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粘附分子CD11a、CD11b、CD62L在恶性淋巴增殖性疾病的表达
The expression of adhesion molecule CD11a,CD11b,CD62L on malignant lymphoproliferative disorders and its clinical implications
【摘要】 目的 :观察恶性淋巴增殖性疾病肿瘤细胞表面 β2 整合素 (CD11a、CD11b)及L 选择素 (CD6 2L)的表达变化及其临床意义。方法 :用流式细胞仪检测 35例初诊或复发急性淋巴白血病 (ALL)、4例慢性淋巴细胞白血病 (CLL)、30例多发性骨髓瘤 (MM)、14例淋巴肉瘤白血病及 2 5例正常人骨髓单个核细胞粘附分子CD11a、CD11b、CD6 2L的表达。结果 :①与正常造血细胞比较 ,CD11b、CD11a在ALL、MM、CLL细胞表达均下降 (P <0 0 1) ,但在淋巴肉瘤白血病细胞表达无明显改变 (P >0 0 5 ) ,CD6 2L在MM、CLL、淋巴肉瘤白血病细胞表达均下降 (P <0 0 5 ) ,但在ALL中表达增强 (P <0 0 5 )。②CD11a在ALL表达明显高于淋巴肉瘤白血病细胞表达 (P <0 0 1) ,CD6 2L在ALL表达明显低于淋巴肉瘤白血病细胞 (P <0 0 1)。③浸润组CD11a在ALL表达高于非浸润组 ,(P <0 0 5 )。④ALL完全缓解组CD11a、CD11b的表达可升至正常范围。结论 :恶性淋巴增殖性疾病肿瘤细胞表面上存在多个粘附分子的表达异常 ,检测粘附分子有助于判断白血病细胞类型及疗效。
【Abstract】 Objective:To investigate the expression of adhesion molecule including CD11a、CD11b、CD62L on malignant lymophoproliferative disorders and its clinical implications.Methods:Adhesion molecule CD11a、CD11b、CD62L of 35 Acute Lymophocytic Leukemia(ALL)、30 multiple myeloma(MM)、4 Chronic Lymophocytic Leukemia(CLL)、14 lymphosarocoma cell leukemia patients and 25 health people were measured by flow cytometric analysis.Results:①CD11a and CD11b expression were lower on ALL、MM、CLL cells than the normal hematopoietic cells.CD62L expression were lower on CLL、MM、lymphosarocoma cell leukemic cells than the normal hematopoietic cells.②The CD11a was lower expressed on ALL than lymphosarocoma cell leukemic cells,CD62L was higher on ALL than lymphosarocoma cells leukemia.③The expression of CD11a in the ALL invasion group was much higher than that in the noninvasive group(P<0 05) (4)The level of CD11a、CD11b were returned to normal levels at remission.Conclusion:The observations suggest that there are abnormalities in the expression of cell adhesion molecules in malignant lymophoproliferative disorders that may help to identify subtypes and object there treatment effect.
【Key words】 Lymphosarocoma cell leukemia Acute leukemia lymophocytic Multiple myeloma Cell adhesion molecule;
- 【文献出处】 中国免疫学杂志 ,Chinese Journal of Immunology , 编辑部邮箱 ,2000年11期
- 【被引频次】5
- 【下载频次】143