Skip to main content
Top
Published in: BMC Medical Genetics 1/2009

Open Access 01-12-2009 | Research article

Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitis

Authors: Edward J Carr, Heather A Niederer, Julie Williams, Lorraine Harper, Richard A Watts, Paul A Lyons, Kenneth GC Smith

Published in: BMC Medical Genetics | Issue 1/2009

Login to get access

Abstract

Background

The genetic contribution to the aetiology of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is not well defined. Across different autoimmune diseases some genes with immunomodulatory roles, such as PTPN22, are frequently associated with multiple diseases, whereas specific HLA associations, such as HLA-B27, tend to be disease restricted. We studied ten candidate loci on the basis of their immunoregulatory role and prior associations with type 1 diabetes (T1D). These included PTPN22, CTLA4 and CD226, which have previously been associated with AAV.

Methods

We genotyped the following 11 SNPs, from 10 loci, in 641 AAV patients using TaqMan genotyping: rs2476601 in PTPN22, rs1990760 in IFIH1, rs3087243 in CTLA4, rs2069763 in IL2, rs10877012 in CYP27B1, rs2292239 in ERBB3, rs3184504 in SH2B3, rs12708716 in CLEC16A, rs1893217 and rs478582 in PTPN2 and rs763361 in CD226. Where possible, we performed a meta-analysis with previous analyses.

Results

Both CTLA4 rs3087243 and PTPN22 rs2476601 showed association with AAV, P = 6.4 × 10-3 and P = 1.4 × 10-4 respectively. The minor allele (A) of CTLA4 rs3087243 is protective (odds ratio = 0.84), whereas the minor allele (A) of PTPN22 rs2476601 confers susceptibility (odds ratio = 1.40). These results confirmed previously described associations with AAV. After meta-analysis, the PTPN22 rs2476601 association was further strengthened (combined P = 4.2 × 10-7, odds ratio of 1.48 for the A allele). The other 9 SNPs, including rs763361 in CD226, showed no association with AAV.

Conclusion

Our study of T1D associated SNPs in AAV has confirmed CTLA4 and PTPN22 as susceptibility loci in AAV. These genes encode two key regulators of the immune response and are associated with many autoimmune diseases, including T1D, autoimmune thyroid disease, celiac disease, rheumatoid arthritis, and now AAV.
Literature
1.
go back to reference Willcocks LC, Lyons PA, Rees AJ, Smith KGC: Pathogenesis of ANCA-associated systemic vasculitis: genetic variation and infections. Arthritis Research & Therapy. 2009, Willcocks LC, Lyons PA, Rees AJ, Smith KGC: Pathogenesis of ANCA-associated systemic vasculitis: genetic variation and infections. Arthritis Research & Therapy. 2009,
2.
go back to reference Knight A, Sandin S, Askling J: Risks and relative risks of Wegener's granulomatosis among close relatives of patients with the disease. Arthritis and Rheumatism. 2008, 58 (1): 302-307. 10.1002/art.23157.CrossRefPubMed Knight A, Sandin S, Askling J: Risks and relative risks of Wegener's granulomatosis among close relatives of patients with the disease. Arthritis and Rheumatism. 2008, 58 (1): 302-307. 10.1002/art.23157.CrossRefPubMed
3.
go back to reference Jagiello P, Gross WL, Epplen JT: Complex genetics of Wegener granulomatosis. Autoimmunity Reviews. 2005, 4 (1): 42-47. 10.1016/j.autrev.2004.06.003.CrossRefPubMed Jagiello P, Gross WL, Epplen JT: Complex genetics of Wegener granulomatosis. Autoimmunity Reviews. 2005, 4 (1): 42-47. 10.1016/j.autrev.2004.06.003.CrossRefPubMed
4.
go back to reference Heckmann M, Holle JU, Arning L, Knaup S, Hellmich B, Nothnagel M, Jagiello P, Gross WL, Epplen JT, Wieczorek S: The Wegener's granulomatosis quantitative trait locus on chromosome 6p21.3 as characterised by tagSNP genotyping. Annals of the Rheumatic Diseases. 2008, 67 (7): 972-979. 10.1136/ard.2007.077693.CrossRefPubMed Heckmann M, Holle JU, Arning L, Knaup S, Hellmich B, Nothnagel M, Jagiello P, Gross WL, Epplen JT, Wieczorek S: The Wegener's granulomatosis quantitative trait locus on chromosome 6p21.3 as characterised by tagSNP genotyping. Annals of the Rheumatic Diseases. 2008, 67 (7): 972-979. 10.1136/ard.2007.077693.CrossRefPubMed
5.
go back to reference Brand O, Gough S, Heward J: HLA, CTLA-4 and PTPN22: the shared genetic master-key to autoimmunity?. Expert Reviews in Molecular Medicine. 2005, 7 (23): 1-15. 10.1017/S1462399405009981.CrossRefPubMed Brand O, Gough S, Heward J: HLA, CTLA-4 and PTPN22: the shared genetic master-key to autoimmunity?. Expert Reviews in Molecular Medicine. 2005, 7 (23): 1-15. 10.1017/S1462399405009981.CrossRefPubMed
6.
go back to reference Todd JA, Walker NM, Cooper JD, Smyth DJ, Downes K, Plagnol V, Bailey R, Nejentsev S, Field SF, Payne F, et al: Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. Nature Genetics. 2007, 39 (7): 857-864. 10.1038/ng2068.CrossRefPubMedPubMedCentral Todd JA, Walker NM, Cooper JD, Smyth DJ, Downes K, Plagnol V, Bailey R, Nejentsev S, Field SF, Payne F, et al: Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. Nature Genetics. 2007, 39 (7): 857-864. 10.1038/ng2068.CrossRefPubMedPubMedCentral
7.
go back to reference Hafler JP, Maier LM, Cooper JD, Plagnol V, Hinks A, Simmonds MJ, Stevens HE, Walker NM, Healy B, Howson JM, et al: CD226 Gly307Ser association with multiple autoimmune diseases. Genes and Immunity. 2009, 10 (1): 5-10. 10.1038/gene.2008.82.CrossRefPubMed Hafler JP, Maier LM, Cooper JD, Plagnol V, Hinks A, Simmonds MJ, Stevens HE, Walker NM, Healy B, Howson JM, et al: CD226 Gly307Ser association with multiple autoimmune diseases. Genes and Immunity. 2009, 10 (1): 5-10. 10.1038/gene.2008.82.CrossRefPubMed
8.
go back to reference Carr EJ, Clatworthy MR, Lowe CE, Todd JA, Wong A, Vyse TJ, Kamesh L, Watts RA, Lyons PA, Smith KGC: Contrasting genetic association of IL2RA with SLE and ANCA-associated vasculitis. BMC Medical Genetics. 2009, 10: 22-10.1186/1471-2350-10-22.CrossRefPubMedPubMedCentral Carr EJ, Clatworthy MR, Lowe CE, Todd JA, Wong A, Vyse TJ, Kamesh L, Watts RA, Lyons PA, Smith KGC: Contrasting genetic association of IL2RA with SLE and ANCA-associated vasculitis. BMC Medical Genetics. 2009, 10: 22-10.1186/1471-2350-10-22.CrossRefPubMedPubMedCentral
9.
go back to reference Giscombe R, Wang X, Huang D, Lefvert AK: Coding sequence 1 and promoter single nucleotide polymorphisms in the CTLA-4 gene in Wegener's granulomatosis. The Journal of Rheumatology. 2002, 29 (5): 950-953.PubMed Giscombe R, Wang X, Huang D, Lefvert AK: Coding sequence 1 and promoter single nucleotide polymorphisms in the CTLA-4 gene in Wegener's granulomatosis. The Journal of Rheumatology. 2002, 29 (5): 950-953.PubMed
10.
go back to reference Slot MC, Sokolowska MG, Savelkouls KG, Janssen RG, Damoiseaux JG, Cohen Tervaert JW: Immunoregulatory gene polymorphisms are associated with ANCA-related vasculitis. Clinical Immunology (Orlando, Fla). 2008, 128 (1): 39-45. 10.1016/j.clim.2008.03.506.CrossRef Slot MC, Sokolowska MG, Savelkouls KG, Janssen RG, Damoiseaux JG, Cohen Tervaert JW: Immunoregulatory gene polymorphisms are associated with ANCA-related vasculitis. Clinical Immunology (Orlando, Fla). 2008, 128 (1): 39-45. 10.1016/j.clim.2008.03.506.CrossRef
11.
go back to reference Jagiello P, Aries P, Arning L, Wagenleiter SE, Csernok E, Hellmich B, Gross WL, Epplen JT: The PTPN22 620W allele is a risk factor for Wegener's granulomatosis. Arthritis and Rheumatism. 2005, 52 (12): 4039-4043. 10.1002/art.21487.CrossRefPubMed Jagiello P, Aries P, Arning L, Wagenleiter SE, Csernok E, Hellmich B, Gross WL, Epplen JT: The PTPN22 620W allele is a risk factor for Wegener's granulomatosis. Arthritis and Rheumatism. 2005, 52 (12): 4039-4043. 10.1002/art.21487.CrossRefPubMed
12.
go back to reference Wieczorek S, Hoffjan S, Chan A, Rey L, Harper L, Fricke H, Holle JU, Gross WL, Epplen JT, Lamprecht P: Novel association of the CD226 (DNAM-1) Gly307Ser polymorphism in Wegener's granulomatosis and confirmation for multiple sclerosis in German patients. Genes and Immunity. 2009, 10 (6): 591-5. 10.1038/gene.2009.44.CrossRefPubMed Wieczorek S, Hoffjan S, Chan A, Rey L, Harper L, Fricke H, Holle JU, Gross WL, Epplen JT, Lamprecht P: Novel association of the CD226 (DNAM-1) Gly307Ser polymorphism in Wegener's granulomatosis and confirmation for multiple sclerosis in German patients. Genes and Immunity. 2009, 10 (6): 591-5. 10.1038/gene.2009.44.CrossRefPubMed
13.
go back to reference Steiner K, Moosig F, Csernok E, Selleng K, Gross WL, Fleischer B, Bröker BM: Increased expression of CTLA-4 (CD152) by T and B lymphocytes in Wegener's granulomatosis. Clinical and Experimental Immunology. 2001, 126 (1): 143-150. 10.1046/j.1365-2249.2001.01575.x.CrossRefPubMedPubMedCentral Steiner K, Moosig F, Csernok E, Selleng K, Gross WL, Fleischer B, Bröker BM: Increased expression of CTLA-4 (CD152) by T and B lymphocytes in Wegener's granulomatosis. Clinical and Experimental Immunology. 2001, 126 (1): 143-150. 10.1046/j.1365-2249.2001.01575.x.CrossRefPubMedPubMedCentral
14.
go back to reference Zhou Y, Huang D, Paris PL, Sauter CS, Prock KA, Hoffman GS: An analysis of CTLA-4 and proinflammatory cytokine genes in Wegener's granulomatosis. Arthritis and Rheumatism. 2004, 50 (8): 2645-2650. 10.1002/art.20385.CrossRefPubMed Zhou Y, Huang D, Paris PL, Sauter CS, Prock KA, Hoffman GS: An analysis of CTLA-4 and proinflammatory cytokine genes in Wegener's granulomatosis. Arthritis and Rheumatism. 2004, 50 (8): 2645-2650. 10.1002/art.20385.CrossRefPubMed
15.
go back to reference Spriewald BM, Witzke O, Wassmuth R, Wenzel RR, Arnold ML, Philipp T, Kalden JR: Distinct tumour necrosis factor alpha, interferon gamma, interleukin 10, and cytotoxic T cell antigen 4 gene polymorphisms in disease occurrence and end stage renal disease in Wegener's granulomatosis. Annals of the Rheumatic Diseases. 2005, 64 (3): 457-461. 10.1136/ard.2004.025809.CrossRefPubMedPubMedCentral Spriewald BM, Witzke O, Wassmuth R, Wenzel RR, Arnold ML, Philipp T, Kalden JR: Distinct tumour necrosis factor alpha, interferon gamma, interleukin 10, and cytotoxic T cell antigen 4 gene polymorphisms in disease occurrence and end stage renal disease in Wegener's granulomatosis. Annals of the Rheumatic Diseases. 2005, 64 (3): 457-461. 10.1136/ard.2004.025809.CrossRefPubMedPubMedCentral
16.
go back to reference Jennette JC, Falk RJ, Andrassy K, Bacon PA, Churg J, Gross WL, Hagen EC, Hoffman GS, Hunder GG, Kallenberg CG: Nomenclature of systemic vasculitides. Proposal of an international consensus conference. Arthritis and Rheumatism. 1994, 37 (2): 187-192. 10.1002/art.1780370206.CrossRefPubMed Jennette JC, Falk RJ, Andrassy K, Bacon PA, Churg J, Gross WL, Hagen EC, Hoffman GS, Hunder GG, Kallenberg CG: Nomenclature of systemic vasculitides. Proposal of an international consensus conference. Arthritis and Rheumatism. 1994, 37 (2): 187-192. 10.1002/art.1780370206.CrossRefPubMed
17.
go back to reference Wellcome Trust Case Control Consortium: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature. 2007, 447 (7145): 661-678. 10.1038/nature05911.CrossRef Wellcome Trust Case Control Consortium: Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature. 2007, 447 (7145): 661-678. 10.1038/nature05911.CrossRef
18.
go back to reference Gonzalez JR, Armengol L, Sole X, Guino E, Mercader JM, Estivill X, Moreno V: SNPassoc: an R package to perform whole genome association studies. Bioinformatics. 2007, 23 (5): 644-645. 10.1093/bioinformatics/btm025.CrossRefPubMed Gonzalez JR, Armengol L, Sole X, Guino E, Mercader JM, Estivill X, Moreno V: SNPassoc: an R package to perform whole genome association studies. Bioinformatics. 2007, 23 (5): 644-645. 10.1093/bioinformatics/btm025.CrossRefPubMed
19.
go back to reference Waterhouse P, Penninger JM, Timms E, Wakeham A, Shahinian A, Lee KP, Thompson CB, Griesser H, Mak TW: Lymphoproliferative disorders with early lethality in mice deficient in Ctla-4. Science (New York, NY). 1995, 270 (5238): 985-988.CrossRef Waterhouse P, Penninger JM, Timms E, Wakeham A, Shahinian A, Lee KP, Thompson CB, Griesser H, Mak TW: Lymphoproliferative disorders with early lethality in mice deficient in Ctla-4. Science (New York, NY). 1995, 270 (5238): 985-988.CrossRef
20.
go back to reference Tivol EA, Borriello F, Schweitzer AN, Lynch WP, Bluestone JA, Sharpe AH: Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4. Immunity. 1995, 3 (5): 541-547. 10.1016/1074-7613(95)90125-6.CrossRefPubMed Tivol EA, Borriello F, Schweitzer AN, Lynch WP, Bluestone JA, Sharpe AH: Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4. Immunity. 1995, 3 (5): 541-547. 10.1016/1074-7613(95)90125-6.CrossRefPubMed
21.
go back to reference Stamper CC, Zhang Y, Tobin JF, Erbe DV, Ikemizu S, Davis SJ, Stahl ML, Seehra J, Somers WS, Mosyak L: Crystal structure of the B7-1/CTLA-4 complex that inhibits human immune responses. Nature. 2001, 410 (6828): 608-611. 10.1038/35069118.CrossRefPubMed Stamper CC, Zhang Y, Tobin JF, Erbe DV, Ikemizu S, Davis SJ, Stahl ML, Seehra J, Somers WS, Mosyak L: Crystal structure of the B7-1/CTLA-4 complex that inhibits human immune responses. Nature. 2001, 410 (6828): 608-611. 10.1038/35069118.CrossRefPubMed
22.
go back to reference Zhang X, Schwartz JC, Almo SC, Nathenson SG: Crystal structure of the receptor-binding domain of human B7-2: insights into organization and signaling. Proceedings of the National Academy of Sciences of the United States of America. 2003, 100 (5): 2586-2591. 10.1073/pnas.252771499.CrossRefPubMedPubMedCentral Zhang X, Schwartz JC, Almo SC, Nathenson SG: Crystal structure of the receptor-binding domain of human B7-2: insights into organization and signaling. Proceedings of the National Academy of Sciences of the United States of America. 2003, 100 (5): 2586-2591. 10.1073/pnas.252771499.CrossRefPubMedPubMedCentral
23.
go back to reference Oaks MK, Hallett KM, Penwell RT, Stauber EC, Warren SJ, Tector AJ: A native soluble form of CTLA-4. Cellular Immunology. 2000, 201 (2): 144-153. 10.1006/cimm.2000.1649.CrossRefPubMed Oaks MK, Hallett KM, Penwell RT, Stauber EC, Warren SJ, Tector AJ: A native soluble form of CTLA-4. Cellular Immunology. 2000, 201 (2): 144-153. 10.1006/cimm.2000.1649.CrossRefPubMed
24.
go back to reference Wing K, Onishi Y, Prieto-Martin P, Yamaguchi T, Miyara M, Fehervari Z, Nomura T, Sakaguchi S: CTLA-4 control over Foxp3+ regulatory T cell function. Science. 2008, 322 (5899): 271-275. 10.1126/science.1160062.CrossRefPubMed Wing K, Onishi Y, Prieto-Martin P, Yamaguchi T, Miyara M, Fehervari Z, Nomura T, Sakaguchi S: CTLA-4 control over Foxp3+ regulatory T cell function. Science. 2008, 322 (5899): 271-275. 10.1126/science.1160062.CrossRefPubMed
25.
go back to reference Rudd CE: The reverse stop-signal model for CTLA4 function. Nature Reviews Immunology. 2008, 8 (2): 153-160. 10.1038/nri2253.CrossRefPubMed Rudd CE: The reverse stop-signal model for CTLA4 function. Nature Reviews Immunology. 2008, 8 (2): 153-160. 10.1038/nri2253.CrossRefPubMed
26.
go back to reference Ueda H, Howson JM, Esposito L, Heward J, Snook H, Chamberlain G, Rainbow DB, Hunter KM, Smith AN, Di Genova G, et al: Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease. Nature. 2003, 423 (6939): 506-511. 10.1038/nature01621.CrossRefPubMed Ueda H, Howson JM, Esposito L, Heward J, Snook H, Chamberlain G, Rainbow DB, Hunter KM, Smith AN, Di Genova G, et al: Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease. Nature. 2003, 423 (6939): 506-511. 10.1038/nature01621.CrossRefPubMed
27.
go back to reference Kavvoura FK, Akamizu T, Awata T, Ban Y, Chistiakov DA, Frydecka I, Ghaderi A, Gough SC, Hiromatsu Y, Ploski R, et al: Cytotoxic T-lymphocyte associated antigen 4 gene polymorphisms and autoimmune thyroid disease: a meta-analysis. The Journal of Clinical Endocrinology and Metabolism. 2007, 92 (8): 3162-3170. 10.1210/jc.2007-0147.CrossRefPubMed Kavvoura FK, Akamizu T, Awata T, Ban Y, Chistiakov DA, Frydecka I, Ghaderi A, Gough SC, Hiromatsu Y, Ploski R, et al: Cytotoxic T-lymphocyte associated antigen 4 gene polymorphisms and autoimmune thyroid disease: a meta-analysis. The Journal of Clinical Endocrinology and Metabolism. 2007, 92 (8): 3162-3170. 10.1210/jc.2007-0147.CrossRefPubMed
28.
go back to reference Smyth DJ, Plagnol V, Walker NM, Cooper JD, Downes K, Yang JH, Howson JM, Stevens H, McManus R, Wijmenga C, et al: Shared and distinct genetic variants in type 1 diabetes and celiac disease. The New England Journal of Medicine. 2008, 359 (26): 2767-2777. 10.1056/NEJMoa0807917.CrossRefPubMedPubMedCentral Smyth DJ, Plagnol V, Walker NM, Cooper JD, Downes K, Yang JH, Howson JM, Stevens H, McManus R, Wijmenga C, et al: Shared and distinct genetic variants in type 1 diabetes and celiac disease. The New England Journal of Medicine. 2008, 359 (26): 2767-2777. 10.1056/NEJMoa0807917.CrossRefPubMedPubMedCentral
29.
go back to reference Daha NA, Kurreeman FA, Marques RB, Stoeken-Rijsbergen G, Verduijn W, Huizinga TW, Toes RE: Confirmation of STAT4, IL2/IL21, and CTLA4 polymorphisms in rheumatoid arthritis. Arthritis and Rheumatism. 2009, 60 (5): 1255-1260. 10.1002/art.24503.CrossRefPubMed Daha NA, Kurreeman FA, Marques RB, Stoeken-Rijsbergen G, Verduijn W, Huizinga TW, Toes RE: Confirmation of STAT4, IL2/IL21, and CTLA4 polymorphisms in rheumatoid arthritis. Arthritis and Rheumatism. 2009, 60 (5): 1255-1260. 10.1002/art.24503.CrossRefPubMed
30.
go back to reference Purohit S, Podolsky R, Collins C, Zheng W, Schatz D, Muir A, Hopkins D, Huang Y, She J: Lack of correlation between the levels of soluble cytotoxic T-lymphocyte associated antigen-4 (CTLA-4) and the CT-60 genotypes. Journal of Autoimmune Diseases. 2005, 2: 8-10.1186/1740-2557-2-8.CrossRefPubMedPubMedCentral Purohit S, Podolsky R, Collins C, Zheng W, Schatz D, Muir A, Hopkins D, Huang Y, She J: Lack of correlation between the levels of soluble cytotoxic T-lymphocyte associated antigen-4 (CTLA-4) and the CT-60 genotypes. Journal of Autoimmune Diseases. 2005, 2: 8-10.1186/1740-2557-2-8.CrossRefPubMedPubMedCentral
31.
go back to reference Wang X, Zhao X, Giscombe R, Lefvert A: A CTLA-4 gene polymorphism at position -318 in the promoter region affects the expression of protein. Genes and Immunity. 2002, 3 (4): 233-234. 10.1038/sj.gene.6363869.CrossRefPubMed Wang X, Zhao X, Giscombe R, Lefvert A: A CTLA-4 gene polymorphism at position -318 in the promoter region affects the expression of protein. Genes and Immunity. 2002, 3 (4): 233-234. 10.1038/sj.gene.6363869.CrossRefPubMed
32.
go back to reference Maier LM, Anderson DE, De Jager PL, Wicker LS, Hafler D: Allelic variant in CTLA4 alters T cell phosphorylation patterns. Proceedings of the National Academy of Sciences of the United States of America. 2007, 104 (47): 18607-18612. 10.1073/pnas.0706409104.CrossRefPubMedPubMedCentral Maier LM, Anderson DE, De Jager PL, Wicker LS, Hafler D: Allelic variant in CTLA4 alters T cell phosphorylation patterns. Proceedings of the National Academy of Sciences of the United States of America. 2007, 104 (47): 18607-18612. 10.1073/pnas.0706409104.CrossRefPubMedPubMedCentral
33.
go back to reference Marson A, Kretschmer K, Frampton GM, Jacobsen ES, Polansky JK, MacIsaac KD, Levine SS, Fraenkel E, von Boehmer H, Young RA: Foxp3 occupancy and regulation of key target genes during T-cell stimulation. Nature. 2007, 445 (7130): 931-935. 10.1038/nature05478.CrossRefPubMedPubMedCentral Marson A, Kretschmer K, Frampton GM, Jacobsen ES, Polansky JK, MacIsaac KD, Levine SS, Fraenkel E, von Boehmer H, Young RA: Foxp3 occupancy and regulation of key target genes during T-cell stimulation. Nature. 2007, 445 (7130): 931-935. 10.1038/nature05478.CrossRefPubMedPubMedCentral
34.
go back to reference Li QJ, Chau J, Ebert PJ, Sylvester G, Min H, Liu G, Braich R, Manoharan M, Soutschek J, Skare P, et al: miR-181a is an intrinsic modulator of T cell sensitivity and selection. Cell. 2007, 129 (1): 147-161. 10.1016/j.cell.2007.03.008.CrossRefPubMed Li QJ, Chau J, Ebert PJ, Sylvester G, Min H, Liu G, Braich R, Manoharan M, Soutschek J, Skare P, et al: miR-181a is an intrinsic modulator of T cell sensitivity and selection. Cell. 2007, 129 (1): 147-161. 10.1016/j.cell.2007.03.008.CrossRefPubMed
35.
go back to reference Vang T, Congia M, Macis MD, Musumeci L, Orrú V, Zavattari P, Nika K, Tautz L, Taskén K, Cucca F, et al: Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant. Nature Genetics. 2005, 37 (12): 1317-1319. 10.1038/ng1673.CrossRefPubMed Vang T, Congia M, Macis MD, Musumeci L, Orrú V, Zavattari P, Nika K, Tautz L, Taskén K, Cucca F, et al: Autoimmune-associated lymphoid tyrosine phosphatase is a gain-of-function variant. Nature Genetics. 2005, 37 (12): 1317-1319. 10.1038/ng1673.CrossRefPubMed
36.
go back to reference Arechiga AF, Habib T, He Y, Zhang X, Zhang ZY, Funk A, Buckner JH: Cutting edge: The PTPN22 allelic variant associated with autoimmunity impairs B cell signaling. Journal of Immunology (Baltimore, Md: 1950). 2009, 182 (6): 3343-3347.CrossRef Arechiga AF, Habib T, He Y, Zhang X, Zhang ZY, Funk A, Buckner JH: Cutting edge: The PTPN22 allelic variant associated with autoimmunity impairs B cell signaling. Journal of Immunology (Baltimore, Md: 1950). 2009, 182 (6): 3343-3347.CrossRef
37.
go back to reference 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 (New York, NY). 2004, 303 (5658): 685-689.CrossRef 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 (New York, NY). 2004, 303 (5658): 685-689.CrossRef
38.
go back to reference Vang T, Miletic AV, Arimura Y, Tautz L, Rickert RC, Mustelin T: Protein tyrosine phosphatases in autoimmunity. Annual Review of Immunology. 2008, 26: 29-55. 10.1146/annurev.immunol.26.021607.090418.CrossRefPubMed Vang T, Miletic AV, Arimura Y, Tautz L, Rickert RC, Mustelin T: Protein tyrosine phosphatases in autoimmunity. Annual Review of Immunology. 2008, 26: 29-55. 10.1146/annurev.immunol.26.021607.090418.CrossRefPubMed
39.
go back to reference Barrett J, Hansoul S, Nicolae DL, Cho JH, Duerr RH, Rioux JD, Brant SR, Silverberg MS, Taylor KD, Barmada MM, et al: Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Nature Genetics. 2008, 40 (8): 955-962. 10.1038/ng.175.CrossRefPubMedPubMedCentral Barrett J, Hansoul S, Nicolae DL, Cho JH, Duerr RH, Rioux JD, Brant SR, Silverberg MS, Taylor KD, Barmada MM, et al: Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Nature Genetics. 2008, 40 (8): 955-962. 10.1038/ng.175.CrossRefPubMedPubMedCentral
40.
go back to reference Criswell LA, Pfeiffer KA, Lum RF, Gonzales B, Novitzke J, Kern M, Moser KL, Begovich AB, Carlton VE, Li W, et al: Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes. American Journal of Human Genetics. 2005, 76 (4): 561-571. 10.1086/429096.CrossRefPubMedPubMedCentral Criswell LA, Pfeiffer KA, Lum RF, Gonzales B, Novitzke J, Kern M, Moser KL, Begovich AB, Carlton VE, Li W, et al: Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes. American Journal of Human Genetics. 2005, 76 (4): 561-571. 10.1086/429096.CrossRefPubMedPubMedCentral
41.
go back to reference Brand OJ, Lowe CE, Heward JM, Franklyn JA, Cooper JD, Todd JA, Gough SC: Association of the interleukin-2 receptor alpha (IL-2Ralpha)/CD25 gene region with Graves' disease using a multilocus test and tag SNPs. Clin Endocrinol (Oxf). 2007, 66 (4): 508-512. Brand OJ, Lowe CE, Heward JM, Franklyn JA, Cooper JD, Todd JA, Gough SC: Association of the interleukin-2 receptor alpha (IL-2Ralpha)/CD25 gene region with Graves' disease using a multilocus test and tag SNPs. Clin Endocrinol (Oxf). 2007, 66 (4): 508-512.
42.
go back to reference Lowe CE, Cooper JD, Brusko T, Walker NM, Smyth DJ, Bailey R, Bourget K, Plagnol V, Field S, Atkinson M, et al: Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes. Nature Genetics. 2007, 39 (9): 1074-1082. 10.1038/ng2102.CrossRefPubMed Lowe CE, Cooper JD, Brusko T, Walker NM, Smyth DJ, Bailey R, Bourget K, Plagnol V, Field S, Atkinson M, et al: Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes. Nature Genetics. 2007, 39 (9): 1074-1082. 10.1038/ng2102.CrossRefPubMed
43.
go back to reference Tait KF, Marshall T, Berman J, Carr-Smith J, Rowe B, Todd JA, Bain SC, Barnett AH, Gough SC: Clustering of autoimmune disease in parents of siblings from the Type 1 diabetes Warren repository. Diabetic Medicine: A Journal of the British Diabetic Association. 2004, 21 (4): 358-362.CrossRef Tait KF, Marshall T, Berman J, Carr-Smith J, Rowe B, Todd JA, Bain SC, Barnett AH, Gough SC: Clustering of autoimmune disease in parents of siblings from the Type 1 diabetes Warren repository. Diabetic Medicine: A Journal of the British Diabetic Association. 2004, 21 (4): 358-362.CrossRef
Metadata
Title
Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitis
Authors
Edward J Carr
Heather A Niederer
Julie Williams
Lorraine Harper
Richard A Watts
Paul A Lyons
Kenneth GC Smith
Publication date
01-12-2009
Publisher
BioMed Central
Published in
BMC Medical Genetics / Issue 1/2009
Electronic ISSN: 1471-2350
DOI
https://doi.org/10.1186/1471-2350-10-121

Other articles of this Issue 1/2009

BMC Medical Genetics 1/2009 Go to the issue