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通过电子显微镜检测到的具有小的过氧化物酶阳性颗粒的白血病原始细胞的免疫表型。

Immunophenotype of leukemic blasts with small peroxidase-positive granules detected by electron microscopy.

作者信息

Vainchenker W, Villeval J L, Tabilio A, Matamis H, Karianakis G, Guichard J, Henri A, Vernant J P, Rochant H, Breton-Gorius J

机构信息

INSERM U 91, Hôpital Henri Mondor, Créteil, France.

出版信息

Leukemia. 1988 May;2(5):274-81.

PMID:2836665
Abstract

Forty-three cases of undifferentiated leukemias by light microscopy examination were diagnosed as acute myeloblastic leukemias by ultrastructural revelation of peroxidase and were subsequently studied by immunological markers. In 41 of these cases, blasts were labeled by at least one of the antimyeloid MoAbs (My 7, My 9, and 80H5). An antimyeloperoxidase polyclonal antibody was used in 23 cases and was clearly positive in 11 of them, while cytochemistry by light microscopy was negative. These myeloblasts were frequently mixed with a minority of blasts from other lineages especially promegakaryoblasts. It is noteworthy that in 6 cases myeloid and lymphoid markers (E rosette receptor, common acute lymphoblastic leukemia antigen (cALLA), CD 9, CD 19 antigens (anti-B4 MoAb] were detected on a fraction of blast cells, suggesting a bilineage leukemia. However, in double labeling experiments, blasts with myeloperoxidase coexpressed lymphoid and myeloid markers including cALLA and CD 19 antigen. In one case, blasts had a typical non-B, non-T acute lymphoblastic leukemia phenotype (HLA-DR, CD 9, CD 19, cALLA positive) without staining by any of the antimyeloid MoAbs. However, 70% of the blasts were labeled by the antimyeloperoxidase antibody and expressed peroxidase-positive granules at ultrastructural level. In conclusion, most of the AML undiagnosed by optical cytochemistry are identified by antimyeloid antibodies. Some of these cases are also stained by some antilymphoid MoAbs. Use of antibodies against myeloperoxidase may improve the diagnosis of difficult cases of acute myeloblastic leukemia.

摘要

通过光学显微镜检查诊断为未分化白血病的43例患者,经超微结构显示过氧化物酶后被诊断为急性髓细胞白血病,随后进行免疫标记研究。在这些病例中,41例原始细胞至少被一种抗髓细胞单克隆抗体(My 7、My 9和80H5)标记。23例使用了抗髓过氧化物酶多克隆抗体,其中11例呈明显阳性,而光学显微镜下的细胞化学检查为阴性。这些原始髓细胞常与少数其他谱系的原始细胞混合,尤其是原始巨核细胞。值得注意的是,在6例中,一部分原始细胞检测到髓系和淋巴系标记(E玫瑰花结受体、普通急性淋巴细胞白血病抗原(cALLA)、CD 9、CD 19抗原(抗B4单克隆抗体),提示为双谱系白血病。然而,在双重标记实验中,带有髓过氧化物酶的原始细胞共表达淋巴系和髓系标记,包括cALLA和CD 19抗原。在1例中,原始细胞具有典型的非B、非T急性淋巴细胞白血病表型(HLA-DR、CD 9、CD 19、cALLA阳性),未被任何抗髓细胞单克隆抗体染色。然而,70%的原始细胞被抗髓过氧化物酶抗体标记,并在超微结构水平表达过氧化物酶阳性颗粒。总之,大多数光学细胞化学未诊断出的急性髓细胞白血病可通过抗髓细胞抗体鉴定。其中一些病例也被一些抗淋巴细胞单克隆抗体染色。使用抗髓过氧化物酶抗体可能会改善急性髓细胞白血病疑难病例的诊断。

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