Literature DB >> 9355958

Infections in IFNGR-1-deficient children.

E Jouanguy1, F Altare, S Lamhamedi-Cherradi, J L Casanova.   

Abstract

Human interferon-gamma receptor 1 (IFNGR-1) deficiency is a newly identified autosomal recessive inherited immune disorder. Children with IFNGR-1 deficiency exhibit a severe, profound and selective susceptibility to weakly virulent mycobacteria, such as bacillus Calmette-Guerin (BCG) vaccine or environmental nontuberculous mycobacteria (NTM). This review compares the infections found in IFNGR-1-deficient children to those in IFN-gamma-deficient or IFNGR-1-deficient mice.

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Year:  1997        PMID： 9355958     DOI： 10.1089/jir.1997.17.583

Source DB:  PubMed          Journal:  J Interferon Cytokine Res        ISSN： 1079-9907            Impact factor:   2.607


  21 in total

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