Dessus-Babus Sophie, Darville Toni L, Cuozzo Francis P, Ferguson Kaethe, Wyrick Priscilla B
Department of Microbiology, James H. Quillen College of Medicine, East Tennessee State University, Johnson City, Tennessee 37684, USA.
Infect Immun. 2002 Jun;70(6):3234-48. doi: 10.1128/IAI.70.6.3234-3248.2002.
The inflammatory response associated with Chlamydia trachomatis genital infections is thought to be initiated by the release of proinflammatory cytokines from infected epithelial cells. This study focuses on the interactions between C. trachomatis-infected HeLa cells and immune cells involved in the early stages of infection, i.e., neutrophils and macrophages. First, we showed that the expression of interleukin-11 (IL-11), an anti-inflammatory cytokine mainly active on macrophages, was upregulated at the mRNA level in the genital tracts of infected mice. Second, incubation of differentiated THP-1 (dTHP-1) cells or monocyte-derived macrophages (MdM) with basal culture supernatants from C. trachomatis serovar E- or serovar L2-infected HeLa cells resulted in macrophage activation with a differential release of tumor necrosis factor alpha (TNF-alpha) and upregulation of indoleamine 2,3-deoxygenase (IDO) but not of Toll-like receptor 2 and 4 mRNA expression. Third, coculture of infected HeLa cells with dTHP-1 cells resulted in a reduction in chlamydial growth, which was more dramatic for serovar E than for L2 and which was partially reversed by the addition of anti-TNF-alpha antibodies for serovar E or exogenous tryptophan for both serovars but was not reversed by the addition of superoxide dismutase or anti-IL-8 or anti-IL-1beta antibodies. A gamma interferon-independent IDO mRNA upregulation was also detected in dTHP-1 cells from infected cocultures. Lastly, with a two-stage coculture system, we found that (i) supernatants from neutrophils added to the apical side of infected HeLa cell cultures were chlamydicidal and induced MdM to express antichlamydial activity and (ii) although polymorphonuclear leukocytes released more proinflammatory cytokines in response to serovar E- than in response to L2-infected cells, MdM were strongly activated by serovar L2 infection, indicating that the early inflammatory response generated with a nondisseminating or a disseminating strain is different.
沙眼衣原体生殖道感染相关的炎症反应被认为是由受感染上皮细胞释放促炎细胞因子引发的。本研究聚焦于沙眼衣原体感染的HeLa细胞与感染早期参与其中的免疫细胞(即中性粒细胞和巨噬细胞)之间的相互作用。首先,我们发现白细胞介素-11(IL-11),一种主要作用于巨噬细胞的抗炎细胞因子,在感染小鼠的生殖道中mRNA水平上调。其次,将分化的THP-1(dTHP-1)细胞或单核细胞衍生的巨噬细胞(MdM)与沙眼衣原体血清型E或血清型L2感染的HeLa细胞的基础培养上清液孵育,导致巨噬细胞活化,肿瘤坏死因子α(TNF-α)释放存在差异,吲哚胺2,3-双加氧酶(IDO)上调,但Toll样受体2和4 mRNA表达未上调。第三,感染的HeLa细胞与dTHP-1细胞共培养导致衣原体生长减少,血清型E比血清型L2更显著,血清型E添加抗TNF-α抗体或两种血清型添加外源性色氨酸可部分逆转这种减少,但添加超氧化物歧化酶或抗IL-8或抗IL-1β抗体不能逆转。在感染共培养的dTHP-1细胞中也检测到γ干扰素非依赖性IDO mRNA上调。最后,使用两阶段共培养系统,我们发现:(i)添加到感染的HeLa细胞培养物顶端的中性粒细胞上清液具有杀衣原体作用,并诱导MdM表达抗衣原体活性;(ii)尽管多形核白细胞对血清型E感染细胞比血清型L2感染细胞释放更多促炎细胞因子,但血清型L2感染强烈激活MdM,表明非传播性或传播性菌株产生的早期炎症反应不同。