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The Pneumococcal Polysaccharide Capsule and Pneumolysin Differentially Affect CXCL8 and IL-6 Release from Cells of the Upper and Lower Respiratory Tract

机译:肺炎球菌多糖胶囊和肺炎球菌溶血素差异影响上呼吸道和下呼吸道细胞的CXCL8和IL-6释放。

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摘要

The polysaccharide capsule and pneumolysin toxin are major virulence factors of the human bacterial pathogen Streptococcus pneumoniae. Colonization of the nasopharynx is asymptomatic but invasion of the lungs can result in invasive pneumonia. Here we show that the capsule suppresses the release of the pro-inflammatory cytokines CXCL8 (IL-8) and IL-6 from the human pharyngeal epithelial cell line Detroit 562. Release of both cytokines was much less from human bronchial epithelial cells (iHBEC) but levels were also affected by capsule. Pneumolysin stimulates CXCL8 release from both cell lines. Suppression of CXCL8 homologue (CXCL2/MIP-2) release by the capsule was also observed in vivo during intranasal colonization of mice but was only discernable in the absence of pneumolysin. When pneumococci were administered intranasally to mice in a model of long term, stable nasopharyngeal carriage, encapsulated S. pneumoniae remained in the nasopharynx whereas the nonencapsulated pneumococci disseminated into the lungs. Pneumococcal capsule plays a role not only in protection from phagocytosis but also in modulation of the pro-inflammatory immune response in the respiratory tract.
机译:多糖荚膜和肺炎球菌溶血素毒素是人细菌病原体肺炎链球菌的主要毒力因子。鼻咽的定殖是无症状的,但肺部的侵袭可导致侵袭性肺炎。在这里,我们显示该胶囊抑制了人类咽上皮细胞系底特律562促炎性细胞因子CXCL8(IL-8)和IL-6的释放。两种细胞因子的释放都远低于人类支气管上皮细胞(iHBEC)但水平也会受到胶囊的影响。肺炎球菌溶血素刺激两种细胞系释放CXCL8。在小鼠鼻内定植的过程中,在体内也观察到了胶囊对CXCL8同源物(CXCL2 / MIP-2)的抑制作用,但只有在没有肺炎球菌溶血素的情况下才能观察到。当在长期,稳定的鼻咽运输模型中向小鼠鼻内给予肺炎球菌时,封装的肺炎链球菌保留在鼻咽中,而未封装的肺炎球菌则扩散到肺中。肺炎球菌胶囊不仅在防止吞噬作用中起作用,而且在呼吸道中调节促炎性免疫应答。

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