Department of Microbiology and Immunology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Cancer Sci. 2010 Feb;101(2):313-20. doi: 10.1111/j.1349-7006.2009.01442.x. Epub 2009 Nov 17.
Dendritic cells (DC) begin maturation in response to complex stimuli consisting of antigens and pattern molecules (PAMP) for the activation of the immune system. Immune adjuvant usually contains PAMP. Infection represents one event that is capable of inducing such a complex set of stimuli. Recently, DC were subdivided into a number of subsets with distinct cell-surface markers, with each subset displaying unique differential maturation in response to pattern molecules to induce various types of effector cells. In the present study, we review how pattern recognition molecules and adaptors in each DC subset drive immune effector cells and their effect in the stimulated DC. Although tumor cells harbor tumor-associated antigens, they usually lack PAMP. Hence, we outline the properties of exogenously-added PAMP in the modulation of raising tumor immunity. In addition, we describe the mechanism by which DC-dependent natural killer activation is triggered for the induction of antitumor immunity.
树突状细胞 (DC) 在对由抗原和模式分子 (PAMP) 组成的复杂刺激物作出反应时开始成熟,这些刺激物可激活免疫系统。免疫佐剂通常含有 PAMP。感染就是能够引发这种复杂刺激的事件之一。最近,DC 被细分为具有不同表面标志物的多个亚群,每个亚群对模式分子的反应显示出独特的差异成熟,以诱导各种类型的效应细胞。在本研究中,我们综述了每个 DC 亚群中的模式识别分子和衔接子如何驱动免疫效应细胞及其在受刺激的 DC 中的作用。尽管肿瘤细胞含有肿瘤相关抗原,但它们通常缺乏 PAMP。因此,我们概述了外源性添加的 PAMP 在提高肿瘤免疫中的调节作用。此外,我们描述了触发 DC 依赖性自然杀伤细胞激活以诱导抗肿瘤免疫的机制。