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本帖最后由 David_2009 于 2011-12-20 00:06 编辑
回复 StephenW 的帖子
Mycrludex, as it claimed, could somehow inhibit the re-infection of HB virion into hepatocyte. However, it's still a problem that it unable to block the intracelluar recycling of HB virion. Thus, the cccDNA still has the chance to be recharged by this way ... Besides, the Mycrludex is just in the Phase I...
On the other side, NA I think could supress the viral retro-transtriptase, hence completely block the cccDNA recharging. This will be followed by the gradually decreasing of cccDNA. e.g Tenofovir, 6 years' clinical data shows no drug tolerance and is commercial available now. Could it be a choice?
Anyway, it is just my expectation and hope
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