Lord E M, Frelinger J G
Department of Microbiology and Immunology, University of Rochester Medical Center, NY 14642, USA.
Cancer Immunol Immunother. 1998 Apr;46(2):75-81. doi: 10.1007/s002620050464.
Increasing the ability of tumor-reactive T cells to mediate tumor regression in vivo has been a major goal of tumor immunologists. Progress toward this goal has been aided by the identification of tumor-associated antigens on both experimental mouse tumors and human tumors. However, the self-like nature and low immunogenicity of these antigens has made it clear that other measures to enhance the effectiveness of the T cells reactive to these antigens are essential if immunotherapy is to be clinically effective. An increased understanding of antigen processing and presentation is an important step in this process, as is the use of cytokines to increase immune responsiveness. Despite recent advances, there is still much to be learned before the specificity of the immune system is safely harnessed to halt malignant cell growth effectively.
提高肿瘤反应性T细胞在体内介导肿瘤消退的能力一直是肿瘤免疫学家的主要目标。在实验小鼠肿瘤和人类肿瘤上鉴定出肿瘤相关抗原,有助于实现这一目标。然而,这些抗原的自身样性质和低免疫原性表明,如果免疫疗法要在临床上有效,采取其他措施来增强对这些抗原产生反应的T细胞的有效性至关重要。增进对抗原加工和呈递的理解是这一过程中的重要一步,使用细胞因子来提高免疫反应性也是如此。尽管最近取得了进展,但在安全利用免疫系统的特异性以有效阻止恶性细胞生长之前,仍有许多需要了解的地方。