Department of Clinical Oncology, Leiden University Medical Center, Netherlands.
Curr Opin Immunol. 2011 Apr;23(2):293-8. doi: 10.1016/j.coi.2010.12.005. Epub 2011 Feb 4.
Defects in MHC-I antigen presentation represent a common feature of cancer and allow evasion from T cell recognition. Recent findings from immunotherapy in melanoma suggested that irreversible MHC-I defects enable escape from immune pressure. Although loss of antigen presentation is known for many years, strategies to counteract these defects are scarce and largely unexamined. Now that the first forms of T-cell-based immunotherapy show clinical efficacy and reach FDA approval, this issue deserves urgent awareness. Here we describe possible roads leading to corrections of MHC-I defects in tumors and describe a salvage pathway for CTL by targeting novel tumor antigens that we recently uncovered.
MHC-I 抗原呈递缺陷是癌症的一个常见特征,使肿瘤细胞逃避 T 细胞的识别。最近黑色素瘤的免疫疗法的发现表明,MHC-I 的不可逆缺陷可使其逃避免疫压力。尽管抗原呈递缺失已被人们认识多年,但针对这些缺陷的策略却很少,且很大程度上尚未被研究。现在,基于 T 细胞的免疫疗法的首次应用已经显示出临床疗效,并获得了 FDA 的批准,因此这个问题值得引起人们的关注。在这里,我们描述了可能的纠正肿瘤中 MHC-I 缺陷的途径,并描述了我们最近发现的一种针对新的肿瘤抗原的 CTL 挽救途径。