ConclusionPreliminary data indicate that lamivudine therapy can significantly improve liver function and effectively inhibit HBV replication, but not to effect the fatality rates.
结论拉米夫定治疗慢性乙型重型肝炎，可缓解病情，改善肝功能，抑制HBV复制，但对病死率无显著影响。
So the biggest challenge for researchers is how the virus is in "sleep" state while using the cocktail therapy to reduce the speed of viral replication.
所以对于研究人员最大的挑战是，如何使病毒处于“休眠”状态，同时使用鸡尾酒疗法降低病毒复制的速度。
Antiviral therapy can inhibit viral replication, recovery and restoration of damaged parts of the immune function.
抗病毒治疗可以抑制病毒复制，恢复和部分恢复受损的免疫功能。
Recent studies have found that by HIV-infected macrophages and dendritic cells may also play a role in drug therapy may not completely prevent virus replication in these cells.
最近研究人员发现，受HIV感染的巨噬细胞和树突状细胞可能也发挥了作用，药物治疗也许并不能完全阻止病毒在这些细胞中复制。
These observations provide evidence that therapy designed to target cells with lytic KSHV replication has activity in KSHV-MCD.
这些观察提供的证据表明，设计针对细胞的KSHV复制裂解疗法对K SHV - MCD有效。
Because at present there is no effective response to HIV drugs, but the use of several drugs combined therapy can inhibit viral replication and to avoid injury in the body's immune system.
因为目前针对艾滋病毒并无特效药物，但利用几种药物进行联合治疗可抑制病毒复制并避免损伤人体免疫系统。
Considering its tumor targeting, replication in tumor tissues and anti-tumor effects, attenuated Salmonella typhimurium has offered a new approach to tumor therapy.
减毒鼠伤寒沙门菌由于具有肿瘤靶向性，能在肿瘤组织中复制并产生抗肿瘤效果的能力，使肿瘤治疗获得了新契机。
He said that the paper written by Dr Nagot and colleagues has "direct clinical implications, suggesting that HIV-1 replication can be reduced with antiviral therapy directed solely at HSV-2."
他认为Nagot博士等撰写的文章对临床治疗有直接的指导作用，提示HIV - 1病毒的复制可直接通过针对HSV - 2的抗病毒的治疗就可以得到抑制。
Accept this kind of therapy if patients infected at the first few months of taking three drugs at the same time, the most effective in inhibiting the proliferation of viral replication.
接受这种疗法的病人如果在感染的最初几个月同时服用三种药物，最能有效地抑制病毒的复制扩散。
Objective: To construct a replication-competent adenovirus vector carrying human endostatin gene, looking for an effective method for the therapy of colon cancer.
目的：构建携带内皮抑素基因的增殖型腺病毒载体，寻找结肠癌的有效治疗方法。
Objective: To construct a replication-competent adenovirus vector carrying human endostatin gene, looking for an effective method for the therapy of colon cancer.
目的：构建携带内皮抑素基因的增殖型腺病毒载体，寻找结肠癌的有效治疗方法。
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