Freni M A, Ajello A, Spadaro A, Fava A, Calapristi I, Marafioti T, Alessi N, Resta M L, Ferraù O
Istituto Pluridisciplinare di Clinica Medica e Terapia Medica Generale e Speciale, Università di Messina, Italy.
Hepatogastroenterology. 1997 Sep-Oct;44(17):1295-301.
BACKGROUND/AIMS: Enhanced hepatocellular display of class I HLA antigens together with rising serum beta-2-microglobulin (a subunit of class I HLA molecule) and transaminases is reported in patients with chronic hepatitis B during treatment with interferon as an index of immune lysis of virus infected cells.
We studied class I HLA antigens and beta-2-microglobulin display in the livers of 23 patients with chronic hepatitis C before and after a 12 month treatment with recombinant alpha interferon. Beta-2-microglobulin serum values were monitored. In all the patients before treatment, class I HLA antigens and beta-2-microglobulin were diffusely displayed in the bile duct epithelium, in the sinusoidal lining cells, in approximately 50% of the inflammatory cells and in the hepatocyte membrane with marked staining in the areas of periportal and lobular necrosis.
At the end of the treatment, class I HLA antigens and beta-2-microglobulin were no longer or only faintly detectable in the hepatocytes of 12 patients who showed clinical and histological improvement. The immunohistochemical pattern was unchanged in the 11 patients who did not respond to the therapy. Baseline serum beta-2-microglobulin values were high in all the patients and decreased significantly only in the group of responders. No peaks of transaminases were registered.
The disappearance or reduction of HLA hepatocellular display without acute increase of serum beta-2-microglobulin values and transaminases during successful treatment with interferon in chronic hepatitis C suggests a clearance of the virus due to direct antiviral rather than immunologically mediated mechanism.
背景/目的:据报道,在慢性乙型肝炎患者接受干扰素治疗期间,I类HLA抗原在肝细胞中的表达增强,同时血清β2-微球蛋白(I类HLA分子的一个亚基)和转氨酶升高,这是病毒感染细胞免疫溶解的一个指标。
我们研究了23例慢性丙型肝炎患者在接受重组α干扰素治疗12个月前后肝脏中I类HLA抗原和β2-微球蛋白的表达情况。监测血清β2-微球蛋白值。在所有治疗前的患者中,I类HLA抗原和β2-微球蛋白在胆管上皮、窦状隙衬里细胞、约50%的炎症细胞以及肝细胞膜中呈弥漫性表达,在汇管区和小叶坏死区域有明显染色。
治疗结束时,12例临床和组织学改善的患者肝细胞中不再能检测到或仅能微弱检测到I类HLA抗原和β2-微球蛋白。11例对治疗无反应的患者免疫组化模式未改变。所有患者基线血清β2-微球蛋白值均较高,仅在有反应的组中显著下降。未记录到转氨酶峰值。
在慢性丙型肝炎患者接受干扰素成功治疗期间,HLA在肝细胞中的表达消失或减少,而血清β2-微球蛋白值和转氨酶未急性升高,这表明病毒清除是由于直接抗病毒机制而非免疫介导机制。