References
[1]谢晓恬.儿童再生障碍性贫血的诊断与治疗[J].实用儿科临床杂志,2009,24(3): 234-237.
[2]何广胜,周玲,吴德沛,孙爱宁,苗瞄,王秀丽,等.CD4+调节性 T细胞在再生障碍性贫血免疫发病中的作用[J].中国实用内科杂志,2007,27(20):1599-1601.
[3]黄永兰,黄绍良,梁蔚文,魏菁.再生障碍性贫血患儿CD4+CD25+T细胞及TGF-β1 Flt-3L水平变化的意义[J].中国实用儿科杂志,2007,22(2):130-133.
[4]李玉云,王卫国,张强,陈乐,马芳,马黎丽.CD4+CD25+Treg细胞和IL-21与再生障碍性贫血发病关系的探讨[J].中国实用儿科杂志,2010,31(4):269-270.
[5]Solomou EE, Rezvani K, Mielke S, Malide D, Keyvanfar K, Visconte V, et al. Deficient CD4+CD25+FOXP3+ T regulatory cells in acquired aplastic anemia[J]. Blood, 2007, 110(5): 1603-1606.
[6]王西阁,王晓格,栾斌,胡姬婷.调节性T细胞及Foxp3基因在再生障碍性贫血患儿外周血中的变化及意义[J].中国当代儿科杂志,2010,12(4): 241-243.
[7]王西阁,曹祎明,王晓格.CD4+CD25int/highCD127low调节性T细胞在再生障碍性贫血患儿中的检测及意义[J].中国当代儿科杂志,2011,13(4):292-295.
[8]许崇艳.再生障碍性贫血的免疫抑制治疗[J]. 中国实验血液学杂志,2005,13(2): 348.
[9]中华医学会儿科分会血液组,中华儿科杂志编委会.小儿再生障碍性贫血的诊疗建议[J].中华儿科杂志, 2001, 39(7): 422-423.
[10]王雪梅,韩梅,肖中平,陈琳.环孢素和雄激素联合治疗再生障碍性贫血疗效观察[J].中国误诊学杂志,2007,7(3): 453.
[11]Fiedler B, Wollert KC. Inter ference of antihypertrophic molecules and signaling pathways with the Ca2+-calcineurin-NFAT cascade in cardiacmy ocytes[J]. Cardiovasc Res, 2004, 63(3): 450-457.
[12]Bayer AL, Yu A, Malek TR. Function of the IL-2R for thymic and peripheral CD4+ CD25+ Foxp3+ T regulatory cells[J]. J Immunol, 2007, 178(7): 4062-4071.
[13]Lutsiak ME, Semnani RT, De Pascalis R, Kashmiri SV, Schlom J, Sabzevari H. Inhibition of CD4+CD25+ T regulatory cell function implicated in enhanced immune response by low-dose cyclophosphamide[J]. Blood, 2005, 105(7): 2862-2868.
[14]Godfrey WR, Spoden DJ, Ge YG, Baker SR, Liu B, Levine BL, et al.Cord blood CD4+CD25+ derived T regulatory cells linesexpress FOXP3 protein and manifest potent suppressor function[J]. Blood, 2005, 105(2): 750-758.
[15]Fontenot JD, Gavin MA, Rudensky AY. Foxp3 programs the development and function of CD4+CD25+ regulatory T cells[J]. Nax Immunol, 2003, 4(4): 330-336.
[16]Khattri R, Cox T, Yasayko SA, Ramsdell F. An essential role for scurfin in CD4+CD25+T regulatory cells[J]. Nat Immunol, 2003, 4(4): 337-342.
[17]Yagi H, Nomura T, Nakamura K, Yamazaki S, Kitawaki T, Hori S, et al. Crucial role of FOXP3 in the development and function of human CD25+CD4+regulatory T cells[J]. Int Immunol, 2004, 16(11): 1643-1656.
[18]Bacchetta R, Passerini L, Gambineri E, Dai M, Allan SE, Perroni L, et al.Defective regulatory and effector T cell functions in patients with FOXP3 mutations[J]. J Clin Invest, 2006, 116(6): 1713-1722.
[19]Gambineri E, Torgerson TR, Ochs HD. Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked inheritance(IPEX), a syndrome of systemic autoimmunity caused by mutations of FOXP3, a critical regulator of T-cell homeostasis[J]. Curr Opin Rheumatol, 2003, 15(4): 430-435.
[20]Unterberger C, Staples KJ, Smallie T, Williams L, Foxwell B, Schaefer A, et al. Role of STAT3 in glucocorticoid induced expression of thehuman IL-10 gene[J]. Mol Immunol, 2008, 45(11): 3230-3237.