Laboratory of Molecular Neuro-Oncology, The Rockefeller University, New York, New York, USA.
Howard Hughes Medical Institute, New York, New York, USA.
JCI Insight. 2017 Nov 2;2(21):96173. doi: 10.1172/jci.insight.96173.
In the course of modeling the naturally occurring tumor immunity seen in patients with paraneoplastic cerebellar degeneration (PCD), we discovered an unexpectedly high threshold for breaking CD8+ cytotoxic T cell (CTL) tolerance to the PCD autoantigen, CDR2. While CDR2 expression was previously found to be strictly restricted to immune-privileged cells (cerebellum, testes, and tumors), unexpectedly we have found that T cells also express CDR2. This expression underlies inhibition of CTL activation; CTLs that respond to epithelial cells expressing CDR2 fail to respond to T cells expressing CDR2. This was a general phenomenon, as T cells presenting influenza (flu) antigen also fail to activate otherwise potent flu-specific CTLs either in vitro or in vivo. Moreover, transfer of flu peptide-pulsed T cells into flu-infected mice inhibits endogenous flu-specific CTLs. Our finding that T cells serve as a site of immune privilege, inhibiting effector CTL function, uncovers an autorepressive loop with general biologic and clinical relevance.
在对副肿瘤性小脑变性 (PCD) 患者中自然发生的肿瘤免疫进行建模的过程中,我们发现打破 CD8+细胞毒性 T 细胞 (CTL) 对 PCD 自身抗原 CDR2 的耐受具有出乎意料的高阈值。虽然先前发现 CDR2 的表达严格限于免疫特权细胞(小脑、睾丸和肿瘤),但出乎意料的是,我们发现 T 细胞也表达 CDR2。这种表达是 CTL 激活抑制的基础;对表达 CDR2 的上皮细胞作出反应的 CTL 无法对表达 CDR2 的 T 细胞作出反应。这是一种普遍现象,因为呈递流感 (flu) 抗原的 T 细胞也无法在体外或体内激活原本有效的 flu 特异性 CTL。此外,将流感肽脉冲 T 细胞转移到流感感染的小鼠中会抑制内源性 flu 特异性 CTL。我们发现 T 细胞作为免疫特权部位,抑制效应 CTL 功能,揭示了具有普遍生物学和临床相关性的自身抑制回路。