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Human Polyclonal Antibodies Produced from Transchromosomal Bovine Provides Prophylactic and Therapeutic Protections Against Zika Virus Infection in STAT2 KO Syrian Hamsters
Zika virus (ZIKV) infection can cause severe congenital diseases, such as microcephaly, ocular defects and arthrogryposis in fetuses, and Guillain–Barré syndrome in adults. Efficacious therapeutic treatments for infected patients, as well as prophylactic treatments to prevent new infections are need...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410148/ https://www.ncbi.nlm.nih.gov/pubmed/30678320 http://dx.doi.org/10.3390/v11020092 |
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author | Siddharthan, Venkatraman Miao, Jinxin Van Wettere, Arnaud J Li, Rong Wu, Hua Sullivan, Eddie Jiao, Jinan Hooper, Jay W. Safronetz, David Morrey, John D. Julander, Justin G. Wang, Zhongde |
author_facet | Siddharthan, Venkatraman Miao, Jinxin Van Wettere, Arnaud J Li, Rong Wu, Hua Sullivan, Eddie Jiao, Jinan Hooper, Jay W. Safronetz, David Morrey, John D. Julander, Justin G. Wang, Zhongde |
author_sort | Siddharthan, Venkatraman |
collection | PubMed |
description | Zika virus (ZIKV) infection can cause severe congenital diseases, such as microcephaly, ocular defects and arthrogryposis in fetuses, and Guillain–Barré syndrome in adults. Efficacious therapeutic treatments for infected patients, as well as prophylactic treatments to prevent new infections are needed for combating ZIKV infection. Here, we report that ZIKV-specific human polyclonal antibodies (SAB-155), elicited in transchromosomal bovine (TcB), provide significant protection from infection by ZIKV in STAT2 knockout (KO) golden Syrian hamsters both prophylactically and therapeutically. These antibodies also prevent testicular lesions in this hamster model. Our data indicate that antibody-mediated immunotherapy is effective in treating ZIKV infection. Because suitable quantities of highly potent human polyclonal antibodies can be quickly produced from the TcB system against ZIKV and have demonstrated therapeutic efficacy in a small animal model, they have the potential as an effective countermeasure against ZIKV infection. |
format | Online Article Text |
id | pubmed-6410148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64101482019-04-01 Human Polyclonal Antibodies Produced from Transchromosomal Bovine Provides Prophylactic and Therapeutic Protections Against Zika Virus Infection in STAT2 KO Syrian Hamsters Siddharthan, Venkatraman Miao, Jinxin Van Wettere, Arnaud J Li, Rong Wu, Hua Sullivan, Eddie Jiao, Jinan Hooper, Jay W. Safronetz, David Morrey, John D. Julander, Justin G. Wang, Zhongde Viruses Article Zika virus (ZIKV) infection can cause severe congenital diseases, such as microcephaly, ocular defects and arthrogryposis in fetuses, and Guillain–Barré syndrome in adults. Efficacious therapeutic treatments for infected patients, as well as prophylactic treatments to prevent new infections are needed for combating ZIKV infection. Here, we report that ZIKV-specific human polyclonal antibodies (SAB-155), elicited in transchromosomal bovine (TcB), provide significant protection from infection by ZIKV in STAT2 knockout (KO) golden Syrian hamsters both prophylactically and therapeutically. These antibodies also prevent testicular lesions in this hamster model. Our data indicate that antibody-mediated immunotherapy is effective in treating ZIKV infection. Because suitable quantities of highly potent human polyclonal antibodies can be quickly produced from the TcB system against ZIKV and have demonstrated therapeutic efficacy in a small animal model, they have the potential as an effective countermeasure against ZIKV infection. MDPI 2019-01-22 /pmc/articles/PMC6410148/ /pubmed/30678320 http://dx.doi.org/10.3390/v11020092 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Siddharthan, Venkatraman Miao, Jinxin Van Wettere, Arnaud J Li, Rong Wu, Hua Sullivan, Eddie Jiao, Jinan Hooper, Jay W. Safronetz, David Morrey, John D. Julander, Justin G. Wang, Zhongde Human Polyclonal Antibodies Produced from Transchromosomal Bovine Provides Prophylactic and Therapeutic Protections Against Zika Virus Infection in STAT2 KO Syrian Hamsters |
title | Human Polyclonal Antibodies Produced from Transchromosomal Bovine Provides Prophylactic and Therapeutic Protections Against Zika Virus Infection in STAT2 KO Syrian Hamsters |
title_full | Human Polyclonal Antibodies Produced from Transchromosomal Bovine Provides Prophylactic and Therapeutic Protections Against Zika Virus Infection in STAT2 KO Syrian Hamsters |
title_fullStr | Human Polyclonal Antibodies Produced from Transchromosomal Bovine Provides Prophylactic and Therapeutic Protections Against Zika Virus Infection in STAT2 KO Syrian Hamsters |
title_full_unstemmed | Human Polyclonal Antibodies Produced from Transchromosomal Bovine Provides Prophylactic and Therapeutic Protections Against Zika Virus Infection in STAT2 KO Syrian Hamsters |
title_short | Human Polyclonal Antibodies Produced from Transchromosomal Bovine Provides Prophylactic and Therapeutic Protections Against Zika Virus Infection in STAT2 KO Syrian Hamsters |
title_sort | human polyclonal antibodies produced from transchromosomal bovine provides prophylactic and therapeutic protections against zika virus infection in stat2 ko syrian hamsters |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410148/ https://www.ncbi.nlm.nih.gov/pubmed/30678320 http://dx.doi.org/10.3390/v11020092 |
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