Ivanov Pavel K, Blokhin Dmitry Y, Chmutin Evgeny F, Grinevich Anatoly S, Perlin Dmitry V, Sokolsky Alexander S, Yakubovskaya Raisa I, Baryshnikov Anatoly Y
Research and Manufacturing Center Medbiospectr Ltd, Moscow, Russia.
Biotechnol J. 2007 Jul;2(7):863-70. doi: 10.1002/biot.200600254.
The N. Blokhin National Cancer Research Center is one of the few Russian scientific institutions in which hybridoma technology of monoclonal antibody (mAb) production has been successfully established. Using this technology, several dozens of mAbs to various antigens of human leukocytes have been elaborated. These mAbs are widely used for immune status evaluation and for differential diagnostics of leukemias. Two mAbs were used to develop therapeutic drugs. Imuteran is a pharmaceutical form of mAb ICO-25 against a mucin-like antigen of human milk fat globules and proposed for treatment of epithelial cell-originating cancers (breast, intestinal, ovarian, lung cancer, etc.). ThePhase II clinical study of this agent is now nearly completed, and preliminary results suggest Imuteran to be a promising anticancer agent with tumor-stabilizing activity, but patients should be carefully monitored for signs of allergic reactions. mAb ICO-90 against the CD3 antigen of human T lymphocytes was used to develop the therapeutic agent Atemonate proposed for treatment of acute transplant rejection. At present, the Phase II clinical study of this agent is over, and the results confirm the drug safety and efficacy for this indication. The drug is being registered at the Ministry of Healthcare and Social Development, and transfer to serial production is expected shortly.
N. 布洛欣国家癌症研究中心是俄罗斯少数成功建立单克隆抗体(mAb)杂交瘤技术的科研机构之一。利用这项技术,已经研制出几十种针对人类白细胞各种抗原的单克隆抗体。这些单克隆抗体广泛用于免疫状态评估和白血病的鉴别诊断。有两种单克隆抗体被用于开发治疗药物。Imuteran是一种针对人乳脂肪球粘蛋白样抗原的单克隆抗体ICO - 25的药物剂型,被提议用于治疗上皮细胞起源的癌症(乳腺癌、肠癌、卵巢癌、肺癌等)。该药物的II期临床研究现已接近完成,初步结果表明Imuteran是一种有前景的具有肿瘤稳定活性的抗癌药物,但应密切监测患者的过敏反应迹象。针对人类T淋巴细胞CD3抗原的单克隆抗体ICO - 90被用于开发治疗药物Atemonate,该药物被提议用于治疗急性移植排斥反应。目前,该药物的II期临床研究已经结束,结果证实了该药物针对这一适应症的安全性和有效性。该药物正在俄罗斯医疗保健和社会发展部进行注册,预计不久将转入批量生产。