Chronic Mucocutaneous Candidiasis Caused by a Gain-of-Function Mutation in the STAT1 DNA-Binding Domain

被引:79
作者
Takezaki, Shunichiro
Yamada, Masafumi [1 ]
Kato, Masahiko [2 ]
Park, Myoung-ja [3 ]
Maruyama, Kenichi [4 ]
Yamazaki, Yasuhiro
Chida, Natsuko [5 ]
Ohara, Osamu [6 ]
Kobayashi, Ichiro
Ariga, Tadashi
机构
[1] Hokkaido Univ, Dept Pediat, Grad Sch Med, Kita Ku, Sapporo, Hokkaido 0608638, Japan
[2] Gunma Childrens Med Ctr, Dept Allergy & Immunol, Shibukawa 3778577, Japan
[3] Gunma Childrens Med Ctr, Dept Hematol Oncol, Shibukawa 3778577, Japan
[4] Gunma Childrens Med Ctr, Dept Nephrol, Shibukawa 3778577, Japan
[5] Hokkaido Univ, Dept Dent Children & Disabled Persons, Grad Sch Dent Med, Sapporo, Hokkaido 0608586, Japan
[6] Kazusa DNA Res Inst, Dept Human Genome Technol, Chiba 2920818, Japan
关键词
D O I
10.4049/jimmunol.1200926
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Chronic mucocutaneous candidiasis (CMC) is a heterogeneous group of primary immunodeficiency diseases characterized by chronic and recurrent Candida infections of the skin, nails, and oropharynx. Gain-of-function mutations in STAT1 were very recently shown to be responsible for autosomal-dominant or sporadic cases of CMC. The reported mutations have been exclusively localized in the coiled-coil domain, resulting in impaired dephosphorylation of STAT1. However, recent crystallographic analysis and direct mutagenesis experiments indicate that mutations affecting the DNA-binding domain of STAT1 could also lead to persistent phosphorylation of STAT1. To our knowledge, this study shows for the first time that a DNA-binding domain mutation of c. 1153C > T in exon 14 (p.T385M) is the genetic cause of sporadic CMC in two unrelated Japanese patients. The underlying mechanisms involve a gain of STAT1 function due to impaired dephosphorylation as observed in the coiled-coil domain mutations. The Journal of Immunology, 2012, 189: 1521-1526.
引用
收藏
页码:1521 / 1526
页数:6
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