Functional role of interleukin-4 (IL-4) and IL-7 in the development of X-linked severe combined immunodeficiency
- PMID: 9885222
Functional role of interleukin-4 (IL-4) and IL-7 in the development of X-linked severe combined immunodeficiency
Abstract
X-linked severe combined immunodeficiency (X-SCID) is characterized by an absent or diminished number of T cells and natural-killer (NK) cells with a normal or elevated number of B cells, and results from mutations of the gammac chain. The gammac chain is shared by interleukin-2 (IL-2), IL-4, IL-7, IL-9, and IL-15 receptors. Recently, a survival signal through the IL-7 receptor alpha (IL-7Ralpha) chain was shown to be important for T-cell development in mice and was suggested to contribute to the X-SCID phenotype. In the present study, we examined function of a mutant gammac chain (A156V) isolated from an X-SCID patient and found that T cells expressing the mutant gammac chain were selectively impaired in their responses to IL-4 or IL-7 compared with the wild-type gammac chain expressing cells although responses to IL-2 or IL-15 were relatively maintained. The result shows that IL-4- and/or IL-7-induced signaling through the gammac chain is critical for T-cell development and plays an important role in the development of the X-SCID phenotype.
Similar articles
-
A novel mutant gammac chain from a patient with typical phenotype of X-linked severe combined immunodeficiency (SCID) has partial signalling function for mediating IL-2 and IL-4 receptor action.Clin Exp Immunol. 1999 Feb;115(2):356-61. doi: 10.1046/j.1365-2249.1999.00792.x. Clin Exp Immunol. 1999. PMID: 9933465 Free PMC article.
-
A partial deficiency of interleukin-7R alpha is sufficient to abrogate T-cell development and cause severe combined immunodeficiency.Blood. 2000 Oct 15;96(8):2803-7. Blood. 2000. PMID: 11023514
-
A novel splice-site mutation in the common gamma chain (gammac) gene IL2RG results in X-linked severe combined immunodeficiency with an atypical NK+ phenotype.Hum Mutat. 2004 May;23(5):522-3. doi: 10.1002/humu.9235. Hum Mutat. 2004. PMID: 15108287
-
Mutations in the gene for the IL-7 receptor result in T(-)B(+)NK(+) severe combined immunodeficiency disease.Curr Opin Immunol. 2000 Aug;12(4):468-73. doi: 10.1016/s0952-7915(00)00122-9. Curr Opin Immunol. 2000. PMID: 10899029 Review.
-
The molecular basis of X-linked severe combined immunodeficiency: the role of the interleukin-2 receptor gamma chain as a common gamma chain, gamma c.Immunol Rev. 1994 Apr;138:61-86. doi: 10.1111/j.1600-065x.1994.tb00847.x. Immunol Rev. 1994. PMID: 8070818 Review.
Cited by
-
A new phenylpyrazoleanilide, y-320, inhibits interleukin 17 production and ameliorates collagen-induced arthritis in mice and cynomolgus monkeys.Pharmaceuticals (Basel). 2013 Dec 23;7(1):1-17. doi: 10.3390/ph7010001. Pharmaceuticals (Basel). 2013. PMID: 24366113 Free PMC article.
-
Self-inactivating gammaretroviral vectors for gene therapy of X-linked severe combined immunodeficiency.Mol Ther. 2008 Mar;16(3):590-8. doi: 10.1038/sj.mt.6300393. Epub 2008 Jan 8. Mol Ther. 2008. PMID: 18180772 Free PMC article.
-
Inborn errors of the development of human natural killer cells.Curr Opin Allergy Clin Immunol. 2013 Dec;13(6):589-95. doi: 10.1097/ACI.0000000000000011. Curr Opin Allergy Clin Immunol. 2013. PMID: 24135998 Free PMC article. Review.
-
Preclinical Development of a Lentiviral Vector for Gene Therapy of X-Linked Severe Combined Immunodeficiency.Mol Ther Methods Clin Dev. 2018 Mar 10;9:257-269. doi: 10.1016/j.omtm.2018.03.002. eCollection 2018 Jun 15. Mol Ther Methods Clin Dev. 2018. PMID: 29707600 Free PMC article.
-
Cell type differences in activity of the Streptomyces bacteriophage phiC31 integrase.Nucleic Acids Res. 2008 Oct;36(17):5462-71. doi: 10.1093/nar/gkn532. Epub 2008 Aug 21. Nucleic Acids Res. 2008. PMID: 18718925 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical