Department of Medicine, Radboud University Nijmegen Medical Centre, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands.
Cytokine. 2012 Dec;60(3):861-9. doi: 10.1016/j.cyto.2012.08.019. Epub 2012 Sep 19.
Bacteroides fragilis, an intestinal flora commensal microorganism, is frequently isolated from abscesses and soft tissue infections. This study aimed to identify pattern recognition receptors (PRRs) involved in B. fragilis recognition and to characterize the induced cytokine profile. Human PBMCs were stimulated with heat-killed B. fragilis and cytokine levels were determined by ELISA. Roles of individual PRRs were assessed using specific blockers of receptor signaling pathways and PBMCs carrying single nucleotide polymorphisms of PRR genes. Cell lines expressing human TLR2 or TLR4 were employed to assess TLR-specificity of B. fragilis. TLR1, TLR2 and NOD2 were the main PRRs responsible for recognition of B. fragilis, while TLR4, TLR6, NOD1 and Dectin-1 were not involved. B. fragilis induced strong IL-6 and IL-8, moderate IL-1β and TNF-α, and poor IL-10, IL-17, IL-23 and IFN-γ production. This study identifies the receptor pathways of the innate immune response to B. fragilis, and thus provides new insights in the host defense against B. fragilis.
脆弱拟杆菌是一种肠道共生微生物,常从脓肿和软组织感染中分离出来。本研究旨在鉴定参与脆弱拟杆菌识别的模式识别受体(PRRs),并描述其诱导的细胞因子谱。用热灭活的脆弱拟杆菌刺激人 PBMCs,通过 ELISA 测定细胞因子水平。使用特定的受体信号通路阻断剂和携带 PRR 基因单核苷酸多态性的 PBMCs 评估个体 PRR 的作用。用人 TLR2 或 TLR4 表达细胞系评估脆弱拟杆菌的 TLR 特异性。TLR1、TLR2 和 NOD2 是识别脆弱拟杆菌的主要 PRRs,而 TLR4、TLR6、NOD1 和 Dectin-1 则不参与。脆弱拟杆菌诱导强烈的 IL-6 和 IL-8、中等强度的 IL-1β 和 TNF-α,以及较弱的 IL-10、IL-17、IL-23 和 IFN-γ产生。本研究确定了固有免疫对脆弱拟杆菌的受体途径,从而为宿主防御脆弱拟杆菌提供了新的见解。