摘要
目的探讨IL-4对HepG2.2.15细胞表达HBsAg和HBeAg及HBVDNA复制的抑制作用,认识IL-4在抗HBV感染中的作用。方法通过MTT比色法检测不同浓度重组IL-4(rIL-4)对HepG2.2.15细胞的细胞毒性作用,用ELISA检测rIL-4对HepG2.2.15细胞不同时相HBsAg和HBe心分泌的作用,用实时荧光定量PCR检测rIL-4对HBVDNA合成的影响。结果rIL-4的各浓度对HepG2.2.15细胞无细胞毒性作用;rIL-4处理HepG2.2.15细胞后,不同浓度组HBsAg、HBeAg及HBVDNA含量在96h的差异具有统计学意义(P〈0.05),但rIL-4的浓度低于100ng/mL的各组,HBsAg和HBVDNA含量在处理48h时,各组间无明显差异(P〉0.05)。此抑制作用随rIL-4浓度的增加而增强。结论rIL-4在体外有直接的抗HBV作用。
Objective To explore the iuhibitory effect of IL-4 on HBsAg, HBeAg and HBV DNA cultured in HepG2.2.15 cell line, and to further provide a theoretical evidence and an experimental basis for investigating the inhibitory effect of IL-4 on HBV infection. Methods The cytotoxic effects of different concentration of recombinant IL-4 (rIL-4) on HepG2.2.15 cells were detected by MTF assay. The inhibition to HBsAg and HBeAg were measured by ELISA. The quantity of HBV DNA was detected with real-time fluorescence quantitative PCR(FQ-PCR). Results MTT showed that different concentration of rlL-4 had no cytotoxic effect on HepG2.2.15 cells..There were statistical differences on HBsAg, HBeAg and HBV DNA levels among different concentration groups at 96 h after rIL-4 treatment( P 〈 0.05). However, there were no differences on HBsAg and HBV DNA levels at 48 h in those groups of 25-100μg/mL rIL-4 concentration. The suppressive effect increased with increasing rIL-4 concentrations. Conclusions These results suggest that rIL-4 at non-cellulotoxic concentration can suppress HBsAg and HBeAg expression and decrease the HBV DNA replication in HepG2.2.15 cell line.
出处
《国际流行病学传染病学杂志》
CAS
2009年第5期293-295,共3页
International Journal of Epidemiology and Infectious Disease