Banchereau Jacques, Palucka A Karolina
Baylor Institute for Immunology Research, 3434 Live Oak, Dallas, Texas 75204, USA.
Nat Rev Immunol. 2005 Apr;5(4):296-306. doi: 10.1038/nri1592.
Mouse studies have shown that the immune system can reject tumours, and the identification of tumour antigens that can be recognized by human T cells has facilitated the development of immunotherapy protocols. Vaccines against cancer aim to induce tumour-specific effector T cells that can reduce the tumour mass, as well as tumour-specific memory T cells that can control tumour relapse. Owing to their capacity to regulate T-cell immunity, dendritic cells are increasingly used as adjuvants for vaccination, and the immunogenicity of antigens delivered by dendritic cells has now been shown in patients with cancer. A better understanding of how dendritic cells regulate immune responses will allow us to better exploit these cells to induce effective antitumour immunity.
小鼠研究表明,免疫系统能够排斥肿瘤,而可被人类T细胞识别的肿瘤抗原的鉴定推动了免疫治疗方案的发展。抗癌疫苗旨在诱导能够缩小肿瘤体积的肿瘤特异性效应T细胞,以及能够控制肿瘤复发的肿瘤特异性记忆T细胞。由于树突状细胞具有调节T细胞免疫的能力,它们越来越多地被用作疫苗接种的佐剂,并且树突状细胞递送抗原的免疫原性现已在癌症患者中得到证实。更好地了解树突状细胞如何调节免疫反应将使我们能够更好地利用这些细胞来诱导有效的抗肿瘤免疫。