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肺的防御:细胞介导免疫作用的研究

The defense of the lung: studies of the role of cell-mediated immunity.

作者信息

Johnson J E, Philp J R

出版信息

Johns Hopkins Med J. 1977 Sep;141(3):126-34.

PMID:330913
Abstract

The defense of the lung against infections, toxins and allergens is accomplished by an excretory transport mechanism and by the interaction of cellular and humoral defense systems. Pulmonary alveolar macrophages represent a common effector pathway for both nonspecific cellular phagocytic defenses and for specifically triggered cell-mediated immunity, via T lymphocytes. Nonspecific activation of macrophages is induced by toxic substances. Studies of the immunocytologic system indicate partial compartmentalization and "local" immunity for both cellular and humoral systems. Further studies on pulmonary cell-mediated immunity have characterized an amplification mechanism by which antigen-induced stimulation of T lymphocytes leads to recruitment of nonsensitive lymphocytes through the production of a low-molecular weight "transfer factor." Other lymphocyte-produced mediators (lymphokines) act to attract, aggregate and accumulate macrophages in areas of inflammation. In addition, macrophages are "activated" and show enhanced microbicidal capabilities as well as enhanced resistance to the cytotoxic effects of certain ingested microorganisms. It is postulated that cellular (nonspecific) and cell-mediated (specific) immune defenses play important roles in protection against several categories of microorganisms in a hierarchy of virulence.

摘要

肺部抵御感染、毒素和过敏原是通过一种排泄转运机制以及细胞防御系统和体液防御系统的相互作用来实现的。肺泡巨噬细胞是通过T淋巴细胞介导的非特异性细胞吞噬防御和特异性触发的细胞介导免疫的共同效应途径。巨噬细胞的非特异性激活由有毒物质诱导。免疫细胞学系统的研究表明,细胞和体液系统都存在部分分隔和“局部”免疫。对肺部细胞介导免疫的进一步研究已经明确了一种放大机制,即抗原诱导的T淋巴细胞刺激通过产生低分子量“转移因子”导致非敏感淋巴细胞的募集。其他淋巴细胞产生的介质(淋巴因子)在炎症区域吸引、聚集和积累巨噬细胞。此外,巨噬细胞被“激活”,显示出增强的杀菌能力以及对某些摄入微生物的细胞毒性作用的增强抵抗力。据推测,细胞(非特异性)和细胞介导(特异性)免疫防御在抵御几类不同毒力等级的微生物中发挥重要作用。

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