Equine rhinopneumonitis vaccine: immunogenicity and safety in foals.
Abstract: Immunogenicity and safety of an equine herpesvirus 1 (ehv-1) vaccine were studied in 111 foals varying in age from 1 to 122 days. Each of 88 principals was given 1 im injection of vaccine. Five of the 88 foals were revaccinated; 69 of the vaccinated principals and 23 nonvaccinated foals (serving as controls) were challenge exposed intranasally with virulent ehv-1.
The vaccine failed to cause adverse local or systemic reaction in 88 principals with serunirneutralization (sn) titers against ehv-1 varying between 0 to 1:256 at time of vaccination. After vaccination, the foals' body temperatures remained normal and peripheral blood leukocyte counts were normal or only slightly depressed. Attenuated ehv-1 was generally isolated from peripheral blood leukocytes obtained from foals after vaccination.
None of 36 vaccinated foals, including those with maternal ehv-1 antibody, had signs of equine rhinopneumonitis (erp) following challenge exposure on experimental day 120. In contrast, all of the nonvaccinated controls had anorexia, depression, nasal discharge, occasional coughing, fever, and marked leukopenia after challenge exposure.
Foals vaccinated when they were 1 to 12 days old and nonvaccinated controls had classic signs of erp after challenge exposure on experimental day 365. Following challenge exposure, vaccinated foals and controls developed fever and leukopenia, and virulent ehv-1 was isolated regularly from nasal and buffy coat specimens.
Foals vaccinated when they were 7 to 42 days old failed to exhibit clinical signs of erp, but did develop mild fever and leukopenia when challenge exposed on experimental day 365. Furthermore, virulent ehv-1 was isolated regularly from paired nasal and blood specimens.
Foals vaccinated at an average age of 122 days not only failed to exhibit clinical signs of erp, but also did not have fever and leukopenia after challenge exposure on experimental day 365. Virulent ehv-1 was not isolated from 42 paired specimens obtained 3 to 14 days after challenge exposure.
Vaccination of foals with low sn titers (1:10 to 1:30) of ehv-1 antibody gave rise to gradual increase in titer over a 35-day period, whereas vaccination of foals with higher sn titers (1:171) produced a decline consistent with maternal antibody decay. Maternal ehv-1 antibody was found to be depleted within 56 to 130 days, depending directly upon the initial sn titer.
Publication Date: 1978-05-01 PubMed ID: 215062
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- Journal Article
Summary
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This research paper evaluates the effectiveness and safety of a vaccine for equine herpesvirus 1 (ehv-1), which can cause equine rhinopneumonitis (erp). It found that the vaccine was safe and did not cause adverse reactions in foals. However, effectiveness varied depending on the age of the foal at the time of vaccination and the presence of maternal antibodies.
Experiment Setup
- The study involved 111 foals aged between 1 and 122 days. Of these, 88 were given an injection of the vaccine, with five receiving a second dose.
- Following vaccination, 69 of the vaccinated foals, along with 23 non-vaccinated foals (used as controls), were intentionally exposed to a virulent strain of ehv-1 to test the vaccine’s effectiveness.
Safety of the Vaccine
- The vaccine was found to be safe, causing no adverse local or systemic reactions in the 88 vaccinated foals.
- Following vaccination, the foals’ body temperatures remained normal and blood leukocyte counts were mostly unaffected.
Vaccine Effectiveness
- The vaccine’s effectiveness varied depending on the age of the foal at the time of vaccination, the presence of maternal antibodies, and the length of time since vaccination.
- After exposure to the virus, none of the vaccinated foals showed signs of erp, regardless of their age at vaccination or the presence of maternal antibodies. This contrasted with the non-vaccinated control group, all of whom developed symptoms of erp following exposure to the virus.
- Foals vaccinated at 1 to 12 days old initially showed no signs of erp but developed symptoms after a year during a second exposure test. Meanwhile, foals vaccinated between 7 to 42 days old experienced only mild symptoms after the second exposure test.
- Foals vaccinated at an average age of 122 days showed no signs of erp or related symptoms, even after the second exposure test a year later.
Impact of Maternal Antibodies
- Maternal ehv-1 antibodies were found to decline over time. Foals with lower antibody levels at the time of vaccination saw an increase in antibody levels over a 35-day period, while those with higher initial levels experienced a decline consistent with typical maternal antibody decay.
- It was concluded that maternal ehv-1 antibody was depleted within 56 to 130 days, dependent on the initial antibody level.
Cite This Article
APA
Purdy CW, Porter RC, Ford SJ.
(1978).
Equine rhinopneumonitis vaccine: immunogenicity and safety in foals.
Am J Vet Res, 39(5), 745-752.
Publication
Researcher Affiliations
MeSH Terms
- Animals
- Antibodies, Viral / analysis
- Antibody Formation
- Female
- Herpesviridae / immunology
- Herpesviridae Infections / prevention & control
- Herpesviridae Infections / veterinary
- Herpesvirus 1, Equid / immunology
- Herpesvirus 1, Equid / pathogenicity
- Horse Diseases / prevention & control
- Horses / immunology
- Immunity, Maternally-Acquired
- Male
- Neutralization Tests
- Viral Vaccines / adverse effects
- Virulence
Citations
This article has been cited 2 times.- Nugent J, Birch-Machin I, Smith KC, Mumford JA, Swann Z, Newton JR, Bowden RJ, Allen GP, Davis-Poynter N. Analysis of equid herpesvirus 1 strain variation reveals a point mutation of the DNA polymerase strongly associated with neuropathogenic versus nonneuropathogenic disease outbreaks. J Virol 2006 Apr;80(8):4047-60.
- Osterrieder K, Dorman DC, Burgess BA, Goehring LS, Gross P, Neinast C, Pusterla N, Hussey GS, Lunn DP. Vaccination for the prevention of equine herpesvirus-1 disease in domesticated horses: A systematic review and meta-analysis. J Vet Intern Med 2024 May-Jun;38(3):1858-1871.
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