Laboratory of Experimental Hematology, Vaccine & Infectious Disease Institute (Vaxinfectio), University of Antwerp, B-2610 Wilrijk, Belgium.
Immunotherapy. 2011 Oct;3(10):1203-22. doi: 10.2217/imt.11.110.
Dendritic cells (DCs) represent the bridging cell compartment between a variety of nonself antigens (i.e., microbial, cancer and vaccine antigens) and adaptive immunity, orchestrating the quality and potency of downstream immune responses. Because of the central role of DCs in the generation and regulation of immunity, the modulation of DC function in order to shape immune responses is gaining momentum. In this respect, recent advances in understanding DC biology, as well as the required molecular signals for induction of T-cell immunity, have spurred many experimental strategies to use DCs for therapeutic immunological approaches for infections and cancer. However, when DCs lose control over such 'protective' responses - by alterations in their number, phenotype and/or function - undesired effects leading to allergy and autoimmune clinical manifestations may occur. Novel therapeutic approaches have been designed and currently evaluated in order to address DCs and silence these immunopathological processes. In this article we present recent concepts of DC biology and some medical implications in view of therapeutic opportunities.
树突状细胞 (DCs) 是连接多种非自身抗原(即微生物、癌症和疫苗抗原)与适应性免疫的桥梁细胞,调控下游免疫反应的质量和效力。由于 DCs 在免疫的产生和调节中发挥着核心作用,因此调控 DC 功能以塑造免疫反应正成为研究热点。在这方面,对 DC 生物学的深入了解以及诱导 T 细胞免疫所需的分子信号的认识,推动了许多利用 DC 进行治疗性免疫方法的实验策略,以用于感染和癌症的治疗。然而,当 DCs 的数量、表型和/或功能发生改变,导致其对这些“保护性”反应失去控制时,可能会出现导致过敏和自身免疫临床表现的不良影响。目前正在设计和评估新的治疗方法,以针对 DCs 并抑制这些免疫病理过程。本文介绍了 DC 生物学的最新概念及其在治疗方面的一些医学意义。