| Literature DB >> 29451984 |
Ivelin S Georgiev1, Michael Gordon Joyce1, Rita E Chen1, Kwanyee Leung1, Krisha McKee1, Aliaksandr Druz1, Joseph G Van Galen1, Masaru Kanekiyo1, Yaroslav Tsybovsky2, Eun Sung Yang1, Yongping Yang1, Priyamvada Acharya1, Marie Pancera1, Paul V Thomas1, Timothy Wanninger1, Hadi M Yassine1, Ulrich Baxa2, Nicole A Doria-Rose1, Cheng Cheng1, Barney S Graham1, John R Mascola1, Peter D Kwong1.
Abstract
Antigen multimerization on a nanoparticle can result in improved neutralizing antibody responses. A platform that has been successfully used for displaying antigens from a number of different viruses is ferritin, a self-assembling protein nanoparticle that allows the attachment of multiple copies (24 monomers or 8 trimers) of a single antigen. Here, we design two-component ferritin variants that allow the attachment of two different antigens on a single particle in a defined ratio and geometric pattern. The two-component ferritin was specifically designed for trimeric antigens, accepting four trimers per particle for each antigen, and was tested with antigens derived from HIV-1 envelope (Env) and influenza hemagglutinin (HA). Particle formation and the presence of native-like antigen conformation were confirmed through negative-stain electron microscopy and antibody-antigen binding analysis. Immunizations in guinea pigs with two-component ferritin particles, displaying diverse Env, HA, or both antigens, elicited neutralizing antibody responses against the respective viruses. The results provide proof-of-principle for the self-assembly of a two-component nanoparticle as a general technology for multimeric presentation of trimeric antigens.Entities:
Keywords: HIV-1; antibody; immunogenicity; influenza; vaccine
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Year: 2018 PMID: 29451984 DOI: 10.1021/acsinfecdis.7b00192
Source DB: PubMed Journal: ACS Infect Dis ISSN: 2373-8227 Impact factor: 5.084