Department of Immunology and Microbiology, Scripps Research, La Jolla, California, United States of America.
Department of Molecular Biosciences, University of Kansas, Lawrence, Kansas, United States of America.
PLoS Pathog. 2024 Mar 21;20(3):e1012095. doi: 10.1371/journal.ppat.1012095. eCollection 2024 Mar.
The 1858C>T allele of the tyrosine phosphatase PTPN22 is present in 5-10% of the North American population and is strongly associated with numerous autoimmune diseases. Although research has been done to define how this allele potentiates autoimmunity, the influence PTPN22 and its pro-autoimmune allele has in anti-viral immunity remains poorly defined. Here, we use single cell RNA-sequencing and functional studies to interrogate the impact of this pro-autoimmune allele on anti-viral immunity during Lymphocytic Choriomeningitis Virus clone 13 (LCMV-cl13) infection. Mice homozygous for this allele (PEP-619WW) clear the LCMV-cl13 virus whereas wildtype (PEP-WT) mice cannot. This is associated with enhanced anti-viral CD4 T cell responses and a more immunostimulatory CD8α- cDC phenotype. Adoptive transfer studies demonstrated that PEP-619WW enhanced anti-viral CD4 T cell function through virus-specific CD4 T cell intrinsic and extrinsic mechanisms. Taken together, our data show that the pro-autoimmune allele of Ptpn22 drives a beneficial anti-viral immune response thereby preventing what is normally a chronic virus infection.
酪氨酸磷酸酶 PTPN22 的 1858C>T 等位基因存在于北美人群的 5-10%中,与许多自身免疫性疾病强烈相关。尽管已经进行了研究来定义该等位基因如何增强自身免疫,但 PTPN22 及其促自身免疫等位基因对抗病毒免疫的影响仍未得到充分定义。在这里,我们使用单细胞 RNA 测序和功能研究来探究该促自身免疫等位基因对淋巴细胞性脉络丛脑膜炎病毒克隆 13(LCMV-cl13)感染期间抗病毒免疫的影响。该等位基因纯合子(PEP-619WW)的小鼠清除了 LCMV-cl13 病毒,而野生型(PEP-WT)小鼠则不能。这与增强的抗病毒 CD4 T 细胞反应和更具免疫刺激性的 CD8α-cDC 表型有关。过继转移研究表明,PEP-619WW 通过病毒特异性 CD4 T 细胞内在和外在机制增强了抗病毒 CD4 T 细胞的功能。总之,我们的数据表明,Ptpn22 的促自身免疫等位基因驱动了有益的抗病毒免疫反应,从而防止了通常是慢性病毒感染。