Presentation of HIV-1 envelope glycoprotein trimers on diverse nanoparticle platforms

被引:24
作者
Brouwer, Philip J. M. [1 ]
Sanders, Rogier W. [1 ,2 ]
机构
[1] Univ Amsterdam, Amsterdam UMC, Dept Med Microbiol, NL-1105 AZ Amsterdam, Netherlands
[2] Cornell Univ, Dept Microbiol & Immunol, Weill Med Coll, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
HIV-1 Env trimer; liposome; nanoparticle presentation; self-assembling protein nanoparticle; virus-like particle; NEUTRALIZING ANTIBODY-RESPONSES; SYNTHETIC VACCINES; ACCURATE DESIGN; DENDRITIC CELLS; IMMUNOGENICITY; BINDING; ENV; PARTICLES; PROTEINS; SURFACE;
D O I
10.1097/COH.0000000000000549
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose of review We will discuss recent advances in the development of nanoparticle vaccines presenting HIV-1 envelope trimer vaccines and the immunological mechanisms by which they act. Recent findings The multivalent presentation of Env trimers on nanoparticles is a promising strategy to increase Env immunogenicity. Recent studies have shed light on how Env nanoparticles increase lymph node trafficking and germinal center formation by using the lectin-mediated complement pathway and enhancing the interaction with naive B cells. Meanwhile, research on different nanoparticle platforms has resulted in improved designs, such as liposomes with improved stability, and the emergence of novel platforms such as protein nanoparticles that self-assemble in vitro. Immmunogenicity studies with these nanoparticles delineate the advantages and expose the limitations of the different nanoparticle platforms. Summary It is becoming increasingly clear that HIV-1 vaccine research might benefit greatly from using nanoparticles presenting Env trimers, particularly during the priming stage of immunization. Among the different nanoparticles that are being pursued, in vitro-assembling nanoparticles allow for greater control of Env quality making them a promising nanoparticle platform.
引用
收藏
页码:302 / 308
页数:7
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