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急性淋巴细胞白血病患者共刺激分子CD86和可溶性细胞毒性T淋巴细胞相关抗原4的表达增加。

Increased expression of costimulatory molecules CD86 and sCTLA-4 in patients with acute lymphoblastic leukemia.

作者信息

Mansour Amany, Elkhodary Tawfik, Darwish Ahmad, Mabed Mohamed

机构信息

Clinical Pathology Department, Mansoura University , Egypt.

出版信息

Leuk Lymphoma. 2014 Sep;55(9):2120-4. doi: 10.3109/10428194.2013.869328. Epub 2014 Mar 7.

Abstract

We herein evaluate the role of the B7-family molecule CD86 and the Cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4) as a possible immunopathogenic factors in patients with ALL. The results of 60 patients with de novo ALL were compared to 40 controls. A significant statistical difference between CD86 expression and sCTLA-4 levels in patients versus their controls has been detected. During follow up period of 28 months, patients suffered from relapse (16 patients) had significantly higher CD86 expression and sCTL-4 levels compared to those remained in complete remission (44 patients) (p = 0.005 and 0.03 respectively). Patients who died from the disease (9 patients) showed significantly higher CD 86 expression and sCTLA-4 levels than surviving patients (51 patients) (p = 0.004 and 0.01 respectively). In conclusion, the higher levels of sCTLA-4 and CD86 in B-ALL patients might be candidate parameters for poor prognosis and may serve to refine treatment stratification with intensification of therapy in those patients prone to relapse.

摘要

我们在此评估B7家族分子CD86和细胞毒性T淋巴细胞相关抗原4(CTLA-4)作为急性淋巴细胞白血病(ALL)患者可能的免疫致病因素的作用。将60例初发ALL患者的结果与40例对照进行比较。已检测到患者与其对照之间CD86表达和可溶性CTLA-4(sCTLA-4)水平存在显著统计学差异。在28个月的随访期内,复发患者(16例)的CD86表达和sCTL-4水平显著高于完全缓解患者(4例)(p值分别为0.005和0.03)。死于该疾病的患者(9例)的CD86表达和sCTLA-4水平显著高于存活患者(51例)(p值分别为0.004和0.01)。总之,B-ALL患者中较高水平的sCTLA-4和CD86可能是预后不良的候选参数,可用于优化治疗分层,对那些易于复发的患者加强治疗。

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