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Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds

SOLOGUREN, Ithaisa ; BOISSON-DUPUIS, Stéphanie ; SANTIAGO, Esther ; XIAOFEI KONG ; JANNIERE, Lucile ; COLINO, Elena ; HERRERA-RAMOS, Estefanía ; FRANCES, Adela ; NAVARRETE, Carmen ; BLANCHE, Stéphane ; FARIA, Emilia ; REMISZEWSKI, Pawet ; PESTANO, Jose ; CORDEIRO, Ana ; FREEMAN, Alexandra ; HOLLAND, Steven ; ABARCA, Katia ; VALERON-LEMAUR, Mónica ; GONCALO-MARQUES, José ; SILVEIRA, Luisa ; GARCIA-CASTELLANO, José Manuel ; CAMINERO, José ; PEREZ-ARELLANO, José Luis ; BENOIT VINCENT, Quentin ; BUSTAMANTE, Jacinta ; ABEL, Laurent ; CASANOVA, Jean-Laurent ; RODRIGUEZ-GALLEGO, Carlos ; FERNANDEZ-PEREZ, Leandro ; CHAPGIER, Ariane ; CARDENES, Maria ; FEINBERG, Jacqueline ; GARCIA-LAORDEN, M. Isabel ; PICARD, Capucine

Human molecular genetics, 2011-04, Vol.20 (8), p.1509-1523 [Periódico revisado por pares]

Oxford: Oxford University Press

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Título:
Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds
Autor: SOLOGUREN, Ithaisa ; BOISSON-DUPUIS, Stéphanie ; SANTIAGO, Esther ; XIAOFEI KONG ; JANNIERE, Lucile ; COLINO, Elena ; HERRERA-RAMOS, Estefanía ; FRANCES, Adela ; NAVARRETE, Carmen ; BLANCHE, Stéphane ; FARIA, Emilia ; REMISZEWSKI, Pawet ; PESTANO, Jose ; CORDEIRO, Ana ; FREEMAN, Alexandra ; HOLLAND, Steven ; ABARCA, Katia ; VALERON-LEMAUR, Mónica ; GONCALO-MARQUES, José ; SILVEIRA, Luisa ; GARCIA-CASTELLANO, José Manuel ; CAMINERO, José ; PEREZ-ARELLANO, José Luis ; BENOIT VINCENT, Quentin ; BUSTAMANTE, Jacinta ; ABEL, Laurent ; CASANOVA, Jean-Laurent ; RODRIGUEZ-GALLEGO, Carlos ; FERNANDEZ-PEREZ, Leandro ; CHAPGIER, Ariane ; CARDENES, Maria ; FEINBERG, Jacqueline ; GARCIA-LAORDEN, M. Isabel ; PICARD, Capucine
Assuntos: Adolescent ; Adult ; Age ; Amino Acid Sequence ; Bacillus ; Biological and medical sciences ; Child ; Child, Preschool ; Children ; Female ; Founder Effect ; Fundamental and applied biological sciences. Psychology ; gamma -Interferon ; Genes, Recessive ; Genetic Predisposition to Disease ; Genetics of eukaryotes. Biological and molecular evolution ; Genotypes ; Haplotypes ; Humans ; Infection ; Interferon gamma Receptor ; Interferon-gamma - metabolism ; Islands ; Male ; Molecular and cellular biology ; Molecular Sequence Data ; Monocytes - metabolism ; Mutation ; Mutation, Missense ; Mycobacteriosis ; Mycobacterium avium ; Mycobacterium bovis ; Mycobacterium Infections - genetics ; Mycobacterium Infections - immunology ; Mycobacterium Infections - microbiology ; Osteomyelitis - genetics ; Osteomyelitis - microbiology ; Pedigree ; Phenotype ; Phosphorylation ; Pneumonia, Bacterial - genetics ; Prophylaxis ; Protein Transport ; Receptors, Interferon - deficiency ; Receptors, Interferon - genetics ; Receptors, Interferon - immunology ; Salmonella ; Salmonella Infections - genetics ; Salmonellosis ; Salmonidae ; STAT1 Transcription Factor - metabolism ; Tuberculosis ; Tuberculosis - genetics ; Tuberculosis - microbiology ; Tuberculosis - mortality ; Young Adult
É parte de: Human molecular genetics, 2011-04, Vol.20 (8), p.1509-1523
Notas: ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
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The authors wish it to be known that, in their opinion, the first two authors should be regarded as joint First Authors.
These two authors should be regarded as Senior Authors.
The authors wish it to be known that, in their opinion, these authors should be regarded as joint Second Authors.
Descrição: We report a series of 14 patients from 11 kindreds with recessive partial (RP)-interferon (IFN)-γR1 deficiency. The I87T mutation was found in nine homozygous patients from Chile, Portugal and Poland, and the V63G mutation was found in five homozygous patients from the Canary Islands. Founder effects accounted for the recurrence of both mutations. The most recent common ancestors of the patients with the I87T and V63G mutations probably lived 1600 (875-2950) and 500 (200-1275) years ago, respectively. The two alleles confer phenotypes that are similar but differ in terms of IFN-γR1 levels and residual response to IFN-γ. The patients suffered from bacillus Calmette-Guérin-osis (n= 6), environmental mycobacteriosis (n= 6) or tuberculosis (n= 1). One patient did not suffer from mycobacterial infections but had disseminated salmonellosis, which was also present in two other patients. Age at onset of the first environmental mycobacterial disease differed widely between patients, with a mean value of 11.25 ± 9.13 years. Thirteen patients survived until the age of 14.82 ± 11.2 years, and one patient died at the age of 7 years, 9 days after the diagnosis of long-term Mycobacterium avium infection and the initiation of antimycobacterial treatment. Up to 10 patients are currently free of infection with no prophylaxis. The clinical heterogeneity of the 14 patients was not clearly related to either IFNGR1 genotype or the resulting cellular phenotype. RP-IFN-γR1 deficiency is, thus, more common than initially thought and should be considered in both children and adults with mild or severe mycobacterial diseases.
Editor: Oxford: Oxford University Press
Idioma: Inglês

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Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds

Oxford: Oxford University Press

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