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慢性黏膜皮肤念珠菌病患者巨噬细胞功能的体外研究(作者译)

[In vitro investigations of microphages function in patients with chronic mucocutaneous candidosis (author's transl)].

作者信息

Djawari D, Gross J, Bischoff T, Hornstein O P, Meinhof W

出版信息

Immun Infekt. 1979 Feb;7(1):24-9.

PMID:374241
Abstract

In five patients with either familial or non-familial type of chronic mucocutaneous candidosis some properties of phagocytic function of the polymorphonuclear leucocytes (PMNL) have been studied in vitro. In each of the patients there were found: a) a decreased chemotactic activity of PMNL, b) a weakness of intake and of intracellular destruction of Candida albicans cells by PMNL, c) an impairment of phagocytosis and intracellular killing of Candida albicans as well of Staphylococcus aureus by PMNL. The rate of phagocytosis of heat-inactivated Candida albicans cells by PMNL was normal in each case. In the serum of two patients a phagocytosis inhibiting factor is supposed to exist. In PMNL of 3 patients a defective activity of NADH-dependent oxidase was found. The occurrence of hereditary CMCC in a father and his two daughters points to an autosomal dominant trait, whereas in most cases of familiar CMCC hitherto described an autosomal recessive mode of transmission was found.

摘要

对5例患有家族性或非家族性慢性黏膜皮肤念珠菌病的患者,在体外研究了多形核白细胞(PMNL)吞噬功能的一些特性。在每例患者中均发现:a)PMNL的趋化活性降低;b)PMNL摄取和细胞内破坏白色念珠菌细胞的能力减弱;c)PMNL对白色念珠菌以及金黄色葡萄球菌的吞噬作用和细胞内杀伤受损。在每种情况下,PMNL对热灭活白色念珠菌细胞的吞噬率均正常。推测两名患者的血清中存在吞噬抑制因子。在3例患者的PMNL中发现NADH依赖性氧化酶活性缺陷。一名父亲及其两个女儿患遗传性慢性黏膜皮肤念珠菌病表明这是一种常染色体显性性状,而迄今为止所描述的大多数家族性慢性黏膜皮肤念珠菌病病例均为常染色体隐性遗传方式。

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