[间质性肺疾病淋巴细胞活化的标志物]。

J F Mornex, G Cordier, J P Revillard
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引用次数: 0

摘要

淋巴细胞性肺泡炎是许多类型间质性肺炎的常见阶段,淋巴细胞积聚在肺泡中,通过调节或激活炎症反应起主要的致病作用,控制愈合、慢性或纤维化的结果。通过对支气管肺泡灌洗淋巴细胞的研究,可以从体外模型的信息中讨论不同参数的功能价值。这些模型表明需要激活信号以顺序的方式作用于功能和反应模式显著不同的细胞。在激活过程中可以定义三个连续的阶段:首先是脂质(花生四烯酸的代谢)和动力学框架发生变化的“膜”阶段,第二阶段对应于“囊胚转化”的开始,淋巴细胞的产生,蛋白质含量和RNA的增加(G1期),然后是细胞分裂前的第三阶段DNA合成(S-G2期);有必要有新的分化标志。细胞周期的阶段和分化的抗原表达的联合研究,由单克隆抗体在异质群体中鉴定,现在受益于细胞荧光技术。这些方法与巨噬细胞产生的介质(白细胞介素)或非特异性激活标记物的测量相结合,应该导致肺泡炎临床免疫学的初始阶段的定义。最后,这些方法允许细胞免疫药理学的发展,从而打开了新的治疗形式的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Markers of lymphocyte activation in interstitial pulmonary disease].

A lymphocytic alveolitis is a common stage in a number of types of interstitial pneumonia where the lymphocytes accumulate in the alveoli and play a major pathogenic role by the regulation or activation of the inflammatory reaction, controlling the outcome either to healing, chronicity or fibrosis. A study of lymphocytes obtained by broncho-alveolar lavage enables the study of different parameters whose functional value is discussed from information derived form in vitro models. These models show the need for activating signals acting in a sequential manner on cells whose function and mode of response are remarkably varied. Three successive phases may be defined during activation: first a "membrane" stage with changes in the lipid (in the metabolism of arachidonic acid) and kinetic framework, a second phase corresponds to the beginning of "blastic transformation" with the production of lymphocytes, an increase in the protein content and RNA (phase G1), then a third stage of DNA synthesis (phase S-G2) preceding cell division; it is necessary to have new markers of differentiation. The joint study of the phases of cell cycles and the antigenic expression of differentiation, identified by monoclonal antibodies within a heterogeneous population nowadays benefit from techniques of cytofluorimetry. The methods combined with a measure of mediators produced (interleukins) or the non-specific markers of activation by macrophages ought to lead to a definition of initial stages of the clinical immunology of alveolitis. Finally these methods permit the development of cellular immunopharmacology which to open the possibilities of new forms of treatment.

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