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Sendai Virus-Vectored Vaccines That Express Envelope Glycoproteins of Respiratory Viruses
Human respiratory syncytial virus (HRSV), human metapneumovirus (HMPV), and human parainfluenza viruses (HPIVs) are leading causes of respiratory disease in young children, the elderly, and individuals of all ages with immunosuppression. Vaccination strategies against these pneumoviruses and paramyx...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230104/ https://www.ncbi.nlm.nih.gov/pubmed/34072332 http://dx.doi.org/10.3390/v13061023 |
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author | Russell, Charles J. Hurwitz, Julia L. |
author_facet | Russell, Charles J. Hurwitz, Julia L. |
author_sort | Russell, Charles J. |
collection | PubMed |
description | Human respiratory syncytial virus (HRSV), human metapneumovirus (HMPV), and human parainfluenza viruses (HPIVs) are leading causes of respiratory disease in young children, the elderly, and individuals of all ages with immunosuppression. Vaccination strategies against these pneumoviruses and paramyxoviruses are vast in number, yet no licensed vaccines are available. Here, we review development of Sendai virus (SeV), a versatile pediatric vaccine that can (a) serve as a Jennerian vaccine against HPIV1, (b) serve as a recombinant vaccine against HRSV, HPIV2, HPIV3, and HMPV, (c) accommodate foreign genes for viral glycoproteins in multiple intergenic positions, (d) induce durable, mucosal, B-cell, and T-cell immune responses without enhanced immunopathology, (e) protect cotton rats, African green monkeys, and chimpanzees from infection, and (f) be formulated into a vaccine cocktail. Clinical phase I safety trials of SeV have been completed in adults and 3–6-year-old children. Clinical testing of SeVRSV, an HRSV fusion (F) glycoprotein gene recombinant, has also been completed in adults. Positive results from these studies, and collaborative efforts with the National Institutes of Health and the Serum Institute of India assist advanced development of SeV-based vaccines. Prospects are now good for vaccine successes in infants and consequent protection against serious viral disease. |
format | Online Article Text |
id | pubmed-8230104 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82301042021-06-26 Sendai Virus-Vectored Vaccines That Express Envelope Glycoproteins of Respiratory Viruses Russell, Charles J. Hurwitz, Julia L. Viruses Review Human respiratory syncytial virus (HRSV), human metapneumovirus (HMPV), and human parainfluenza viruses (HPIVs) are leading causes of respiratory disease in young children, the elderly, and individuals of all ages with immunosuppression. Vaccination strategies against these pneumoviruses and paramyxoviruses are vast in number, yet no licensed vaccines are available. Here, we review development of Sendai virus (SeV), a versatile pediatric vaccine that can (a) serve as a Jennerian vaccine against HPIV1, (b) serve as a recombinant vaccine against HRSV, HPIV2, HPIV3, and HMPV, (c) accommodate foreign genes for viral glycoproteins in multiple intergenic positions, (d) induce durable, mucosal, B-cell, and T-cell immune responses without enhanced immunopathology, (e) protect cotton rats, African green monkeys, and chimpanzees from infection, and (f) be formulated into a vaccine cocktail. Clinical phase I safety trials of SeV have been completed in adults and 3–6-year-old children. Clinical testing of SeVRSV, an HRSV fusion (F) glycoprotein gene recombinant, has also been completed in adults. Positive results from these studies, and collaborative efforts with the National Institutes of Health and the Serum Institute of India assist advanced development of SeV-based vaccines. Prospects are now good for vaccine successes in infants and consequent protection against serious viral disease. MDPI 2021-05-29 /pmc/articles/PMC8230104/ /pubmed/34072332 http://dx.doi.org/10.3390/v13061023 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Russell, Charles J. Hurwitz, Julia L. Sendai Virus-Vectored Vaccines That Express Envelope Glycoproteins of Respiratory Viruses |
title | Sendai Virus-Vectored Vaccines That Express Envelope Glycoproteins of Respiratory Viruses |
title_full | Sendai Virus-Vectored Vaccines That Express Envelope Glycoproteins of Respiratory Viruses |
title_fullStr | Sendai Virus-Vectored Vaccines That Express Envelope Glycoproteins of Respiratory Viruses |
title_full_unstemmed | Sendai Virus-Vectored Vaccines That Express Envelope Glycoproteins of Respiratory Viruses |
title_short | Sendai Virus-Vectored Vaccines That Express Envelope Glycoproteins of Respiratory Viruses |
title_sort | sendai virus-vectored vaccines that express envelope glycoproteins of respiratory viruses |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230104/ https://www.ncbi.nlm.nih.gov/pubmed/34072332 http://dx.doi.org/10.3390/v13061023 |
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