Department of Physiological Sciences, Institute of Veterinary Medicine, Warsaw University of Life Sciences (SGGW), Nowoursynowska 159, 02-776 Warsaw, Poland.
Department of Small Animal Diseases and Clinic, Institute of Veterinary Medicine, Warsaw University of Life Sciences (SGGW), Nowoursynowska 159, 02-776 Warsaw, Poland.
Int J Mol Sci. 2023 Jul 18;24(14):11616. doi: 10.3390/ijms241411616.
Canine atopic dermatitis (cAD) is a genetic, chronic, and recurrent inflammatory and pruritic skin disorder. Allergen-specific immunotherapy (ASIT) is presently recognized as the only clinically effective disease-modifying treatment for allergies. The aim of our study was to analyze the changes in gene expression observed in the peripheral blood nuclear cells of cAD patients subjected to ASIT. Blood samples designated for transcriptomic analyses were collected from AD dogs twice, before and six months after ASIT, and also from healthy dogs. Statistical analysis revealed 521 differentially expressed transcripts, among which 241 transcripts represented genes with well-described functions. Based on the available literature, we chose nine differentially expressed genes (, , , , , , , , and ) which may be important in the context of the dysregulated immune response observed in cAD patients. The expressions of five out of the nine described genes (, , , , and ) changed after the application of ASIT. The expressions of three of these genes returned to the level observed in the healthy control group. The genes listed above need further investigation to determine details of their role in the molecular mechanism of immune tolerance induction in response to allergen-specific immunotherapy.
犬特应性皮炎(cAD)是一种遗传的、慢性的、复发性的炎症性和瘙痒性皮肤病。过敏原特异性免疫疗法(ASIT)目前被认为是治疗过敏的唯一具有临床疗效的疾病修正治疗方法。我们的研究目的是分析接受 ASIT 的 cAD 患者外周血核细胞中观察到的基因表达变化。用于转录组分析的血液样本从 AD 犬身上采集两次,分别在 ASIT 前和 ASIT 后 6 个月,也从健康犬身上采集。统计分析显示有 521 个差异表达的转录本,其中 241 个转录本代表具有明确功能的基因。根据现有文献,我们选择了九个差异表达的基因(,,,,,,,和),这些基因在 cAD 患者中观察到的失调免疫反应中可能很重要。在应用 ASIT 后,其中 5 个描述基因(,,,,和)的表达发生了变化。其中 3 个基因的表达恢复到健康对照组观察到的水平。上述基因需要进一步研究,以确定它们在过敏原特异性免疫治疗诱导免疫耐受的分子机制中的作用细节。