Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, UK.
Immunology. 2009 Sep;128(1 Suppl):e385-94. doi: 10.1111/j.1365-2567.2008.02987.x. Epub 2008 Dec 16.
The T helper type 2 (Th2) mediated expulsion of the gastrointestinal nematode Trichinella spiralis requires interleukin-4 receptor alpha (IL-4Ralpha) expression on both bone-marrow-derived and non-bone-marrow-derived cells. To more definitively investigate the role of IL-4/IL-13 responsiveness in the development of protective immunity to T. spiralis, cell-specific IL-4Ralpha signalling on CD4(+) T cells (Lck(cre) IL-4Ralpha(-/flox)) and macrophages/neutrophils (LysM(cre) IL-4Ralpha(-/flox)) was analysed on the BALB/c background. Infection of wild-type and control IL-4Ralpha(-/flox) mice induced a Th2-type immune response with elevated IL-4 cytokine production, parasite-specific immunoglobulin G1 (IgG1), total IgE, intestinal mastocytosis and enteropathy. In contrast, global IL-4Ralpha-deficient BALB/c mice showed reduced worm expulsion, antibody production, intestinal mastocytosis and gut pathology. BALB/c mice generated with cell-specific deletion of IL-4Ralpha on CD4(+) T lymphocytes or macrophages/neutrophils, controlled gastrointestinal helminth infection by eliciting a protective immune response comparable to that observed with wild-type and IL-4Ralpha(-/flox) controls. Together, this shows that the development of host protective Th2 responses accompanied by parasite loss is independent of IL-4Ralpha expression on CD4(+) T cells and macrophages/neutrophils.
辅助性 T 细胞 2 型(Th2)介导的胃肠道寄生虫旋毛虫的排出需要骨髓来源细胞和非骨髓来源细胞上的白细胞介素 4 受体 alpha(IL-4Ralpha)表达。为了更明确地研究 IL-4/IL-13 反应性在旋毛虫保护性免疫中的作用,在 BALB/c 背景下分析了 CD4(+) T 细胞(Lck(cre) IL-4Ralpha(-/flox)和巨噬细胞/中性粒细胞(LysM(cre) IL-4Ralpha(-/flox)上的细胞特异性 IL-4Ralpha 信号。野生型和对照 IL-4Ralpha(-/flox) 小鼠的感染诱导了 Th2 型免疫反应,产生了升高的 IL-4 细胞因子产生、寄生虫特异性免疫球蛋白 G1(IgG1)、总 IgE、肠道肥大细胞和肠病。相比之下,全局 IL-4Ralpha 缺陷型 BALB/c 小鼠显示出减少的蠕虫排出、抗体产生、肠道肥大细胞和肠道病理学。在 BALB/c 小鼠中,通过在 CD4(+) T 淋巴细胞或巨噬细胞/中性粒细胞上特异性缺失 IL-4Ralpha,产生了与野生型和 IL-4Ralpha(-/flox) 对照相似的保护性免疫反应,从而控制了胃肠道蠕虫感染。总之,这表明宿主保护性 Th2 反应的发展伴随着寄生虫的丧失,而不依赖于 CD4(+) T 细胞和巨噬细胞/中性粒细胞上的 IL-4Ralpha 表达。