[1] World Health Organization, 2013. Global tuberculosis report 2013[EB/OL].[2015-06-12]. http://apps.who.int/iris/bitstream/10665/91355/1/9789241564656_eng.pdf.[2] Dye C, Williams B G. The population dynamics and control of tuberculosis[J]. Science, 2010,328(5980):856-861.[3] Thye T, Vannberg F O, Wong S H, et al. Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2[J]. Nat Genet, 2010,42(9):739-741.[4] Motulsky A G. Metabolic polymorphisms and the role of infectious diseases in human evolution[J]. Hum Biol, 1960,32:28-62.[5] Stead W W, Senner J W, Reddick W T, et al. Racial differences in susceptibility to infection by Mycobacterium tuberculosis[J]. N Engl J Med, 1990,322(7):422-427.[6] Comstock G W. Tuberculosis in twins: a re-analysis of the Prophit survey[J]. Am Rev Respir Dis, 1978,117(4):621-624.[7] Sorensen T I, Nielsen G G, Andersen P K, et al. Genetic and environmental influences on premature death in adult adoptees[J]. N Engl J Med, 1988,318(12):727-732.[8] Simonds B. The collection of 300 twin index cases for a study of tuberculosis in twins and their families[J]. Acta Genet Stat Med, 1957,7(1):42-47.[9] Newport M J, Goetghebuer T, Weiss H A, et al. Genetic regulation of immune responses to vaccines in early life[J]. Genes Immun, 2004,5(2):122-129.[10] Jenkins K A, Mansell A. TIR-containing adaptors in Toll-like receptor signalling[J]. Cytokine, 2010,49(3):237-244.[11] 周燕,郑瑞娟,胡忠义.Toll样受体基因多态性与结核病易感性的研究进展[J].中华预防医学杂志,2011,45(1):73-76.[12] Bernard N J, O'Neill L A. Mal, more than a bridge to MyD88[J]. IUBMB Life, 2013,65(9):777-786.[13] Leavy O. Innate immune signalling: TIRAP diversifies the sites of TLR signalling[J]. Nat Rev Immunol, 2014 ,14(4):211.[14] Jenkins K A, Mansell A. TIR-containing adaptors in Toll-like receptor signalling[J]. Cytokine, 2010,49(3):237-244.[15] 江载芳,赵顺英.儿童肺结核的临床诊断标准和治疗方案(试行)[J].中华儿科杂志,2006,44(4):249-251.[16] Horng T, Barton G M, Medzhitov R. TIRAP: an adapter molecule in the Toll signaling pathway[J]. Nat Immunol, 2001,2(9):835-841.[17] Khor C C, Chapman S J, Vannberg F O, et al. A Mal functional variant is associated with protection against invasive pneumococcal disease, bacteremia, malaria and tuberculosis[J]. Nat Genet, 2007,39(4):523-528.[18] Castiblanco J, Varela D C, Castano-Rodriguez N, et al. TIRAP(MAL) S180L polymorphism is a common protective factor against developing tuberculosis and systemic lupus erythematosus[J]. Infect Genet Evol, 2008,8(5):541-544.[19] Hawn T R, Dunstan S J, Thwaites G E, et al. A polymorphism in Toll-interleukin 1 receptor domain containing adaptor protein is associated with susceptibility to meningeal tuberculosis[J]. J Infect Dis, 2006,194(8):1127-1134.[20] Zhang Y X, Xue Y, Liu J Y, et al. Association of TIRAP(MAL) gene polymorhisms with susceptibility to tuberculosis in a Chinese population[J]. Genet Mol Res, 2011,10(1):7-15.[21] Cooke G S, Hill A V. Genetics of susceptibility to human infectious disease[J]. Nat Rev Genet, 2001,2(12):967-977.[22] Basu Roy R, Whittaker E, Kampmann B. Current understanding of the immune response to tuberculosis in children[J]. Curr Opin Infect Dis, 2012,25(3):250-257.[23] Qi H, Sun L, Wu X, et al. Toll-like receptor 1(TLR1) Gene SNP rs5743618 is associated with increased risk for tuberculosis in Han Chinese children[J]. Tuberculosis(Edinb), 2015,95(2):197-203.[24] Sun L, Jin Y Q, Shen C, et al. Genetic contribution of CISH promoter polymorphisms to susceptibility to tuberculosis in Chinese children[J]. PLoS One, 2014,9(3):e92020.[25] Qi H, Sun L, Jin Y Q, et al. Rs2243268 and rs2243274 of Interleukin-4(IL-4) gene are associated with reduced risk for extrapulmonary and severe tuberculosis in Chinese Han children[J]. Infect Genet Evol, 2014,23:121-128.[26] Shen C, Wu X R, Jiao W W, et al. A functional promoter polymorphism of IFITM3 is associated with susceptibility to pediatric tuberculosis in Han Chinese population[J]. PLoS One, 2013,8(7):e67816.[27] Feng W X, Mokrousov I, Wang B B, et al. Tag SNP polymorphism of CCL2 and its role in clinical tuberculosis in Han Chinese pediatric population[J]. PLOS One, 2011,6(2):e14652.[28] Mokrousov I, Wu X R, Vyazovaya A, et al. Polymorphism of 3'UTR region of TNFR2 coding gene and its role in clinical tuberculosis in Han Chinese pediatric population[J]. Infect Genet Evol, 2011,11(6):1312-1318.[29] Jin J, Sun L, Jiao W, et al. SLC11A1(Formerly NRAMP1) gene polymorphisms associated with pediatric tuberculosis in China[J]. Clin Infect Dis, 2009,48(6):733-738.[30] Xiao J, Sun L, Jiao W W, et al. Lack of association between polymorphisms in the P2X7 gene and tuberculosis in a Chinese Han population[J]. FEMS Immunol Med Microbiol, 2009,55(1):107-111.[31] 李洁琼,谢兰品,董雅坤,等.TLR4基因多态性与中国汉族儿童结核病易感性的关联研究[J].山西医科大学学报,2014,42(12):1151-1158.[32] 徐放,谢兰品,董雅坤,等.TLR2基因多态性与中国汉族儿童结核病易感性的关联研究[J].中国循证儿科杂志,2014,9(6):417-422.[33] 焦伟伟,李兆娜,孙琳,等.维生素D受体基因多态性与中国汉族儿童结核病易感性的研究[J].中国实用儿科杂志,2009,24(4):264-266.[34] 陈晓.儿童结核病78例临床特点及误诊分析[J].临床误诊误治,2013,26(12):1-3.[35] 胡杰,王琳,隗慧林,等.肺结核即时诊断技术研究进展[J].解放军医药杂志,2012,24(8):4-6. |