摘要
目的 :探讨用免疫分型结合免疫球蛋白重链 (Ig H )及 T细胞受体γ(TCRγ)基因重排对急性淋巴细胞白血病 (AL L )的分型诊断及预后的判断价值。方法 :免疫分型采用碱性磷酸酶抗碱性磷酸酶复合物 (APAAP)免疫组化法 ,基因重排采用多聚酶链反应技术 (PCR法 )检测 5 8例初治成人 AL L 患者。结果 :1通过免疫分型检测 ,5 8例 AL L 中 ,43例 (74.1% )为不带髓系相关标记的 AL L(My- AL L) ,15例 (2 5 .9% )为带髓系相关标记的AL L(My+ AL L) ,以 CD1 5 最常见。 2采用 PCR法检测 Ig H基因重排和 TCR 基因重排发现 ,5 8例 AL L 中有79.3% (4 6 /5 8)免疫分型与基因重排结果完全吻合 ,即 T- AL L 出现 TCR 基因重排阳性 ,B- AL L 出现 Ig H基因重排阳性 ,2 0 .7% (12 /5 8)基因重排结果与免疫分型不能完全吻合。 3 5 8例 AL L经 DOL P或 DOCP方案 1个疗程后 ,My- AL L CR为 72 .1% (31/43) ,My+ AL L为 6 6 .7% (10 /15 ) ;AL L不同阶段 CR率分别是 :T- AL L为82 .4% (14/17) ,Pro B- AL L为 5 0 .0 % (3/6 ) ,C- AL L为 90 .5 % (19/2 1) ,Pre B- AL L为 33.3% (4 /12 ) ,成熟 B- AL L为 5 0 .0 % (1/2 ) ;经基因重排检测与免疫分型吻合的 AL L CR率为 71.7% (33/46 ) ,不吻合的 AL L 为 6 6 .7% (8/12 )。
Objective:To analyze the typing diagnosis and prognosis of acute lymphoblastic lekemia (ALL) by immune typing (IT) binding immunoglobulin heavy chain (IgH) and T cell receptor γ(TCRγ) gene rearrangement (GA). Method:58 cases of de nove adult ALL were detected by alkaline phosphatase antialkaline phosphatase compound (APAAP) immunohistochemistry and polymerase chain reaction (PCR).Result:① It was detected in all 58 patients,43( 74.1 %) cases didn′t express myeloid associated markers (My -ALL), 15( 25.9 %) expressing them (My +ALL).Among the markers,CD15 + was the most often expressed.② The detection of IgH and TCR showed that GA in 79.3 % (46/58) cases were complete accordance with IT,that was,T ALL were positive in TCR,B All in IgH,but GA in 20.7 % (12/58) cases didn′t completely coincide with IT.③After one course of treatment of ALL cases by DOLP/DOCP,the complete remission rate (CR) of My -ALL was 71.3 % (31/43) and My +ALL was 66.7 % (10/15).The CR of different stages of ALL were 82.4 % (14/17,T ALL), 50.0 % (3/6,proB ALL), 90.5 % (13/21,C ALL), 33.3 % (4/12,pre B ALL) and 50.0 % (1/2,mature B ALL) respectively.CR was 71.7 % (33/46) in cases of ALL whose IT were in accordance with GA,but CR in cases whose IT didn′t coincide with GA was 66.7 % (8/12).Conclusion:In regard to the typing of leukemia,IT should be added on the basis of FAB typing,which might improve the positive rate of diagnosis and have value in prognosis.GA was only a reference in diagnosis,yet it had no guiding significance in prognosis.
出处
《临床血液学杂志》
CAS
2001年第2期51-53,共3页
Journal of Clinical Hematology