Patents on enhancing the potency and longevity of highly valuable protein hormones.

Fuad Fares, Eyal Fima, Avri Havron
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引用次数: 4

Abstract

One major issue regarding the clinical use of many peptides is their short half-life span in the body, due to the rapid clearance from the circulation. Thus, at the clinical level, there is a need for a regime of frequent injections of the peptides into the patients to overcome this low stability factor. The major strategies for overcoming this problem by pharmaceutical companies are based on chemical techniques and using specific peptidase inhibitors or cocktails. For this purpose, the cassette gene contains the sequence of the carboxyl-terminal peptide (CTP) of human chorionic gonadotropin β subunit which was ligated to the coding sequence of follitropin (FSH), erythropoietin (EPO), growth hormone (GH) and thus to increase the longevity and bioactivity of these proteins in vivo. Interestingly, FSH-CTP and GH-CTP were found to be not immunogenic in humans. FSH-CTP was approved by The European Commission. In addition, GH-CTP is not toxic and it passed successfully clinical trials Phase II in adults. Thus, using this technology seems to be promising in designing long acting peptides. Development of long acting peptides will diminish the cost of these drugs and perhaps reduce the number of injections in the clinical protocols. The article also summarizes some relevant patents.

提高高价值蛋白质激素效力和寿命的专利。
关于许多多肽的临床应用的一个主要问题是它们在体内的半衰期短,由于从循环中迅速清除。因此,在临床水平上,有必要对患者进行频繁的多肽注射,以克服这种低稳定因子。制药公司克服这一问题的主要策略是基于化学技术和使用特定的肽酶抑制剂或鸡尾酒。为此,卡式基因含有人绒毛膜促性腺激素β亚基的羧基末端肽(CTP)序列,该序列与卵泡素(FSH)、促红细胞生成素(EPO)、生长激素(GH)的编码序列相连接,从而增加这些蛋白在体内的寿命和生物活性。有趣的是,FSH-CTP和GH-CTP在人类中没有免疫原性。FSH-CTP获得欧盟委员会批准。此外,GH-CTP是无毒的,并且成功地通过了成人II期临床试验。因此,使用这种技术在设计长效肽方面似乎很有希望。长作用肽的开发将降低这些药物的成本,并可能减少临床方案中的注射次数。文章还对相关专利进行了综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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