bnAb lineage, V033-a. A single immunization with a germline-targeting native-like trimer, Q23-APEX-GT1, recapitulated the ontogeny of the mature rhesus bnAb in KI mice, including rare, disfavored somatic mutations. Resulting antibodies exhibited potent neutralization against a broad panel of heterologous HIV-1 strains. Boosting with Env escape mutant trimers further improved breadth and potency, and cryo-electron microscopy analysis revealed the structural basis for heterologous neutralization breadth. Nonhuman primate and mouse models combined with structure can serve as a platform for identifying and validating immunogens that streamline HIV vaccination regimens.
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