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17型辅助性T细胞和调节性T细胞活性在鼠柠檬酸杆菌侵袭及炎性损伤中的作用

Involvement of T helper type 17 and regulatory T cell activity in Citrobacter rodentium invasion and inflammatory damage.

作者信息

Symonds E L, Riedel C U, O'Mahony D, Lapthorne S, O'Mahony L, Shanahan F

机构信息

Alimentary Pharmabiotic Centre, NUI Cork, Ireland.

出版信息

Clin Exp Immunol. 2009 Jul;157(1):148-54. doi: 10.1111/j.1365-2249.2009.03934.x.

Abstract

Citrobacter rodentium is a murine pathogen that transiently colonizes the lumen of the large intestine. C. rodentium induces colitis, but the relative importance and temporal induction of the T helper type 17 (Th17) and regulatory T cell (T(reg)) pathways in protection from the infection and inflammation have not been assessed. Our aim was to investigate the key immunological signalling events associated with successful clearance of C. rodentium. Mice were challenged with luminescent-tagged C. rodentium and killed at days 3 (early infection), 10 (peak infection) and 21 (late infection) post-infection. Bioluminescent imaging and bacterial culture determined levels of C. rodentium. Distal colon mRNA expression of interleukin (IL)-17, IL-6, IL-1beta, tumour necrosis factor (TNF)-alpha, forkhead box P3 (FoxP3) and ghrelin were assessed using real-time polymerase chain reaction. Results were compared with age-matched non-infected mice. Low levels of C. rodentium were found at day 3, high levels at day 10, with clearance from the majority of the mice by day 21. In the distal colon, there was up-regulation of TNF-alpha and FoxP3 throughout the study and increases in IL-6 and IL-17 during the peak and late stages of infection. Ghrelin expression was increased at the peak and late stages of infection. This study has characterized changes to the T helper cell pathways, following the course of C. rodentium infection in mice. There were significant immunological changes, with up-regulation of the Th17 and T(reg) pathways in the distal colon and an increase in ghrelin expression compared with non-infected control mice. These changes may play a role in the pathology and clearance of C. rodentium.

摘要

鼠柠檬酸杆菌是一种可短暂定殖于大肠肠腔的鼠类病原体。鼠柠檬酸杆菌可诱发结肠炎,但17型辅助性T细胞(Th17)和调节性T细胞(Treg)途径在抗感染和炎症中的相对重要性及时序诱导情况尚未得到评估。我们的目的是研究与成功清除鼠柠檬酸杆菌相关的关键免疫信号事件。用荧光标记的鼠柠檬酸杆菌感染小鼠,并在感染后第3天(早期感染)、第10天(感染高峰期)和第21天(晚期感染)处死小鼠。通过生物发光成像和细菌培养确定鼠柠檬酸杆菌的水平。使用实时聚合酶链反应评估远端结肠中白细胞介素(IL)-17、IL-6、IL-1β、肿瘤坏死因子(TNF)-α、叉头框P3(FoxP3)和胃饥饿素的mRNA表达。将结果与年龄匹配的未感染小鼠进行比较。在第3天发现鼠柠檬酸杆菌水平较低,第10天水平较高,到第21天大多数小鼠体内的该菌被清除。在整个研究过程中,远端结肠中TNF-α和FoxP3上调,在感染高峰期和晚期IL-6和IL-17增加。胃饥饿素表达在感染高峰期和晚期增加。本研究描述了小鼠感染鼠柠檬酸杆菌过程中辅助性T细胞途径的变化。与未感染的对照小鼠相比,出现了显著的免疫变化,远端结肠中Th17和Treg途径上调,胃饥饿素表达增加。这些变化可能在鼠柠檬酸杆菌的病理过程和清除中发挥作用。

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