Ogawa Y
Third Department of Internal Medicine, Ehime University School of Medicine, Japan.
Gastroenterol Jpn. 1988 Jun;23(3):279-86. doi: 10.1007/BF02779471.
The in vivo activity of the interferon (IFN) system was studied in 39 patients with chronic hepatitis B (CHB) and in 24 patients with chronic hepatitis type non-A, non-B (CHNANB). 2',5'-Oligoadenylate synthetase (2-5 A synthetase) activity was monitored in the liver and peripheral blood mononuclear cells (PBMCs). Liver 2-5 A synthetase activity was higher in HBeAg-positive CHB and CHNANB patients than in HBeAg-negative CHB patients or controls. The IFN system appeared to be preserved in CH patients. In HBeAg-positive CHB patients the changes in DNA-P activity indicated that PBMC 2-5 A synthetase activity depended on replication of hepatitis B virus(HBV). Exogenous IFN administration in patients with HBeAg-positive CHB significantly elevated 2-5 A synthetase activity in PBMCs, as well as in the liver. In measurement of 2-5 A synthetase activity of CHB patients, the IFN system seems to be important in regulating HBV replication and in the exacerbation of liver inflammatory activity.
对39例慢性乙型肝炎(CHB)患者和24例非甲非乙型慢性肝炎(CHNANB)患者的体内干扰素(IFN)系统活性进行了研究。监测了肝脏和外周血单个核细胞(PBMC)中的2',5'-寡腺苷酸合成酶(2-5A合成酶)活性。HBeAg阳性的CHB和CHNANB患者的肝脏2-5A合成酶活性高于HBeAg阴性的CHB患者或对照组。CH患者的IFN系统似乎是完整的。在HBeAg阳性的CHB患者中,DNA-P活性的变化表明PBMC的2-5A合成酶活性取决于乙型肝炎病毒(HBV)的复制。对HBeAg阳性的CHB患者给予外源性IFN可显著提高PBMC以及肝脏中的2-5A合成酶活性。在检测CHB患者的2-5A合成酶活性时,IFN系统似乎在调节HBV复制和加剧肝脏炎症活动方面具有重要作用。