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A broadly neutralizing monoclonal antibody induces broad protection against heterogeneous PRRSV strains in piglets

机译:宽度中和单克隆抗体诱导仔猪异质PRRSV菌株的广泛保护

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Neutralizing antibodies (NAbs) have attracted attention as tools for achieving PRRSV control and prevention, but viral antigenic variation undermines the abilities of NAbs elicited by attenuated PRRSV vaccines to confer full protection against heterogeneous PRRSV field isolates. As demonstrated in this study, the monoclonal antibody (mAb) mAb-PN9cx3 exhibited broad-spectrum recognition and neutralizing activities against PRRSV-1 and PRRSV-2 strains in vitro. Furthermore, in vivo experiments revealed that the administration of two 10-mg doses of mAb-PN9cx3 before and after the inoculation of piglets with heterologous PRRSV isolates (HP-PRRSV-JXA1 or PRRSV NADC30-like strain HNhx) resulted in significant reduction of the PRRSV-induced pulmonary pathological changes and virus loads in porcine alveolar macrophages (PAMs) compared with the results obtained with mAb-treated isotype controls. Moreover, minimal hilar lymph node PRRSV antigen levels were observed in mAb-PN9cx3-treated piglets. A transcriptome profile analysis of PAMs extracted from lung tissues of piglets belonging to different groups (except for antibody-isotype controls) indicated that mAb-PN9cx3 treatment reversed the PRRSV infection-induced alterations in expression profiles. A gene ontology (GO) enrichment analysis of these genes traced their functions to pathways that included the immune response, inflammatory response, and response to steroid hormone, and their functions in oogenesis and positive regulation of angiogenesis have been implicated in PRRSV pathogenesis. Overall, NADC30-like HNhx infection affected more gene pathways than HP-PRRSV infection. In conclusion, our research describes a novel immunologic approach involving the use of mAbs that confer cross-protection against serious illness resulting from infection with heterogeneous PRRSV-2 isolates, which is a feat that has not yet been achieved through vaccination. Ultimately, mAb-PN9cx3 will be a powerful addition to our current arsenal for achieving PRRSV prevention and eradication.
机译:中和抗体(NABs)引起了易于实现PRRSV控制和预防的工具的注意,但病毒抗原变异破坏了通过减毒PRRSV疫苗引发的NAB的能力,以赋予全面的PRRSV野外分离株全面保护。如本研究所证明的,单克隆抗体(MAB)MAB-PN9CX3在体外表现出对PRRSV-1和PRRSV-2菌株的广谱识别和中和活性。此外,在体内实验表明,用异源PRRSV分离物(HP-PRRSV-JXA1或PRRSV NADC30样菌株HNHX)在接种仔猪之前和之后给药两次10mg剂量的MAB-PN9CX3导致与用MAB处理的同种型对照获得的结果相比,PRRSV诱导的肺病理学变化和病毒载荷,与猪肺泡巨噬细胞(PAMS)相比。此外,在MAB-PN9CX3处理的仔猪中观察到最小的HILAR淋巴结PRRSV抗原水平。从属于不同组的仔猪组织中提取的PAM的转录组谱分析(抗体 - 同种型对照除外)表明MAB-PN9CX3治疗反转表达谱中PRRSV感染诱导的改变。这些基因的基因本体(GO)富集分析追溯其对包括免疫应答,炎症反应和对类固醇激素的反应的途径的功能,并且它们在血管生成的ocofis作用中的功能涉及PRRSV发病机制。总体而言,NADC30样HNHX感染影响比HP-PRRSV感染更多的基因途径。总之,我们的研究描述了一种新的免疫方法,涉及使用赋予交叉保护的MAB对具有异质性PRRSV-2分离株导致的严重疾病,这是通过疫苗接种尚未实现的壮举。最终,MAB-PN9CX3将是我们目前的阿森纳,以实现PRRSV预防和消除的强大补充。

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