Péchiné Séverine, Janoir Claire, Collignon Anne
a EA4043 Faculté de Pharmacie , Univ Paris-Sud, Université Paris-Saclay , Chatenay-Malabry , France.
Expert Opin Biol Ther. 2017 Apr;17(4):415-427. doi: 10.1080/14712598.2017.1300655. Epub 2017 Mar 5.
Clostridium difficile infections are characterized by a high recurrence rate despite antibiotic treatments and there is an urgent need to develop new treatments such as fecal transplantation and immonotherapy. Besides active immunotherapy with vaccines, passive immunotherapy has shown promise, especially with monoclonal antibodies. Areas covered: Herein, the authors review the different assays performed with monoclonal antibodies against C. difficile toxins and surface proteins to treat or prevent primary or recurrent episodes of C. difficile infection in animal models and in clinical trials as well. Notably, the authors lay emphasis on the phase III clinical trial (MODIFY II), which allowed bezlotoxumab to be approved by the Food and Drug Administration and the European Medicines Agency. They also review new strategies for producing single domain antibodies and nanobodies against C. difficile and new approaches to deliver them in the digestive tract. Expert opinion: Only two human Mabs against TcdA and TcdB have been tested alone or in combination in clinical trials. However, many animal model studies have provided rationale for the use of Mabs and nanobodies in C. difficile infection and pave the way for further clinical investigation.
艰难梭菌感染的特点是尽管进行了抗生素治疗,但复发率仍然很高,因此迫切需要开发新的治疗方法,如粪便移植和免疫疗法。除了用疫苗进行主动免疫治疗外,被动免疫治疗也显示出了前景,尤其是单克隆抗体。涵盖领域:在此,作者回顾了用针对艰难梭菌毒素和表面蛋白的单克隆抗体进行的不同检测,这些检测用于在动物模型和临床试验中治疗或预防艰难梭菌感染的初次发作或复发。值得注意的是,作者着重介绍了III期临床试验(MODIFY II),该试验使贝佐妥单抗获得了美国食品药品监督管理局和欧洲药品管理局的批准。他们还回顾了生产针对艰难梭菌的单域抗体和纳米抗体的新策略,以及将它们递送至消化道的新方法。专家观点:在临床试验中,仅对两种针对TcdA和TcdB的人源单克隆抗体进行了单独或联合测试。然而,许多动物模型研究为在艰难梭菌感染中使用单克隆抗体和纳米抗体提供了理论依据,并为进一步的临床研究铺平了道路。