Invariant natural killer T cells recognize a fungal glycosphingolipid that can induce airway hyperreactivity

被引:114
作者
Albacker, Lee A. [1 ]
Chaudhary, Vinod [2 ]
Chang, Ya-Jen [1 ]
Kim, Hye Young [1 ]
Chuang, Ya-Ting [1 ]
Pichavant, Muriel [1 ]
DeKruyff, Rosemarie H. [1 ]
Savage, Paul B. [2 ]
Umetsu, Dale T. [1 ]
机构
[1] Harvard Univ, Childrens Hosp, Sch Med, Div Immunol & Allergy, Boston, MA 02115 USA
[2] Brigham Young Univ, Dept Chem & Biochem, Provo, UT 84602 USA
基金
美国国家卫生研究院;
关键词
ALLERGIC BRONCHOPULMONARY ASPERGILLOSIS; ACTIVATE NKT CELLS; LYMPHOID-CELLS; ADAPTIVE IMMUNITY; RECEPTOR DECTIN-1; TYPE-2; IMMUNITY; AIRBORNE FUNGI; SEVERE ASTHMA; BETA-GLUCANS; MURINE MODEL;
D O I
10.1038/nm.3321
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aspergillus fumigatus is a saprophytic fungus that is ubiquitous in the environment and is commonly associated with allergic sensitization and severe asthma in humans. Although A. fumigatus is recognized by multiple microbial pattern-recognition receptors, we found that an A. fumigatus-derived glycosphingolipid, asperamide B, directly activates invariant natural killer T (iNKT) cells in vitro in a CD1d-restricted, MyD88-independent and dectin-1-independent fashion. Moreover, asperamide B, when loaded onto CD1d, directly stained, and was sufficient to activate, human and mouse iNKT cells. In vivo, asperamide B rapidly induced airway hyperreactivity, which is a cardinal feature of asthma, by activating pulmonary iNKT cells in an interleukin-33 (IL-33)-ST2-dependent fashion. Asperamide B is thus the first fungal glycolipid found to directly activate iNKT cells. These results extend the range of microorganisms that can be directly detected by iNKT cells to the kingdom of fungi and may explain how A. fumigatus can induce severe chronic respiratory diseases in humans.
引用
收藏
页码:1297 / +
页数:9
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