Restoration of Pattern Recognition Receptor Costimulation to Treat Chromoblastomycosis, a Chronic Fungal Infection of the Skin

被引:119
作者
da Gloria Sousa, Maria [1 ]
Reid, Delyth M. [1 ]
Schweighoffer, Edina [2 ]
Tybulewicz, Victor [2 ]
Ruland, Juergen [3 ,4 ]
Langhorne, Jean [2 ]
Yamasaki, Sho [5 ]
Taylor, Philip R. [6 ]
Almeida, Sandro R. [7 ]
Brown, Gordon D. [1 ]
机构
[1] Univ Aberdeen, Inst Med Sci, Sect Immunol & Infect, Aberdeen Fungal Grp, Aberdeen AB25 2ZD, Scotland
[2] Natl Inst Med Res, London NW7 1AA, England
[3] Tech Univ Munich, Klinikum Rechts Isar, Inst Mol Immunol, D-81675 Munich, Germany
[4] German Res Ctr Environm Hlth, Helmholtz Zentrum Munchen, Lab Signaling Immune Syst, D-85764 Neuherberg, Germany
[5] Kyushu Univ, Med Inst Bioregulat, Div Mol Immunol, Fukuoka 8128582, Japan
[6] Cardiff Univ, Sch Med, Dept Infect Immun & Biochem, Cardiff CF14 4XN, S Glam, Wales
[7] Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Anal Clin & Toxicol, BR-05508900 Sao Paulo, Brazil
基金
英国惠康基金;
关键词
C-TYPE LECTINS; SYK KINASE; DECTIN-1; INFLAMMATION; MACROPHAGES; INDUCTION; CELLS; MICE;
D O I
10.1016/j.chom.2011.04.005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Chromoblastomycosis is a chronic skin infection caused by the fungus Fonsecaea pedrosoi. Exploring the reasons underlying the chronic nature of F. pedrosoi infection in a murine model of chromoblastomycosis, we find that chronicity develops due to a lack of pattern recognition receptor (PRR) costimulation. F. pedrosoi was recognized primarily by C-type lectin receptors (CLRs), but not by Toll-like receptors (TLRs), which resulted in the defective induction of proinflammatory cytokines. Inflammatory responses to F. pedrosoi could be reinstated by TLR costimulation, but also required the CLR Mincle and signaling via the Syk/CARD9 pathway. Importantly, exogenously administering TLR ligands helped clear F. pedrosoi infection in vivo. These results demonstrate how a failure in innate recognition can result in chronic infection, highlight the importance of coordinated PRR signaling, and provide proof of the principle that exogenously applied PRR agonists can be used therapeutically.
引用
收藏
页码:436 / 443
页数:8
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