Title of article :
Effect of Antifungal-Treated Host Macrophages on Candida glabrata
Author/Authors :
Li, Hong-Bin Department of Dermatology and Venereology - First Affiliated Hospital of Kunming Medical University, Yunnan, China , Li, Na Department of Dermatology and Venereology - First Affiliated Hospital of Kunming Medical University, Yunnan, China , Wen, Shu-Ran Department of Dermatology and Venereology - First Affiliated Hospital of Kunming Medical University, Yunnan, China , Qiang, Ming-Yue Department of Dermatology and Venereology - First Affiliated Hospital of Kunming Medical University, Yunnan, China , Yang, Zheng-Hui Department of Dermatology and Venereology - First Affiliated Hospital of Kunming Medical University, Yunnan, China , Dong, Tian-Xiang Department of Dermatology and Venereology - First Affiliated Hospital of Kunming Medical University, Yunnan, China , Li, Yu-Ye Department of Dermatology and Venereology - First Affiliated Hospital of Kunming Medical University, Yunnan, China , Kuang, Yi-Qun NHC Key Laboratory of Drug Addiction Medicine - First Affiliated Hospital of Kunming Medical University - Kunming Medical University, Yunnan, China
Pages :
8
From page :
1
To page :
8
Abstract :
Objective Candida glabrata (C. glabrata) causes infections associated with severe sepsis and high mortality. This study describes the effects of micafungin (MCF), itraconazole (ICZ), and amphotericin B (AmB) on the function of macrophages during C. glabrata infection. Methods RAW264.1 macrophages were treated with MCF, ICZ, or AmB and then challenged with C. glabrata. Cytokines from infected macrophage supernatants and the levels of superoxide dismutase (SOD) in macrophages were measured at different time points after phagocytosis. Results The activity of SOD was significantly increased in RAW264.1 cells that phagocytized C. glabrata and reached a peak level at 6 hours (P < 0.05). ICZ and AmB did not affect the SOD activity in cells that phagocytized C. glabrata versus that in untreated macrophage. C. glabrata stimulated macrophages to secrete cytokines. Neither ICZ nor AmB affected the secretion of interleukin-6 (IL-6), interleukin-8 (IL-8), or tumor necrosis factor-α (TNF-α) by C. glabrata-infected macrophages. However, MCF downregulated the secretion of TNF-α by infected macrophages and reduced the SOD activity of C. glabrata compared with those in untreated controls. Conclusion Echinocandins may increase their antifungal efficacy by altering the innate immune response of macrophages and attenuating antioxidants of this organism.
Keywords :
Effect of Antifungal-Treated , Host Macrophages , Candida glabrata
Journal title :
Canadian Journal of Infectious Diseases and Medical Microbiology
Serial Year :
2021
Full Text URL :
Record number :
2618889
Link To Document :
بازگشت