期刊文献+

脐血间充质干细胞移植治疗多发性肌炎/皮肌炎:Th细胞因子的变化 被引量:6

Umbilical cord blood mesenchymal stem cells transplantion for polymyositis/dermatomyositis:variation of Th cytokines
下载PDF
导出
摘要 背景:近年来,应用干细胞治疗免疫性疾病已成为研究热点,国内外有关脐血间充质干细胞移植治疗多发性肌炎/皮肌炎的报道较少。目的:观察脐血间充质干细胞移植治疗多发性肌炎/皮肌炎患者血清干扰素γ、白细胞介素4、白细胞介素17水平变化,探讨Th细胞因子在多发性肌炎/皮肌炎发生发展中的免疫机制。方法:81例多发性肌炎/皮肌炎患者,其中44例为常规治疗组,给予糖皮质激素联合免疫抑制剂治疗,37例为脐血间充质干细胞移植组,静脉输注脐血间充质干细胞(3.5-5.2)×107,用药方案与常规治疗组相同。随访治疗后1,3,6个月肌酸激酶、肌力变化及治疗后3,6个月肺部影像学改变,并在治疗前及治疗后3,6个月检测移植组Th细胞因子水平。结果与结论:1两组治疗后1,3,6个月与治疗前比较肌酸激酶值明显下降、肌力评分明显增高(均P<0.001);移植组治疗后各时间点肌酸激酶值较常规治疗组低、肌力评分较常规治疗组高(均P<0.001)。2脐血间充质干细胞移植治疗能明显改善肺部影像学异常,且安全性好。3移植治疗后6个月干扰素γ水平显著升高,而白细胞介素4水平显著下降(均P<0.01);移植治疗后3,6个月白细胞介素17水平显著下降(均P<0.01)。4移植治疗后6个月白细胞介素4、白细胞介素17水平与肌酸激酶水平成正相关(r=0.467和0.488,均P<0.05);干扰素γ水平与肌酸激酶水平无明显相关(r=0.213,P>0.05)。结果表明给予糖皮质激素及免疫抑制剂治疗同时,联合脐血间充质干细胞移植治疗多发性肌炎/皮肌炎安全、有效,可调节多发性肌炎/皮肌炎患者免疫网络效应、改善免疫耐受。 BACKGROUND:In recent years, the application of stem cel s to treat autoimmune diseases has become a hot spot. But, studies on umbilical cord blood mesenchymal stem cel s transplantation for the treatment of polymyositis/dermatomyositis are rarely reported. OBJECTIVE:To explore the immunologic mechanism of Th cytokines on the occurrence and development of polymyositis/dermatomyositis by observing the changes in serum interferon-γ, interleukin-4 and interleukin-17 in patients after umbilical cord blood mesenchymal stem cel s transplantation. METHODS:Eighty-one polymyositis/dermatomyositis patients were selected and divided into conventional therapy group (n=44) undergoing glucocorticoid and immunosuppressants therapy and cel transplantation group (n=37) undergoing intravenous infusion of umbilical cord blood mesenchymal stem cel s at a density of (3.5-5.2 )&#215;107 . Dosing regimen was same in the two groups. After fol ow-up of 1, 3, 6 months, the changes of creatine kinase and myodynamia were evaluated;after fol ow-up of 3 and 6 months, lung imaging was evaluated;in the cel transplantation group, interferon-γ, interleukin-4 and interleukin-17 levels were detected before treatment and at 3 and 6 months after treatment. RESULTS AND CONCLUSION:At 1, 3, 6 months after treatment, the creatine kinase level was significantly decreased, and the muscle force grade was significantly increased in both groups (both P〈0.001). Compared with the conventional therapy group, the creatine kinase level was lower and the muscle force grade was higher in the cel transplantation group (both P〈0.001). Results from lung imaging test showed a remarkable improvement after cel transplantation, and it indicated that umbilical cord blood mesenchymal stem cel s transplantation had good stability. At 6 months after transplantation, the level of interferon-γwas significantly increased, while the interleukin-4 level was decreased significantly (both P〈0.01);at 3, 6 months after cel transplantation, the
出处 《中国组织工程研究》 CAS 北大核心 2015年第14期2186-2191,共6页 Chinese Journal of Tissue Engineering Research
基金 福建省医学创新课题(2011-CXB-29) 福建医科大学非直属附属医院科学研究发展专项基金(FZS13011Y) 福建省龙岩市重点科技项目(2012LY116)~~
关键词 干细胞 移植 多发性肌炎/皮肌炎 脐血间充质干细胞 TH细胞因子 干扰素γ 白细胞介素4 白细胞介素17 Polymyositis Dermatomyositis Cord Blood Stem Cell Transplantation Interferon-gamma Interleukin-4 Interleukin-17
  • 相关文献

参考文献31

  • 1陈光辉.牛丰南.炎症性肌病[A]//李作汉,张平辟中经肌肉疾病的临床与病理[M].北京:人民卫生出版社,2007:162-192. 被引量:1
  • 2Dalakas MC. Polymyositis, dermatomyositis and inclusion-body myositis. N Engl J Med. 1991;325(21 ): 1487-1498. 被引量:1
  • 3Mastaglia FL, Phillips BA. Idiopathic inflammatory myopathies epidemiology, classification, and diagnostic criteria. Rheum Dis Cin North Am. 2002;28(4):723-741. 被引量:1
  • 4Reed AM, Ernste F. The inflammatory milieu in idiopathic inflammatory myositis. Curt Rheumatol Rep. 2009; 11 (4): 295-301. 被引量:1
  • 5McGuckin CP, Forraz N, AIIouard Q, et al. Umbilical cord blood stem cells can expand hematopoietic and neuroglial progenitors in vitro. Exp Cell Res. 2004;295(2):350-359. 被引量:1
  • 6Lu FZ, Fujino M, Kitazawa , et al. Characterization and gene transfer in mesenchymal stem cells derived from human umbilical-cord blood. J Lab Clin Med. 2005;146(5):271-278. 被引量:1
  • 7Hao L, Gao L, Chen XH, et al. Human umbilical cord blood-derived stromal cells prevent graft-versus-host disease in mice following haplo-identical stem cell transplantation. Cytotherapy. 2011 ;13(1 ):83-91. 被引量:1
  • 8Bohan A, Peter JB. Polymyositis and dermatornyositis (first of two parts). N Engl J Med. 1975;292(7):344-347. 被引量:1
  • 9HughesAL, Nei M. Evolution of the major histocompatibility complex: independent origin of nonclassical class I genes in different groups of mammals. Mol Biol Evol. 1989;6(6):559-579. 被引量:1
  • 10Miller FW, Rider LG, Chung YL, et al. Proposed preliminary core set measures for disease outcome assessment in adult and juvenile idiopathic inflammatory myopathies. Rheumatology (Oxford). 2001 ;40(11 ):1262-1273. 被引量:1

二级参考文献88

  • 1吕璐璐,刘拥军,许贞书,王彤,张浪辉,朱雄鹏,梁琳慧,王晗,陈志哲,韩忠朝.脐带源间充质干细胞的分离和生物学性状[J].福建医科大学学报,2006,40(2):99-104. 被引量:38
  • 2Thomas Korn,Estelle Bettelli,Mohamed Oukka,et al.IL-17and Th17 Cells[J].Annu.Rev.Immunol,2009,27:485-517 被引量:1
  • 3Jiang jiao Xie,Yan Cheng,Xiang Cheng,et al.The Th17/Treg functional imbalance during atherogenesis in ApoE/mice[J].Cytokine,2010,49:185-193 被引量:1
  • 4Wang W,Shao S,Jiao Z,et al.The Th17/Treg imbalance and cytokine environment in peripheral blood of patients with rheumatoid arthritis[J].Rheumatol Int,2011,Jan11[Epub ahead of print] 被引量:1
  • 5Shen H,Xia L,Lu J,Xiao W.Interleukin-17and interleukin-23in patients with polymyositis and dermatomyositis[J].Scand J Rheu-matol,2011,40:217-220 被引量:1
  • 6Tzartos J S,Friese M A,Craner M J,et al.Interleukin-17production in central nervous system-infiltrating T cells and glial cells is associated with active disease in multiple sclerosis[J].Am J Pathol,2008,172(1):146-155 被引量:1
  • 7Liu Xue-bin,Stewart Leung,Jian Hong,et al.Crucial role of interleukin-7in T helper type17survival and expansion in autoimmune disease[J].Nature medicine,2010,16(2):191-197 被引量:1
  • 8Strauss L,Czystowska M,Szajnik M,et al.Differential responses of human regulatory T cells(Treg)and effector T cells to rapamycin[J].PLoS One,2009,4(6):e5994 被引量:1
  • 9Mai J,Wang H,Yang X F.Th17cells interplay with Foxp3+Tregs in regulation of inflammation and autoimmunity[J].Front Biosci,2010,15:986-1006 被引量:1
  • 10Mai J,Wang H,Yang X F.,et al.Th17cells interplay with Foxp3+Tregs in regulation of inflammation and autoimmunity[J].Front Biosci,2010,15:986-1006 被引量:1

共引文献58

同被引文献41

引证文献6

二级引证文献38

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部