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PMID: 9355958 Published · ppublish English Journal Article Review

Infections in IFNGR-1-deficient children.

Jouanguy E, Altare F, Lamhamedi-Cherradi S, Casanova JL

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.

MeSH Terms
Animals Bacterial Infections/physiopathology Child Humans Infections/physiopathology Interferon-gamma Mice Parasitic Diseases/physiopathology Receptors, Interferon/deficiency Virus Diseases/physiopathology
Chemicals
Receptors, Interferon interferon gamma receptor Interferon-gamma
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Jouanguy E
INSERM U429, Hôpital Necker-Enfants Malades, Paris, France.
Altare F
Lamhamedi-Cherradi S
Casanova J L
Article Info
Journal
Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research
Abbr.
J Interferon Cytokine Res
ISSN
1079-9907
Published
1997-10-00
Pages
583-7
Language
English
Region
United States
NLM ID
9507088
Subset
IM
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