Leprince C, Blumenfeld N, Flandrin G, Galanaud P, Sigaux F, Richard Y
Inserm U 131, Clamari, France.
Blood. 1990 Feb 15;75(4):963-71.
The purpose of this study was to analyze the expression of B8.7 antigen and its implication in the low molecular weight B-Cell growth factor (LMW BCGF) proliferative pathway at the early stages of the human B-cell differentiation. After an overnight incubation in culture medium of B-cell precursor acute lymphoblastic leukemias (ALL), we demonstrated the presence of B8.7 antigen in 18 of 25 cases (72%). Such an incubation also induced a significant increase in the LMW BCGF responsiveness of ALL cells (P less than 0.03). In addition, we showed a significant correlation between B8.7 expression and the ability of pre-B ALL cells to respond to LMW BCGF. As previously described for normal B cells, the anti-B8.7 monoclonal antibody inhibited the LMW BCGF-dependent proliferation of pre-B ALL cells in a dose-dependent manner. These data indicate that B8.7 antigen is expressed and may be functionally related to the LMW BCGF pathway at the pre-B cell stages of differentiation. These results also suggest that human B-cell precursor ALL are not only phenotypically similar to their normal B lymphocyte counterparts, but are also sensitive to the same immunoregulatory cytokines that control normal cell growth.
本研究的目的是分析B8.7抗原在人B细胞分化早期阶段的表达及其在低分子量B细胞生长因子(LMW BCGF)增殖途径中的意义。在B细胞前体急性淋巴细胞白血病(ALL)的培养基中孵育过夜后,我们在25例中的18例(72%)中证实了B8.7抗原的存在。这样的孵育还导致ALL细胞对LMW BCGF的反应性显著增加(P小于0.03)。此外,我们显示B8.7表达与前B ALL细胞对LMW BCGF的反应能力之间存在显著相关性。如先前对正常B细胞所描述的,抗B8.7单克隆抗体以剂量依赖性方式抑制前B ALL细胞依赖LMW BCGF的增殖。这些数据表明,B8.7抗原在分化的前B细胞阶段表达,并且可能在功能上与LMW BCGF途径相关。这些结果还表明,人B细胞前体ALL不仅在表型上与其正常B淋巴细胞对应物相似,而且对控制正常细胞生长的相同免疫调节细胞因子也敏感。