Bayry Jagadeesh, Lacroix-Desmazes Sébastien, Kazatchkine Michel D, Hermine Olivier, Tough David F, Kaveri Srini V
The Edward Jenner Institute for Vaccine Research, Berkshire, United Kingdom.
J Immunol. 2005 Jul 1;175(1):15-20. doi: 10.4049/jimmunol.175.1.15.
Investigating the signals that regulate the function of dendritic cells (DC), the sentinels of the immune system, is critical to understanding the role of DC in the regulation of immune responses. Accumulating lines of evidence indicate that in addition to innate stimuli and T cell-derived signals, B lymphocytes exert a profound regulatory effect in vitro and in vivo on the Ag-presenting function of DC. The identification of B cells as a cellular source of cytokines, chemokines, and autoantibodies that are critically involved in the process of maturation, migration, and function of DC provides a rationale for immunotherapeutic intervention of autoimmune and inflammatory conditions by targeting B cells. Conversely, efficient cross-presentation of Ags by DC pulsed with immune complexes provides an alternative approach in the immunotherapy of cancer and infectious diseases.
研究调节树突状细胞(DC)功能的信号至关重要,DC是免疫系统的哨兵,对于理解DC在免疫反应调节中的作用意义重大。越来越多的证据表明,除了先天刺激和T细胞衍生信号外,B淋巴细胞在体外和体内对DC的抗原呈递功能都具有深远的调节作用。将B细胞鉴定为细胞因子、趋化因子和自身抗体的细胞来源,这些物质在DC的成熟、迁移和功能过程中起着关键作用,这为通过靶向B细胞对自身免疫和炎症性疾病进行免疫治疗干预提供了理论依据。相反,用免疫复合物脉冲处理的DC对抗原进行高效交叉呈递,为癌症和传染病的免疫治疗提供了另一种方法。