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Increased surface expression of HIV-1 envelope is associated with improved antibody response in vaccinia prime/protein boost immunization.


ABSTRACT: HIV-1 envelope (Env)-based vaccines have so far largely failed to induce antibodies that prevent HIV-1 infection. One factor proposed to limit the immunogenicity of cell-associated Env is its low level of expression on the cell surface, restricting accessibility to antibodies. Using a vaccinia prime/protein boost protocol in mice, we explored the immunologic effects of mutations in the Env cytoplasmic tail (CT) that increased surface expression, including partial truncation and ablation of a tyrosine-dependent endocytosis motif. After vaccinia primes, CT-modified Envs induced up to 7-fold higher gp120-specific IgG, and after gp120 protein boosts, they elicited up to 16-fold greater Tier-1 HIV-1 neutralizing antibody titers, although results were variable between isolates. These data indicate that the immunogenicity of HIV-1 Env in a prime/boost vaccine can be enhanced in a strain-dependent manner by CT mutations that increase Env surface expression, thus highlighting the importance of the prime in this vaccine format.

SUBMITTER: Hogan MJ 

PROVIDER: S-EPMC5770335 | biostudies-literature | 2018 Jan

REPOSITORIES: biostudies-literature

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Increased surface expression of HIV-1 envelope is associated with improved antibody response in vaccinia prime/protein boost immunization.

Hogan Michael J MJ   Conde-Motter Angela A   Jordan Andrea P O APO   Yang Lifei L   Cleveland Brad B   Guo Wenjin W   Romano Josephine J   Ni Houping H   Pardi Norbert N   LaBranche Celia C CC   Montefiori David C DC   Hu Shiu-Lok SL   Hoxie James A JA   Weissman Drew D  

Virology 20171122


HIV-1 envelope (Env)-based vaccines have so far largely failed to induce antibodies that prevent HIV-1 infection. One factor proposed to limit the immunogenicity of cell-associated Env is its low level of expression on the cell surface, restricting accessibility to antibodies. Using a vaccinia prime/protein boost protocol in mice, we explored the immunologic effects of mutations in the Env cytoplasmic tail (CT) that increased surface expression, including partial truncation and ablation of a tyr  ...[more]

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