Georgiades J A
Georgiades Foundation for Therapy of Chronic Diseases, Stafford, TX 77477, USA.
Arch Immunol Ther Exp (Warsz). 1996;44(1):11-22.
A literature review of patients chronically infected with hepatitis B virus (HBV) treated with natural human interferon alpha (nHuIFN-alpha) given parenterally every day for 28 days revelated that even the daily dose of (5 x 10(6)IU) of IFN-alpha inhibits cellular metabolism. As a result of metabolic block, the number of blood elements were diminished. Furthermore treated patients recorded several different adverse reactions. In contrast, among patients treated with the oral form of nHuIFN-alpha non metabolic block occurred and no adverse reactions were seen, even though the therapy lasted much longer. Two years after initiation of parenteral IFN-alpha therapy, the loss of HBV-BeAg was 53.8% and 28.8% of the patients had undergone seroconversion. In contrast, 77% of patients on oral interferon lost HBV-BeAg and 74% serconverted and normalized their biochemical liver function. The results suggest that the nHuIFN-alpha given orally and parenterally activate two different mechanisms responsible for virus elimination.
一项关于慢性感染乙肝病毒(HBV)患者的文献综述显示,每天经肠胃外给予天然人干扰素α(nHuIFN-α)持续28天,即便干扰素α的每日剂量为(5×10⁶IU)也会抑制细胞代谢。由于代谢阻滞,血液成分数量减少。此外,接受治疗的患者出现了几种不同的不良反应。相比之下,口服nHuIFN-α治疗的患者未发生代谢阻滞,且未观察到不良反应,尽管治疗持续时间长得多。肠胃外干扰素α治疗开始两年后,HBV - e抗原消失率为53.8%,28.8%的患者发生了血清转换。相比之下,口服干扰素治疗的患者中77%的患者HBV - e抗原消失,74%的患者血清转换且肝功能生化指标恢复正常。结果表明,口服和肠胃外给予nHuIFN-α激活了两种不同的病毒清除机制。