Max Planck Unit for the Science of Pathogens, Berlin, Germany; Max Planck Institute for Infection Biology, Berlin, Germany.
Department of Infectious Diseases and Pulmonary Medicine, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany; German Center for Lung Research (DZL), Berlin, Germany.
Curr Opin Immunol. 2019 Feb;56:60-66. doi: 10.1016/j.coi.2018.09.018. Epub 2018 Oct 24.
Immune detection of microbial viability is increasingly recognized as a potent driver of innate and adaptive immune responses. Here we describe recent mechanistic insights into the process of how the immune system discriminates between viable and non-viable microbial matter. Accumulating evidence suggests a key role for microbial RNA as a widely conserved viability associated PAMP (vita-PAMP) and a molecular signal of increased infectious threat. Toll-like receptor 8 (TLR8) has recently emerged as a critical sensor for viable bacteria, ssRNA viruses, and archaea in human antigen presenting cells (APC). We discuss the role of microbial RNA, and other potential vita-PAMPs in antimicrobial immunity and vaccine responses.
免疫检测微生物的存活能力正逐渐被视为先天和适应性免疫反应的有力驱动因素。在这里,我们描述了免疫系统如何区分有活力和无活力的微生物物质的最新机制见解。越来越多的证据表明,微生物 RNA 作为一种广泛保守的存活相关 PAMP(vita-PAMP)和传染性威胁增加的分子信号,起着关键作用。Toll 样受体 8(TLR8)最近被认为是人类抗原呈递细胞(APC)中细菌、单链 RNA 病毒和古菌的关键传感器。我们讨论了微生物 RNA 以及其他潜在的 vita-PAMPs 在抗菌免疫和疫苗反应中的作用。