Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea.
Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea; GENOME INSIGHT Inc., Daejeon 34051, Republic of Korea.
J Hepatol. 2024 Nov;81(5):806-818. doi: 10.1016/j.jhep.2024.06.011. Epub 2024 Jun 13.
BACKGROUND & AIMS: Chronic HCV infection results in abnormal immunological alterations, which are not fully normalized after viral elimination by direct-acting antiviral (DAA) treatment. Herein, we longitudinally examined phenotypic, transcriptomic, and epigenetic alterations in peripheral blood regulatory T (Treg) cells from patients with chronic HCV infection before, during, and after DAA treatment.
Patients with chronic genotype 1b HCV infection who achieved sustained virologic response by DAA treatment and age-matched healthy donors were recruited. Phenotypic characteristics of Treg cells were investigated through flow cytometry analysis. Moreover, the transcriptomic and epigenetic landscapes of Treg cells were analyzed using RNA sequencing and ATAC-seq (assay for transposase-accessible chromatin with sequencing) analysis.
The Treg cell population - especially the activated Treg cell subpopulation - was expanded in peripheral blood during chronic HCV infection, and this expansion was sustained even after viral clearance. RNA sequencing analysis revealed that viral clearance did not abrogate the inflammatory features of these Treg cells, such as Treg activation and TNF signaling. Moreover, ATAC-seq analysis showed inflammatory imprinting in the epigenetic landscape of Treg cells from patients, which remained after treatment. These findings were further confirmed by intracellular cytokine staining, demonstrating that Treg cells exhibited inflammatory features and TNF production in chronic HCV infection that were maintained after viral clearance.
Overall, our results showed that during chronic HCV infection, the expanded Treg cell population acquired inflammatory features at phenotypic, transcriptomic, and epigenetic levels, which were maintained even after successful viral elimination by DAA treatment. Further studies are warranted to examine the clinical significance of sustained inflammatory features in the Treg cell population after recovery from chronic HCV infection.
During chronic HCV infection, several immune components are altered both quantitatively and qualitatively. The recent introduction of direct-acting antivirals has led to high cure rates. Nevertheless, we have demonstrated that inflammatory features of Treg cells are maintained at phenotypic, transcriptomic, and epigenetic levels even after successful DAA treatment. Further in-depth studies are required to investigate the long-term clinical outcomes of patients who have recovered from chronic HCV infection.
慢性 HCV 感染导致免疫异常,这些异常在直接作用抗病毒 (DAA) 治疗清除病毒后并未完全恢复正常。在此,我们纵向研究了慢性 HCV 感染患者在 DAA 治疗前、治疗中和治疗后外周血调节性 T (Treg) 细胞的表型、转录组和表观遗传改变。
招募了慢性基因型 1b HCV 感染并通过 DAA 治疗获得持续病毒学应答的患者和年龄匹配的健康供体。通过流式细胞术分析研究 Treg 细胞的表型特征。此外,还通过 RNA 测序和 ATAC-seq(用于转座酶可及染色质测序的分析)分析研究了 Treg 细胞的转录组和表观遗传景观。
在慢性 HCV 感染期间,外周血中 Treg 细胞群体 - 特别是激活的 Treg 细胞亚群 - 扩增,并且这种扩增在病毒清除后仍持续存在。RNA 测序分析表明,病毒清除并未消除这些 Treg 细胞的炎症特征,如 Treg 激活和 TNF 信号。此外,ATAC-seq 分析显示患者 Treg 细胞的表观遗传景观中存在炎症印迹,并且在治疗后仍然存在。这些发现通过细胞内细胞因子染色进一步得到证实,表明在慢性 HCV 感染中 Treg 细胞表现出炎症特征和 TNF 产生,并且在病毒清除后仍然存在。
总的来说,我们的结果表明,在慢性 HCV 感染期间,扩增的 Treg 细胞群体在表型、转录组和表观遗传水平上获得了炎症特征,并且在 DAA 治疗成功清除病毒后仍然存在。需要进一步研究以检查慢性 HCV 感染后从恢复中 Treg 细胞群体持续炎症特征的临床意义。
在慢性 HCV 感染期间,多个免疫成分在数量和质量上都发生了改变。直接作用抗病毒药物的最近引入导致了高治愈率。然而,我们已经证明,即使在成功的 DAA 治疗后,Treg 细胞的炎症特征在表型、转录组和表观遗传水平上仍然存在。需要进一步深入研究以调查从慢性 HCV 感染中恢复的患者的长期临床结局。