Department of Ophthalmology, Kresge Eye Institute, Wayne State University School of Medicine, Detroit, Michigan, USA.
Invest Ophthalmol Vis Sci. 2011 May 10;52(6):3074-82. doi: 10.1167/iovs.10-5928.
This study was conducted to investigate whether flagellin, the sole ligand of Toll-like receptor-5 (TLR5), induces an innate defense that is sufficient to protect injured corneas from Candida albicans.
Scarified corneas of adult B6, TLR5(-/-), Camp(-/-) (cathelicidin-related antimicrobial peptide), or PMN-depleted mice were pretreated with Pseudomonas aeruginosa flagellin or a mutant and then were inoculated with C. albicans. The corneas were compared for disease progression, cytokine and Camp expression, and PMN infiltration before and after C. albicans infection. Disease progress was recorded by digital photography and clinical scoring, cytokine levels were determined by ELISA, the levels of Camp gene product were assessed by Western blot, and PMN infiltration was measured by MPO determination and immunohistochemistry.
Topical application of flagellin induced profound protection against Candida keratitis in a TLR5-dependent manner. The improved disease outcome including reduced tissue inflammation and rapid functional recovery can be attributed to a marked decrease in fungal burden at the early stage of C. albicans infection in flagellin-exposed B6 mouse corneas. Although both PMN infiltration and Camp upregulation contributed to corneal innate defense against fungal infection, Camp ablation totally, and PMN depletion partially, abrogated flagellin-induced fungal clearance in B6 mouse corneas.
Flagellin induces a strong innate defense and promotes robust resistance to C. albicans infection in the cornea. Topical flagellin or its mimetic may become a new prophylactic agent for preventing contact lens or trauma/injury-associated microbial keratitis.
本研究旨在探讨鞭毛蛋白(Toll 样受体 5(TLR5)的唯一配体)是否能诱导先天防御,从而足以保护受损的角膜免受白色念珠菌的侵害。
成年 B6、TLR5(-/-)、Camp(-/-)(抗菌肽相关 Cathelicidin)或PMN 耗竭小鼠的划痕角膜先用铜绿假单胞菌鞭毛蛋白或突变体预处理,然后接种白色念珠菌。比较接种白色念珠菌前后角膜的疾病进展、细胞因子和 Camp 表达以及 PMN 浸润情况。通过数字摄影和临床评分记录疾病进展,通过 ELISA 测定细胞因子水平,通过 Western blot 评估 Camp 基因产物水平,通过 MPO 测定和免疫组织化学测定 PMN 浸润。
鞭毛蛋白的局部应用以 TLR5 依赖的方式对白色念珠菌角膜炎产生了深刻的保护作用。早期白色念珠菌感染时真菌负荷明显减少,导致组织炎症减轻和功能快速恢复,从而改善了疾病结局。虽然 PMN 浸润和 Camp 上调都有助于角膜对真菌感染的先天防御,但 Camp 消融完全,PMN 耗竭部分,可消除 TLR5 敲除小鼠角膜中鞭毛蛋白诱导的真菌清除作用。
鞭毛蛋白诱导强烈的先天防御,并促进角膜对白色念珠菌感染的强大抵抗力。鞭毛蛋白或其类似物可能成为预防隐形眼镜或创伤/损伤相关微生物角膜炎的新预防剂。