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皮肤利什曼病中单核细胞的募集、抗原降解及定位

Monocyte recruitment, antigen degradation and localization in cutaneous leishmaniasis.

作者信息

Ridley M J, Ridley D S

出版信息

Br J Exp Pathol. 1986 Apr;67(2):209-18.

Abstract

The relationship between the destruction of Leishmania, the recruitment of monocytes and macrophage activity in the lesions of cutaneous leishmaniasis (CL) was studied in 53 biopsies representing the phases of evolution of the infection. Lysozyme, amastigotes and their degradation products were located by their specific antibodies. A rising level of monocyte influx was found to correlate with the degradation and solubilization of antigen, a falling level with final clearance. Differences in the results supported the previous concept of macrophage activation and macrophage lysis as alternative mechanisms for the elimination of Leishmania. Macrophage activation appeared to coincide with re-phagocytosis of externalized antigenic products of different type and origin. Macrophage lysis was a fully effective mechanism only when the antigen was contained within a focalized granuloma before mass lysis. Failing this, degradation and clearance of antigen were incomplete, and residues were sequestered on the periphery of the lesion where they bound to collagen and epidermis with consequential tissue damage. Antigen was demonstrated on the surface of lightly parasitized macrophages but not heavily infected ones. Other cells bound antigen without ingesting it, a process which might allow antigen presentation though it would also favour survival of parasites within the cell.

摘要

在53份代表皮肤利什曼病(CL)感染演变阶段的活检样本中,研究了利什曼原虫的破坏、单核细胞的募集与病变中巨噬细胞活性之间的关系。通过特异性抗体定位溶菌酶、无鞭毛体及其降解产物。发现单核细胞流入水平的上升与抗原的降解和溶解相关,水平下降与最终清除相关。结果的差异支持了先前关于巨噬细胞活化和巨噬细胞裂解作为消除利什曼原虫的替代机制的概念。巨噬细胞活化似乎与不同类型和来源的外在化抗原产物的再吞噬同时发生。巨噬细胞裂解只有在抗原在大量裂解前包含在局限性肉芽肿内时才是一种完全有效的机制。否则,抗原的降解和清除是不完全的,残留物被隔离在病变周边,在那里它们与胶原蛋白和表皮结合,从而导致组织损伤。在轻度寄生的巨噬细胞表面可检测到抗原,但在重度感染的巨噬细胞表面则未检测到。其他细胞结合抗原但不摄取,这一过程可能允许抗原呈递,尽管这也有利于寄生虫在细胞内的存活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/34fa/2013155/8ab8577702de/brjexppathol00014-0058-a.jpg

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