Stabilizing HIV-1 envelope glycoprotein trimers to induce neutralizing antibodies

被引:34
|
作者
de la Pena, Alba Torrents [1 ]
Sanders, Rogier W. [1 ,2 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Med Microbiol, NL-1105 AZ Amsterdam, Netherlands
[2] Cornell Univ, Weill Med Coll, Dept Micro Biol & Immunol, New York, NY 10021 USA
基金
欧洲研究理事会; 美国国家卫生研究院;
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; CRYO-EM STRUCTURE; CRYSTAL-STRUCTURE; STRUCTURAL DETERMINANTS; AFFINITY MATURATION; GERMLINE PRECURSORS; NONHUMAN-PRIMATES; VACCINE DESIGN; AMINO-ACIDS; GP120;
D O I
10.1186/s12977-018-0445-y
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
An effective HIV-1 vaccine probably will need to be able to induce broadly neutralizing HIV-1 antibodies (bNAbs) in order to be efficacious. The many bNAbs that have been isolated from HIV-1 infected patients illustrate that the human immune system is able to elicit this type of antibodies. The elucidation of the structure of the HIV-1 envelope glycoprotein (Env) trimer has further fueled the search for Env immunogens that induce bNAbs, but while native Env trimer mimetics are often capable of inducing strain-specific neutralizing antibodies (NAbs) against the parental virus, they have not yet induced potent bNAb responses. To improve the performance of Env trimer immunogens, researchers have studied the immune responses that Env trimers have induced in animals; they have evaluated how to best use Env trimers in various immunization regimens; and they have engineered increasingly stabilized Env trimer variants. Here, we review the different approaches that have been used to increase the stability of HIV-1 Env trimer immunogens with the aim of improving the induction of NAbs. In particular, we draw parallels between the various approaches to stabilize Env trimers and ones that have been used by nature in extremophile microorganisms in order to survive in extreme environmental conditions.
引用
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页数:11
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