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Efficacy of a cold‐adapted, intranasal, equine influenza vaccine: challenge trials

Identifieur interne : 001408 ( Istex/Corpus ); précédent : 001407; suivant : 001409

Efficacy of a cold‐adapted, intranasal, equine influenza vaccine: challenge trials

Auteurs : H. G. G. Townsend ; S. J. Penner ; T. C. Watts ; A. Cook ; J. Bogdan ; D. M. Haines ; S. Griffin ; T. Chambers ; R. E. Holland ; P. Whitaker-Dowling ; J. S. Youngner ; R. W. Sebring

Source :

RBID : ISTEX:DDD3E75B61BC5F924443D0530DC0CBBFDDC3922F

English descriptors

Abstract

A randomised, controlled, double‐blind, influenza virus, aerosol challenge of horses was undertaken to determine the efficacy of a cold‐adapted, temperature sensitive, modified‐live virus, intranasal, equine influenza vaccine. Ninety 11‐month‐old influenza‐naïve foals were assigned randomly to 3 groups (20 vaccinates and 10 controls per group) and challenged 5 weeks, 6 and 12 months after a single vaccination. Challenges were performed on Day 0 in a plastic‐lined chamber. Between Days 1 and 10, animals were examined daily for evidence of clinical signs of influenza. Nasal swabs for virus isolation were obtained on Day 1 and Days 1 to 8 and blood samples for serology were collected on Days 1, 7 and 14. There was no adverse response to vaccination in any animal. Following challenge at 5 weeks and 6 months, vaccinates had significantly lower clinical scores (P = 0.0001 and 0.005, respectively), experienced smaller increases in rectal temperature (P = 0.0008 and 0.0007, respectively) and shed less virus (P<0.0001 and P = 0.03, respectively) over fewer days (P<0.0001 and P = 0.002, respectively) than did the controls. After the 12 month challenge, rectal temperatures (P = 0.006) as well as the duration (P = 0.03) and concentration of virus shed (P = 0.04) were significantly reduced among vaccinated animals. The results of this study showed that 6 months after a single dose of vaccine the duration and severity of clinical signs were markedly reduced amongst vaccinated animals exposed to a severe live‐virus challenge. Appropriate use of this vaccine should lead to a marked reduction in the frequency, severity and duration of outbreaks of equine influenza in North America.

Url:
DOI: 10.2746/042516401776249354

Links to Exploration step

ISTEX:DDD3E75B61BC5F924443D0530DC0CBBFDDC3922F

Le document en format XML

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<p>A randomised, controlled, double‐blind, influenza virus, aerosol challenge of horses was undertaken to determine the efficacy of a cold‐adapted, temperature sensitive, modified‐live virus, intranasal, equine influenza vaccine. Ninety 11‐month‐old influenza‐naïve foals were assigned randomly to 3 groups (20 vaccinates and 10 controls per group) and challenged 5 weeks, 6 and 12 months after a single vaccination. Challenges were performed on Day 0 in a plastic‐lined chamber. Between Days 1 and 10, animals were examined daily for evidence of clinical signs of influenza. Nasal swabs for virus isolation were obtained on Day 1 and Days 1 to 8 and blood samples for serology were collected on Days 1, 7 and 14. There was no adverse response to vaccination in any animal. Following challenge at 5 weeks and 6 months, vaccinates had significantly lower clinical scores (P = 0.0001 and 0.005, respectively), experienced smaller increases in rectal temperature (P = 0.0008 and 0.0007, respectively) and shed less virus (P<0.0001 and P = 0.03, respectively) over fewer days (P<0.0001 and P = 0.002, respectively) than did the controls. After the 12 month challenge, rectal temperatures (P = 0.006) as well as the duration (P = 0.03) and concentration of virus shed (P = 0.04) were significantly reduced among vaccinated animals. The results of this study showed that 6 months after a single dose of vaccine the duration and severity of clinical signs were markedly reduced amongst vaccinated animals exposed to a severe live‐virus challenge. Appropriate use of this vaccine should lead to a marked reduction in the frequency, severity and duration of outbreaks of equine influenza in North America.</p>
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<p>A randomised, controlled, double‐blind, influenza virus, aerosol challenge of horses was undertaken to determine the efficacy of a cold‐adapted, temperature sensitive, modified‐live virus, intranasal, equine influenza vaccine. Ninety 11‐month‐old influenza‐naïve foals were assigned randomly to 3 groups (20 vaccinates and 10 controls per group) and challenged 5 weeks, 6 and 12 months after a single vaccination. Challenges were performed on Day 0 in a plastic‐lined chamber. Between Days 1 and 10, animals were examined daily for evidence of clinical signs of influenza. Nasal swabs for virus isolation were obtained on Day 1 and Days 1 to 8 and blood samples for serology were collected on Days 1, 7 and 14. There was no adverse response to vaccination in any animal. Following challenge at 5 weeks and 6 months, vaccinates had significantly lower clinical scores (P = 0.0001 and 0.005, respectively), experienced smaller increases in rectal temperature (P = 0.0008 and 0.0007, respectively) and shed less virus (P<0.0001 and P = 0.03, respectively) over fewer days (P<0.0001 and P = 0.002, respectively) than did the controls. After the 12 month challenge, rectal temperatures (P = 0.006) as well as the duration (P = 0.03) and concentration of virus shed (P = 0.04) were significantly reduced among vaccinated animals. The results of this study showed that 6 months after a single dose of vaccine the duration and severity of clinical signs were markedly reduced amongst vaccinated animals exposed to a severe live‐virus challenge. Appropriate use of this vaccine should lead to a marked reduction in the frequency, severity and duration of outbreaks of equine influenza in North America.</p>
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<title>Efficacy of a cold‐adapted, intranasal, equine influenza vaccine: challenge trials</title>
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<title>Efficacy of a cold‐adapted, intranasal, equine influenza vaccine: challenge trials</title>
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<name type="personal">
<namePart type="given">H. G. G.</namePart>
<namePart type="family">TOWNSEND</namePart>
<affiliation>Department of Large Animal Clinical Sciences, University of Saskatchewan, Saskatoon, Saskatchewan, Canada S7N 5B4</affiliation>
<affiliation>Correspondence address: Department of Large Animal Clinical Sciences, University of Saskatchewan, Saskatoon, Saskatchewan, Canada S7N 5B4</affiliation>
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<affiliation>Department of Veterinary Science, University of Kentucky, 108 Gluck Equine Research Center, Lexington, Kentucky 40546</affiliation>
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<affiliation>Department of Molecular Genetics and Biochemistry, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, USA</affiliation>
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<namePart type="given">J. S.</namePart>
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<affiliation>Department of Molecular Genetics and Biochemistry, School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania 15261, USA</affiliation>
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<dateIssued encoding="w3cdtf">2001-11</dateIssued>
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<abstract lang="en">A randomised, controlled, double‐blind, influenza virus, aerosol challenge of horses was undertaken to determine the efficacy of a cold‐adapted, temperature sensitive, modified‐live virus, intranasal, equine influenza vaccine. Ninety 11‐month‐old influenza‐naïve foals were assigned randomly to 3 groups (20 vaccinates and 10 controls per group) and challenged 5 weeks, 6 and 12 months after a single vaccination. Challenges were performed on Day 0 in a plastic‐lined chamber. Between Days 1 and 10, animals were examined daily for evidence of clinical signs of influenza. Nasal swabs for virus isolation were obtained on Day 1 and Days 1 to 8 and blood samples for serology were collected on Days 1, 7 and 14. There was no adverse response to vaccination in any animal. Following challenge at 5 weeks and 6 months, vaccinates had significantly lower clinical scores (P = 0.0001 and 0.005, respectively), experienced smaller increases in rectal temperature (P = 0.0008 and 0.0007, respectively) and shed less virus (P<0.0001 and P = 0.03, respectively) over fewer days (P<0.0001 and P = 0.002, respectively) than did the controls. After the 12 month challenge, rectal temperatures (P = 0.006) as well as the duration (P = 0.03) and concentration of virus shed (P = 0.04) were significantly reduced among vaccinated animals. The results of this study showed that 6 months after a single dose of vaccine the duration and severity of clinical signs were markedly reduced amongst vaccinated animals exposed to a severe live‐virus challenge. Appropriate use of this vaccine should lead to a marked reduction in the frequency, severity and duration of outbreaks of equine influenza in North America.</abstract>
<subject lang="en">
<genre>keywords</genre>
<topic>horse</topic>
<topic>influenza</topic>
<topic>cold‐adapted</topic>
<topic>vaccine</topic>
<topic>challenge trial</topic>
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<identifier type="ISSN">0425-1644</identifier>
<identifier type="eISSN">2042-3306</identifier>
<identifier type="DOI">10.1001/(ISSN)2042-3306</identifier>
<identifier type="PublisherID">EVJ</identifier>
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<date>2001</date>
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<number>33</number>
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<title>Derivation and characterisation of a live attenuated equine influenza vaccine virus</title>
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