Hołowiecki J, Stella-Hołowiecka B, Krawczyk-Kuliś M, Wiechnik E, Japa J, Jarczok K, Rudzka E, Duraj M
Arch Immunol Ther Exp (Warsz). 1984;32(1):43-9.
The specificity and the clinical usefulness of the hybridoma derived monoclonal antibodies raised against the differentiation antigens of granulocytes (VIM-D5, VIM-C6), monocytes (VIM-D2), B lymphocytes (VIB-C5, VIC-Y1), erythrocytes (VIE-G4) and CALLA (VIL-A1) was studied in leukemic cells isolated from peripheral blood and bone marrow of 41 adults with acute leukemia by using indirect fluorescence method. The VIL-A1 positivity was observed in 4/9 of ALL and in none of myeloid leukemia. It was accompanied in 3/4 of cases by VIB-C5 positivity and in one case by VIE-G4 positivity. It is important that 2 out 3 unclassifiable cases (PAS-) could be diagnosed as common ALL due to their VIL-A1 positivity. VIM-D5 like VIM-C6 reacted specifially with granulocytic cells only and gave positive results in 20/30 of acute myeloid leukemias. When classified according to the FAB scheme, the proportion of VIM-D5 + patients rose from M1 toward more mature subtypes, including M4/5. It allowed to identify as AML 2/6 of unclassifiable-Mo leukemias, VIC-Y1 appeared to be helpful in characterization of B cell malignancies and of myelomonocytic leukemias. It is concluded that the monoclonal antibodies of VI series are specific and allow a more precise definition of leukemia, thus helping in optimalization of treatment.
采用间接荧光法,对41例急性白血病成年患者外周血和骨髓中分离出的白血病细胞,研究了针对粒细胞(VIM-D5、VIM-C6)、单核细胞(VIM-D2)、B淋巴细胞(VIB-C5、VIC-Y1)、红细胞(VIE-G4)和CALLA(VIL-A1)分化抗原产生的杂交瘤衍生单克隆抗体的特异性及临床实用性。在9例急性淋巴细胞白血病(ALL)中有4例观察到VIL-A1阳性,而在髓系白血病中均未观察到。在4例中的3例伴有VIB-C5阳性,1例伴有VIE-G4阳性。重要的是,3例无法分类的病例(PAS-)中有2例因其VIL-A1阳性可被诊断为普通型ALL。VIM-D5与VIM-C6一样,仅与粒细胞特异性反应,在30例急性髓系白血病中有20例呈阳性结果。根据FAB分型方案分类时,VIM-D5阳性患者的比例从M1型向更成熟的亚型上升,包括M4/5型。它能将6例无法分类的M0白血病中的2例鉴定为AML,VIC-Y1似乎有助于B细胞恶性肿瘤和骨髓单核细胞白血病的特征化。结论是,VI系列单克隆抗体具有特异性,能更精确地定义白血病,从而有助于优化治疗。