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对从白色念珠菌中提取的口服葡聚糖免疫佐剂活性的初步评估。

Preliminary evaluation of immunoadjuvant activity of an orally administered glucan extracted from Candida albicans.

作者信息

Nicoletti A, Nicoletti G, Ferraro G, Palmieri G, Mattaboni P, Germogli R

机构信息

Institute of Microbiology, University of Catania, Italy.

出版信息

Arzneimittelforschung. 1992 Oct;42(10):1246-50.

PMID:1472146
Abstract

The immunoadjuvant activity of an orally administered glucan (Glucanil, Gluimmun) was investigated in mice. Glucan was extracted from Candida albicans ATCC 20955 and purified by an alkali-acid and detergent treatment. In this study the chronic intravenous infection with Candida albicans (treated or not with amphotericin B) or Staphylococcus aureus was the experimental model. Moreover the production of interleukin-2 was evaluated in treated animals. Oral treatment with glucan at 1 mg/mouse/day repeated doses, starting from 10 days before the experimental infection, significantly increased polymorphonuclear leukocytes and peripheral monocytes number. A significant increase in number and in vitro candidacidal activity was also observed for alveolar macrophages. The resistance towards systemic infection with Candida albicans or Staphylococcus aureus increased, significantly reducing the growth of microorganisms in the kidneys of infected animals. Glucan significantly increased the candidacidal spleen cells activity and synergized with amphotericin B chemotherapeutic action. Higher doses (eg. 2 or 5 mg/mouse) were not effective. A 10 days oral treatment with 1 mg/mouse/d significantly increased the interleukin-2 production. Toxicological studies showed that glucan is highly tolerated.

摘要

在小鼠中研究了口服葡聚糖(Glucanil,Gluimmun)的免疫佐剂活性。葡聚糖从白色念珠菌ATCC 20955中提取,并通过酸碱和去污剂处理进行纯化。在本研究中,白色念珠菌(用或不用两性霉素B治疗)或金黄色葡萄球菌的慢性静脉感染作为实验模型。此外,还评估了治疗动物中白细胞介素-2的产生。从实验感染前10天开始,以1mg/小鼠/天的重复剂量口服葡聚糖治疗,显著增加了多形核白细胞和外周单核细胞数量。肺泡巨噬细胞的数量和体外杀念珠菌活性也显著增加。对白色念珠菌或金黄色葡萄球菌全身感染的抵抗力增强,显著降低了感染动物肾脏中微生物的生长。葡聚糖显著增加了杀念珠菌脾细胞活性,并与两性霉素B的化疗作用协同。更高剂量(例如2或5mg/小鼠)无效。以1mg/小鼠/天进行10天的口服治疗显著增加了白细胞介素-2的产生。毒理学研究表明葡聚糖具有高度耐受性。

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