Department of Oncology, Medical Sciences Division, University of Oxford, Oxford, United Kingdom.
Centre for Medicines Discovery, Nuffield Department of Medicine, Medical Sciences Division, University of Oxford, Oxford, United Kingdom.
Front Immunol. 2021 Jun 30;12:696791. doi: 10.3389/fimmu.2021.696791. eCollection 2021.
Peptide-based cancer vaccines rely upon the strong activation of the adaptive immune response to elicit its effector function. They have shown to be highly specific and safe, but have yet to prove themselves as an efficacious treatment for cancer in the clinic. This is for a variety of reasons, including tumour heterogeneity, self-tolerance, and immune suppression. Importance has been placed on the overall design of peptide-based cancer vaccines, which have evolved from simple peptide derivatives of a cancer antigen, to complex drugs; incorporating overlapping regions, conjugates, and delivery systems to target and stimulate different components of antigen presenting cells, and to bolster antigen cross-presentation. Peptide-based cancer vaccines are increasingly becoming more personalised to an individual's tumour antigen repertoire and are often combined with existing cancer treatments. This strategy ultimately aids in combating the shortcomings of a more generalised vaccine strategy and provides a comprehensive treatment, taking into consideration cancer cell variability and its ability to avoid immune interrogation.
基于肽的癌症疫苗依赖于适应性免疫反应的强烈激活来发挥其效应功能。它们已被证明具有高度的特异性和安全性,但尚未在临床上证明自己是一种有效的癌症治疗方法。这是由于多种原因造成的,包括肿瘤异质性、自身耐受性和免疫抑制。基于肽的癌症疫苗的整体设计受到了重视,这些疫苗已经从癌症抗原的简单肽衍生物发展为复杂的药物;结合了重叠区域、缀合物和递药系统,以靶向和刺激抗原呈递细胞的不同成分,并增强抗原交叉呈递。基于肽的癌症疫苗越来越针对个体的肿瘤抗原库进行个性化定制,并且经常与现有的癌症治疗方法联合使用。这种策略最终有助于克服更普遍的疫苗策略的缺点,并提供全面的治疗,考虑到癌细胞的可变性及其逃避免疫检测的能力。