Tailored Immunogens Direct Affinity Maturation toward HIV Neutralizing Antibodies

Bryan Briney(Scripps Research Institute), Devin Sok(Scripps Research Institute), Joseph G. Jardine(Scripps Research Institute), Daniel W. Kulp(Scripps Research Institute), Patrick Skog(Scripps Research Institute), Sergey Menis(Scripps Research Institute), Ronald Jacak(Scripps Research Institute), Oleksandr Kalyuzhniy(Scripps Research Institute), Natalia de Val(Scripps Research Institute), Fabian Sesterhenn(Scripps Research Institute), Khoa Le(Scripps Research Institute), Alejandra Ramos(Scripps Research Institute), Meaghan Jones(Scripps Research Institute), Karen L. Saye-Francisco(Scripps Research Institute), Tanya R. Blane(Scripps Research Institute), Skye Spencer(Scripps Research Institute), Erik Georgeson(Scripps Research Institute), Xiaozhen Hu(Scripps Research Institute), Gabriel Ozorowski(Scripps Research Institute), Yumiko Adachi(Scripps Research Institute), Michael Kubitz(Scripps Research Institute), Anita Sarkar(Scripps Research Institute), Ian A. Wilson(Scripps Research Institute), Andrew B. Ward(Scripps Research Institute), David Nemazee(Scripps Research Institute), Dennis R. Burton(Scripps Research Institute), William R. Schief(Scripps Research Institute)
Cell
September 1, 2016
Cited by 280Open Access
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Abstract

Induction of broadly neutralizing antibodies (bnAbs) is a primary goal of HIV vaccine development. VRC01-class bnAbs are important vaccine leads because their precursor B cells targeted by an engineered priming immunogen are relatively common among humans. This priming immunogen has demonstrated the ability to initiate a bnAb response in animal models, but recall and maturation toward bnAb development has not been shown. Here, we report the development of boosting immunogens designed to guide the genetic and functional maturation of previously primed VRC01-class precursors. Boosting a transgenic mouse model expressing germline VRC01 heavy chains produced broad neutralization of near-native isolates (N276A) and weak neutralization of fully native HIV. Functional and genetic characteristics indicate that the boosted mAbs are consistent with partially mature VRC01-class antibodies and place them on a maturation trajectory that leads toward mature VRC01-class bnAbs. The results show how reductionist sequential immunization can guide maturation of HIV bnAb responses.


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