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Coordination of Candida albicans Invasion and Infection Functions by Phosphoglycerol Phosphatase Rhr2

Interleukin 17-Mediated Host Defense against Candida albicans

Section of Immunology, Institute of Virology, University of Zürich, Winterthurerstrasse 266a, Zürich, CH-8057, Switzerland
Author to whom correspondence should be addressed.
Academic Editor: Sarah Gaffen
Pathogens 2015, 4(3), 606-619;
Received: 17 July 2015 / Revised: 6 August 2015 / Accepted: 7 August 2015 / Published: 12 August 2015
(This article belongs to the Special Issue Candida Albicans Infections)
Candida albicans is part of the normal microbiota in most healthy individuals. However, it can cause opportunistic infections if host defenses are breached, with symptoms ranging from superficial lesions to severe systemic disease. The study of rare congenital defects in patients with chronic mucocutaneous candidiasis led to the identification of interleukin-17 (IL-17) as a key factor in host defense against mucosal fungal infection. Experimental infections in mice confirmed the critical role of IL-17 in mucocutaneous immunity against C. albicans. Research on mouse models has also contributed importantly to our current understanding of the regulation of IL-17 production by different cellular sources and its effector functions in distinct tissues. In this review, we highlight recent findings on IL-17-mediated immunity against C. albicans in mouse and man. View Full-Text
Keywords: interleukin 17; chronic mucocutaneous candidiasis; mouse models interleukin 17; chronic mucocutaneous candidiasis; mouse models
MDPI and ACS Style

Sparber, F.; LeibundGut-Landmann, S. Interleukin 17-Mediated Host Defense against Candida albicans. Pathogens 2015, 4, 606-619.

AMA Style

Sparber F, LeibundGut-Landmann S. Interleukin 17-Mediated Host Defense against Candida albicans. Pathogens. 2015; 4(3):606-619.

Chicago/Turabian Style

Sparber, Florian, and Salomé LeibundGut-Landmann. 2015. "Interleukin 17-Mediated Host Defense against Candida albicans" Pathogens 4, no. 3: 606-619.

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