Pharmacovigilance Department, Poison Center and Claude Bernard University, Lyon, France.
MAbs. 2009 Mar-Apr;1(2):104-11. doi: 10.4161/mabs.1.2.7909. Epub 2009 Mar 19.
Monoclonal antibodies (mAbs) are large molecules intended to bind to specific targets often expressed on the immune system, and to treat various immunopathological conditions. Therefore, mAbs can be considered to have a high potential for immunotoxicity, which is reflected in the clinical experience accumulated on mAbs-induced adverse effects related to immunosuppression, immunostimulation and hypersensitivity (immunogenicity). So far, non clinical immunotoxicity studies have been inadequate to address all safety issues in relation to the possible immunotoxicity of mAbs, because they are fraught with limitations and pitfalls primarily related to the lack of relevant animal species. In addition, clinical studies rarely include validated end-points dedicated to the prediction of immunotoxicity. With the ongoing development of mAbs as novel therapeutic strategies for a wide variety of diseases, efforts should be paid to improve our understanding of mAbs-induced immunotoxic effects and design dedicated strategies to assess their immunological safety, both non clinically and clinically.
单克隆抗体(mAbs)是一种旨在与免疫系统上经常表达的特定靶标结合的大型分子,并用于治疗各种免疫病理学病症。因此,mAbs 可能具有较高的免疫毒性潜力,这反映在 mAbs 诱导的与免疫抑制、免疫刺激和过敏(免疫原性)相关的不良反应的临床经验积累中。到目前为止,非临床免疫毒性研究还不足以解决与 mAbs 可能的免疫毒性相关的所有安全问题,因为它们存在局限性和陷阱,主要与缺乏相关动物物种有关。此外,临床研究很少包括专门用于预测免疫毒性的验证终点。随着 mAbs 作为治疗各种疾病的新型治疗策略的不断发展,应努力提高我们对 mAbs 诱导的免疫毒性作用的理解,并设计专门的策略来评估它们的免疫安全性,无论是在非临床还是临床环境中。