过敏毒素:在疾病中的可能作用。

W Vogt
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引用次数: 125

摘要

过敏毒素,特别是C3a和C5a,具有多种生物活性,提示其作为炎症反应介质的作用:它们引起平滑肌收缩、组胺释放、毛细血管通透性增加、白细胞粘附血管内皮、白细胞趋化、血小板和白细胞聚集。大多数这些作用是由其他介质的协同作用支持的,特别是花生四烯酸衍生物,它可能由过敏毒素刺激的细胞,如白细胞或内皮细胞产生。补体肽在体内的作用很大程度上取决于它们产生的位置:在血管内释放到全身循环中,主要是由于白细胞的激活、聚集和它们在肺血管中的积累,导致成人呼吸窘迫综合征和肺休克等不良症状。血管内释放可由某些药物引起,也可由血液与旁路或透析装置表面接触引起。局部炎症和防御反应的诱导需要在组织间隙释放过敏毒素。组织液与血浆补体成分的浓度在数量上不同。这就提出了一些问题,即如何在病变部位获得C3a和C5a的有效浓度,以产生能够吸引血液白细胞的趋化梯度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anaphylatoxins: possible roles in disease.

Anaphylatoxins, in particular C3a and C5a, have various biological activities which suggest a role as mediators of inflammatory reactions: they cause contraction of smooth muscle, histamine release, increase in capillary permeability, adhesion of leukocytes to vascular endothelium, leukocyte chemotaxis, and aggregation of platelets and leukocytes. Most of these effects are supported by the cooperation of other mediators, in particular arachidonic acid derivatives which may be produced by anaphylatoxin-stimulated cells, e.g. leukocytes or endothelium. In vivo effects of the complement peptides depend very much on the site of their generation: intravascular release in the general circulation leads to adverse symptoms such as adult respiratory distress syndrome and shock lung, mainly due to leukocyte activation, aggregation and their accumulation in lung vessels. Intravascular release may be induced by certain drugs, and by contact of blood with the surfaces of bypass or dialysis apparatus. Induction of local inflammatory and defense reactions requires release of anaphylatoxins in tissue spaces. Tissue fluid differs quantitatively from blood plasma in its concentration of complement components. This raises some problems of how efficient concentrations of C3a and C5a can be attained at the site of a lesion to generate a chemotactic gradient capable of attracting blood leukocytes.

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