Vapniarsky Natalia, Simpson David L, Arzi Boaz, Taechangam Nopmanee, Walker Naomi J, Garrity Carissa, Bulkeley Evelyn, Borjesson Dori L
School of Veterinary Medicine, Veterinary Institute for Regenerative Cures, University of California, Davis, Davis, CA, United States.
Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, Davis, CA, United States.
Front Vet Sci. 2020 Jun 3;7:310. doi: 10.3389/fvets.2020.00310. eCollection 2020.
Feline chronic gingivostomatitis (FCGS) is an immune-mediated inflammatory condition affecting the oral mucosa that results in substantial pain and suffering. The goal of this study was to complete an in-depth immunohistochemistry analysis of affected FCGS mucosa, to perform and compare immune cell phenotypes in the blood of FCGS and healthy controls cats, and to determine a transcriptomic profile of the affected and normal oral mucosa of FCGS cats. We hypothesized that cats with FCGS would have circulating activated CD8+ T cells and that tissues would be infiltrated with activated B and T cells with a highly proinflammatory transcriptome. We found that oral mucosal tissues from cats with FCGS have high tissue infiltration of B cells and that T cells include both CD4+ and CD8+ lymphocytes. Cells positive for CD25 (IL2 receptor, indicative of lymphocyte activation) and FOXP3 (indicative of regulatory T cells) were scattered throughout the mucosa. Compared to healthy individuals, cats with FCGS had high circulating CD8+ effector memory cells with a concurrent decrease in central memory cells and evidence of circulating activated CD8+ T cells (CD25+, CD62L-). Gene expression in the affected tissues was enriched for genes associated with T-cell signaling, cell adhesion molecules, leukocyte migration, inflammatory signaling pathways, extracellular matrix-receptor interactions, cytokine-cytokine receptor interactions, and natural killer cell-mediated cytotoxicity, among others. These data are essential to understand disease pathogenesis, to inform mechanism of action studies for future and current therapies, and to help select prognostic biomarkers and potency assays for stem cell treatment of FCGS.
猫慢性龈口炎(FCGS)是一种影响口腔黏膜的免疫介导性炎症疾病,会导致严重的疼痛和痛苦。本研究的目的是对受影响的FCGS黏膜进行深入的免疫组织化学分析,对FCGS猫和健康对照猫的血液中的免疫细胞表型进行检测和比较,并确定FCGS猫受影响和正常口腔黏膜的转录组概况。我们假设患有FCGS的猫会有循环活化的CD8 + T细胞,并且组织会被具有高度促炎转录组的活化B细胞和T细胞浸润。我们发现,患有FCGS的猫的口腔黏膜组织有大量B细胞浸润,并且T细胞包括CD4 +和CD8 +淋巴细胞。CD25(IL2受体,指示淋巴细胞活化)和FOXP3(指示调节性T细胞)阳性的细胞散布在整个黏膜中。与健康个体相比,患有FCGS的猫有高循环CD8 +效应记忆细胞,同时中央记忆细胞减少,并有循环活化CD8 + T细胞(CD25 +,CD62L -)的证据。受影响组织中的基因表达富集了与T细胞信号传导、细胞粘附分子、白细胞迁移、炎症信号通路、细胞外基质 - 受体相互作用、细胞因子 - 细胞因子受体相互作用以及自然杀伤细胞介导的细胞毒性等相关的基因。这些数据对于理解疾病发病机制、为未来和当前治疗的作用机制研究提供信息以及帮助选择FCGS干细胞治疗的预后生物标志物和效力测定至关重要。