Niikura Mamoru, Inoue Shin-Ichi, Kobayashi Fumie
Department of Infectious Diseases, Kyorin University School of Medicine, Tokyo 181-8611, Japan.
J Biomed Biotechnol. 2011;2011:383962. doi: 10.1155/2011/383962. Epub 2011 Nov 13.
Interleukin- (IL-) 10, anti-inflammatory cytokine, is known to inhibit the protective immune responses against malaria parasites and to be involved in exacerbating parasitemia during Plasmodium infection. In contrast, IL-10 is regarded as necessary for suppressing severe pathology during Plasmodium infection. Here, we summarize the role of IL-10 during murine malaria infection, focusing especially on coinfection with lethal and nonlethal strains of malaria parasites. Recent studies have demonstrated that the major sources of IL-10 are subpopulations of CD4+ T cells in humans and mice infected with Plasmodium. We also discuss the influence of innate immunity on the induction of CD4+ T cells during murine malaria coinfection.
白细胞介素-(IL-)10是一种抗炎细胞因子,已知它可抑制针对疟原虫的保护性免疫反应,并在疟原虫感染期间参与加重寄生虫血症。相比之下,IL-10被认为是疟原虫感染期间抑制严重病理反应所必需的。在此,我们总结了IL-10在鼠疟感染过程中的作用,尤其关注与致死性和非致死性疟原虫菌株的共感染情况。最近的研究表明,IL-10的主要来源是感染疟原虫的人和小鼠体内的CD4+ T细胞亚群。我们还讨论了天然免疫对鼠疟共感染期间CD4+ T细胞诱导的影响。