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从针对主要包膜蛋白表面表位的抗体中分离出猪繁殖与呼吸综合征病毒中和抗体。

Dissociation of porcine reproductive and respiratory syndrome virus neutralization from antibodies specific to major envelope protein surface epitopes.

机构信息

Department of Veterinary and Biomedical Sciences, University of Minnesota, St. Paul, MN 55108, USA.

出版信息

Virology. 2012 Nov 25;433(2):367-76. doi: 10.1016/j.virol.2012.08.026. Epub 2012 Sep 12.

Abstract

Glycoprotein 5 (GP5) and membrane (M) protein are the major proteins in the envelope of porcine reproductive and respiratory syndrome virus (PRRSV). Although viral neutralization epitopes are reported in GP5 and M of type 2 PRRSV, their significance as targets of porcine humoral immunity is not well described. Thus, we constructed recombinant polypeptides containing ectodomain neutralization epitopes to examine their involvement in porcine antibody neutralization and antiviral immunity. PRRSV infection elicited ectodomain-specific antibodies, whose titers did not correlate with the neutralizing antibody (NA) response. Ectodomain-specific antibodies from PRRSV-neutralizing serum bound virus but did not neutralize infectivity. Furthermore, immunization of pigs with ectodomain polypeptides raised specific antibodies and provided partial protection without a detectable NA response. Finally the polypeptides did not block infection of porcine macrophages. These results suggest that the GP5/M ectodomain peptide epitopes are accessible for host antibody recognition, but are not associated with antibody-mediated virus neutralization.

摘要

糖蛋白 5(GP5)和膜(M)蛋白是猪繁殖与呼吸综合征病毒(PRRSV)包膜中的主要蛋白。虽然已报道在 2 型 PRRSV 的 GP5 和 M 中存在病毒中和表位,但它们作为猪体液免疫靶标的重要性尚未得到很好描述。因此,我们构建了含有外结构域中和表位的重组多肽,以研究它们在猪抗体中和和抗病毒免疫中的作用。PRRSV 感染诱导出针对外结构域的特异性抗体,其滴度与中和抗体(NA)反应无关。来自 PRRSV 中和血清的外结构域特异性抗体结合病毒,但不能中和感染性。此外,用外结构域多肽免疫猪可产生特异性抗体,并提供部分保护,而不会检测到 NA 反应。最后,这些多肽不能阻止猪巨噬细胞的感染。这些结果表明,GP5/M 外结构域肽表位可被宿主抗体识别,但与抗体介导的病毒中和无关。

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