Center for Convergent Research of Emerging Virus Infection, Korea Research Institute of Chemical Technology, 141 Gajeong-ro, Yuseong-gu, Daejeon-si 34114, Korea.
Anticancer Agent Research Center, Korea Research Institute of Bioscience & Biotechnology, 30 Yeongudanji-ro, Ochang-eup, Cheongwon-gu, Cheongju-si, Chungbuk 28116, Korea.
Viruses. 2018 Apr 20;10(4):211. doi: 10.3390/v10040211.
Nucleoside analogs have been frequently identified as antiviral agents. In recent years, gemcitabine, a cytidine analog in clinical use for the treatment of many solid tumors, was also shown to have antiviral activity against a broad range of viruses. Nucleoside analogs generally interfere with cellular nucleos(t)ide synthesis pathways, resulting in the depletion or imbalance of (d)NTP pools. Intriguingly, a few recent reports have shown that some nucleoside analogs, including gemcitabine, activated innate immunity, inducing the expression of interferon-stimulated genes, through nucleos(t)ide synthesis inhibition. The precise crosstalk between these two independent processes remains to be determined. Nonetheless, we summarize the current knowledge of nucleos(t)ide synthesis inhibition-related innate immunity and propose it as a newly emerging antiviral mechanism of nucleoside analogs.
核苷类似物已被广泛鉴定为抗病毒药物。近年来,在临床中用于治疗多种实体瘤的胞苷类似物吉西他滨也被证明具有广谱抗病毒活性。核苷类似物通常干扰细胞核苷(t)合成途径,导致(d)NTP 池的耗竭或失衡。有趣的是,最近有几项报告表明,包括吉西他滨在内的一些核苷类似物通过核苷酸合成抑制激活了先天免疫,诱导干扰素刺激基因的表达。这两个独立过程之间的确切串扰仍有待确定。尽管如此,我们总结了核苷酸合成抑制相关先天免疫的现有知识,并提出它作为核苷类似物新出现的抗病毒机制。