| Literature DB >> 28237764 |
Saikat Banerjee1, Heliang Shi1, Marisa Banasik1, Hojin Moon1, William Lees2, Yali Qin1, Andrew Harley1, Adrian Shepherd2, Michael W Cho3.
Abstract
The membrane proximal external region (MPER) of HIV-1 gp41 is targeted by broadly neutralizing antibodies (bnAbs) 4E10 and 10E8. In this proof-of-concept study, we evaluated a novel multi-immunogen vaccine strategy referred to as Incremental, Phased Antigenic Stimulation for Rapid Antibody Maturation (IPAS-RAM) to induce 4E10/10E8-like bnAbs. Rabbits were immunized sequentially, but in a phased manner, with three immunogens that are progressively more native (gp41-28×3, gp41-54CT, and rVV-gp160DH12). Although nAbs were not induced, epitope-mapping analyses indicated that IPAS-RAM vaccination was better able to target antibodies towards the 4E10/10E8 epitopes than homologous prime-boost immunization using gp41-28×3 alone. MPER-specific rabbit monoclonal antibodies were generated, including 9F6. Although it lacked neutralizing activity, the target epitope profile of 9F6 closely resembled those of 4E10 and 10E8 (671NWFDITNWLWYIK683). B-cell repertoire analyses suggested the importance of co-immunizations for maturation of 9F6, which warrants further evaluation of our IPAS-RAM vaccine strategy using an improved priming immunogen.Entities:
Keywords: Antibody maturation; HIV-1; MPER; NGS; Neutralizing antibody; Next-generation sequencing; Rabbit; Vaccine; gp41
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Year: 2017 PMID: 28237764 PMCID: PMC5385849 DOI: 10.1016/j.virol.2017.02.015
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616