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Volumn 68, Issue 5, 2006, Pages 432-438

Multiplex family-based study in systemic lupus erythematosus: Association between the R620W polymorphism of PTPN22 and the FcγRIIa (CD32A) R131 allele

Author keywords

Autoimmunity; Families; Fc RIIa (CD32A); PTPN22; Systemic lupus erythematosus

Indexed keywords

CD32 ANTIGEN; DNA; IMMUNOGLOBULIN FC FRAGMENT; MANNOSE BINDING LECTIN;

EID: 33750695297     PISSN: 00012815     EISSN: 13990039     Source Type: Journal    
DOI: 10.1111/j.1399-0039.2006.00695.x     Document Type: Article
Times cited : (16)

References (30)
  • 1
    • 1642512496 scopus 로고    scopus 로고
    • Antihistone and anti-double-stranded deoxyribonucleic acid antibodies are associated with renal disease in systemic lupus erythematosus
    • Cortes-Hernandez J, Ordi-Ros J, Labrador M et al. Antihistone and anti-double-stranded deoxyribonucleic acid antibodies are associated with renal disease in systemic lupus erythematosus. Am J Med 2004: 116: 165-73.
    • (2004) Am J Med , vol.116 , pp. 165-173
    • Cortes-Hernandez, J.1    Ordi-Ros, J.2    Labrador, M.3
  • 2
    • 4143105691 scopus 로고    scopus 로고
    • Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE
    • Kyogoku C, Langefeld CD, Ortmann WA et al. Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE. Am J Hum Genet 2004: 75: 504-7.
    • (2004) Am J Hum Genet , vol.75 , pp. 504-507
    • Kyogoku, C.1    Langefeld, C.D.2    Ortmann, W.A.3
  • 3
    • 3242713277 scopus 로고    scopus 로고
    • A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis
    • Begovich AB, Carlton VE, Honigberg LA et al. A missense single-nucleotide polymorphism in a gene encoding a protein tyrosine phosphatase (PTPN22) is associated with rheumatoid arthritis. Am J Hum Genet 2004: 75: 330-7.
    • (2004) Am J Hum Genet , vol.75 , pp. 330-337
    • Begovich, A.B.1    Carlton, V.E.2    Honigberg, L.A.3
  • 4
    • 0942279640 scopus 로고    scopus 로고
    • PEST domain-enriched tyrosine phosphatase (PEP) regulation of effector/memory T cells
    • Hasegawa K, Martin F, Huang G, Tumas D, Diehl L, Chan AC. PEST domain-enriched tyrosine phosphatase (PEP) regulation of effector/memory T cells. Science 2004: 303: 685-9.
    • (2004) Science , vol.303 , pp. 685-689
    • Hasegawa, K.1    Martin, F.2    Huang, G.3    Tumas, D.4    Diehl, L.5    Chan, A.C.6
  • 5
    • 12144291502 scopus 로고    scopus 로고
    • A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes
    • Bottini N, Musumeci L, Alonso A et al. A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes. Nat Genet 2004: 36: 337-8.
    • (2004) Nat Genet , vol.36 , pp. 337-338
    • Bottini, N.1    Musumeci, L.2    Alonso, A.3
  • 6
    • 28444469783 scopus 로고    scopus 로고
    • Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant
    • Vang T, Congia M, Macis MD et al. Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant. Nat Genet 2005: 37: 1317-9.
    • (2005) Nat Genet , vol.37 , pp. 1317-1319
    • Vang, T.1    Congia, M.2    Macis, M.D.3
  • 7
    • 8744266374 scopus 로고    scopus 로고
    • The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease
    • Velaga MR, Wilson V, Jennings CE et al. The codon 620 tryptophan allele of the lymphoid tyrosine phosphatase (LYP) gene is a major determinant of Graves' disease. J Clin Endocrinol Metab 2004: 89: 5862-5.
    • (2004) J Clin Endocrinol Metab , vol.89 , pp. 5862-5865
    • Velaga, M.R.1    Wilson, V.2    Jennings, C.E.3
  • 8
    • 20144387851 scopus 로고    scopus 로고
    • Analysis of families in the Multiple Autoimmune Disease Genetics Consortium (MADGC) Collection: The PTPN22 620W allele associates with multiple autoimmune phenotypes
    • Criswell LA, Pfeiffer KA, Lum RF et al. Analysis of families in the Multiple Autoimmune Disease Genetics Consortium (MADGC) Collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes. Am J Hum Genet 2005: 76: 561-71.
    • (2005) Am J Hum Genet , vol.76 , pp. 561-571
    • Criswell, L.A.1    Pfeiffer, K.A.2    Lum, R.F.3
  • 9
    • 27844531635 scopus 로고    scopus 로고
    • A single-nucleotide polymorphism in the gene encoding lymphoid protein tyrosine phosphatase (PTPN22) confers susceptibility to generalised vitiligo
    • Canton I, Akhtar S, Gavalas NG et al. A single-nucleotide polymorphism in the gene encoding lymphoid protein tyrosine phosphatase (PTPN22) confers susceptibility to generalised vitiligo. Genes Immun 2005: 6: 584-7.
    • (2005) Genes Immun , vol.6 , pp. 584-587
    • Canton, I.1    Akhtar, S.2    Gavalas, N.G.3
  • 10
    • 0029855639 scopus 로고    scopus 로고
    • Informed consent in human experimentation before the Nuremberg code
    • Vollmann J, Winau R. Informed consent in human experimentation before the Nuremberg code. BMJ 1996: 313: 1445-9.
    • (1996) BMJ , vol.313 , pp. 1445-1449
    • Vollmann, J.1    Winau, R.2
  • 11
    • 0031229830 scopus 로고    scopus 로고
    • Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus
    • Hochberg MC. Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum 1997: 40: 1725.
    • (1997) Arthritis Rheum , vol.40 , pp. 1725
    • Hochberg, M.C.1
  • 13
    • 0033924133 scopus 로고    scopus 로고
    • Mannose binding lectin (MBL) genotype distributions with relation to serum levels in UK Caucasoids
    • Crosdale DJ, Ollier WE, Thomson W et al. Mannose binding lectin (MBL) genotype distributions with relation to serum levels in UK Caucasoids. Eur J Immunogenet 2000: 27: 111-7.
    • (2000) Eur J Immunogenet , vol.27 , pp. 111-117
    • Crosdale, D.J.1    Ollier, W.E.2    Thomson, W.3
  • 14
    • 0029045792 scopus 로고
    • Interplay between promoter and structural gene variants control basal serum level of mannan-binding protein
    • Madsen HO, Garred P, Thiel S et al. Interplay between promoter and structural gene variants control basal serum level of mannan-binding protein. J Immunol 1995: 155: 3013-20.
    • (1995) J Immunol , vol.155 , pp. 3013-3020
    • Madsen, H.O.1    Garred, P.2    Thiel, S.3
  • 15
    • 0023780367 scopus 로고
    • The first international standard for antibodies to double stranded DNA
    • Feltkamp TE, Kirkwood TB, Maini RN, Aarden LA. The first international standard for antibodies to double stranded DNA. Ann Rheum Dis 1988: 47: 740-6.
    • (1988) Ann Rheum Dis , vol.47 , pp. 740-746
    • Feltkamp, T.E.1    Kirkwood, T.B.2    Maini, R.N.3    Aarden, L.A.4
  • 16
    • 0029858544 scopus 로고    scopus 로고
    • The TDT and other family-based tests for linkage disequilibrium and association
    • Spielman RS, Ewens WJ. The TDT and other family-based tests for linkage disequilibrium and association. Am J Hum Genet 1996: 59: 983-9.
    • (1996) Am J Hum Genet , vol.59 , pp. 983-989
    • Spielman, R.S.1    Ewens, W.J.2
  • 17
    • 19944433325 scopus 로고    scopus 로고
    • Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus
    • Orozco G, Sanchez E, Gonzalez-Gay MA et al. Association of a functional single-nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with rheumatoid arthritis and systemic lupus erythematosus. Arthritis Rheum 2005: 52: 219-24.
    • (2005) Arthritis Rheum , vol.52 , pp. 219-224
    • Orozco, G.1    Sanchez, E.2    Gonzalez-Gay, M.A.3
  • 18
    • 11144292728 scopus 로고    scopus 로고
    • The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis
    • Begovich AB, Caillier SJ, Alexander HC et al. The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis. Am J Hum Genet 2005: 76: 184-7.
    • (2005) Am J Hum Genet , vol.76 , pp. 184-187
    • Begovich, A.B.1    Caillier, S.J.2    Alexander, H.C.3
  • 19
    • 20844452226 scopus 로고    scopus 로고
    • Association analysis of the 1858C>T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases
    • Viken MK, Amundsen SS, Kvien TK et al. Association analysis of the 1858C>T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases. Genes Immun 2005: 6: 271-3.
    • (2005) Genes Immun , vol.6 , pp. 271-273
    • Viken, M.K.1    Amundsen, S.S.2    Kvien, T.K.3
  • 20
    • 27844441996 scopus 로고    scopus 로고
    • No evidence for association between 1858 C/T single-nucleotide polymorphism of PTPN22 gene and primary Sjogren's syndrome
    • Ittah M, Gottenberg JE, Proust A et al. No evidence for association between 1858 C/T single-nucleotide polymorphism of PTPN22 gene and primary Sjogren's syndrome. Genes Immun 2005: 6: 457-8.
    • (2005) Genes Immun , vol.6 , pp. 457-458
    • Ittah, M.1    Gottenberg, J.E.2    Proust, A.3
  • 21
    • 22244442459 scopus 로고    scopus 로고
    • Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations
    • van Oene M, Wintle RF, Liu X et al. Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations. Arthritis Rheum 2005: 52: 1993-8.
    • (2005) Arthritis Rheum , vol.52 , pp. 1993-1998
    • Van Oene, M.1    Wintle, R.F.2    Liu, X.3
  • 22
    • 23444454030 scopus 로고    scopus 로고
    • Lack of association of a functional single nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with susceptibility to biopsy-proven giant cell arteritis
    • Gonzalez-Gay MA, Oliver J, Orozco G, Garcia-Porrua C, Lopez-Nevot MA, Martin J. Lack of association of a functional single nucleotide polymorphism of PTPN22, encoding lymphoid protein phosphatase, with susceptibility to biopsy-proven giant cell arteritis. J Rheumatol 2005: 32: 1510-2.
    • (2005) J Rheumatol , vol.32 , pp. 1510-1512
    • Gonzalez-Gay, M.A.1    Oliver, J.2    Orozco, G.3    Garcia-Porrua, C.4    Lopez-Nevot, M.A.5    Martin, J.6
  • 23
    • 23644432242 scopus 로고    scopus 로고
    • Association analysis of the R620W polymorphism of protein tyrosine phosphatase PTPN22 in systemic lupus erythematosus families: Increased T allele frequency in systemic lupus erythematosus patients with autoimmune thyroid disease
    • Wu H, Cantor RM, Graham DS et al. Association analysis of the R620W polymorphism of protein tyrosine phosphatase PTPN22 in systemic lupus erythematosus families: increased T allele frequency in systemic lupus erythematosus patients with autoimmune thyroid disease. Arthritis Rheum 2005: 52: 2396-402.
    • (2005) Arthritis Rheum , vol.52 , pp. 2396-2402
    • Wu, H.1    Cantor, R.M.2    Graham, D.S.3
  • 24
    • 0035748530 scopus 로고    scopus 로고
    • Association of mannose-binding lectin gene variation with disease severity and infections in a population-based cohort of systemic lupus erythematosus patients
    • Garred P, Voss A, Madsen HO, Junker P. Association of mannose-binding lectin gene variation with disease severity and infections in a population-based cohort of systemic lupus erythematosus patients. Genes Immun 2001: 2: 442-50.
    • (2001) Genes Immun , vol.2 , pp. 442-450
    • Garred, P.1    Voss, A.2    Madsen, H.O.3    Junker, P.4
  • 25
    • 0034803432 scopus 로고    scopus 로고
    • Mannose binding lectin and FcgammaRIIa (CD32) polymorphism in Spanish systemic lupus erythematosus patients
    • Villarreal J, Crosdale D, Ollier W et al. Mannose binding lectin and FcgammaRIIa (CD32) polymorphism in Spanish systemic lupus erythematosus patients. Rheumatology (Oxford) 2001: 40: 1009-12.
    • (2001) Rheumatology (Oxford) , vol.40 , pp. 1009-1012
    • Villarreal, J.1    Crosdale, D.2    Ollier, W.3
  • 26
    • 13344279426 scopus 로고
    • Skewed distribution of IgG Fc receptor IIa (CD32) polymorphism is associated with renal disease in systemic lupus erythematosus patients
    • Duits AJ, Bootsma H, Derksen RH et al. Skewed distribution of IgG Fc receptor IIa (CD32) polymorphism is associated with renal disease in systemic lupus erythematosus patients. Arthritis Rheum 1995: 38: 1832-6.
    • (1995) Arthritis Rheum , vol.38 , pp. 1832-1836
    • Duits, A.J.1    Bootsma, H.2    Derksen, R.H.3
  • 27
    • 0035555022 scopus 로고    scopus 로고
    • The genetics of complex autoimmune diseases: Non-MHC susceptibility genes
    • Wandstrat A, Wakeland E. The genetics of complex autoimmune diseases: non-MHC susceptibility genes. Nat Immunol 2001: 2: 802-9.
    • (2001) Nat Immunol , vol.2 , pp. 802-809
    • Wandstrat, A.1    Wakeland, E.2
  • 28
    • 11144266638 scopus 로고    scopus 로고
    • Association of the single nucleotide polymorphism C1858T of the PTPN22 gene with type 1 diabetes
    • Ladner MB, Bottini N, Valdes AM, Noble JA. Association of the single nucleotide polymorphism C1858T of the PTPN22 gene with type 1 diabetes. Hum Immunol 2005: 66: 60-4.
    • (2005) Hum Immunol , vol.66 , pp. 60-64
    • Ladner, M.B.1    Bottini, N.2    Valdes, A.M.3    Noble, J.A.4
  • 29
    • 0035988858 scopus 로고    scopus 로고
    • FcgammaRIIA, FcgammaRIIIA and FcgammaRIIIB polymorphisms in Spanish patients with systemic lupus erythematosus
    • Gonzalez-Escribano MF, Aguilar F, Sanchez-Roman J, Nunez-Roldan A. FcgammaRIIA, FcgammaRIIIA and FcgammaRIIIB polymorphisms in Spanish patients with systemic lupus erythematosus. Eur J Immunogenet 2002: 29: 301-6.
    • (2002) Eur J Immunogenet , vol.29 , pp. 301-306
    • Gonzalez-Escribano, M.F.1    Aguilar, F.2    Sanchez-Roman, J.3    Nunez-Roldan, A.4
  • 30
    • 1842835171 scopus 로고    scopus 로고
    • FC gamma RIIa polymorphism in patients with rheumatoid arthritis
    • Pawlik A, Ostanek L, Brzosko I et al. FC gamma RIIa polymorphism in patients with rheumatoid arthritis. Clin Exp Rheumatol 2002: 20: 841-4.
    • (2002) Clin Exp Rheumatol , vol.20 , pp. 841-844
    • Pawlik, A.1    Ostanek, L.2    Brzosko, I.3


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