Petit-Jentreau Laetitia, Tailleux Ludovic, Coombes Janine L
Institute of Infection and Global Health, Department of Infection Biology, University of LiverpoolLiverpool, United Kingdom.
Mycobacterial Genetics Unit, Institut PasteurParis, France.
Front Cell Infect Microbiol. 2017 Aug 7;7:347. doi: 10.3389/fcimb.2017.00347. eCollection 2017.
Immune responses are essential for the protection of the host against external dangers or infections and are normally efficient in the clearance of invading microbes. However, some intracellular pathogens have developed strategies to replicate and survive within host cells resulting in latent infection associated with strong inflammation. This excessive response can cause cell and tissue damage and lead to the release of the intracellular content, in particular the nucleotide pool, into the extracellular space. Over the last decade, new studies have implicated metabolites from the purinergic pathway in shaping the host immune response against intracellular pathogens and proved their importance in the outcome of the infection. This review aims to summarize how the immune system employs the purinergic system either to fight the pathogen, or to control collateral tissue damage. This will be achieved by focusing on the macrophage response against two intracellular pathogens, the human etiologic agent of tuberculosis, and the protozoan parasite, .
免疫反应对于保护宿主抵御外部危险或感染至关重要,并且通常能有效地清除入侵的微生物。然而,一些细胞内病原体已经发展出在宿主细胞内复制和存活的策略,导致与强烈炎症相关的潜伏感染。这种过度反应会导致细胞和组织损伤,并导致细胞内物质,特别是核苷酸池释放到细胞外空间。在过去十年中,新的研究表明嘌呤能途径的代谢产物在塑造宿主针对细胞内病原体的免疫反应中发挥作用,并证明了它们在感染结果中的重要性。本综述旨在总结免疫系统如何利用嘌呤能系统对抗病原体或控制附带的组织损伤。这将通过关注巨噬细胞对两种细胞内病原体的反应来实现,这两种病原体分别是人类结核病病原体和原生动物寄生虫。