Department of Medical Genetics, University of Oslo and Oslo University Hospital, Oslo, Norway.
K. G. Jebsen Inflammation Research Centre, University of Oslo, Oslo, Norway.
Front Immunol. 2021 Nov 18;12:713611. doi: 10.3389/fimmu.2021.713611. eCollection 2021.
Methotrexate (MTX) is the first line treatment of rheumatoid arthritis (RA), and methylation changes in bulk T cells have been reported after treatment with MTX. We have investigated cell-type specific DNA methylation changes across the genome in naïve and memory CD4 T cells before and after MTX treatment of RA patients. DNA methylation profiles of newly diagnosed RA patients (N=9) were assessed by reduced representation bisulfite sequencing.
We found that MTX treatment significantly influenced DNA methylation levels at multiple CpG sites in both cell populations. Interestingly, we identified differentially methylated sites annotated to two genes; and , previously reported to predict treatment outcome in RA patients when measured in bulk T cells. Furthermore, several of the genes, including , annotated to the significant CpG sites are relevant for RA susceptibility or the action of MTX.
We detected CpG sites that were associated with MTX treatment in CD4 naïve and memory T cells isolated from RA patients. Several of these sites overlap genetic regions previously associated with RA risk and MTX treatment outcome.
甲氨蝶呤(MTX)是类风湿关节炎(RA)的一线治疗药物,并且在接受 MTX 治疗后, bulk T 细胞中的甲基化变化已有报道。我们研究了 RA 患者接受 MTX 治疗前后 naïve 和记忆 CD4 T 细胞中整个基因组的细胞类型特异性 DNA 甲基化变化。通过简化代表性亚硫酸氢盐测序评估了新诊断的 RA 患者(N=9)的 DNA 甲基化图谱。
我们发现 MTX 治疗在两种细胞群中的多个 CpG 位点显著影响 DNA 甲基化水平。有趣的是,我们鉴定了两个基因中注释的差异甲基化位点; 和 ,当在 bulk T 细胞中测量时,先前报道可预测 RA 患者的治疗结果。此外,包括 在内的几个注释到显著 CpG 位点的基因与 RA 易感性或 MTX 的作用有关。
我们在从 RA 患者中分离的 CD4 naïve 和记忆 T 细胞中检测到与 MTX 治疗相关的 CpG 位点。其中一些位点与先前与 RA 风险和 MTX 治疗结果相关的遗传区域重叠。