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卡氏肺孢子虫囊肿壁的酵母聚糖:化疗的绝佳靶点。

Yeast glucan of Pneumocystis carinii cyst wall: an excellent target for chemotherapy.

作者信息

Matsumoto Y, Yamada M, Amagai T

机构信息

Department of Applied Immunology, Faculty of Agriculture, University of Tokyo.

出版信息

J Protozool. 1991 Nov-Dec;38(6):6S-7S.

PMID:1818205
Abstract

Pneumocystis pneumonia is the most serious opportunistic infection in immunocompromised patients, particularly those with AIDS. Approved therapy is limited to pentamidine and inhibitors of folic acid synthesis, but these drugs show a high rate of adverse reactions in AIDS patients emphasizing the urgent need for additional effective therapies. Progress has, however, been hindered by lack of knowledge about this parasite's cellular characteristics. Previously we reported that beta (1,3)glucan is a major component of the Pneumocystis carinii cyst wall. This study shows that administration of aculeacin A, an inhibitor of beta (1,3)glucan biosynthesis, affects cyst wall formation, inhibits cyst maturation, and prevents severe pneumonia in steroid-treated rats. Thus this study not only demonstrates that beta (1,3)glucan is indispensable for growth of the parasite in rats, but suggests a new therapeutic strategy for human pneumocystosis.

摘要

肺孢子菌肺炎是免疫功能低下患者,尤其是艾滋病患者最严重的机会性感染。批准使用的治疗方法仅限于喷他脒和叶酸合成抑制剂,但这些药物在艾滋病患者中显示出很高的不良反应发生率,这凸显了对其他有效治疗方法的迫切需求。然而,由于对这种寄生虫的细胞特征缺乏了解,研究进展受到了阻碍。此前我们报道,β(1,3)-葡聚糖是卡氏肺孢子虫包囊壁的主要成分。本研究表明,给予β(1,3)-葡聚糖生物合成抑制剂阿库拉霉素A,会影响包囊壁形成,抑制包囊成熟,并预防类固醇治疗大鼠的严重肺炎。因此,本研究不仅证明β(1,3)-葡聚糖对大鼠体内该寄生虫的生长不可或缺,还为人类肺孢子菌病提出了一种新的治疗策略。

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