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Multi-Envelope HIV-1 Vaccine Development: Two Targeted Immune Pathways, One Desired Protective Outcome

机译:多包络HIV-1疫苗开发:两个有针对性的免疫途径,一个所需的保护性结果

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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.
机译:2016年,患有HIV-1,〜180万新HIV-1感染的人数超过3000多万人,根据艾滋病规划署(UNAIDS.ORG),〜100万HIV-1相关死亡。因此,预防的HIV-1疫苗仍然是全球优先级。 HIV-1的变体包络具有疫苗发育的显着障碍,并且疫苗领域已经意识到用单个HIV-1包络蛋白免疫不足以产生宽度中和抗体。在这里,我们描述了两个非矫直类靶向途径,其中多封套HIV-1疫苗可能产生针对变体HIV-1的保护性免疫应答。途径包括(i)诱导多克隆免疫应答,包括具有副反应性和交叉反应性特异性的多型抗体,一起能够中和各种HIV-1(在本报告中称为Poly-Nab)和(ii)诱导一种或多种单克隆抗体,每个抗体具有宽度中和特异性(BNAB)。考虑到每一条途径,我们描述了可能最终支持HIV-1疫苗成功的挑战和策略。

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