Innate Immunity: Mechanisms Linking with Adaptive Immunity

描述（由申请人提供）：本提案旨在请求支持由Luke A. J.奥尼尔、Kate A.菲茨杰拉德和阿韦里尔岛马，将于2010年6月7日至12日在都柏林，爱尔兰举行。在过去的5年里，我们对先天免疫的分子基础的理解取得了显着的进展。我们现在有相当多的细节，对主要类别的先天免疫受体，感觉病原体和挑起免疫和炎症反应。这些包括Toll样受体（TLR）、NOD样受体（NLR）和RIG-I样受体（RLR）。这些受体在宿主防御微生物中的作用已被研究，它们的信号通路已被阐明，它们在感染性和炎症性疾病中的作用也已被详细研究。除了通过诱导各种效应机制刺激先天免疫外，这些受体还参与建立适应性免疫。这通过诱导关键细胞因子以促进T和B细胞发育和活化，以及通过诱导树突细胞表面上的共刺激分子，特别是CD 80和CD 86来发生。最后一个方面涉及佐剂--激活这些受体的微生物或合成试剂充当建立记忆反应所需的强大佐剂。先天性免疫和适应性免疫之间的界面继续揭示新的组件和机制，最终可能有助于治疗操作。新的感受病原体（特别是核酸）的受体和激活它们的机制正在被发现。从适应性免疫回到先天免疫的负反馈回路正在被揭示。进化方面也为复杂的哺乳动物免疫系统是如何形成的提供了见解。本次会议将汇集研究这些受体激活的先天免疫机制的科学家，并将重点关注这些受体的能力及其引发的促进适应性免疫的反应。因此，会议将对许多对免疫感兴趣的研究人员以及免疫系统在疾病中的作用感兴趣。近年来，我们在理解微生物入侵者如何被先天免疫系统识别以及传感如何转化为最终导致免疫应答基因转录调控的信号通路方面取得了相当大的进展。关于先天免疫的Keystone研讨会会议：与适应性免疫相关的机制将汇集世界知名的科学家，致力于先天免疫传感机制和适应性免疫，并将对研究免疫，传染病以及免疫系统在自身免疫和炎症性疾病中的作用的研究人员感兴趣。

DESCRIPTION (provided by applicant): This proposal is to request support for a Keystone Symposia meeting entitled Innate Immunity: Mechanisms Linking with Adaptive Immunity, organized by Luke A.J. O'Neill, Kate A. Fitzgerald and Averil I. Ma, which will be held in Dublin, Ireland from June 7 - 12, 2010. In the past 5 years there have been remarkable advances in our understanding of the molecular basis of innate immunity. We now have considerable detail on the major classes of innate immune receptors that sense pathogens and provoke immune and inflammatory responses. These include the Toll-like receptors (TLRs), NOD-like receptors (NLRs) and RIG-I-like receptors (RLRs). The role these receptors play in host defense against microbes has been studied, their signaling pathways elucidated, and their roles in infectious and inflammatory diseases examined in detail. As well as stimulating innate immunity via induction of various effector mechanisms, these receptors also participate in the establishment of adaptive immunity. This occurs via the induction of key cytokines to promote T and B cell development and activation, and also via the induction of co-stimulatory molecules on the surface of dendritic cells, notably CD80 and CD86. A final aspect concerns adjuvancy - microbial or synthetic agents that activate these receptors act as powerful adjuvants required for the establishment of memory responses. The interface between innate and adaptive immunity continues to reveal novel components and mechanisms which might ultimately lend themselves to therapeutic manipulation. New receptors that sense pathogens (particularly nucleic acids) and the mechanisms that activate them are being uncovered. Negative feedback loops from adaptive immunity back to innate immunity are being revealed. Evolutionary aspects are also providing insights into how the complex mammalian immune system was formed. This conference will bring together scientists working on innate immune mechanisms activated by these receptors, and will have as a key focus the ability of these receptors and the responses they elicit to promote adaptive immunity. The conference will therefore be of interest to many investigators interested in immunity and the role the immune system plays in disease. Considerable progress has been made in recent years in our understanding of how microbial invaders are recognized by the innate immune system and how sensing translates into signaling pathways that culminate in the transcriptional regulation of immune response genes. The Keystone Symposia meeting on Innate Immunity: Mechanisms Linking with Adaptive Immunity will bring together world-renowned scientists working on innate immune sensing mechanisms and adaptive immunity, and will be of interest to researchers investigating immunity, infectious disease and the role the immune system plays in autoimmune and inflammatory diseases.