Haks Mariëlle C, Bottazzi Barbara, Cecchinato Valentina, De Gregorio Corinne, Del Giudice Giuseppe, Kaufmann Stefan H E, Lanzavecchia Antonio, Lewis David J M, Maertzdorf Jeroen, Mantovani Alberto, Sallusto Federica, Sironi Marina, Uguccioni Mariagrazia, Ottenhoff Tom H M
Department of Infectious Diseases, Leiden University Medical Center, Leiden, Netherlands.
Humanitas Clinical and Research Center, Rozzano, Italy.
Front Immunol. 2017 Nov 15;8:1563. doi: 10.3389/fimmu.2017.01563. eCollection 2017.
Vaccinology aims to understand what factors drive vaccine-induced immunity and protection. For many vaccines, however, the mechanisms underlying immunity and protection remain incompletely characterized at best, and except for neutralizing antibodies induced by viral vaccines, few correlates of protection exist. Recent omics and systems biology big data platforms have yielded valuable insights in these areas, particularly for viral vaccines, but in the case of more complex vaccines against bacterial infectious diseases, understanding is fragmented and limited. To fill this gap, the EC supported ADITEC project (http://www.aditecproject.eu/; http://stm.sciencemag.org/content/4/128/128cm4.full) featured a work package on "Molecular signatures of immunity and immunogenicity," aimed to identify key molecular mechanisms of innate and adaptive immunity during effector and memory stages of immune responses following vaccination. Specifically, technologies were developed to assess the human immune response to vaccination and infection at the level of the transcriptomic and proteomic response, T-cell and B-cell memory formation, cellular trafficking, and key molecular pathways of innate immunity, with emphasis on underlying mechanisms of protective immunity. This work intersected with other efforts in the ADITEC project. This review summarizes the main achievements of the work package.
疫苗学旨在了解驱动疫苗诱导的免疫和保护作用的因素。然而,对于许多疫苗而言,免疫和保护作用的潜在机制充其量仍未得到充分表征,除了病毒疫苗诱导的中和抗体外,几乎不存在保护作用的相关指标。最近的组学和系统生物学大数据平台在这些领域提供了有价值的见解,特别是对于病毒疫苗,但对于针对细菌感染性疾病的更复杂疫苗而言,相关认识仍支离破碎且有限。为填补这一空白,欧盟委员会支持的ADITEC项目(http://www.aditecproject.eu/; http://stm.sciencemag.org/content/4/128/128cm4.full)有一个关于“免疫和免疫原性的分子特征”的工作包,旨在确定接种疫苗后免疫反应的效应阶段和记忆阶段先天免疫和适应性免疫的关键分子机制。具体而言,开发了一些技术,用于在转录组和蛋白质组反应、T细胞和B细胞记忆形成、细胞转运以及先天免疫的关键分子途径层面评估人类对疫苗接种和感染的免疫反应,重点关注保护性免疫的潜在机制。这项工作与ADITEC项目中的其他工作相互交叉。本综述总结了该工作包的主要成果。