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慢性丙型肝炎感染患者在干扰素和利巴韦林治疗前及治疗期间T淋巴细胞亚群的变化。

Modifications of T-lymphocyte subsets before and during interferon and ribavirin treatment for chronic hepatitis C infection.

作者信息

Neau-Cransac Martine, Foucher Juliette, Ledinghen Victor De, Bernard Pierre-Henri, Legrand Elisabeth, Lafon Marie-Edith

机构信息

Immunology Laboratory, Pellegrin Hospital, Place Amélie Raba Léon, 33076 Bordeaux, France.

出版信息

Viral Immunol. 2005;18(1):197-204. doi: 10.1089/vim.2005.18.197.

Abstract

Our purpose was to determine in HCV-infected patients whether T-lymphocyte sub-populations were modified before and during interferon-alpha and ribavirin treatment, and whether this correlated with virological response. Twenty-two naive patients were given IFN-alpha 3 Million Units three times per week for 24 or 48 weeks and ribavirin. Sustained virological response corresponded to undetectable serum HCV RNA at treatment completion and 6 months later. Total blood lymphocyte counts and CD3(+)CD4(+), CD3(+)CD8(+), CD3(+)CD4(+)HLA-DR(+), and CD3(+)CD8(+)HLA-DR(+) lymphocyte subsets evaluated before, during, and after treatment were compared to values from 37 healthy subjects. At inclusion, patients and controls had similar total lymphocyte counts. CD3(+)CD4(+) counts and percentages were significantly higher in HCV patients. HLA-DR expression was also increased in CD4(+) (p < 0.0001) and CD8(+) T-cells (p = 0.0008) as compared with controls. During treatment, all lymphocyte subset counts and percentage decreased except the CD3(+)CD4(+) T-cell percentage which increased. Moreover, after 1 month of treatment, virological responders exhibited higher CD4(+) counts than nonresponders (p = 0.025), whereas they did not differ at inclusion or during the 2nd to 6th months of treatment. After treatment completion, all populations returned to baseline values. These results suggest that CD3(+)CD4(+) T-lymphocyte percentage increase under treatment could be related to IFN immunomodulation and associated with virological response.

摘要

我们的目的是确定在丙型肝炎病毒(HCV)感染患者中,α干扰素和利巴韦林治疗前及治疗期间T淋巴细胞亚群是否发生改变,以及这是否与病毒学应答相关。22例初治患者接受每周3次、每次300万单位的α干扰素治疗,疗程为24或48周,并同时服用利巴韦林。持续病毒学应答定义为治疗结束时及6个月后血清HCV RNA检测不到。将治疗前、治疗期间及治疗后的全血淋巴细胞计数以及CD3(+)CD4(+)、CD3(+)CD8(+)、CD3(+)CD4(+)HLA-DR(+)和CD3(+)CD8(+)HLA-DR(+)淋巴细胞亚群与37名健康受试者的值进行比较。纳入研究时,患者和对照组的总淋巴细胞计数相似。HCV患者的CD3(+)CD4(+)计数和百分比显著更高。与对照组相比,CD4(+)(p < 0.0001)和CD8(+) T细胞(p = 0.0008)中的HLA-DR表达也增加。治疗期间,除CD3(+)CD4(+) T细胞百分比增加外,所有淋巴细胞亚群的计数和百分比均下降。此外,治疗1个月后,病毒学应答者的CD4(+)计数高于无应答者(p = 0.025),而在纳入研究时或治疗的第2至6个月期间两者无差异。治疗结束后,所有群体均恢复至基线值。这些结果表明,治疗期间CD3(+)CD4(+) T淋巴细胞百分比增加可能与干扰素免疫调节有关,并与病毒学应答相关。

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