Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a model
Détails
ID Serval
serval:BIB_529FEA8EE33F
Type
Article: article d'un périodique ou d'un magazine.
Sous-type
Synthèse (review): revue aussi complète que possible des connaissances sur un sujet, rédigée à partir de l'analyse exhaustive des travaux publiés.
Collection
Publications
Institution
Titre
Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a model
Périodique
Immunol Rev
ISSN
0105-2896 (Print)
ISSN-L
0105-2896
Statut éditorial
Publié
Date de publication
12/2000
Volume
178
Pages
39-48
Langue
anglais
Notes
Notarangelo, L D
Giliani, S
Mazza, C
Mella, P
Savoldi, G
Rodriguez-Perez, C
Mazzolari, E
Fiorini, M
Duse, M
Plebani, A
Ugazio, A G
Vihinen, M
Candotti, F
Schumacher, R F
eng
E.0668/Telethon/Italy
Research Support, Non-U.S. Gov't
Review
England
Immunol Rev. 2000 Dec;178:39-48.
Giliani, S
Mazza, C
Mella, P
Savoldi, G
Rodriguez-Perez, C
Mazzolari, E
Fiorini, M
Duse, M
Plebani, A
Ugazio, A G
Vihinen, M
Candotti, F
Schumacher, R F
eng
E.0668/Telethon/Italy
Research Support, Non-U.S. Gov't
Review
England
Immunol Rev. 2000 Dec;178:39-48.
Résumé
Cytokines play a major role in lymphoid development. Defects of the common gamma chain (gamma(c)) or of the JAK3 protein in humans have been shown to result in a severe combined immune deficiency (SCID), with a profound defect in T and natural killer (NK)-cell development, whereas B-cell generation is apparently unaffected (T-B+NK-SCID). While extensive molecular and biochemical analysis of these patients has been instrumental in understanding better the biological properties of the gamma(c) and JAK3 protein, an unexpected phenotypic heterogeneity of gamma(c) and JAK3 deficiency has emerged, indicating the need for appropriate and extensive investigations even in patients with atypical presentations. At the same time, characterization of the defects has been instrumental in the development of novel therapeutic approaches, from in utero hematopoietic stem cell transplantation to gene therapy.
Mots-clé
Cytokines/immunology, Female, Humans, Janus Kinase 3, Killer Cells, Natural/immunology, Male, Models, Biological, Mutation, Phenotype, Protein-Tyrosine Kinases/chemistry/*genetics/metabolism, Receptors, Interleukin-2/genetics, Severe Combined Immunodeficiency/*genetics/*immunology/therapy, Signal Transduction, T-Lymphocytes/immunology
Pubmed
Création de la notice
01/11/2017 10:29
Dernière modification de la notice
20/08/2019 14:08