Burdin N, Moingeon P
Département Recherche et Développement, Aventis Pasteur, Marcy l'Etoile, France.
Cell Biol Toxicol. 2001;17(2):67-75. doi: 10.1023/a:1010944003649.
Dendritic cells (DCs) can be used as an antigen presentation platform for vaccination against cancer. In this approach, DCs are expanded in vitro from monocyte-derived progenitors, and subsequently loaded with well-characterized tumor-associated antigens (TAAs). TAAs can be incubated with DCs in various forms, including peptides, recombinant proteins, plasmid DNA, formulated RNA, or recombinant viruses. Advantages and limitations of DC-based cellular vaccines against cancers, as well as preliminary results of clinical studies already performed in humans, are discussed. Importantly, significant advances in our understanding of the biology of DCs can be used to support the design of new vaccines or adjuvants in order to elicit TH1 cellular immune responses.
树突状细胞(DCs)可作为癌症疫苗接种的抗原呈递平台。在这种方法中,DCs从单核细胞衍生的祖细胞在体外进行扩增,随后负载特征明确的肿瘤相关抗原(TAAs)。TAAs可以与DCs以多种形式孵育,包括肽、重组蛋白、质粒DNA、配制的RNA或重组病毒。本文讨论了基于DC的细胞疫苗用于癌症治疗的优缺点,以及已经在人体中进行的临床研究的初步结果。重要的是,我们对DC生物学的理解取得的重大进展可用于支持新型疫苗或佐剂的设计,以引发TH1细胞免疫反应。