Harnessing calcineurin as a novel anti-infective agent against invasive fungal infections

被引:251
作者
Steinbach, William J. [1 ]
Reedy, Jennifer L.
Cramer, Robert A.
Perfect, John R.
Heitman, Joseph
机构
[1] Duke Univ, Ctr Med, Div Pediat Infect Dis, Dept Pediat, Durham, NC 27710 USA
[2] Duke Univ, Ctr Med, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
[3] Duke Univ, Ctr Med, Div Infect Dis & Int Hlth, Dept Med, Durham, NC 27710 USA
[4] Duke Univ, Ctr Med, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA
关键词
D O I
10.1038/nrmicro1680
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The number of immunocompromised patients with invasive fungal infections continues to increase and new antifungal therapies are not keeping pace with the growing incidence of these infections and their associated mortality. Calcineurin inhibition is currently used to exert effective immunosuppression following organ transplantation and in treating various other conditions. However, the calcineurin pathway is also intricately involved in the growth and pathogenesis of the three major fungal pathogens of humans, Cryptococcus neoformans, Candida albicans and Aspergillus fumigatus, and the exploitation of fungal calcineurin pathways holds great promise for the future development of novel antifungal agents. This Review summarizes our current understanding of calcineurin biology in these fungal species, and its exciting potential role in treating invasive fungal infections.
引用
收藏
页码:418 / 430
页数:13
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