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Effects of Formalin-Inactivated Respiratory Syncytial Virus (FI-RSV) in the Perinatal Lamb Model of RSV

Respiratory syncytial virus (RSV) is the most frequent cause of bronchiolitis in infants and children worldwide. There are currently no licensed vaccines or effective antivirals. The lack of a vaccine is partly due to increased caution following the aftermath of a failed clinical trial of a formalin...

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Autores principales: Derscheid, Rachel J., Gallup, Jack M., Knudson, Cory J., Varga, Steven M., Grosz, Drew D., van Geelen, Albert, Hostetter, Shannon J., Ackermann, Mark R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855688/
https://www.ncbi.nlm.nih.gov/pubmed/24324695
http://dx.doi.org/10.1371/journal.pone.0081472
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author Derscheid, Rachel J.
Gallup, Jack M.
Knudson, Cory J.
Varga, Steven M.
Grosz, Drew D.
van Geelen, Albert
Hostetter, Shannon J.
Ackermann, Mark R.
author_facet Derscheid, Rachel J.
Gallup, Jack M.
Knudson, Cory J.
Varga, Steven M.
Grosz, Drew D.
van Geelen, Albert
Hostetter, Shannon J.
Ackermann, Mark R.
author_sort Derscheid, Rachel J.
collection PubMed
description Respiratory syncytial virus (RSV) is the most frequent cause of bronchiolitis in infants and children worldwide. There are currently no licensed vaccines or effective antivirals. The lack of a vaccine is partly due to increased caution following the aftermath of a failed clinical trial of a formalin-inactivated RSV vaccine (FI-RSV) conducted in the 1960’s that led to enhanced disease, necessitating hospitalization of 80% of vaccine recipients and resulting in two fatalities. Perinatal lamb lungs are similar in size, structure and physiology to those of human infants and are susceptible to human strains of RSV that induce similar lesions as those observed in infected human infants. We sought to determine if perinatal lambs immunized with FI-RSV would develop key features of vaccine-enhanced disease. This was tested in colostrum-deprived lambs immunized at 3–5 days of age with FI-RSV followed two weeks later by RSV infection. The FI-RSV-vaccinated lambs exhibited several key features of RSV vaccine-enhanced disease, including reduced RSV titers in bronchoalveolar lavage fluid and lung, and increased infiltration of peribronchiolar and perivascular lymphocytes compared to lambs either undergoing an acute RSV infection or naïve controls; all features of RSV vaccine-enhanced disease. These results represent a first step proof-of-principle demonstration that the lamb can develop altered responses to RSV following FI-RSV vaccination. The lamb model may be useful for future mechanistic studies as well as the assessment of RSV vaccines designed for infants.
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spelling pubmed-38556882013-12-09 Effects of Formalin-Inactivated Respiratory Syncytial Virus (FI-RSV) in the Perinatal Lamb Model of RSV Derscheid, Rachel J. Gallup, Jack M. Knudson, Cory J. Varga, Steven M. Grosz, Drew D. van Geelen, Albert Hostetter, Shannon J. Ackermann, Mark R. PLoS One Research Article Respiratory syncytial virus (RSV) is the most frequent cause of bronchiolitis in infants and children worldwide. There are currently no licensed vaccines or effective antivirals. The lack of a vaccine is partly due to increased caution following the aftermath of a failed clinical trial of a formalin-inactivated RSV vaccine (FI-RSV) conducted in the 1960’s that led to enhanced disease, necessitating hospitalization of 80% of vaccine recipients and resulting in two fatalities. Perinatal lamb lungs are similar in size, structure and physiology to those of human infants and are susceptible to human strains of RSV that induce similar lesions as those observed in infected human infants. We sought to determine if perinatal lambs immunized with FI-RSV would develop key features of vaccine-enhanced disease. This was tested in colostrum-deprived lambs immunized at 3–5 days of age with FI-RSV followed two weeks later by RSV infection. The FI-RSV-vaccinated lambs exhibited several key features of RSV vaccine-enhanced disease, including reduced RSV titers in bronchoalveolar lavage fluid and lung, and increased infiltration of peribronchiolar and perivascular lymphocytes compared to lambs either undergoing an acute RSV infection or naïve controls; all features of RSV vaccine-enhanced disease. These results represent a first step proof-of-principle demonstration that the lamb can develop altered responses to RSV following FI-RSV vaccination. The lamb model may be useful for future mechanistic studies as well as the assessment of RSV vaccines designed for infants. Public Library of Science 2013-12-06 /pmc/articles/PMC3855688/ /pubmed/24324695 http://dx.doi.org/10.1371/journal.pone.0081472 Text en © 2013 Derscheid et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Derscheid, Rachel J.
Gallup, Jack M.
Knudson, Cory J.
Varga, Steven M.
Grosz, Drew D.
van Geelen, Albert
Hostetter, Shannon J.
Ackermann, Mark R.
Effects of Formalin-Inactivated Respiratory Syncytial Virus (FI-RSV) in the Perinatal Lamb Model of RSV
title Effects of Formalin-Inactivated Respiratory Syncytial Virus (FI-RSV) in the Perinatal Lamb Model of RSV
title_full Effects of Formalin-Inactivated Respiratory Syncytial Virus (FI-RSV) in the Perinatal Lamb Model of RSV
title_fullStr Effects of Formalin-Inactivated Respiratory Syncytial Virus (FI-RSV) in the Perinatal Lamb Model of RSV
title_full_unstemmed Effects of Formalin-Inactivated Respiratory Syncytial Virus (FI-RSV) in the Perinatal Lamb Model of RSV
title_short Effects of Formalin-Inactivated Respiratory Syncytial Virus (FI-RSV) in the Perinatal Lamb Model of RSV
title_sort effects of formalin-inactivated respiratory syncytial virus (fi-rsv) in the perinatal lamb model of rsv
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3855688/
https://www.ncbi.nlm.nih.gov/pubmed/24324695
http://dx.doi.org/10.1371/journal.pone.0081472
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