Meyer P R, Krugliak L, Neely S, Levine A, Parker J W, Kaplan B, Taylor C R
Am J Clin Pathol. 1986 Oct;86(4):461-8. doi: 10.1093/ajcp/86.4.461.
Blast cells from ten patients (seven adults, three children) with acute lymphoblastic leukemias (ALL) contained immunoreactive cytoplasmic alpha-1-anti-trypsin (alpha-1-AT) and alpha-1-antichymotrypsin (alpha-1-ACT). Cytochemically positive reactions for block-like periodic acid-Schiff and a localized acid phosphatase suggested that the cells were of lymphoid origin rather than myeloid origin: negative for sudan black-B, nonspecific esterase, chloroacetate esterase, and myeloperoxidase. By surface phenotype, the leukemia showed positive reactions for both lymphoid (common acute lymphoblastic leukemia antigen, Ia, OKT-10) and myeloid (OKM-1, Leu M-1) antigens. Three of three patients tested portrayed the Philadelphia chromosome. Nine patients were Mexican-American and one was Japanese: all were of Asian ethnic derivation. Both myeloid and lymphoid treatment regimens were employed, with survival less than expected. Early granulocytic differentiation detectable by cytoplasmic alpha-1-AT and alpha-1-ACT in lymphoid blasts is discussed.
来自10例急性淋巴细胞白血病(ALL)患者(7名成人,3名儿童)的原始细胞含有免疫反应性细胞质α-1-抗胰蛋白酶(α-1-AT)和α-1-抗糜蛋白酶(α-1-ACT)。细胞化学显示块状过碘酸希夫反应和局部酸性磷酸酶呈阳性反应,提示这些细胞起源于淋巴细胞而非髓细胞:苏丹黑B、非特异性酯酶、氯乙酸酯酶和髓过氧化物酶呈阴性。从表面表型来看,白血病对淋巴细胞(常见急性淋巴细胞白血病抗原、Ia、OKT-10)和髓细胞(OKM-1、Leu M-1)抗原均呈阳性反应。检测的3例患者中有3例呈现费城染色体。9例患者为墨西哥裔美国人,1例为日本人:所有患者均为亚洲血统。采用了髓细胞和淋巴细胞治疗方案,但生存率低于预期。文中讨论了通过淋巴细胞原始细胞中的细胞质α-1-AT和α-1-ACT检测到的早期粒细胞分化情况。