Functional Genomics and Systems Biology Group, Department of Bioinformatics, Biocenter, Julius-Maximilians-University Würzburg, Würzburg, Germany.
Institute of Immunology, Jena University Hospital, Friedrich-Schiller-University, Jena, Germany.
Commun Biol. 2024 Jul 18;7(1):879. doi: 10.1038/s42003-024-06563-1.
In clinical situations, peripheral blood accessible CD3CD4CXCR5 T-follicular helper (T) cells may have to serve as a surrogate indicator for dysregulated germinal center responses in tissues. To determine the heterogeneity of T cells in peripheral blood versus tonsils, CD3CD4CD45RACXCR5 cells of both origins were sorted. Transcriptomes, TCR repertoires and cell-surface protein expression were analysed by single-cell RNA sequencing, flow cytometry and immunohistochemistry. Reassuringly, all blood-circulating CD3CD4CXCR5 T-cell subpopulations also appear in tonsils, there with some supplementary T characteristics, while peripheral blood-derived T cells display markers of proliferation and migration. Three further subsets of T cells, however, with bona fide T-follicular gene expression patterns, are exclusively found in tonsils. One additional, distinct and oligoclonal CD4CXCR5 subpopulation presents pronounced cytotoxic properties. Those 'killer T (T) cells' can be discovered in peripheral blood as well as among tonsillar cells but are located predominantly outside of germinal centers. They appear terminally differentiated and can be distinguished from all other T subsets by expression of NKG7 (TIA-1), granzymes, perforin, CCL5, CCR5, EOMES, CRTAM and CX3CR1. All in all, this study provides data for detailed CD4CXCR5 T-cell assessment of clinically available blood samples and extrapolation possibilities to their tonsil counterparts.
在临床情况下,外周血中可获得的 CD3CD4CXCR5 T 滤泡辅助 (Tfh) 细胞可能不得不作为组织中失调的生发中心反应的替代指标。为了确定外周血与扁桃体中 T 细胞的异质性,对两种来源的 CD3CD4CD45RACXCR5 细胞进行了分选。通过单细胞 RNA 测序、流式细胞术和免疫组织化学分析了转录组、TCR 库和细胞表面蛋白表达。令人欣慰的是,所有外周血循环中的 CD3CD4CXCR5 T 细胞亚群也出现在扁桃体中,具有一些补充的 T 特征,而外周血来源的 T 细胞显示出增殖和迁移的标志物。然而,还有另外三个具有真正 T 滤泡基因表达模式的 T 细胞亚群仅在扁桃体中发现。一个额外的、独特的和寡克隆的 CD4CXCR5 亚群表现出明显的细胞毒性。这些“杀伤性 T (T) 细胞”可以在外周血以及扁桃体细胞中发现,但主要位于生发中心之外。它们表现出终末分化,可以通过表达 NKG7(TIA-1)、颗粒酶、穿孔素、CCL5、CCR5、EOMES、CRTAM 和 CX3CR1 与所有其他 T 亚群区分开来。总而言之,这项研究为详细评估临床可用的血液样本中的 CD4CXCR5 T 细胞提供了数据,并为推断其扁桃体对应物提供了可能性。