Partial interferon-γ receptor signaling chain deficiency in a patient with bacille Calmette-Guerin and Mycobacterium abscessus infection

被引:141
作者
Döffinger, R
Jouanguy, E
Dupuis, S
Fondanèche, MC
Stephan, JL
Emile, JF
Lamhamedi-Cherradi, S
Altare, F
Pallier, A
Barcenas-Morales, G
Meinl, E
Krause, C
Pestka, S
Schreiber, RD
Novelli, F
Casanova, JL
机构
[1] Hop Necker Enfants Malad, INSERM, U429, F-75015 Paris, France
[2] Hop Necker Enfants Malad, Unite Immunol & Hematol Pediat, F-75015 Paris, France
[3] Hop Univ St Etienne, Serv Pediat, St Etienne, France
[4] Hop Paul Brousse, Serv Anat Pathol, Villejuif, France
[5] Univ Nacl Autonoma Mexico, Fac Estudios Super Cuautitlan, Immunol Lab, Mexico City 04510, DF, Mexico
[6] Univ Erlangen Nurnberg, Inst Klin & Mol Virol, D-8520 Erlangen, Germany
[7] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Mol Genet & Microbiol, Piscataway, NJ 08854 USA
[8] Washington Univ, Dept Pathol, St Louis, MO 63130 USA
[9] Univ Turin, Dipartimento Sci Clin & Biol, Orbassano, Italy
关键词
D O I
10.1086/315197
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Complete deficiency of either of the two human interferon (IFN)-gamma receptor components, the ligand-binding IFN-gamma R1 chain and the signaling IFN-gamma R2 chain, is invariably associated with early-onset infection caused by bacille Calmeete-Guerin vaccines and/or environmental nontuberculous mycobacteria, poor granuloma formation, and a fatal outcome in childhood, Partial IFN-gamma R1 deficiency is associated with a milder histopathologic and clinical phenotype, Cells from a 20-year-old healthy person with a history of curable infections due to bacille Calmette-Guerin and Mycobacterium abscessus and mature granulomas in childhood were investigated, There was a homozygous nucleotide substitution in IFNGR2, causing an amino acid substitution in the extracellular region of the encoded receptor, Cell surface IFN-gamma R2 were detected by flow cytometry, Cellular responses to IFN-gamma were impaired but not abolished, Transfection with the wild-type IFNGR2 gene restored full responsiveness to IFN-gamma, This is the first demonstration of partial IFN-gamma R2 deficiency in humans.
引用
收藏
页码:379 / 384
页数:6
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