Department of Infectious Diseases, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China.
Can J Gastroenterol Hepatol. 2017;2017:3612403. doi: 10.1155/2017/3612403. Epub 2017 May 8.
Up to now, little was known about the immunological changes of chronic hepatitis C (CHC) patients treated with direct-acting antiviral agents (DAAs); we try to explore the effect of DAAs on the frequency of monocytes, NK cells, and cytokines that promote their activation.
15 treatment-naive CHC patients and 10 healthy controls were recruited. Patients were examined before DAAs therapy (0 w) and at week 4 (4 w) and week 12 (12 w) of therapy. Percentage of monocytes and NK cells of the peripheral blood was analyzed by flow cytometry. Serum cytokines IL-12, IL-18, CXCL10, CXCL11, sCD14, and sCD163 were measured by enzyme linked immunosorbent assay.
The frequency of CD3CD16CD56 NK cells and classic CD14CD16 monocytes decreased, while CD14CD16 monocytes and cytokines IL-12, IL-18, CXCL10, CXCL11, sCD14, and sCD163 increased at 0 w compared to healthy controls. During DAAs treatment, the decreased NK cells and classic monocytes gradually increased to normal levels; the increased inflammatory monocytes and cytokines IL-12 and CXCL11 decreased to normal levels, but the increased cytokines IL-18, CXCL10, sCD14, and sCD163 still remained at high levels at 12 w though they decreased rapidly from 0 w.
Our results showed that DAAs treatment attenuated the activation of monocytes and NK cells in CHC patients. Trial registration number is NCT03063723.
目前,我们对于直接作用抗病毒药物(DAAs)治疗慢性丙型肝炎(CHC)患者的免疫变化知之甚少;我们试图探讨 DAAs 对单核细胞、NK 细胞频率以及促进其激活的细胞因子的影响。
招募了 15 名未经治疗的 CHC 患者和 10 名健康对照者。在 DAAs 治疗前(0 周)以及治疗第 4 周(4 周)和第 12 周(12 周)对患者进行检查。通过流式细胞术分析外周血单核细胞和 NK 细胞的比例。通过酶联免疫吸附试验测量血清细胞因子 IL-12、IL-18、CXCL10、CXCL11、sCD14 和 sCD163。
与健康对照组相比,0 周时 CD3CD16CD56 NK 细胞和经典 CD14CD16 单核细胞频率降低,而 CD14CD16 单核细胞和细胞因子 IL-12、IL-18、CXCL10、CXCL11、sCD14 和 sCD163 增加。在 DAAs 治疗期间,减少的 NK 细胞和经典单核细胞逐渐增加至正常水平;增加的炎性单核细胞和细胞因子 IL-12 和 CXCL11 降低至正常水平,但增加的细胞因子 IL-18、CXCL10、sCD14 和 sCD163 在 12 周时仍保持在高水平,尽管它们从 0 周开始迅速下降。
我们的结果表明,DAAs 治疗减轻了 CHC 患者单核细胞和 NK 细胞的激活。试验注册号为 NCT03063723。