Trapero-Marugán M, García-Buey L, Muñoz C, Quintana N E, Moreno-Monteagudo J A, Borque M J, Fernández M J, Salvanés F R, Medina J, Moreno-Otero R
Gastroenterology and Hepatology Service, Hospital Universitario de La Princesa, Madrid, Spain.
Aliment Pharmacol Ther. 2006 Jul 1;24(1):117-28. doi: 10.1111/j.1365-2036.2006.02954.x.
An impairment of cellular immune response may contribute to the persistency of hepatitis C virus infection.
To analyse the Th1/Th2 cytokine profile in peripheral blood CD4(+) and CD8(+) T cells from patients with chronic hepatitis C (CHC) during treatment with pegylated interferon-alpha2a plus ribavirin and to correlate the Th1/Th2 balance with virological response (SVR).
Prospective longitudinal study: 44 naïve genotype 1 CHC patients received PEG-IFNalpha2a plus ribavirin for 48 weeks: 26 (59.1%) achieved a SVR, 13 relapsed (29.5%) and 5 (11.4%) were non-responders. Sixteen healthy controls were analysed. The production of IL-4, IFNgamma and TNFalpha by CD4(+) and CD8(+) T cells was measured using flow cytometry, both in resting and phorbol-ester-stimulated cells.
First three months of treatment: the synthesis of TNFalpha by phorbol-ester-stimulated-CD4(+) T cells was higher in patients with SVR (P < 0.01). At the end of treatment, SVR was associated with higher intracellular expression of IFNgamma by stimulated-CD4(+) and CD8(+) T cells (P < 0.05). At the end of follow-up, a higher intracellular expression of IFNgamma by CD4(+) T cells was associated with a SVR.
A Th1-type immune response was associated with achievement of a SVR, as indicated by the persistent elevation of intracellular IFNgamma and TNFalpha.
细胞免疫反应受损可能导致丙型肝炎病毒感染持续存在。
分析慢性丙型肝炎(CHC)患者在接受聚乙二醇化干扰素-α2a联合利巴韦林治疗期间外周血CD4(+)和CD8(+) T细胞中的Th1/Th2细胞因子谱,并将Th1/Th2平衡与病毒学应答(SVR)相关联。
前瞻性纵向研究:44例初治基因1型CHC患者接受聚乙二醇干扰素-α2a联合利巴韦林治疗48周:26例(59.1%)实现SVR,13例复发(29.5%),5例(11.4%)无应答。分析了16名健康对照者。使用流式细胞术测量静息和佛波酯刺激细胞中CD4(+)和CD8(+) T细胞产生的IL-4、IFNγ和TNFα。
治疗的前三个月:SVR患者中佛波酯刺激的CD4(+) T细胞产生的TNFα更高(P < 0.01)。治疗结束时,SVR与刺激的CD4(+)和CD8(+) T细胞中IFNγ的细胞内表达较高相关(P < 0.05)。随访结束时,CD4(+) T细胞中IFNγ的细胞内表达较高与SVR相关。
如细胞内IFNγ和TNFα持续升高所示,Th1型免疫反应与实现SVR相关。