Department of Embryology, Medical University of Gdańsk, 80-211 Gdansk, Poland.
Department of Clinical Immunology and Transplantology, Medical University of Gdańsk, 80-211 Gdansk, Poland.
Molecules. 2018 Feb 14;23(2):414. doi: 10.3390/molecules23020414.
During recent decades, the market for peptide-based drugs, including antimicrobial peptides, has vastly extended and evolved. These drugs can be useful in treatment of various types of disorders, e.g., cancer, autoimmune diseases, infections, and non-healing wounds. Although peptides are less immunogenic than other biologic therapeutics, they can still induce immune responses and cause allergies. It is important to evaluate the immunogenic and allergic potential of peptides before they are forwarded to the expensive stages of clinical trials. The process of the evaluation of immunogenicity and cytotoxicity is complicated, as in vitro models and bioinformatics tools cannot fully simulate situations in the clinic. Nevertheless, several potentially promising tests for the preclinical evaluation of peptide drugs have been implemented (e.g., cytotoxicity assays, the basophil activation test, and lymphocyte activation assays). In this review, we focus on strategies for evaluation of the allergic potential of peptide-based therapeutics.
近几十年来,包括抗菌肽在内的基于肽的药物市场已经大大扩展和发展。这些药物可用于治疗各种类型的疾病,例如癌症、自身免疫性疾病、感染和难以愈合的伤口。尽管肽比其他生物治疗药物的免疫原性低,但它们仍可能引起免疫反应和过敏。在肽类药物进入昂贵的临床试验阶段之前,评估其免疫原性和过敏潜力非常重要。评估免疫原性和细胞毒性的过程很复杂,因为体外模型和生物信息学工具不能完全模拟临床情况。尽管如此,已经实施了几种有希望的肽类药物临床前评估的潜在测试(例如,细胞毒性测定、嗜碱性粒细胞活化试验和淋巴细胞活化试验)。在这篇综述中,我们重点介绍了评估基于肽的治疗药物过敏潜力的策略。