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Pre- and postexposure protection by passive immunoglobulin but no enhancement of infection with a flavivirus in a mouse model.

机译:被动免疫球蛋白在接触前和接触后的保护但在小鼠模型中未增强黄病毒的感染。

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摘要

Antibody-dependent enhancement of flavivirus infection, which except for dengue virus is without clear proof in vivo, is still under debate. Recently, postexposure immunoglobulin prophylaxis against tick-borne encephalitis virus, a flavivirus, was claimed to possibly have worsened the outcome of infection due to antibody-dependent enhancement. In the present study, antibody-dependent enhancement and pre- or postexposure protection by passive administration of tick-borne encephalitis virus immunoglobulin were evaluated in a mouse model. Preexposure treatment with homologous murine or heterologous human immunoglobulin provided complete protection against lethal challenge with tick-borne encephalitis virus. For postexposure treatment with antibody, the degree of protection correlated with the amount of immunoglobulin administered and was inversely related to the time interval between infection and treatment. Indications of enhancement of infection would have been increased lethality or reduced mean survival time, but neither was observed under the conditions used in our experiments despite the broad range of immunoglobulin and virus challenge doses applied. In contrast to these in vivo results, antibody-dependent enhancement of tick-borne encephalitis virus infection of murine peritoneal macrophages was readily demonstrable in vitro. Thus, antibody-dependent enhancement of viral infection in vitro does not necessarily predict enhancement in vivo.
机译:除登革热病毒在体内尚无明确证据外,黄病毒感染的抗体依赖性增强作用仍在争论中。最近,据称暴露后预防滴虫传播性脑炎病毒(一种黄病毒)的免疫球蛋白可能由于抗体依赖性增强而使感染的结果恶化。在本研究中,在小鼠模型中评估了tick虫性脑炎病毒免疫球蛋白的被动给药对抗体的依赖性增强作用以及接触前或接触后的保护作用。用同源鼠或异源人类免疫球蛋白进行暴露前处理可完全保护tick虫脑炎病毒致死性攻击。对于用抗体进行的暴露后治疗,保护程度与免疫球蛋白的施用量相关,与感染和治疗之间的时间间隔成反比。增强感染的指征会增加致死率或缩短平均存活时间,但尽管免疫球蛋白和病毒攻击剂量范围广泛,但在我们的实验条件下均未观察到。与这些体内结果相反,在体外容易证明抗体依赖性增强小鼠腹膜巨噬细胞对tick传脑炎病毒的感染。因此,体外病毒感染的抗体依赖性增强不一定预示体内增强。

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