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

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 t...

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Autores principales: Zhang, Zhigang, Zhai, Tianshu, Li, Mingshuo, Zhang, Kun, Li, Jingrui, Zheng, Xu, Tian, Chaonan, Chen, Rui, Dong, Jianhui, Zhou, En-Min, Nan, Yuchen, Wu, Chunyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962380/
https://www.ncbi.nlm.nih.gov/pubmed/33726857
http://dx.doi.org/10.1186/s13567-021-00914-0
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author Zhang, Zhigang
Zhai, Tianshu
Li, Mingshuo
Zhang, Kun
Li, Jingrui
Zheng, Xu
Tian, Chaonan
Chen, Rui
Dong, Jianhui
Zhou, En-Min
Nan, Yuchen
Wu, Chunyan
author_facet Zhang, Zhigang
Zhai, Tianshu
Li, Mingshuo
Zhang, Kun
Li, Jingrui
Zheng, Xu
Tian, Chaonan
Chen, Rui
Dong, Jianhui
Zhou, En-Min
Nan, Yuchen
Wu, Chunyan
author_sort Zhang, Zhigang
collection PubMed
description 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13567-021-00914-0.
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spelling pubmed-79623802021-03-16 A broadly neutralizing monoclonal antibody induces broad protection against heterogeneous PRRSV strains in piglets Zhang, Zhigang Zhai, Tianshu Li, Mingshuo Zhang, Kun Li, Jingrui Zheng, Xu Tian, Chaonan Chen, Rui Dong, Jianhui Zhou, En-Min Nan, Yuchen Wu, Chunyan Vet Res Research Article 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13567-021-00914-0. BioMed Central 2021-03-16 2021 /pmc/articles/PMC7962380/ /pubmed/33726857 http://dx.doi.org/10.1186/s13567-021-00914-0 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Zhang, Zhigang
Zhai, Tianshu
Li, Mingshuo
Zhang, Kun
Li, Jingrui
Zheng, Xu
Tian, Chaonan
Chen, Rui
Dong, Jianhui
Zhou, En-Min
Nan, Yuchen
Wu, Chunyan
A broadly neutralizing monoclonal antibody induces broad protection against heterogeneous PRRSV strains in piglets
title A broadly neutralizing monoclonal antibody induces broad protection against heterogeneous PRRSV strains in piglets
title_full A broadly neutralizing monoclonal antibody induces broad protection against heterogeneous PRRSV strains in piglets
title_fullStr A broadly neutralizing monoclonal antibody induces broad protection against heterogeneous PRRSV strains in piglets
title_full_unstemmed A broadly neutralizing monoclonal antibody induces broad protection against heterogeneous PRRSV strains in piglets
title_short A broadly neutralizing monoclonal antibody induces broad protection against heterogeneous PRRSV strains in piglets
title_sort broadly neutralizing monoclonal antibody induces broad protection against heterogeneous prrsv strains in piglets
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962380/
https://www.ncbi.nlm.nih.gov/pubmed/33726857
http://dx.doi.org/10.1186/s13567-021-00914-0
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