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针对猪内源性逆转录病毒(PERVs)产生中和抗体。

Generation of neutralising antibodies against porcine endogenous retroviruses (PERVs).

机构信息

Robert Koch Institute, Nordufer 20, D.13353 Berlin, Germany.

出版信息

Virology. 2011 Mar 1;411(1):78-86. doi: 10.1016/j.virol.2010.12.032. Epub 2011 Jan 14.

Abstract

Antibodies neutralising porcine endogenous retroviruses (PERVs) were induced in different animal species by immunisation with the transmembrane envelope protein p15E. These antibodies recognised epitopes, designated E1, in the fusion peptide proximal region (FPPR) of p15E, and E2 in the membrane proximal external region (MPER). E2 is localised in a position similar to that of an epitope in the transmembrane envelope protein gp41 of the human immunodeficiency virus-1 (HIV-1), recognised by the monoclonal antibody 4E10 that is broadly neutralising. To detect neutralising antibodies specific for PERV, a novel assay was developed, which is based on quantification of provirus integration by real-time PCR. In addition, for the first time, highly effective neutralising antibodies were obtained by immunisation with the surface envelope protein of PERV. These data indicate that neutralising antibodies can be induced by immunisation with both envelope proteins.

摘要

不同动物物种通过用跨膜包膜蛋白 p15E 免疫,诱导产生中和猪内源性逆转录病毒 (PERV) 的抗体。这些抗体识别 p15E 的融合肽近端区域 (FPPR) 中的表位,命名为 E1,以及膜近端外部区域 (MPER) 中的 E2。E2 定位于类似于人类免疫缺陷病毒 1 (HIV-1) 的跨膜包膜蛋白 gp41 中一个表位的位置,该表位被广泛中和的单克隆抗体 4E10 识别。为了检测针对 PERV 的中和抗体,开发了一种新的基于实时 PCR 定量测定前病毒整合的测定法。此外,首次通过用 PERV 的表面包膜蛋白免疫获得了高效的中和抗体。这些数据表明,用包膜蛋白免疫可以诱导中和抗体。

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