Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Department of Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.
Science. 2018 Nov 9;362(6415):694-699. doi: 10.1126/science.aat5030.
During the process of cross-presentation, viral or tumor-derived antigens are presented to CD8 T cells by dependent CD8α/XCR1 classical dendritic cells (cDC1s). We designed a functional CRISPR screen for previously unknown regulators of cross-presentation, and identified the BEACH domain-containing protein WDFY4 as essential for cross-presentation of cell-associated antigens by cDC1s in mice. However, WDFY4 was not required for major histocompatibility complex class II presentation, nor for cross-presentation by monocyte-derived dendritic cells. In contrast to mice, mice displayed normal lymphoid and nonlymphoid cDC1 populations that produce interleukin-12 and protect against infection. However, similar to mice, mice failed to prime virus-specific CD8 T cells in vivo or induce tumor rejection, revealing a critical role for cross-presentation in antiviral and antitumor immunity.
在交叉呈递过程中,病毒或肿瘤衍生抗原由依赖 CD8α/XCR1 的经典树突状细胞 (cDC1) 呈递给 CD8 T 细胞。我们设计了一个功能性 CRISPR 筛选,用于寻找未知的交叉呈递调节因子,发现含有 BEACH 结构域的蛋白 WDFY4 是 cDC1 呈递细胞相关抗原所必需的。然而,WDFY4 对于 MHC Ⅱ类呈递以及单核细胞衍生树突状细胞的交叉呈递并非必需。与 小鼠不同, 小鼠显示正常的淋巴样和非淋巴样 cDC1 群体,能够产生白细胞介素-12 并抵抗 感染。然而,与 小鼠类似, 小鼠未能在体内诱导病毒特异性 CD8 T 细胞或诱导肿瘤排斥,揭示了交叉呈递在抗病毒和抗肿瘤免疫中的关键作用。