期刊文献+

骨髓增生异常综合征患者CD4^+ CD25^+调节性T细胞、调控基因FOXP3的表达及意义 被引量:5

Expression and Significance of CD4^+ CD25^+ Treg,FOXP3 Gene in the Myelodysplastic Syndrome
下载PDF
导出
摘要 目的探讨骨髓增生异常综合征(MDS)患者CD4+ CD25+调节性T细胞(CD4+ CD25+ Treg细胞)和调控基因FOXP3的表达及意义。方法分离22例MDS患者[MDS组,根据MDS分型标准分为:难治性贫血组(RA组)6例、难治性血细胞减少伴有多系发育异常组(RCMD组)11例、难治性贫血伴原始细胞增多组(RAEB组)5例]和8例正常健康者骨髓单个核细胞,采用免疫荧光标记和流式细胞仪检测CD4+ CD25+ Treg细胞占CD4+ T细胞比例;提取骨髓单个核细胞RNA,采用RT-PCR检测FOXP3基因的表达水平。结果MDS组CD4+ CD25+ Treg细胞比例、FOXP3基因表达水平与正常对照组比较,差异均无统计学意义(均P>0.05);RA组、RAEB组CD4+ CD25+ Treg细胞比例、FOXP3基因表达水平与正常对照组比较,差异均有统计学意义(均P<0.01);RCMD组CD4+ CD25+ Treg细胞比例、FOXP3基因表达水平与正常对照组比较,差异均无统计学意义(均P>0.05);RCMD组、RAEB组CD4+ CD25+ Treg细胞比例、FOXP3基因表达水平与RA组比较,差异均有统计学意义(均P<0.01);RA组、RCMD组CD4+ CD25+ Treg比例、FOXP3基因表达水平与RAEB组比较,差异均有统计学意义(均P<0.01)。结论MDS患者CD4+ CD25+ Treg占CD4+ T细胞比例及FOXP3基因表达水平随预后危险级别的升高而升高,提示免疫异常是MDS疾病的发生、发展的一个促进因素。 Objective To explore the expression levels and the clinic significance of CD4^+CD25^+ regulatory T cell (CD4^+ CD25^+ Treg cell) and regulator and control gene FOXP3 in the myelodysplastic syndrome (MDS) patients.Methods The expression levels of CD4^+ CD25^+ Treg was detected by means of immunofluorescence and flow cytometry in 24 patients with MDS [MDS group:divide by the standard of MDS grouping:refractory anemia group (RA group) 6 examples,refractory cytopenia with multilineage dysplasia group (RCMD group) 11 examples,refractory anemia with excess blasts group(RAEB group) 5 examples] and 8 normal controls,respectively,that of FOXP3 by real-time quantitative RT-PCR.Results The expression levels of CD4^+ CD25^+ Treg and FOXP3 in the MDS group were not obviously different with the normal control group(all P〈0.05);patients with RA group and RAEB group,The expression levels of CD4^+ CD25^+ Treg and FOXP3 were obviously different with the normal control group (all P〈0.01);The expression levels of CD4^+ CD25^+ Treg and FOXP3 in the RCMD group were not obviously different with the normal control group (all P〈0.05);patients with RCMD group and RAEB group,The expression levels of CD4^+ CD25^+ Treg and FOXP3 were obviously different with the RA group(all P〈0.01);patients with RA group and RCMD group,The expression levels of CD4^+ CD25^+ Treg and FOXP3 were obviously different with the RAEB group(all P〈0.01).Conclusion The percentage of CD4^+ CD25^+ Treg in CD4^+T cell and the expression level of FOXP3 depends on the risk category of MDS;higher risk indicates more percentages and expressions,suggesting that immunologic abnormality is a promoting factor in the onset and progression.
出处 《实用临床医学(江西)》 CAS 2010年第1期5-7,10,共4页 Practical Clinical Medicine
关键词 骨髓增生异常综合征 CD4+ CD25+调节性T细胞 FOXP3基因 检测 myelodysplastic syndrome CD4^+ CD25^+ regulatory T cell FOXP3 gene detection
  • 相关文献

参考文献8

  • 1Maciejewski J P,Selleri C,Sato T,et al.A severe and consistent deficit in marrow and circulating primitive hematopoietic cells (long term culture-initiating cells) in acquired aplastic anemia[J].Blood,1996,88(6):1983-1991.
  • 2Leving M K,Sangregorio R,Roncarolo M G,et al.Human CD4^+ CD25^+ regulatory T cells suppress naive and memory T cell proliferation and can be expanded in vitro without loss of function[J].J Exp Med,2001,193(11):1295-1302.
  • 3陈书长,张之南.协和血液病学[M].北京:人民卫生出版社.2004:420-431.
  • 4Khattri R,Cox T,Yasayko S A,et al.An essential role for scurfin in CD4+CD25+ T regulatory cells[J].In Immunol,2003,4(4):337-342.
  • 5Yagi H,Nomura T,Nakamura K,et al.Crucial role of FOXP3 in the development and function of human CD25+ CD4+ regulatory T cells[J].Int Immunol,2007,16(11):1643-1656.
  • 6Bacchetta R,Passerini L,Gambineri E,et al.Defective regulatory and effector T cell functions in patients with FOXP3 mutations[J].J Clin Invest,2006,116(6):1713-1722.
  • 7Gambineri E,Torgerson T R,Ochs H D.Immune dysregulation,polyeodocrinopathy,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.
  • 8Solomou E E,Rezvani K,Midke S,et al.Deficient CD4+ CD25+ FOXP3+ T regulatory cells in acquired aplastic anemia[J].Blood,2007,110(5):1603-1606.

同被引文献48

  • 1李晓,陈怀增,叶枫,吕卫国,洪蝶,陈小君,谢幸.卵巢癌细胞培养上清诱导CD4^+CD25^-T细胞分化为CD4^+CD25^+调节性T细胞[J].中华微生物学和免疫学杂志,2006,26(2):121-124. 被引量:5
  • 2卢洁,金洁.三氧化二砷体内诱导人骨髓增生异常综合征荷瘤小鼠细胞凋亡机制的研究[J].中华儿科杂志,2006,44(10):782-786. 被引量:5
  • 3Gambineri E, Torgerson T R, Ochs H D. Immune dysregulation, polyen- doerinopathy, enteropathy, and X-linked inheritance ( IPEX ), a syndrome of systemic autoimmunity caused by mutations of FOXP3, a critical regula- tor of T-cell homeostasis [J]. Curr Opin Rheumatol, 2003; 15 (4) : 430- 435.
  • 4Fontenot J D, Gavin M A, Rudernky A Y. Foxp3 programs the development and function of CD4 + CD25 + regulatory T cells[J] .Nat Immtmol,2003;4 (4) :330-336.
  • 5Zhou X, Bailey-Bucktmut S, Jeker L T et al. Plasticity of CD4( + ) FoxP3.( + ) T cells[J] .Curt Opin Immunol,2009;21(3) :281-285.
  • 6Ikemoto T, Yamaguchi T, Morine Y et al. Clinical roles of increased popu- lations of Foxp3 + CIM + T cells in peripheral blood from advanced pancre- atic cancer patients[J] .Pancreas,2006;33(4) :386-390.
  • 7Gabaglia C R, DeLaney A, Gee Jet al. Treatment combining RU486 and Ad5IL-12 vector attenuates the growth of experimentally formed prostate tumors and induces changes in the sentinel lymph nodes of mice [ J ]. J Transl Med, 2010; 8 : 98.
  • 8Gu T, Rowswell-Tumer R B,Kilinc M O et al. Central role of IFN gam- ma-indoleamine 2,3-dioxygenase axis in regulation of interleukin-12-me- diated antitttmor immunity[J]. Cancer Res,2010; 70( 1 ) : 129-138.
  • 9Tam WF, Hahnel PS, Schuler A, et al. STATS is crucial to main- tain leukemic stem cells in acute myelogenous leukemias induced by MOZ-TIF2[J]. Cancer Res,2013,73(1):373-84.
  • 10Ogawa C, Tone Y, Tsuda M, et al. TGF-beta-mediated Foxp3 gene expression is cooperatively regulated by Stat5, Creb, and AP-1 through CNS2[J]. J Immunol,2014,192(1):475-83.

引证文献5

二级引证文献27

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