两篇JCI证实靶向干扰素或可提高抗逆转录病毒药物治疗HIV的疗效

2016-12-14 佚名 生物谷

尽管联合抗逆转录病毒疗法(cART)能够协助HIV-1阳性病人有效地管控他们的感染病情,但是一些病人会经历免疫系统不断地激活,从而能够恶化病情发展。这种长期激活归因于I型干扰素(IFN-I)的持续信号转导,其中IFN-I是结合到IFN受体上来调节免疫系统的蛋白。 本周,两项新的研究证实在HIV-1感染的人源化小鼠模型中,靶向IFN-I信号的抗体能够加强cART的疗效。相关研究结果均于2016年1


尽管联合抗逆转录病毒疗法(cART)能够协助HIV-1阳性病人有效地管控他们的感染病情,但是一些病人会经历免疫系统不断地激活,从而能够恶化病情发展。这种长期激活归因于I型干扰素(IFN-I)的持续信号转导,其中IFN-I是结合到IFN受体上来调节免疫系统的蛋白。

本周,两项新的研究证实在HIV-1感染的人源化小鼠模型中,靶向IFN-I信号的抗体能够加强cART的疗效。相关研究结果均于2016年12月12日在线发表在Journal of Clinical Investigation期刊上,论文标题分别为“Targeting type I interferon–mediated activation restores immune function in chronic HIV infection”和“The interferon paradox: can inhibiting an antiviral mechanism advance an HIV cure?”。

在美国加州大学洛杉矶分校科学家Scott Kitchen领导的一项研究中,研究人员利用一种阻断人IFN受体2的抗体治疗被HIV-1感染的小鼠。他们观察到T细胞耗竭和病毒载量下降的迹象,这表明慢性免疫激活下降和感染管控得到改善。

在另一项研究中,美国北卡罗来纳大学Lishan Su实验室开发出一种不同的靶向人IFNα/β受体的抗体,并且观察到它也会逆转HIV-1感染的人源化小鼠体内的免疫过度激活。

在这两项研究中,相比于单独接受cART治疗的HIV-1感染的人源化小鼠,与cART治疗协同进行的IFN-I信号阻断会导致更好的治疗结果。这两项研究的结果强烈支持将IFN-I阻断作为cART治疗的一种辅助手段进行进一步评价。

原始出处

Anjie Zhen,1 Valerie Rezek,1 Cindy Youn,1 Brianna Lam,1 Nelson Chang,1 Jonathan Rick,1 Mayra Carrillo,1 Heather Martin,1 Saro Kasparian,1 Philip Syed,1 Nicholas Rice,1 David G. Brooks,2,3 and Scott G. Kitchen1.Targeting type I interferon–mediated activation restores immune function in chronic HIV infection.JCI.2016

Steven G. Deeks,1 Pamela M. Odorizzi,1 and Rafick-Pierre Sekaly2The interferon paradox: can inhibiting an antiviral mechanism advance an HIV cure?.JCI.2016


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    2017-08-30 mjldent
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    2017-03-24 hxj0117