Schmatz D M, Romancheck M A, Pittarelli L A, Schwartz R E, Fromtling R A, Nollstadt K H, Vanmiddlesworth F L, Wilson K E, Turner M J
Department of Biochemical Parasitology, Merck Sharp & Dohme Research Laboratories, Rahway, NJ 07065.
Proc Natl Acad Sci U S A. 1990 Aug;87(15):5950-4. doi: 10.1073/pnas.87.15.5950.
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-beta-glucan as a major constituent. Based on this, several proposed 1,3-beta-glucan synthesis inhibitors were evaluated for their ability to control P. carinii pneumonia in vivo. Compounds from two classes of 1,3-beta-glucan synthesis inhibitors, the echinocandins and papulacandins, were found to be effective against P. carinii.
卡氏肺孢子虫肺炎是美国艾滋病患者死亡的主要原因。由于不良反应发生率高,目前可用的治疗方法用途有限。因此,迫切需要一种更安全的治疗和预防这种疾病的方法。最近的证据表明,卡氏肺孢子虫与真菌有关,并且包囊形式的壁含有1,3-β-葡聚糖作为主要成分。基于此,对几种提议的1,3-β-葡聚糖合成抑制剂在体内控制卡氏肺孢子虫肺炎的能力进行了评估。发现两类1,3-β-葡聚糖合成抑制剂,即棘白菌素类和丘疹霉素类的化合物对卡氏肺孢子虫有效。