中华皮肤科杂志
中華皮膚科雜誌
중화피부과잡지
Chinese Journal of Dermatology
2013年
6期
404-407
,共4页
陈柳青%陈金波%段逸群%李东升%董碧麟%张红梅%俞鑫
陳柳青%陳金波%段逸群%李東升%董碧麟%張紅梅%俞鑫
진류청%진금파%단일군%리동승%동벽린%장홍매%유흠
基因重排,γ链T细胞抗原受体%肉芽肿,蕈样%聚合酶链反应
基因重排,γ鏈T細胞抗原受體%肉芽腫,蕈樣%聚閤酶鏈反應
기인중배,γ련T세포항원수체%육아종,심양%취합매련반응
Gene rearrangement,gamma-chain T-cell antigen receptor%Mycosis fungoides%Polymerase chain reaction
目的 探讨BIOMED-2系统T细胞受体(TCR)γ引物组合在蕈样肉芽肿(MF)患者不同来源标本中TCRγ基因重排检测中的价值.方法 收集28例MF患者15份石蜡组织样本、14份新鲜皮损及18份全血组织样本,提取DNA,利用BIOMED-2系统TCRγ引物组合进行TCRγ基因重排检测,比较3组不同来源样本的检出率并进行统计学分析.用SPSS13.0软件进行统计分析.各组之间阳性率采用x2检验或Fisher确切概率法检验.结果 15份石蜡包埋组织标本3份TCRγ基因重排阳性,18份血液标本11份阳性,14份新鲜皮损标本12份阳性,3组之间阳性率差异有统计学意义(x2=13.047,P< 0.01),新鲜皮损TCRγ基因重排阳性率显著高于石蜡组织.201 1年的6例石蜡标本3份基因重排阳性,阳性率显著高于其余9例2011年之前的石蜡标本(Fisher精确概率法,P=0.044),与14例新鲜组织标本TCRγ基因重排阳性率(12/14)相比差异无统计学意义(Fisher精确概率法,P=0.131).血液标本TCRγ基因重排阳性率低于新鲜皮损,两组之间差异无统计学意义(x2=2.358,P>0.05).结论 BIOMED-2系统TCRγ引物组合适用于检测MF患者不同组织样本的TCR基因重排,更适用于新鲜的组织标本.
目的 探討BIOMED-2繫統T細胞受體(TCR)γ引物組閤在蕈樣肉芽腫(MF)患者不同來源標本中TCRγ基因重排檢測中的價值.方法 收集28例MF患者15份石蠟組織樣本、14份新鮮皮損及18份全血組織樣本,提取DNA,利用BIOMED-2繫統TCRγ引物組閤進行TCRγ基因重排檢測,比較3組不同來源樣本的檢齣率併進行統計學分析.用SPSS13.0軟件進行統計分析.各組之間暘性率採用x2檢驗或Fisher確切概率法檢驗.結果 15份石蠟包埋組織標本3份TCRγ基因重排暘性,18份血液標本11份暘性,14份新鮮皮損標本12份暘性,3組之間暘性率差異有統計學意義(x2=13.047,P< 0.01),新鮮皮損TCRγ基因重排暘性率顯著高于石蠟組織.201 1年的6例石蠟標本3份基因重排暘性,暘性率顯著高于其餘9例2011年之前的石蠟標本(Fisher精確概率法,P=0.044),與14例新鮮組織標本TCRγ基因重排暘性率(12/14)相比差異無統計學意義(Fisher精確概率法,P=0.131).血液標本TCRγ基因重排暘性率低于新鮮皮損,兩組之間差異無統計學意義(x2=2.358,P>0.05).結論 BIOMED-2繫統TCRγ引物組閤適用于檢測MF患者不同組織樣本的TCR基因重排,更適用于新鮮的組織標本.
목적 탐토BIOMED-2계통T세포수체(TCR)γ인물조합재심양육아종(MF)환자불동래원표본중TCRγ기인중배검측중적개치.방법 수집28례MF환자15빈석사조직양본、14빈신선피손급18빈전혈조직양본,제취DNA,이용BIOMED-2계통TCRγ인물조합진행TCRγ기인중배검측,비교3조불동래원양본적검출솔병진행통계학분석.용SPSS13.0연건진행통계분석.각조지간양성솔채용x2검험혹Fisher학절개솔법검험.결과 15빈석사포매조직표본3빈TCRγ기인중배양성,18빈혈액표본11빈양성,14빈신선피손표본12빈양성,3조지간양성솔차이유통계학의의(x2=13.047,P< 0.01),신선피손TCRγ기인중배양성솔현저고우석사조직.201 1년적6례석사표본3빈기인중배양성,양성솔현저고우기여9례2011년지전적석사표본(Fisher정학개솔법,P=0.044),여14례신선조직표본TCRγ기인중배양성솔(12/14)상비차이무통계학의의(Fisher정학개솔법,P=0.131).혈액표본TCRγ기인중배양성솔저우신선피손,량조지간차이무통계학의의(x2=2.358,P>0.05).결론 BIOMED-2계통TCRγ인물조합괄용우검측MF환자불동조직양본적TCR기인중배,경괄용우신선적조직표본.
Objective To estimate the value of BIOMED-2 primers for the detection of T cell receptor γ (TCR-γ) gene rearrangements in different types of specimens from patients with mycosis fungoides (MF).Methods Totally,15 paraffin-embedded tissue specimens,14 fresh tissue specimens and 18 whole blood specimens were obtained from 28 patients with MF,and subjected to DNA extraction.BIOMED-2 multiplex PCR tubes TCRγ (A+B) were used for the analysis of TCRγgene rearrangements.Data were processed by SPSS 13.0 software,and statistical analysis was done by chi-square test and Fisher's exact probability test.Results TCR-γ gene rearrangements were detected in 3 paraffin-embedded tissue specimens,11 fresh tissue specimens and 12 blood specimens,with significant differences in the detection rate between the three samples (x2 =13.047,P < 0.01).The fresh tissue samples showed a significantly higher detection rate than the paraffin-embedded tissue samples (X2 =12.523,P < 0.01).The detection rate of TCRγgene rearrangements was 3/6 in paraffin-embedded tissue samples collected in 2011,significantly higher than that in the other 9 paraffin-embedded tissue samples collected before 2011 (Fisher's exact probability test,P =0.044),but similar to that in 14 fresh tissue specimens (12/14,Fisher's exact probability test,P =0.044).Decreased detection rate of TCRγ gene rearrangements was observed in blood samples compared with fresh tissue specimens,but no statistical difference was observed between the two types of specimens (x2 =2.358,P > 0.05).Conclusions BIOMED-2 multiplex PCR tubes TCRγ(A+B) are suitable for the detection of clonal rearrangements of TCRγgene in different types of specimens,especially in fresh tissue specimens,from patients with MF.