Hurwitz Julia L, Bonsignori Mattia
1 Department of Infectious Diseases, St. Jude Children's Research Hospital , Memphis, Tennessee.
2 Department of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center , Memphis, Tennessee.
Viral Immunol. 2018 Mar;31(2):124-132. doi: 10.1089/vim.2017.0144. Epub 2018 Jan 9.
In 2016, there were more than 30 million individuals living with HIV-1, ∼1.8 million new HIV-1 infections, and ∼1 million HIV-1-related deaths according to UNAIDS ( unaids.org ). Hence, a preventive HIV-1 vaccine remains a global priority. The variant envelopes of HIV-1 present a significant obstacle to vaccine development and the vaccine field has realized that immunization with a single HIV-1 envelope protein will not be sufficient to generate broadly neutralizing antibodies. Here we describe two nonmutually exclusive, targeted pathways with which a multi-envelope HIV-1 vaccine may generate protective immune responses against variant HIV-1. Pathways include (i) the induction of a polyclonal immune response, comprising a plethora of antibodies with subset-reactive and cross-reactive specificities, together able to neutralize diverse HIV-1 (termed Poly-nAb in this report) and (ii) the induction of one or a few monoclonal antibodies, each with a broadly neutralizing specificity (bnAb). With each pathway in mind, we describe challenges and strategies that may ultimately support HIV-1 vaccine success.
根据联合国艾滋病规划署(unaids.org)的数据,2016年,全球有超过3000万人感染了HIV-1,约180万例新发HIV-1感染,以及约100万例与HIV-1相关的死亡。因此,开发预防性HIV-1疫苗仍然是全球的优先事项。HIV-1的变异包膜给疫苗研发带来了重大障碍,疫苗领域已经认识到,仅用单一的HIV-1包膜蛋白进行免疫不足以产生广泛中和抗体。在此,我们描述了两种并非相互排斥的靶向途径,多包膜HIV-1疫苗可通过这些途径产生针对变异HIV-1的保护性免疫反应。这些途径包括:(i)诱导多克隆免疫反应,产生大量具有亚型反应性和交叉反应性特异性的抗体,共同作用以中和多种HIV-1(本报告中称为多克隆中和抗体);(ii)诱导一种或几种具有广泛中和特异性的单克隆抗体(bnAb)。考虑到每种途径,我们描述了可能最终支持HIV-1疫苗成功的挑战和策略。