中华检验医学杂志
中華檢驗醫學雜誌
중화검험의학잡지
CHINESE JOURNAL OF LABORATORY MEDICINE
2008年
11期
1215-1220
,共6页
袁向亮%王剑%李美星%张通通%薛剑%沈立松
袁嚮亮%王劍%李美星%張通通%薛劍%瀋立鬆
원향량%왕검%리미성%장통통%설검%침립송
流式细胞术%白血病%淋巴瘤%免疫分型
流式細胞術%白血病%淋巴瘤%免疫分型
류식세포술%백혈병%림파류%면역분형
Flow eybometty%Leukemia%Lymphoma%Immunophenotyping
目的 建立五色流式细胞术分析白血病和淋巴瘤免疫表型方案,并评价其临床应用价值.方法 对73例急性白血病和30例淋巴瘤患者,采用五色流式免疫表型分析方案中系列敏感指标组合(CD7/CD33/CD19/CD13/CD45)进行第一轮筛选,系列特异指标(cMPO/cCD79a/cCD3/CD117/CD45)组合做确认检测,并根据确认试验结果进行第二轮检测.结果 用仪器软件自动程序可方便地得到理想的五色荧光补偿值.五色流式表型分析结果显示,急性B淋巴细胞性白血病(B-ALL)中CD19阳性率100%(27/27),cCD79a阳性率92.6%(25/27),根据CD34、CD10、cμ、sIgM等表达情况可对B-ALL进行确切分期诊断;急性T淋巴细胞性白血病(T-ALL)中均表达CD7(8/8)和cCD3(8/8),根据CD2、CD1a、CD3、CD4、CD8等表达情况可对T-ALL进行确切分期;急性髓细胞性白血病(AML)中髓系细胞系列相对特异抗原cMPO表达率89.5%(34/38)、CD117为81.6%(31/38),26.3%(10/38)的AML混合表达淋系抗原CD7,结合形态学等可进行亚型辅助诊断.采用五色抗体组合并用CD19/SSC设门可对B细胞淋巴瘤进行鉴别诊断.开展五色流式表型分析节省检测的上样管数,由原来三色方案的12管减少到6管,同时可节省20%的抗体用量.结论 五色流式表型分析方案提高了免疫表型分析的准确性,降低了成本,适合临床实验室开展白血病和淋巴瘤的免疫表型分析.
目的 建立五色流式細胞術分析白血病和淋巴瘤免疫錶型方案,併評價其臨床應用價值.方法 對73例急性白血病和30例淋巴瘤患者,採用五色流式免疫錶型分析方案中繫列敏感指標組閤(CD7/CD33/CD19/CD13/CD45)進行第一輪篩選,繫列特異指標(cMPO/cCD79a/cCD3/CD117/CD45)組閤做確認檢測,併根據確認試驗結果進行第二輪檢測.結果 用儀器軟件自動程序可方便地得到理想的五色熒光補償值.五色流式錶型分析結果顯示,急性B淋巴細胞性白血病(B-ALL)中CD19暘性率100%(27/27),cCD79a暘性率92.6%(25/27),根據CD34、CD10、cμ、sIgM等錶達情況可對B-ALL進行確切分期診斷;急性T淋巴細胞性白血病(T-ALL)中均錶達CD7(8/8)和cCD3(8/8),根據CD2、CD1a、CD3、CD4、CD8等錶達情況可對T-ALL進行確切分期;急性髓細胞性白血病(AML)中髓繫細胞繫列相對特異抗原cMPO錶達率89.5%(34/38)、CD117為81.6%(31/38),26.3%(10/38)的AML混閤錶達淋繫抗原CD7,結閤形態學等可進行亞型輔助診斷.採用五色抗體組閤併用CD19/SSC設門可對B細胞淋巴瘤進行鑒彆診斷.開展五色流式錶型分析節省檢測的上樣管數,由原來三色方案的12管減少到6管,同時可節省20%的抗體用量.結論 五色流式錶型分析方案提高瞭免疫錶型分析的準確性,降低瞭成本,適閤臨床實驗室開展白血病和淋巴瘤的免疫錶型分析.
목적 건립오색류식세포술분석백혈병화림파류면역표형방안,병평개기림상응용개치.방법 대73례급성백혈병화30례림파류환자,채용오색류식면역표형분석방안중계렬민감지표조합(CD7/CD33/CD19/CD13/CD45)진행제일륜사선,계렬특이지표(cMPO/cCD79a/cCD3/CD117/CD45)조합주학인검측,병근거학인시험결과진행제이륜검측.결과 용의기연건자동정서가방편지득도이상적오색형광보상치.오색류식표형분석결과현시,급성B림파세포성백혈병(B-ALL)중CD19양성솔100%(27/27),cCD79a양성솔92.6%(25/27),근거CD34、CD10、cμ、sIgM등표체정황가대B-ALL진행학절분기진단;급성T림파세포성백혈병(T-ALL)중균표체CD7(8/8)화cCD3(8/8),근거CD2、CD1a、CD3、CD4、CD8등표체정황가대T-ALL진행학절분기;급성수세포성백혈병(AML)중수계세포계렬상대특이항원cMPO표체솔89.5%(34/38)、CD117위81.6%(31/38),26.3%(10/38)적AML혼합표체림계항원CD7,결합형태학등가진행아형보조진단.채용오색항체조합병용CD19/SSC설문가대B세포림파류진행감별진단.개전오색류식표형분석절성검측적상양관수,유원래삼색방안적12관감소도6관,동시가절성20%적항체용량.결론 오색류식표형분석방안제고료면역표형분석적준학성,강저료성본,괄합림상실험실개전백혈병화림파류적면역표형분석.
Objective To establish a five-color flow cytometric immunophenotyping protocol and valuate its clinical application in leukemia and lymphoma. Methods Samples from 73 cases of acute leukemia and 30 cases of lymphoma were analyzed using a comprehensive antibody panel with five-color combination. The antibody combination CD7/CD33/CD19/CD13/CD45 and MPO/cCD79a/cCD3/CD117/CD45,composed of different lineage distinctive and lineage sensitive markers of B, T and myeloid cells, were applied to determine the lineage originality of leukemia and lymphoma celia. The markers used in the second step analysis were based on the findings of the first step. Results Five-color compensation can be performed automatically and easily with the advanced digital compensation program. The results showed that the expression ratio of CD19 in B-ALL was 100% (27/27), cCD79, pesitivity was 92.6% (25/27) and CD7,cCD3 was expressed in all T-ALL cases (8/8). The B-ALL could be staged depending on the expression level of CD34 ,CD10 ,cμ,sIgM and the T-ALL could be dearly staged dependent on the expression level of CD2,CD1a,,CD4,CD4,CD8. The expression ratio of cMPO, CD117 was 89. 5% (34/38) and 81.6% (31/38) in AML respectively, however CD7 was also expressed in 26.3% (10/38) of AML cases. Combined with morphology, immanophenotypes could be used for diagnosing AML with subtyping. The CD19/SSC gating can be used for immunophenotyping of B cell lymphoma with differential diagnosis. The number of robes required was significantly reduced with our panel from 12 tubes of 3-color to 6 tubes of 5-color. Implementation of the five-color protocol had resulted in 20% reduction in reagent costs. Conclusions The application of fivecolor staining protocol significantly improve the sensitivity and accuracy of measurement of immunophenotypes of acute leukemia and lymphoma. It reduces the cost and can be widely applied in the clinical laboratory diagnosis.