A point mutation in a domain of gamma interferon receptor 1 provokes severe immunodeficiency - PubMed (original) (raw)
Case Reports
A point mutation in a domain of gamma interferon receptor 1 provokes severe immunodeficiency
L M Allende et al. Clin Diagn Lab Immunol. 2001 Jan.
Abstract
Gamma interferon (IFN-gamma) and the cellular responses induced by it are essential for controlling mycobacterial infections. Most patients bearing an IFN-gamma receptor ligand-binding chain (IFN-gammaR1) deficiency present gross mutations that truncate the protein and prevent its expression, giving rise to severe mycobacterial infections and, frequently, a fatal outcome. In this report a new mutation that affects the IFN-gammaR1 ligand-binding domain in a Spanish patient with mycobacterial disseminated infection and multifocal osteomyelitis is characterized. The mutation generates an amino acid change that does not abrogate protein expression on the cellular surface but that severely impairs responses after the binding of IFN-gamma (CD64 and HLA class II induction and tumor necrosis factor alpha and interleukin-12 production). A patient's younger brother, who was also probably homozygous for the mutation, died from meningitis due to Mycobacterium bovis. These findings suggest that a point mutation may be fatal when it affects functionally important domains of the receptor and that the severity is not directly related to a lack of IFN-gamma receptor expression. Future research on these nontruncating mutations will make it possible to develop new therapeutical alternatives in this group of patients.
Figures
FIG. 1
New mutation Val63Gly in the ligand-binding domain of IFN-γR1. (a) Sequence of the new mutation boundaries. Italics, amino acids implicated in the binding of IFN-γ to its receptor ; roman amino acids conserved in murine IFN-γR1 . (b) Pedigree and SSCP intrafamilial segregation of the Val63Gly mutation compared with a control.
FIG. 2
Cytofluorographic analysis of CD119 expression in the patient and family. Dotted lines, isotypic control fluorescence; solid lines, positive fluorescence. The graph shows expression in peripheral blood lymphocytes; similar results were obtained in peripheral monocytes and granulocytes (data not shown).
FIG. 3
Immune function parameters of the mutated IFN-γR1. (a) TNF-α production by monocytes stimulated with medium, LPS, and LPS plus rhIFN-γ; (b) induction of CD64 in monocytes after stimulation with IFN-γ. ▵, isotypic control fluorescence; ○, expression of CD64 after 24 h of stimulation with medium alone; □, expression of CD64 after 24 h of stimulation with 1,000 IU of rhIFN-γ/ml.
FIG. 3
Immune function parameters of the mutated IFN-γR1. (a) TNF-α production by monocytes stimulated with medium, LPS, and LPS plus rhIFN-γ; (b) induction of CD64 in monocytes after stimulation with IFN-γ. ▵, isotypic control fluorescence; ○, expression of CD64 after 24 h of stimulation with medium alone; □, expression of CD64 after 24 h of stimulation with 1,000 IU of rhIFN-γ/ml.
Similar articles
- Novel mutation in the interferon-gamma-receptor gene and susceptibility to mycobacterial infections.
Storgaard M, Varming K, Herlin T, Obel N. Storgaard M, et al. Scand J Immunol. 2006 Aug;64(2):137-9. doi: 10.1111/j.1365-3083.2006.01775.x. Scand J Immunol. 2006. PMID: 16867158 - Mutation in the signal-transducing chain of the interferon-gamma receptor and susceptibility to mycobacterial infection.
Dorman SE, Holland SM. Dorman SE, et al. J Clin Invest. 1998 Jun 1;101(11):2364-9. doi: 10.1172/JCI2901. J Clin Invest. 1998. PMID: 9616207 Free PMC article. - Disseminated Mycobacterium avium complex infection in a child with partial dominant interferon gamma receptor 1 deficiency in India.
Sharma VK, Pai G, Deswarte C, Lodha R, Singh S, Kang LW, Yin CC, Casanova JL, Bustamante J, Kabra SK. Sharma VK, et al. J Clin Immunol. 2015 Jul;35(5):459-62. doi: 10.1007/s10875-015-0173-1. Epub 2015 Jun 9. J Clin Immunol. 2015. PMID: 26054576 - Granulomatous skin lesions, severe scrotal and lower limb edema due to mycobacterial infections in a child with complete IFN-γ receptor-1 deficiency.
Edeer Karaca N, Boisson-Dupuis S, Aksu G, Bustamante J, Kandiloglu G, Ozsan N, Hekimgil M, Casanova JL, Kutukculer N. Edeer Karaca N, et al. Immunotherapy. 2012 Nov;4(11):1121-7. doi: 10.2217/imt.12.111. Immunotherapy. 2012. PMID: 23194362 Free PMC article. Review. - Genetically determined susceptibility to mycobacterial infection.
Patel SY, Doffinger R, Barcenas-Morales G, Kumararatne DS. Patel SY, et al. J Clin Pathol. 2008 Sep;61(9):1006-12. doi: 10.1136/jcp.2007.051201. Epub 2008 Mar 6. J Clin Pathol. 2008. PMID: 18326015 Review.
Cited by
- Transcriptome and ultrastructural changes in dystrophic Epidermolysis bullosa resemble skin aging.
Breitenbach JS, Rinnerthaler M, Trost A, Weber M, Klausegger A, Gruber C, Bruckner D, Reitsamer HA, Bauer JW, Breitenbach M. Breitenbach JS, et al. Aging (Albany NY). 2015 Jun;7(6):389-411. doi: 10.18632/aging.100755. Aging (Albany NY). 2015. PMID: 26143532 Free PMC article. - Inherited interleukin-12 deficiency: IL12B genotype and clinical phenotype of 13 patients from six kindreds.
Picard C, Fieschi C, Altare F, Al-Jumaah S, Al-Hajjar S, Feinberg J, Dupuis S, Soudais C, Al-Mohsen IZ, Génin E, Lammas D, Kumararatne DS, Leclerc T, Rafii A, Frayha H, Murugasu B, Wah LB, Sinniah R, Loubser M, Okamoto E, Al-Ghonaium A, Tufenkeji H, Abel L, Casanova JL. Picard C, et al. Am J Hum Genet. 2002 Feb;70(2):336-48. doi: 10.1086/338625. Epub 2001 Dec 17. Am J Hum Genet. 2002. PMID: 11753820 Free PMC article. - The monogenic basis of human tuberculosis.
Boisson-Dupuis S. Boisson-Dupuis S. Hum Genet. 2020 Jun;139(6-7):1001-1009. doi: 10.1007/s00439-020-02126-6. Epub 2020 Feb 13. Hum Genet. 2020. PMID: 32055999 Free PMC article. Review. - A novel form of cell type-specific partial IFN-gammaR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon.
Kong XF, Vogt G, Chapgier A, Lamaze C, Bustamante J, Prando C, Fortin A, Puel A, Feinberg J, Zhang XX, Gonnord P, Pihkala-Saarinen UM, Arola M, Moilanen P, Abel L, Korppi M, Boisson-Dupuis S, Casanova JL. Kong XF, et al. Hum Mol Genet. 2010 Feb 1;19(3):434-44. doi: 10.1093/hmg/ddp507. Epub 2009 Oct 31. Hum Mol Genet. 2010. PMID: 19880857 Free PMC article. - Partial recessive IFN-γR1 deficiency: genetic, immunological and clinical features of 14 patients from 11 kindreds.
Sologuren I, Boisson-Dupuis S, Pestano J, Vincent QB, Fernández-Pérez L, Chapgier A, Cárdenes M, Feinberg J, García-Laorden MI, Picard C, Santiago E, Kong X, Jannière L, Colino E, Herrera-Ramos E, Francés A, Navarrete C, Blanche S, Faria E, Remiszewski P, Cordeiro A, Freeman A, Holland S, Abarca K, Valerón-Lemaur M, Gonçalo-Marques J, Silveira L, García-Castellano JM, Caminero J, Pérez-Arellano JL, Bustamante J, Abel L, Casanova JL, Rodríguez-Gallego C. Sologuren I, et al. Hum Mol Genet. 2011 Apr 15;20(8):1509-23. doi: 10.1093/hmg/ddr029. Epub 2011 Jan 25. Hum Mol Genet. 2011. PMID: 21266457 Free PMC article.
References
- Aguet M, Dembic Z, Merlin G. Molecular cloning and expression of the human interferon-γ receptor. Cell. 1988;55:273–280. - PubMed
- Altare F, Durandy A, Lammas D, Emile J F, Lamhamedi S, Le Deist F, Drysdale P, Jouanguy E, Döffinger R, Bernaudin F, Jeppsson O, Gollob J A, Meinl E, Segal A W, Fischer A, Kumararatne D, Casanova J L. Impairment of mycobacterial immunity in human interleukin 12 receptor deficiency. Science. 1998;280:1432–1435. - PubMed
- Altare F, Jouanguy E, Lamhamedi S, Döffinger R, Fischer A, Casanova J L. Mendelian susceptibility to mycobacterial infection in man. Curr Opin Immunol. 1998;10:413–417. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials