Wang Rong-Fu
The Center for Cell and Gene Therapy and Department of Immunology, Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA.
Immunol Rev. 2002 Oct;188:65-80. doi: 10.1034/j.1600-065x.2002.18807.x.
The importance of T-cell-mediated antitumor immunity has been demonstrated in both animal models and human cancer therapy. The identification of major histocompatibility complex (MHC) class I-restricted tumor antigens has generated a resurgence of interest in immunotherapy for cancer. However, recent studies suggest that therapeutic strategies that have mainly focused on the use of CD8+ T cells (and MHC class I-restricted tumor antigens) may not be effective in eliminating cancer cells in patients. Novel strategies have been developed for enhancing T-cell responses against cancer by prolonging antigen presentation of dendritic cells to T cells and the inclusion of MHC class II-restricted tumor antigens. identification of MHC class II-restricted tumor antigens, which are capable of stimulating CD4+ T cells, not only aids our understanding of the host immune responses against cancer antigens, but also provides opportunities for developing effective cancer vaccines.
T细胞介导的抗肿瘤免疫的重要性已在动物模型和人类癌症治疗中得到证实。主要组织相容性复合体(MHC)I类限制性肿瘤抗原的鉴定引发了对癌症免疫疗法的再度关注。然而,最近的研究表明,主要侧重于使用CD8 + T细胞(以及MHC I类限制性肿瘤抗原)的治疗策略可能无法有效消除患者体内的癌细胞。通过延长树突状细胞向T细胞的抗原呈递以及纳入MHC II类限制性肿瘤抗原,已开发出增强T细胞对癌症反应的新策略。能够刺激CD4 + T细胞的MHC II类限制性肿瘤抗原的鉴定,不仅有助于我们理解宿主针对癌症抗原的免疫反应,还为开发有效的癌症疫苗提供了机会。