Regulation of TH2 memory/effector cells during allergic inflammation

描述（由申请人提供）：临床和实验研究表明，过敏原特异性TH 2记忆/效应细胞存在于肺中，并有助于哮喘的持续和进展。最近，已经确定了CD 4 + TH 17细胞在调节过敏性炎症中的病理作用;然而，在TH 2免疫应答的背景下可以分泌IL-17的细胞类型仍然难以捉摸。我们已经发现了一种新的人类TH 2记忆/效应细胞亚群，其特征是同时产生TH 17和TH 2细胞因子以及GATA 3和ROR？T细胞在单细胞水平共表达;称为IL-17-TH 2细胞。与人类中的发现相似，IL-17-TH 2细胞主要存在于发炎的肺中，但不存在于其他淋巴器官中，并且在过敏性肺病小鼠模型中，在气道炎症的慢性阶段作为主要的IL-17产生T细胞持续存在。此外，我们发现细胞因子IL-12和IL-21能够诱导IL-17和IL-21，同时促进TH 2记忆/效应细胞产生TH 2细胞因子。用IL-12处理TH 2记忆/效应细胞诱导IRF 4（干扰素调节因子4）的显著上调，IRF 4是产生TH 2和TH 17免疫应答的关键因子。这些发现表明，大量的可塑性存在于CD 4 + TH 2记忆/效应细胞，这可以通过局部炎症线索控制。值得注意的是，我们观察到，总的CD 4 + TH 2记忆/效应细胞池中的循环IL-17-TH 2细胞的频率在特应性哮喘患者的血液中显著升高。在小鼠中，我们证明了抗原特异性IL-17-TH 2细胞与仅由经典TH 2或TH 17细胞诱导的那些相比，触发了更显著的炎性白细胞流入、杯状增生和粘蛋白产生。总的来说，这些初步研究导致了我们的中心假设，即IL-12和IL-21诱导肺部驻留的CD 4 + TH 2记忆/效应细胞获得TH 17炎症特性，并且这种产生的IL-17-TH 2细胞有助于慢性过敏性哮喘的恶化。在目的1中，我们专注于确定IL-12诱导IL-17-TH 2细胞的潜在机制。我们假设IL-12诱导TH 2记忆/效应细胞中IRF 4的上调，导致IL-17和IL-21细胞因子的产生。目的2：研究IL-21对IL-17-TH 2细胞的诱导和功能的调节作用。我们假设自分泌IL-21与IL-12协同作用，增强IL-17-TH 2细胞的诱导和效应功能。在目的3中，我们将确定IL-17-TH 2细胞在慢性过敏性哮喘免疫发病机制中的生物学相关性。我们推测，IL-17-TH 2细胞触发不同的趋化因子的产生，导致异质性炎症白细胞的浸润和病理变化，在慢性过敏性哮喘肺。我们相信，这些研究将拓宽我们对IL-17-TH 2细胞的炎症特性以及IL-17-TH 2、经典TH 2和TH 17细胞在慢性过敏性炎症中的相互关系的认识，从而为哮喘和特应性疾病的治疗提供更具体的方法。 公共卫生相关性：该项目的目标是确定调节新型IL-17产生TH 2记忆/效应细胞亚群的诱导和功能的潜在机制，并确定其在慢性过敏性炎症免疫发病机制中的生物学相关性。通过研究这种新的TH 2记忆/效应细胞亚群，我们将了解促炎细胞因子如何调节组织驻留TH 2记忆/效应细胞，以获得独特的炎症特性，并了解TH 2和TH 17细胞之间的相互关系，这有助于慢性过敏性哮喘的异质性，持久性和严重性。

DESCRIPTION (provided by applicant): Clinical and experimental investigations suggest that allergen-specific TH2 memory/effector cells reside in the lung and contribute to the persistence and progression of asthma. Recently, a pathological role for CD4+TH17 cells in the regulation of allergic inflammation has been identified; however, the cell types that can secrete IL-17 within the context of TH2 immune responses remain elusive. We have discovered a novel subset of human TH2 memory/effector cells featuring concurrent TH17 and TH2 cytokine production and GATA3 and ROR?t co-expression at a single cell level; termed IL-17-TH2 cells. Mirroring the findings in humans, IL-17-TH2 cells could be found primarily in inflamed lung, but not other lymphoid organs, and persist as the dominant IL-17-producing T cells at the chronic stage of airway inflammation in a mouse model of allergic lung diseases. Furthermore, we found that the cytokine IL-12 and IL-21 are capable of inducing IL-17 and IL-21, while promoting TH2 cytokine production by TH2 memory /effector cells. The treatment of TH2 memory/effector cells with IL-12 induces a significant up-regulation of IRF4 (interferon regulatory factor 4), a critical factor for the development of TH2 and TH17 immune responses. These findings suggest that substantial plasticity exists within CD4+TH2 memory/effector cells and this can be controlled by local inflammatory cues. Notably, we observed that the frequency of circulating IL-17-TH2 cells within total CD4+TH2 memory/effector cell pool is significantly elevated in blood of patients with atopic asthma. In mouse, we demonstrated that antigen specific IL-17-TH2 cells triggered much prominent influx of inflammatory leukocytes, goblet hyperplasia and mucin production compared with those induced only by classical TH2 or TH17 cells. Collectively, these preliminary studies lead to our central hypothesis that IL-12 and IL-21 induce lung resident CD4+ TH2 memory/effector cells to acquire TH17 inflammatory properties, and that such generated IL-17-TH2 cells contribute to the exacerbation of chronic allergic asthma. In Aim 1, we focus on determining the underlying mechanisms by which IL-12 induce IL-17-TH2 cells. We hypothesize that IL-12 induces up-regulation of IRF4 in TH2 memory/effector cells, leading to IL-17 and IL-21 cytokine production. In Aim 2, we will determine the role of IL-21 in regulating the induction and function of IL-17-TH2 cells. We hypothesize that autocrine IL-21 synergizes with IL-12 to enhance the induction and effector function of IL-17-TH2 cells. In Aim 3, we will define the biological relevance of IL-17-TH2 cells in the immunopathogenesis of chronic allergic asthma. We hypothesize that IL-17-TH2 cells trigger diverse chemokine production, leading to the infiltration of heterogeneous inflammatory leukocytes and pathological changes in lung during chronic allergic asthma. We believe that the proposed studies will broaden our views of the inflammatory properties of IL-17-TH2 cells and the inter-relationship between IL-17-TH2, classical TH2 and TH17 cells during chronic allergic inflammation, and thus provide more specific approaches for the treatments in asthma and atopy. PUBLIC HEALTH RELEVANCE: The goal of this project is to determine the underlying mechanisms that regulate the induction and function of a novel IL-17-producing TH2 memory/effector cell subset and define their biological relevance in the immunopathogenesis of chronic allergic inflammation. By examining this novel TH2 memory/effector cell subset, we will learn how the proinflammatory cytokines modulate tissue resident TH2 memory/effector cells to acquire distinctive inflammatory properties and understand the inter-relationship between TH2 and TH17 cells, that contribute to the heterogeneity, persistence and severity of chronic allergic asthma.