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人源化抗神经节苷脂GM2抗体可有效诱导肺癌患者单核细胞中的抗体依赖性细胞介导的细胞毒性。

Humanized anti-ganglioside GM2 antibody is effective to induce antibody-dependent cell-mediated cytotoxicity in mononuclear cells from lung cancer patients.

作者信息

Parajuli P, Yanagawa H, Hanibuchi M, Takeuchi E, Miki T, Yano S, Sone S

机构信息

Third Department of Internal Medicine, The University of Tokushima School of Medicine, 3-18-15 Kuramoto-cho, 770-8503, Tokushima, Japan.

出版信息

Cancer Lett. 2001 Apr 26;165(2):179-84. doi: 10.1016/s0304-3835(01)00427-x.

Abstract

Ganglioside GM2 is one of the major gangliosides expressed on the cell surface of human tumors including lung cancer. We have previously reported that a mouse-human chimeric monoclonal antibody (mAb), KM966, against GM2 promotes the lysis of lung cancer cells by human blood mononuclear cells (MNC) of healthy donors. In this study, we examined antibody-dependent cell-mediated cytotoxicity (ADCC) of MNC, using KM966 mAb and its humanized counterpart, KM8969, in 16 lung cancer patients and 18 control patients. The ADCC activity was assessed by 4-h (51)Cr release from GM2 positive SBC-3 small cell lung cancer cells. MNC from lung cancer patients exhibited similar ADCC activity to those from control patients when KM966 and KM8969 were used as mAb. Moreover, effective ADCC activity was observed even in MNC from advanced lung cancer patients. These observations suggest the potential activity of humanized anti-GM2 mAb (KM8969), as well as chimeric KM966, in biological therapy for lung cancer patients.

摘要

神经节苷脂GM2是包括肺癌在内的人类肿瘤细胞表面表达的主要神经节苷脂之一。我们之前报道过,一种针对GM2的鼠-人嵌合单克隆抗体(mAb)KM966可促进健康供体的人血单核细胞(MNC)对肺癌细胞的裂解作用。在本研究中,我们使用KM966单克隆抗体及其人源化对应物KM8969,检测了16例肺癌患者和18例对照患者中MNC的抗体依赖性细胞介导的细胞毒性(ADCC)。通过检测GM2阳性的SBC-3小细胞肺癌细胞4小时的(51)Cr释放来评估ADCC活性。当使用KM966和KM8969作为单克隆抗体时,肺癌患者的MNC表现出与对照患者相似的ADCC活性。此外,即使在晚期肺癌患者的MNC中也观察到了有效的ADCC活性。这些观察结果表明,人源化抗GM2单克隆抗体(KM8969)以及嵌合抗体KM966在肺癌患者的生物治疗中具有潜在活性。

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