Hardy B, Galli M, Rivlin E, Goren L, Novogrodsky A
Felsenstein Medical Research Center, Petah-Tikva, Israel.
Cancer Immunol Immunother. 1995 Jun;40(6):376-82. doi: 10.1007/BF01525388.
A novel monoclonal antibody (BAT) to the B-lymphoblastoid cell line activates murine lymphocytes and exhibits a striking antitumor activity in mice. In order to evaluate the potential use of this antibody against human cancer, we have investigated its immuno-stimulatory properties on human peripheral blood lymphocytes (PBL). Our findings demonstrate that BAT mAb induces proliferation and cytotoxicity in human PBL against natural-killer-cell-sensitive and natural-killer-cell-resistant tumor cell lines. Interleukin-2 at a low concentration synergizes with BAT mAb in eliciting these effects. BAT mAb binds to human peripheral T cells as revealed by a double-labelling technique using anti-CD3 and BAT mAb. The molecular mass of the antigen recognized by BAT mAb was 48-50 kDa under reducing and non-reducing conditions. This study provides a basis for future experiments to evaluate the use of BAT mAb in the immunotherapy of cancer.
一种针对B淋巴母细胞系的新型单克隆抗体(BAT)可激活小鼠淋巴细胞,并在小鼠体内展现出显著的抗肿瘤活性。为了评估该抗体在人类癌症治疗中的潜在用途,我们研究了其对人外周血淋巴细胞(PBL)的免疫刺激特性。我们的研究结果表明,BAT单克隆抗体可诱导人PBL增殖并对自然杀伤细胞敏感和自然杀伤细胞抗性的肿瘤细胞系产生细胞毒性。低浓度的白细胞介素-2与BAT单克隆抗体协同作用引发这些效应。使用抗CD3和BAT单克隆抗体的双标记技术显示,BAT单克隆抗体与人外周T细胞结合。在还原和非还原条件下,BAT单克隆抗体识别的抗原分子量为48 - 50 kDa。本研究为未来评估BAT单克隆抗体在癌症免疫治疗中的应用提供了实验基础。