Magalhaes Joao Gamelas, Fritz Jörg H, Le Bourhis Lionel, Sellge Gernot, Travassos Leonardo H, Selvanantham Thirumahal, Girardin Stephen E, Gommerman Jennifer L, Philpott Dana J
Department of Immunology, University of Toronto, Toronto, Ontario, Canada.
J Immunol. 2008 Dec 1;181(11):7925-35. doi: 10.4049/jimmunol.181.11.7925.
While a number of microbial-associated molecular patterns have been known for decades to act as adjuvants, the mechanisms and the signaling pathways underlying their action have remained elusive. Here, we examined the unfolding of the adaptive immune response induced by Nod2 in vivo upon activation by its specific ligand, muramyl dipeptide, a component of peptidoglycan. Our findings demonstrate that this bacterial sensor triggers a potent Ag-specific immune response with a Th2-type polarization profile, characterized by the induction of IL-4 and IL-5 by T cells and IgG1 Ab responses. Nod2 was also found to be critical for the induction of both Th1- and Th2-type responses following costimulation with TLR agonists. Importantly, the synergistic responses to Nod2 and TLR agonists seen in vivo were recapitulated by dendritic cells in vitro, suggesting that these cells likely play a central role in the integration of Nod2- and TLR-dependent signals for driving the adaptive immune response. Taken together, our results identify Nod2 as a critical mediator of microbial-induced potentiation and polarization of Ag-dependent immunity. Moreover, these findings affect our understanding of Crohn's diseases pathogenesis, where lack of Nod2-dependent Th2 signaling in a subset of these patients might explain heightened Th1-mediated inflammation at the level of the intestinal mucosa.
虽然几十年来已知多种微生物相关分子模式可作为佐剂,但其作用的机制和信号通路仍不清楚。在此,我们研究了Nod2在体内被其特异性配体胞壁酰二肽(肽聚糖的一种成分)激活后所诱导的适应性免疫反应的展开情况。我们的研究结果表明,这种细菌传感器触发了一种具有Th2型极化特征的强效抗原特异性免疫反应,其特征是T细胞诱导IL-4和IL-5以及IgG1抗体反应。还发现Nod2在用TLR激动剂共刺激后对诱导Th1型和Th2型反应都至关重要。重要的是,体内观察到的对Nod2和TLR激动剂的协同反应在体外树突状细胞中得到了重现,这表明这些细胞可能在整合Nod2和TLR依赖性信号以驱动适应性免疫反应中发挥核心作用。综上所述,我们的结果确定Nod2是微生物诱导的抗原依赖性免疫增强和极化的关键介质。此外,这些发现影响了我们对克罗恩病发病机制的理解,在这些患者的一部分中,缺乏Nod2依赖性Th2信号可能解释了肠道黏膜水平上Th1介导的炎症加剧。