Yu Shaoxiong, Ge Hailiang, Li Su, Qiu Hua-Ji
State Key Laboratory of Veterinary Biotechnology, National African Swine Fever Para-Reference Laboratory, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Harbin, China.
Front Microbiol. 2022 Feb 11;13:839585. doi: 10.3389/fmicb.2022.839585. eCollection 2022.
Macrophages are professional antigen-presenting cells and serve as the first line of defense against invading pathogens. Macrophages are polarized toward the proinflammatory classical (M1) or anti-inflammatory alternative (M2) phenotype upon viral infections. M1-polarized macrophages exert critical roles in antiviral responses different mechanisms. Within the long competitive history between viruses and hosts, viruses have evolved various immune evasion strategies, inhibiting macrophage acquisition of an antiviral phenotype, impairing the antiviral responses of activated macrophages, and/or exploiting macrophage phenotypes for efficient replication. This review focuses on the sophisticated regulation of macrophage polarization utilized by viruses and is expected to provide systematic insights into the regulatory mechanisms of macrophage polarization by viruses and further facilitate the design of therapeutic targets for antivirals.
巨噬细胞是专业的抗原呈递细胞,是抵御入侵病原体的第一道防线。在病毒感染时,巨噬细胞会向促炎经典(M1)或抗炎替代(M2)表型极化。M1极化的巨噬细胞通过不同机制在抗病毒反应中发挥关键作用。在病毒与宿主漫长的竞争历史中,病毒进化出了各种免疫逃避策略,抑制巨噬细胞获得抗病毒表型,损害活化巨噬细胞的抗病毒反应,和/或利用巨噬细胞表型进行高效复制。本综述聚焦于病毒对巨噬细胞极化的复杂调控,有望为病毒调控巨噬细胞极化的机制提供系统的见解,并进一步促进抗病毒治疗靶点的设计。