Hayata T, Nakano Y, Yoshizawa K, Sodeyama T, Kiyosawa K
Second Department of Internal Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
Hepatology. 1991 Jun;13(6):1022-8.
We investigated the effects of interferon therapy on hepatocyte human leukocyte antigen class I and class II antigen expression and intrahepatic lymphocyte subsets in patients with chronic viral hepatitis B (n = 11) and C (n = 10). Interferon-alpha was administered intramuscularly in doses ranging from 3 to 18 million international units daily for 4 wk. Liver biopsy specimens were obtained just before and immediately after treatment, and the specimens were stained by the indirect immunoperoxidase method for evaluation of human leukocyte antigen expression and lymphocyte subsets. Before therapy, no significant difference was noted between hepatitis B and C in human leukocyte antigen class I antigen expression on hepatocytes or in the lymphocyte subsets in the intralobular and portal areas. After interferon-alpha treatment, hepatocyte expression of human leukocyte antigen class I antigens and serum beta 2-microglobulin levels were virtually unchanged in chronic viral hepatitis C patients, but both were increased in chronic viral hepatitis B patients. Human leukocyte antigen class II antigens were not expressed during treatment. The mean number of intralobular CD3+ and CD8+ cells and the mean serum ALT level decreased significantly in chronic viral hepatitis C patients (p less than 0.05) but not in chronic viral hepatitis B patients. The mean number of intralobular CD4+ cells was unaffected by interferon therapy in both groups. In all 21 patients, the changes in CD8+ cell numbers paralleled the changes in serum ALT levels. Our findings suggest that T-cell cytotoxicity may play an important role in hepatocyte damage in both chronic viral hepatitis C and chronic viral hepatitis B and that the response to interferon-alpha differs in these two types of hepatitis.
我们研究了干扰素治疗对慢性乙型病毒性肝炎患者(n = 11)和慢性丙型病毒性肝炎患者(n = 10)肝细胞人类白细胞抗原I类和II类抗原表达以及肝内淋巴细胞亚群的影响。α干扰素通过肌肉注射给药,剂量为每日300万至1800万国际单位,共4周。在治疗前和治疗后立即获取肝活检标本,并用间接免疫过氧化物酶法对标本进行染色,以评估人类白细胞抗原表达和淋巴细胞亚群。治疗前,慢性乙型和丙型肝炎在肝细胞人类白细胞抗原I类抗原表达或小叶内和门管区的淋巴细胞亚群方面未观察到显著差异。α干扰素治疗后,慢性丙型病毒性肝炎患者肝细胞人类白细胞抗原I类抗原的表达和血清β2-微球蛋白水平基本未变,但慢性乙型病毒性肝炎患者两者均升高。治疗期间未表达人类白细胞抗原II类抗原。慢性丙型病毒性肝炎患者小叶内CD3 +和CD8 +细胞的平均数量以及血清ALT平均水平显著下降(p < 0.05),而慢性乙型病毒性肝炎患者则未下降。两组中小叶内CD4 +细胞的平均数量不受干扰素治疗的影响。在所有21例患者中,CD8 +细胞数量的变化与血清ALT水平的变化平行。我们的研究结果表明,T细胞细胞毒性可能在慢性丙型病毒性肝炎和慢性乙型病毒性肝炎的肝细胞损伤中起重要作用,并且这两种类型的肝炎对α干扰素的反应有所不同。