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Partial Interferon‐γ Receptor Signaling Chain Deficiency in a Patient with Bacille Calmette‐Guérin andMycobacterium abscessusInfection
Author(s) -
Rainer Döffinger,
Emmanuelle Jouanguy,
Stéphanie BoissonDupuis,
MarieClaude Fondanèche,
Jean-Louis Stéphan,
JeanFrançois Emile,
Salma LamhamediCherradi,
Frédéric Altare,
Annaïck Pallier,
Gabriela BarcenasMorales,
Edgar Meinl,
Christopher Krause,
Sidney Pestka,
Robert D. Schreiber,
Francesco Novelli,
JeanLaurent Casanova
Publication year - 2000
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/315197
Subject(s) - mycobacterium bovis , immunology , interferon gamma , biology , nontuberculous mycobacteria , interferon , mycobacterium abscessus , flow cytometry , mycobacterium , receptor , immunodeficiency , microbiology and biotechnology , cytokine , medicine , immune system , tuberculosis , mycobacterium tuberculosis , pathology , bacteria , genetics
Complete deficiency of either of the two human interferon (IFN)-gamma receptor components, the ligand-binding IFN-gammaR1 chain and the signaling IFN-gammaR2 chain, is invariably associated with early-onset infection caused by bacille Calmette-Guérin vaccines and/or environmental nontuberculous mycobacteria, poor granuloma formation, and a fatal outcome in childhood. Partial IFN-gammaR1 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-Guérin 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-gammaR2 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-gammaR2 deficiency in humans.

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