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慢性髓性白血病急变期的免疫表型特征

Immunophenotypic characteristics of the blast crisis in chronic myeloid leukemia.

作者信息

López-Karpovitch X, Cárdenas R, Piedras J

机构信息

Departamento de Hematología y Oncología, Instituto Nacional de la Nutrición Salvador Zubirán, México, D.F.

出版信息

Rev Invest Clin. 1997 Jan-Feb;49(1):31-6.

PMID:9229753
Abstract

OBJECTIVE

To characterize the immunophenotype of blast crisis (BC) in Mexican patients with chronic myeloid leukemia (CML).

MATERIAL AND METHODS

Mononuclear cells of 17 patients with CML in BC were immunophenotyped employing a panel of 18 monoclonal antibodies: CD5, CD10, CD14, CD22, and anti-HLA-DR used in all patients; CD2, CD15, CD19, CD34, and CD41 in 13 to 16 patients; and CD3, CD7, CD13, CD20, CD21, CD33, CD42b, and CD61 in less than 10 patients.

RESULTS

Myeloid was the most frequent type (9/17 cases) followed by lymphoid (6/17) and hybrid or mixed lineage (2/17). Four of the myeloid BC expressed megakaryocyte/platelet associated antigens; 5 of 6 cases with lymphoid BC showed an early precursor B cell immunophenotype (HLA-DR+, CD10+), and the other was an uncommon case of lymphoid B/T transformation (CD19+, CD5+). The CD34 antigen was present in 6 out of 15 cases: 4 patients with lymphoid BC, 1 with myeloid transformation, and 1 with megakaryoblastic BC.

CONCLUSIONS

Our findings are comparable to those found in the literature comprising 192 patients. The present study confirms the lineage heterogeneity of CML BC and suggests that extensive immunophenotyping may allow insight for a more precise recognition of normal and leukemic ontogenesis.

摘要

目的

对墨西哥慢性髓系白血病(CML)患者急变期(BC)的免疫表型进行特征分析。

材料与方法

采用一组18种单克隆抗体对17例CML急变期患者的单核细胞进行免疫表型分析:所有患者均使用CD5、CD10、CD14、CD22和抗HLA - DR;13至16例患者使用CD2、CD15、CD19、CD34和CD41;少于10例患者使用CD3、CD7、CD13、CD20、CD21、CD33、CD42b和CD61。

结果

髓系是最常见的类型(9/17例),其次是淋系(6/17)和混合或混合谱系(2/17)。4例髓系急变期表达巨核细胞/血小板相关抗原;6例淋系急变期中有5例表现为早期前体B细胞免疫表型(HLA - DR +,CD10 +),另一例是罕见的淋系B/T转化病例(CD19 +,CD5 +)。15例中有6例存在CD34抗原:4例淋系急变期患者,1例髓系转化患者,1例巨核母细胞性急变期患者。

结论

我们的研究结果与文献中192例患者的结果相当。本研究证实了CML急变期的谱系异质性,并表明广泛的免疫表型分析可能有助于更精确地识别正常和白血病的发生过程。

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