Gahr M, Ranti J, Schröter W
Eur J Pediatr. 1978 Mar 13;127(3):173-9. doi: 10.1007/BF00442058.
A new defect of chemotaxis and random motility of polymorphonuclear leukocytes is described in a patient with severe recurrent bacterial infections since early childhood. This defect seems to be intrinsic to the cells. The patient's plasma did not contain an inhibitor of chemotaxis. Addition of plasma to the patient's cells restored their chemotactic activity. High concentrations of immunoglobulin E were found in the patient's plasma. Phagocytosis, bacterial killing, and reduction of nitroblue tetrazolium salt were normal. Histological examination of lung tissue revealed a pattern similar to that observed in chronic granulomatous disease.
一名自幼年起就患有严重复发性细菌感染的患者,其多形核白细胞的趋化性和随机运动出现了一种新的缺陷。这种缺陷似乎是细胞固有的。患者血浆中不含趋化性抑制剂。向患者的细胞中添加血浆可恢复其趋化活性。在患者血浆中发现了高浓度的免疫球蛋白E。吞噬作用、细菌杀伤以及硝基蓝四氮唑盐还原均正常。肺组织的组织学检查显示出一种与慢性肉芽肿病中观察到的模式相似的情况。