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Advances in understanding pulmonary host defense mechanisms: dendritic cell function and immunomodulation.

机译:在理解肺部宿主防御机制方面的进展:树突状细胞功能和免疫调节。

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摘要

Mucosal host immunity in the respiratory tract can probably be manipulated to better improve defense against microbes and other antigens or particulates that cause infection and respiratory illness. An evolving strategy is to target the extensive network of dendritic cells in the lungs, especially dendritic cells located in the airway epithelium, which are super antigen-presenting cells that can initiate specific T-lymphocyte immune responses. Also, dendritic cells can elaborate cytokines such as interleukin 12 which drive other components of the immune response including antibody production. However, dendritic cells can be counter-regulated by inhibitory cytokines or certain microbes that create a dynamic interplay. This review emphasizes human studies and relevant animal models that provide a framework for future planning of experimental approaches to enhancing antimicrobial immunity and respiratory host defense.
机译:可以操纵呼吸道中的粘膜宿主免疫力,以更好地改善对引起感染和呼吸系统疾病的微生物和其他抗原或微粒的防御能力。一种发展中的策略是靶向肺中的树突状细胞的广泛网络,尤其是位于气道上皮的树突状细胞,它们是可以启动特定T淋巴细胞免疫反应的超抗原呈递细胞。而且,树突状细胞可以形成细胞因子,例如白介素12,其驱动免疫应答的其他成分,包括抗体产生。然而,树突状细胞可以被抑制性细胞因子或某些产生动态相互作用的微生物反调节。这篇综述强调了人类研究和相关的动物模型,这些模型为将来计划增强抗菌素免疫力和呼吸道宿主防御的实验方法提供了框架。

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