Significant Association Between Fc Receptor-Like 3 Polymorphisms (-1901A>G and -658C>T) and Neuromyelitis Optica (NMO) Susceptibility in the Chinese Population (original) (raw)
References
Asgari N, Lillevang ST, Skejoe HPB, Falah M, Stenager E, Kyvik KO (2011) A population-based study of neuromyelitis optica in Caucasians. Neurology 76(18):1589–1595 ArticleCASPubMedPubMed Central Google Scholar
Cabrera-Gómez JA, Kurtzke JF, González-Quevedo A, Lara-Rodríguez R (2009) An epidemiological study of neuromyelitis optica in Cuba. J Neurol 256(1):35–44 ArticlePubMed Google Scholar
Cossburn M, Tackley G, Baker K, Ingram G, Burtonwood M, Malik G, Pickersgill T, te Water Naudé J, Robertson N (2012) The prevalence of neuromyelitis optica in South East Wales. Eur J Neurol 19(4):655–659 ArticleCASPubMed Google Scholar
Mealy MA, Wingerchuk DM, Greenberg BM, Levy M (2012) Epidemiology of neuromyelitis optica in the United States: a multicenter analysis. Arch Neurol 69(9):1176–1180 ArticlePubMed Google Scholar
Rivera JF, Kurtzke JF, Booth VJA, Corona VT (2008) Characteristics of Devic’s disease (neuromyelitis optica) in Mexico. J Neurol 255(5):710–715 ArticlePubMed Google Scholar
Jarius S, Wildemann B, Paul F (2014) Neuromyelitis optica: clinical features, immunopathogenesis and treatment. Clin Exp Immunol 176(2):149–164 ArticleCASPubMedPubMed Central Google Scholar
Wingerchuk DM, Hogancamp WF, O’Brien PC, Weinshenker BG (1999) The clinical course of neuromyelitis optica (Devic’s syndrome). Neurology 53(5):1107–1114 ArticleCASPubMed Google Scholar
Lennon VA, Kryzer TJ, Pittock SJ, Verkman AS, Hinson SR (2005) IgG marker of optic-spinal multiple sclerosis binds to the aquaporin-4 water channel. J Exp Med 202(4):473–477 ArticleCASPubMedPubMed Central Google Scholar
Lennon VA, Wingerchuk DM, Kryzer TJ, Pittock SJ, Lucchinetti CF, Fujihara K, Nakashima I, Weinshenker BG (2004) A serum autoantibody marker of neuromyelitis optica: distinction from multiple sclerosis. Lancet 364(9451):2106–2112 ArticleCASPubMed Google Scholar
Ratelade J, Verkman AS (2012) Neuromyelitis optica: aquaporin-4 based pathogenesis mechanisms and new therapies. Int J Biochem Cell Biol 44(9):1519–1530 ArticleCASPubMedPubMed Central Google Scholar
Davis RS, Dennis G Jr, Odom MR, Gibson AW, Kimberly RP, Burrows PD, Cooper MD (2002) Fc receptor homologs: newest members of a remarkably diverse Fc receptor gene family. Immunol Rev 190:123–136 ArticleCASPubMed Google Scholar
Song GG, Bae SC, Kim JH, Kim YH, Choi SJ, Ji JD, Lee YH (2013) Association between functional Fc receptor-like 3 (FCRL3) -169 C/T polymorphism and susceptibility to seropositive rheumatoid arthritis in Asians: a meta-analysis. Hum Immunol 74(9):1206–1213. doi:10.1016/j.humimm.2013.05.018 ArticleCASPubMed Google Scholar
Kochi Y, Yamada R, Suzuki A, Harley JB, Shirasawa S, Sawada T, Bae SC, Tokuhiro S, Chang X, Sekine A, Takahashi A, Tsunoda T, Ohnishi Y, Kaufman KM, Kang CP, Kang C, Otsubo S, Yumura W, Mimori A, Koike T, Nakamura Y, Sasazuki T, Yamamoto K (2005) A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities. Nat Genet 37(5):478–485. doi:10.1038/ng1540 ArticleCASPubMedPubMed Central Google Scholar
Han SW, Sa KH, Kim SI, Lee SI, Park YW, Lee SS, Yoo WH, Kang JY, Soe JS, Nam EJ, Lee J, Park JY, Kang YM (2012) FCRL3 gene polymorphisms contribute to the radiographic severity rather than susceptibility of rheumatoid arthritis. Hum Immunol 73(5):537–542. doi:10.1016/j.humimm.2012.02.011 ArticleCASPubMed Google Scholar
Bajpai UD, Swainson LA, Mold JE, Graf JD, Imboden JB, McCune JM (2012) A functional variant in FCRL3 is associated with higher Fc receptor-like 3 expression on T cell subsets and rheumatoid arthritis disease activity. Arthritis Rheum 64(8):2451–2459. doi:10.1002/art.34457 ArticleCASPubMedPubMed Central Google Scholar
Zhao SX, Liu W, Zhan M, Song ZY, Yang SY, Xue LQ, Pan CM, Gu ZH, Liu BL, Wang HN, Liang L, Liang J, Zhang XM, Yuan GY, Li CG, Chen MD, Chen JL, Gao GQ, Song HD (2013) A refined study of FCRL genes from a genome-wide association study for Graves’ disease. PLoS One 8(3):7 Google Scholar
Inoue N, Watanabe M, Yamada H, Takemura K, Hayashi F, Yamakawa N, Akahane M, Shimizuishi Y, Hidaka Y, Iwatani Y (2012) Associations between autoimmune thyroid disease prognosis and functional polymorphisms of susceptibility genes, CTLA4, PTPN22, CD40, FCRL3, and ZFAT, previously revealed in genome-wide association studies. J Clin Immunol 32(6):1243–1252 ArticleCASPubMed Google Scholar
Chen JY, Wang CM, Wu YJ, Kuo SN, Shiu CF, Chang SW, Lin YT, Ho HH, Wu J (2011) Disease phenotypes and gender association of FCRL3 single-nucleotide polymorphism -169 T/C in Taiwanese patients with systemic lupus erythematosus and rheumatoid arthritis. J Rheumatol 38(2):264–270. doi:10.3899/jrheum.100437 ArticleCASPubMed Google Scholar
Sanchez E, Callejas JL, Sabio JM, de Haro M, Camps M, de Ramon E, Garcia-Hernandez FJ, Koeleman B, Martin J, Gonzalez-Escribano MF (2006) Polymorphisms of the FCRL3 gene in a Spanish population of systemic lupus erythematosus patients. Rheumatology (Oxford) 45(8):1044–1046. doi:10.1093/rheumatology/kel160 ArticleCAS Google Scholar
You Y, Wang Z, Deng G, Hao F (2008) Lack of association between Fc receptor-like 3 gene polymorphisms and systemic lupus erythematosus in Chinese population. J Dermatol Sci 52(2):118–122. doi:10.1016/j.jdermsci.2008.04.011 ArticleCASPubMed Google Scholar
Piotrowski P, Lianeri M, Prokop E, Wudarski M, Olesinska M, Jagodzinski PP (2014) The FCRL3 -169T>C polymorphism might be associated with some autoantibody presence in patients with SLE in a Polish population. Mod Rheumatol 24(2):296–299. doi:10.3109/14397595.2013.854066 ArticleCASPubMed Google Scholar
Tanaka A, Ohira H, Kikuchi K, Nezu S, Shibuya A, Bianchi I, Podda M, Invernizzi P, Takikawa H (2011) Genetic association of Fc receptor-like 3 polymorphisms with susceptibility to primary biliary cirrhosis: ethnic comparative study in Japanese and Italian patients. Tissue Antigens 77(3):239–243. doi:10.1111/j.1399-0039.2010.01600.x ArticleCASPubMed Google Scholar
Mendoza JL, Lana R, Martin MC, de la Concha EG, Urcelay E, Diaz-Rubio M, Abreu MT, Mitchell AA (2009) FcRL3 gene promoter variant is associated with peripheral arthritis in Crohn’s disease. Inflamm Bowel Dis 15(9):1351–1357. doi:10.1002/ibd.20895 ArticlePubMed Google Scholar
Plagnol V, Howson JM, Smyth DJ, Walker N, Hafler JP, Wallace C, Stevens H, Jackson L, Simmonds MJ, Bingley PJ, Gough SC, Todd JA (2011) Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. PLoS Genet 7(8):e1002216. doi:10.1371/journal.pgen.1002216 ArticleCASPubMedPubMed Central Google Scholar
Howson JM, Krause S, Stevens H, Smyth DJ, Wenzlau JM, Bonifacio E, Hutton J, Ziegler AG, Todd JA, Achenbach P (2012) Genetic association of zinc transporter 8 (ZnT8) autoantibodies in type 1 diabetes cases. Diabetologia 55(7):1978–1984. doi:10.1007/s00125-012-2540-2 ArticleCASPubMedPubMed Central Google Scholar
Matesanz F, Fernandez O, Milne RL, Fedetz M, Leyva L, Guerrero M, Delgado C, Lucas M, Izquierdo G, Alcina A (2008) The high producer variant of the Fc-receptor like-3 (FCRL3) gene is involved in protection against multiple sclerosis. J Neuroimmunol 195(1–2):146–150. doi:10.1016/j.jneuroim.2008.01.004 ArticleCASPubMed Google Scholar
Li K, Zhao M, Hou S, Du L, Kijlstra A, Yang P (2008) Association between polymorphisms of FCRL3, a non-HLA gene, and Behcet’s disease in a Chinese population with ophthalmic manifestations. Mol Vis 14:2136–2142 CASPubMedPubMed Central Google Scholar
Wingerchuk DM, Lennon VA, Pittock SJ, Lucchinetti CF, Weinshenker BG (2006) Revised diagnostic criteria for neuromyelitis optica. Neurology 66(10):1485–1489 ArticleCASPubMed Google Scholar
Kochi Y, Myouzen K, Yamada R, Suzuki A, Kurosaki T, Nakamura Y, Yamamoto K (2009) FCRL3, an autoimmune susceptibility gene, has inhibitory potential on B-cell receptor-mediated signaling. J Immunol 183(9):5502–5510. doi:10.4049/jimmunol.0901982 ArticleCASPubMed Google Scholar
Swainson LA, Mold JE, Bajpai UD, McCune JM (2010) Expression of the autoimmune susceptibility gene FcRL3 on human regulatory T cells is associated with dysfunction and high levels of programmed cell death-1. J Immunol 184(7):3639–3647. doi:10.4049/jimmunol.0903943 ArticleCASPubMedPubMed Central Google Scholar