HIV-1 envelope glycoprotein immunogens to induce broadly neutralizing antibodies

被引:42
|
作者
Sliepen, Kwinten [1 ]
Sanders, Rogier W. [1 ,2 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Med Microbiol, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[2] Cornell Univ, Weill Med Coll, Dept Microbiol & Immunol, New York, NY 10021 USA
基金
欧洲研究理事会;
关键词
nanoparticle vaccines; vaccination strategies; envelope glycoprotein; immunogen design; sequential vaccination; broadly neutralizing antibodies; HIV-1; vaccines; IMMUNODEFICIENCY-VIRUS TYPE-1; PROXIMAL EXTERNAL REGION; HUMORAL IMMUNE-RESPONSE; STRUCTURE-BASED DESIGN; OUTER DOMAIN; AFFINITY MATURATION; CRYSTAL-STRUCTURE; GP140; TRIMERS; BINDING-SITE; ENV TRIMERS;
D O I
10.1586/14760584.2016.1129905
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The long pursuit for a vaccine against human immunodeficiency virus 1 (HIV-1) has recently been boosted by a number of exciting developments. An HIV-1 subunit vaccine ideally should elicit potent broadly neutralizing antibodies (bNAbs), but raising bNAbs by vaccination has proved extremely difficult because of the characteristics of the HIV-1 envelope glycoprotein complex (Env). However, the isolation of bNAbs from HIV-1-infected patients demonstrates that the human humoral immune system is capable of making such antibodies. Therefore, a focus of HIV-1 vaccinology is the elicitation of bNAbs by engineered immunogens and by using vaccination strategies aimed at mimicking the bNAb maturation pathways in HIV-infected patients. Important clues can also be taken from the successful subunit vaccines against hepatitis B virus and human papillomavirus. Here, we review the different types of HIV-1 immunogens and vaccination strategies that are being explored in the search for an HIV-1 vaccine that induces bNAbs.
引用
收藏
页码:349 / 365
页数:17
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