Woodring Therese, Dewey Colin N, Santos Dias Lucas Dos, He Xin, Dobson Hannah E, Wüthrich Marcel, Klein Bruce
Departments of Pediatrics, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, Madison WI, USA.
Biostatistics and Medical Informatics, University of Wisconsin School of Medicine and Public Health, University of Wisconsin-Madison, Madison WI, USA.
iScience. 2022 Aug 13;25(9):104934. doi: 10.1016/j.isci.2022.104934. eCollection 2022 Sep 16.
Memory T cells underpin vaccine-induced immunity but are not yet fully understood. To distinguish features of memory cells that confer protective immunity, we used single cell transcriptome analysis to compare antigen-specific CD4T cells recalled to lungs of mice that received a protective or nonprotective subunit vaccine followed by challenge with a fungal pathogen. We unexpectedly found populations specific to protection that expressed a strong type I interferon response signature, whose distinctive transcriptional signature appeared unconventionally dependent on IFN-γ receptor. We also detected a unique population enriched in protection that highly expressed the gene for the natural killer cell marker NKG7. Lastly, we detected differences in TCR gene use and in Th1- and Th17-skewed responses after protective and nonprotective vaccine, respectively, reflecting heterogeneous - and expressing populations. Our findings highlight key features of transcriptionally diverse and distinctive antigen-specific T cells associated with protective vaccine-induced immunity.
记忆T细胞是疫苗诱导免疫的基础,但尚未被完全理解。为了区分赋予保护性免疫的记忆细胞特征,我们使用单细胞转录组分析来比较被召回至接受保护性或非保护性亚单位疫苗接种后再用真菌病原体攻击的小鼠肺部的抗原特异性CD4 T细胞。我们意外地发现了与保护相关的细胞群体,它们表达强烈的I型干扰素反应特征,其独特的转录特征非常规地依赖于IFN-γ受体。我们还检测到一个在保护中富集的独特细胞群体,其高度表达自然杀伤细胞标志物NKG7的基因。最后,我们分别检测到保护性和非保护性疫苗接种后TCR基因使用以及Th1和Th17偏向反应的差异,反映了异质性和表达群体。我们的研究结果突出了与保护性疫苗诱导免疫相关的转录多样且独特的抗原特异性T细胞的关键特征。