a Mater Research - University of Queensland, Translational Research Institute , Queensland , Australia.
b Mater Research - University of Queensland , Queensland , Australia.
Gut Microbes. 2018 Mar 4;9(2):175-178. doi: 10.1080/19490976.2017.1387343. Epub 2017 Oct 17.
Thiopurines are analogues of endogenous purines. They are pro-drugs which require the purine salvage pathway to convert them to the active drug nucleotides (TGN). These drugs are used to maintain clinical remission in patients with inflammatory bowel diseases. In our recent Gut paper, we showed that thioguanine worked quickly to improve colitis in the absence in the host animal of the key guanine salvage enzyme, hypoxanthine-guanine-phosphoribosyltransferase (HPRT). Current evidence favours the proposition that active drug delivery to the host lacking HPRT requires translocation of TGN-loaded bacteria across the inflamed mucosal barrier, and most likely delivery by phagocytosis. Alternatively, the efficacy of thioguanine in treating colitis could be mediated by modulation of the community of the microbiota in the intestine, or there are novel host pathways for conversion of the thioguanine pro-drug to TGN.
硫嘌呤是内源性嘌呤的类似物。它们是前体药物,需要嘌呤补救途径将其转化为活性药物核苷酸 (TGN)。这些药物用于维持炎症性肠病患者的临床缓解。在我们最近的 Gut 论文中,我们表明,硫鸟嘌呤在缺乏关键嘌呤补救酶次黄嘌呤-鸟嘌呤-磷酸核糖转移酶 (HPRT) 的宿主动物中迅速发挥作用,改善结肠炎。目前的证据支持这样的观点,即缺乏 HPRT 的宿主中活性药物的递送至需要负载 TGN 的细菌穿过炎症性黏膜屏障的易位,并且很可能通过吞噬作用进行递送。或者,硫鸟嘌呤治疗结肠炎的疗效可能是通过调节肠道微生物群落来介导的,或者存在将硫鸟嘌呤前体药物转化为 TGN 的新的宿主途径。