TREATMENT OF PNEUMOCYSTIS-CARINII PNEUMONIA WITH 1,3-BETA-GLUCAN SYNTHESIS INHIBITORS

被引:165
作者
SCHMATZ, DM
ROMANCHECK, MA
PITTARELLI, LA
SCHWARTZ, RE
FROMTLING, RA
NOLLSTADT, KH
VANMIDDLESWORTH, FL
WILSON, KE
TURNER, MJ
机构
[1] MERCK SHARP & DOHME LTD,DEPT NAT PROD CHEM,RAHWAY,NJ 07065
[2] MERCK SHARP & DOHME LTD,DEPT MICROBIOL,RAHWAY,NJ 07065
关键词
AIDS; antifungal drug; Candida; echinocandin; opportunistic infection; papulacandin;
D O I
10.1073/pnas.87.15.5950
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Pneumocystis carinii pneumonia is a major cause of death in AIDS patients in the United States. The presently available treatments have limited use due to a high incidence of adverse reactions. Therefore, there is an urgent need for a safer method for treatment and prevention of this disease. Recent evidence has suggested that P. carinii is related to fungi and that the wall of the cyst form contains 1,3-β-glucan as a major constituent. Based on this, several proposed 1,3-β-glucan synthesis inhibitors were evaluated for their ability to control P. carinii pneumonia in vivo. Compounds from two classes of 1,3-β-glucan synthesis inhibitors, the echinocandins and papulacandins, were found to be effective against P. carinii.
引用
收藏
页码:5950 / 5954
页数:5
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