Trials of an inactivated equid herpesvirus 1 vaccine: challenge with a subtype 2 virus.
Abstract: Serological responses following two and three doses of an inactivated equid herpesvirus 1 ( EHV -1) vaccine containing a subtype 1 strain were examined in yearling ponies. Complement fixing antibody responses were significantly higher against the subtype 1 vaccine strain than against a subtype 2 virus. Complement fixing antibody responses declined rapidly after the second dose of vaccine and had returned to almost pre-vaccination levels eight weeks after the second dose of vaccine. Complement fixing antibody titres to the heterologous subtype 2 strain increased after each successive dose of vaccine. The neutralising antibody responses following vaccination were weak although less strain specific than the complement fixing antibody responses. When challenged with a subtype 2 strain, 15 ponies which had received three doses of vaccine, two, eight and 12 weeks previously resisted challenge infection. However, 11 out of 15 ponies which had received two doses of vaccine eight and 12 weeks previously were susceptible to infection. While two doses of vaccine did not reduce duration of virus excretion or febrile responses in ponies challenged eight weeks after the second dose, the amount of virus excreted was significantly reduced.
Publication Date: 1984-04-14 PubMed ID: 6328729DOI: 10.1136/vr.114.15.375Google Scholar: Lookup
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- Clinical Trial
- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research article focuses on testing an inactivated equid herpesvirus 1 (EHV-1) vaccine in yearling ponies and the subsequent immune responses elicited by it, especially when faced with a subtype 2 of the virus challenge.
Subject and Vaccine Administered
- The research carried out trials with a vaccine against equid herpesvirus 1 (EHV-1), a significant pathogen in horses, mules, and donkeys leading to much economic loss due to its detrimental effects. The subtype 1 strain of the EHV-1 was incorporated into the inactivated vaccine.
- The trials were conducted on ponies that were a year old to observe the immune response to vaccination.
- Two groups received the vaccine: one group got two doses, while the other got three doses. The timing of the doses and the subsequent challenge with subtype 2 of the virus varied for each group.
Serological Response
- The serological responses, or the production of antibodies in response to the vaccine, were studied.
- A significant increase in complement fixing antibodies was observed against the subtype 1 virus included in the vaccine. These antibodies are involved in eliminating infected cells and combatting the virus.
- An interesting observation was that these antibodies declined rapidly after the second dose and almost reverted to pre-vaccination levels eight weeks post the second dose.
- The amount of complement fixing antibodies against the subtype 2 virus showed an increase with each additional dose of vaccine.
- The vaccine-induced neutralising antibody responses were weak, suggesting lower effectiveness of the vaccine against neutralising the virus. However, this response was less strain-specific than the complement fixing ones.
Challenge Infection Outcomes
- The vaccinated ponies were then challenged with a subtype 2 virus to study the vaccine’s effectiveness.
- Ponies administered three doses of the vaccine showed resistance to the subtype 2 virus, indicating the benefits of a third dose in providing immunity against a heterologous virus.
- Conversely, out of the ponies that received two doses, most were still susceptible to subtype 2 virus infection, indicating that two doses may not offer complete protection.
- While two doses did not lower the duration of virus excretion or fever responses when ponies were faced with a subtype 2 challenge, the viral load was significantly reduced.
Implications
- The study provides insights on EHV-1 vaccine’s effectiveness, showing the benefit of a three-dose regimen in equine immunity against homologous and heterologous viruses.
- The findings highlight the need for further research to optimize the vaccine dosage and its delivery schedule for comprehensive protection against EHV-1 and its subtypes.
Cite This Article
APA
Mumford JA, Bates J.
(1984).
Trials of an inactivated equid herpesvirus 1 vaccine: challenge with a subtype 2 virus.
Vet Rec, 114(15), 375-381.
https://doi.org/10.1136/vr.114.15.375 Publication
Researcher Affiliations
MeSH Terms
- Animals
- Antibodies, Viral / analysis
- Antibodies, Viral / biosynthesis
- Clinical Trials as Topic / veterinary
- Complement Fixation Tests / veterinary
- Herpesviridae / immunology
- Herpesviridae Infections / immunology
- Herpesviridae Infections / prevention & control
- Herpesviridae Infections / veterinary
- Herpesvirus 1, Equid / immunology
- Horse Diseases / immunology
- Horse Diseases / prevention & control
- Horses
- Neutralization Tests
- Respiratory Tract Infections / immunology
- Respiratory Tract Infections / veterinary
- Vaccination / veterinary
- Vaccines, Attenuated / immunology
- Viral Vaccines / immunology
Citations
This article has been cited 5 times.- Warda FF, Ahmed HES, Shafik NG, Mikhael CA, Abd-ElAziz HMG, Mohammed WA, Shosha EA. Application of equine herpesvirus-1 vaccine inactivated by both formaldehyde and binary ethylenimine in equine.. Vet World 2021 Jul;14(7):1815-1821.
- Charan S, Palmer K, Chester P, Mire-Sluis AR, Meager A, Edington N. Transforming growth factor-beta induced by live or ultraviolet-inactivated equid herpes virus type-1 mediates immunosuppression in the horse.. Immunology 1997 Apr;90(4):586-91.
- Allen G, Yeargan M, Costa LR, Cross R. Major histocompatibility complex class I-restricted cytotoxic T-lymphocyte responses in horses infected with equine herpesvirus 1.. J Virol 1995 Jan;69(1):606-12.
- Bridges CG, Ledger N, Edington N. The characterization of equine herpes virus-1-infected cell polypeptides recognized by equine lymphocytes.. Immunology 1988 Feb;63(2):193-8.
- Bridges CG, Edington N. Genetic restriction of cytolysis during equid herpesvirus 1 subtype 2 infection.. Clin Exp Immunol 1987 Nov;70(2):276-82.
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