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ID:36535405
大小:42.50 KB
页数:13页
时间:2019-05-11
《非霍奇金淋巴瘤患者外周血CD4CD25high调节性T细胞研究》由会员上传分享,免费在线阅读,更多相关内容在学术论文-天天文库。
1、非霍奇金淋巴瘤患者外周血CD4+CD25high调节性T细胞研究作者:刘莉,姚军霞,丁乾,黄士昂【摘要】本研究分析B细胞非霍奇金淋巴瘤(B-NHL)患者外周血T细胞亚群及CD4+CD25high调节T(Tr)细胞比例及其变化规律,初步探讨B-NHL免疫抑制机制,以及化疗对此免疫抑制功能的影响。采用流式细胞术检测42例初治B-NHL患者、36例化疗后达CR/PR患者及15例正常健康者(对照组)外周血CD3+、CD4+、CD8+和CD4+CD25highT细胞的比例。结果显示: B-NHL患者CD3+及CD4+T细胞比例、CD4/CD8比值均低于正常对照组,它们依次为(68.
2、33±15.27)%,对照(72.06±9.26)%;(34.47±12.84)%,对照(42.45±9.2)%;1.36±0.26,对照1.92±0.20,但CD4+CD25highTr细胞比例明显高于正常对照组,为(4.10±1.21)%,对照(2.04±1.03)%,(P<0.001)。化疗后组CD4/CD8比值低于化疗前组(P<0.05);而外周血CD4+CD25highTr细胞比例,显著高于化疗前组和对照组(P<0.01)。结论:B-NHL初治化疗前及化疗后患者外周血CD4+CD25highTr细胞比例都显著升高,提示CD4+CD25highT
3、r细胞可能是B-NHL患者免疫抑制的重要原因之一。【关键词】非霍奇金淋巴瘤13 CD4+CD25highRegulatoryTCellsinPeripheralBloodofPatientswithBCellNon-Hodgkin’sLymphoma AbstractThisstudywasaimedtoanalyzetheproportionofTcellsubsets,CD4+CD25highregulatongTcells(Tr)inperipheralbloodofB-NHLpatientsandthierchangeregularity,andtoinves
4、tigatetheimmunosuppressionmechanismandinfluenceofchemotherapyonimmunosuppressionfunctionofB-NHLpatients.Theperipheralbloodwascollectedfrom42patientswithB-NHL,36patientswithB-NHLwhoachievedpartialremission(PR)orcompleteremission(CR)after4-6cyclesofchemotherapyand15healthycontrols.Byusingmo
5、noclonalantibodies,thebloodsampleswereevaluatedwiththeflowcytometryforlymphocytesubsetsandTrcells.TheresultsshowedthattheproportionofCD3+andCD4+Tcells,andtheratioofCD4/CD8inpatientswithB-NHLgroupwassignificantlylessthanthoseinthehealthycontrols,i.e.(68.33±15.27)%versus(72.06±9.26)%;(34.47
6、±12.84)%versus(42.45±9.2)%;1.36±0.26versus1.92±0.20,buttheprevalenceoftheCD4+CD25highTrcellswassignificantlyhigherthanthoseinthehealthygroup〖(4.10±1.21)%versus(2.04±1.03)%,P<0.001].TheratioofCD4/13CD8inchemotherapygroupwaslowerthanthatincontrol,buttheproportionofCD4+CD25highTregcellsin
7、chemotherapygroupwashigherthanthosebeforechemo-/radio-therapyandthecontrol.ItisconcludedthattherelativeincreaseofCD4+CD25highTrcellsinperipheralbloodofB-NHLparientsmayberelatedtoimmunosuppressionandtumorprogression. Keywordsnon-Hodgkin′slymphoma;T-cellsubset;chemot
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