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抗磷脂酰丝氨酸抗体在晚期出血性沙粒病毒感染豚鼠模型中的保护作用

Protective Effect of Anti-Phosphatidylserine Antibody in a Guinea Pig Model of Advanced Hemorrhagic Arenavirus Infection.

作者信息

Thomas John M, Thorpe Philip E

机构信息

The University of Texas Rio Grande Valley Department of Biology; School of Medicine 1201 W. University Drive, Edinburg, Texas 78539, USA.

The University of Texas Southwestern Medical Center Department of Pharmacology 2201 Inwood Road, Dallas, Texas 75390, USA.

出版信息

Open Microbiol J. 2017 Oct 30;11:303-315. doi: 10.2174/1874285801711010303. eCollection 2017.

Abstract

OBJECTIVE

Host derived markers on virally infected cells or virions may provide targets for the generation of antiviral agents. Recently, we identified phosphatidylserine (PS) as a host marker of virions and virally-infected cells.

METHODS AND MATERIALS

Under normal physiological conditions, PS is maintained on the inner leaflet of the plasma membrane facing the cytosol. Following viral infection, activation or pre-apoptotic changes cause PS to become externalized. We have previously shown that bavituximab, a chimeric human-mouse antibody that binds PS complexed with β2-glycoprotein I (β2GP1), protected rodents against lethal Pichinde virus and cytomegalovirus infections.

RESULTS

Here, we determined the antiviral activity of a fully human monoclonal antibody, PGN632, that directly binds to PS. Treatment with PGN632 protected 20% of guinea pigs with advanced infections of the hemorrhagic arenavirus, Pichinde, from death. Combining PGN632 with ribavirin improved the antiviral activity of both agents, such that the combination rescued 50% of animals from death.

CONCLUSION

The major mechanisms of action of PGN632 appear to be opsonization of virus and antibody-dependent cellular cytotoxicity of virally-infected cells. PS-targeting agents may have utility in the treatment of viral diseases.

摘要

目的

病毒感染细胞或病毒粒子上的宿主衍生标记物可能为抗病毒药物的研发提供靶点。最近,我们鉴定出磷脂酰丝氨酸(PS)是病毒粒子和病毒感染细胞的一种宿主标记物。

方法和材料

在正常生理条件下,PS维持在质膜面向胞质溶胶的内膜层。病毒感染后,激活或凋亡前变化会导致PS外化。我们之前已表明,巴维昔单抗是一种与人β2糖蛋白I(β2GP1)复合的PS结合嵌合人鼠抗体,可保护啮齿动物免受致死性皮钦德病毒和巨细胞病毒感染。

结果

在此,我们测定了一种直接结合PS的全人单克隆抗体PGN632的抗病毒活性。用PGN632治疗可使20%患有出血性沙粒病毒皮钦德晚期感染的豚鼠免于死亡。将PGN632与利巴韦林联合使用可提高两种药物的抗病毒活性,联合用药使50%的动物免于死亡。

结论

PGN632的主要作用机制似乎是病毒的调理作用和病毒感染细胞的抗体依赖性细胞毒性。靶向PS的药物可能在病毒性疾病治疗中具有应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/440b/5737030/f0797d9791ac/TOMICROJ-11-303_F1.jpg

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