Uchida K, Yamamoto Y, Klein T W, Friedman H, Yamaguchi H
Research Center for Medical Mycology, Teikyo University School of Medicine, Tokyo, Japan.
J Med Vet Mycol. 1992;30(4):293-300. doi: 10.1080/02681219280000381.
Administration of recombinant human granulocyte-colony stimulating factor (G-CSF), which induces hemopoietic precursor cells to proliferate and differentiate into neutrophils, protected leukopenic mice infected with opportunistic fungi. Mice were injected with cyclophosphamide and were then subcutaneously (s.c.) or intravenously (i.v.) administered 15-120 micrograms G-CSF kg-1 day-1 for 3 days. The number of peripheral blood neutrophils in the G-CSF treated mice was significantly increased 48 h after G-CSF administration. All leukopenic mice infected with either Candida albicans, Cryptococcus neoformans or Aspergillus fumigatus were significantly protected by treatment with the G-CSF. Moreover, G-CSF treatment caused a decrease in the number of viable yeasts in kidneys of Candida infected mice. These data suggest that prophylactic therapy with G-CSF may be useful against fungal infections in an immunocompromised host.
重组人粒细胞集落刺激因子(G-CSF)可诱导造血前体细胞增殖并分化为中性粒细胞,给感染机会性真菌的白细胞减少小鼠注射该因子可起到保护作用。给小鼠注射环磷酰胺,然后皮下(s.c.)或静脉内(i.v.)给予15 - 120微克G-CSF·kg⁻¹·天⁻¹,持续3天。给予G-CSF后48小时,接受G-CSF治疗的小鼠外周血中性粒细胞数量显著增加。所有感染白色念珠菌、新型隐球菌或烟曲霉的白细胞减少小鼠通过G-CSF治疗均得到显著保护。此外,G-CSF治疗使念珠菌感染小鼠肾脏中活酵母数量减少。这些数据表明,G-CSF预防性治疗可能对免疫受损宿主的真菌感染有效。