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In Vitro Inhibition of Hepatitis C Virus by Antisense Oligonucleotides in PBMC Compared to Hepatoma Cells

机译:与肝癌细胞相比,PBMC中反义寡核苷酸体外抑制丙型肝炎病毒

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摘要

Aim. To assess the efficiency of phosphorothioate antisense oligodeoxynucleotide 1 (S-ODN1) on HCV translation inhibition in PBMC compared to hepatoma cells in vitro for the first time. Materials and Methods. The study included 34 treatment naive HCV patients. IRES domain III and IV sequence variations were tested in 45 clones from 9 HCV patients. PBMC of HCV positive patients were subjected to S-ODN in vitro. Concomitantly HepG2 cells infected by the same patients serum were also treated with S-0DN1 for 24 and 48 hours. Cellular RNA was tested for HCV plus and minus strands by reverse transcription polymerase chain reaction (RT-PCR). Results. Sequence variations were seen in HCV IRES domain III only while domain IV was conserved among all the tested patient s clones. S-ODN1 successfully inhibited HCV translation in HepG2 cells, while in PBMC inhibition was partial. Conclusion. HCV IRES domain IV is more conserved than domain IIId in genotype 4 HCV patients. S-ODN against HCV IRES domain IV was not efficient to inhibit HCV translation in PBMC under the study conditions. Further studies testing other S-ODN targeting other HCV IRES domains in PBMC should be done.
机译:目标。为了评估硫代磷酸反义寡聚脱氧核苷酸1(S-ODN1)在体外首次与肝癌细胞相比对PBMC中HCV翻译抑制的效率。材料和方法。该研究包括34名初治HCV患者。在来自9位HCV患者的45个克隆中测试了IRES结构域III和IV序列变异。 HCV阳性患者的PBMC在体外接受S-ODN。同时,用相同的患者血清感染的HepG2细胞也用S-0DN1处理24和48小时。通过逆转录聚合酶链反应(RT-PCR)测试了细胞RNA的HCV正负链。结果。仅在HCV IRES结构域III中观察到序列变异,而结构域IV在所有测试的患者克隆中均保守。 S-ODN1成功抑制HepG2细胞中的HCV翻译,而在PBMC中则部分抑制。结论。 HCV IRES结构域IV在基因型4 HCV患者中比结构域IIId更保守。在研究条件下,针对HCV IRES结构域IV的S-ODN无法有效抑制PBMC中的HCV翻译。应该做进一步的研究来测试针对PBMC中其他HCV IRES域的其他S-ODN。

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