Dai Zhen-sheng, Chen Qin-fen, Lu Hong-zhou, Xie Yi
Department of Infectious Disease, Shanghai Public Health Clinical Center affiliated to Fudan University, Jinshan District, Shanghai, People's Republic of China.
Int J Hematol. 2009 Jun;89(5):656-63. doi: 10.1007/s12185-009-0320-7. Epub 2009 May 9.
Malignant monoclonal B cells of chronic B cell lymphocytic leukemia (B-CLL) usually fail to be cleared, which indicates important costimulatory molecules may be lacking. Among those costimulatory signals, B7-1/CD80 and B7-2/CD86 caused utmost attention. In this study, B7-1 and B7-2 expression on B cells in chronic B cell lymphocytic leukemia patients were detected. Data showed that B7-2 expression in chronic B cell lymphocytic leukemia patients is significantly lower than in normal people, which suggests defective B7-2 expression may be one of the pathogenic mechanisms of chronic B cell lymphocytic leukemia. Further, we confirmed interferon-gamma could induce B7-2 expression slightly and promote T-cell response against chronic B cell lymphocytic leukemia cells, indicating interferon-gamma has clinical value in chronic leukemia immunotherapy based on modulating B7-2 expression.
慢性B淋巴细胞白血病(B-CLL)的恶性单克隆B细胞通常无法被清除,这表明可能缺乏重要的共刺激分子。在这些共刺激信号中,B7-1/CD80和B7-2/CD86引起了极大关注。在本研究中,检测了慢性B淋巴细胞白血病患者B细胞上B7-1和B7-2的表达。数据显示,慢性B淋巴细胞白血病患者的B7-2表达明显低于正常人,这表明B7-2表达缺陷可能是慢性B淋巴细胞白血病的致病机制之一。此外,我们证实干扰素-γ可轻微诱导B7-2表达,并促进T细胞对慢性B淋巴细胞白血病细胞的反应,表明干扰素-γ在基于调节B7-2表达的慢性白血病免疫治疗中具有临床价值。