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Veterinary microbiology2025; 310; 110732; doi: 10.1016/j.vetmic.2025.110732

Vaccination against Hendra virus of previously unvaccinated mares and their foals demonstrates the effectiveness of the current prime and boost vaccination schedule for foals.

Abstract: Hendra virus (HeV) is a high consequence pathogen that causes severe respiratory and/or neurological disease in both horses and humans with high mortality. The equine vaccine, Equivac® HeV, is a recombinant soluble version of the G glycoprotein of HeV (HeV-sG) that elicits a potent HeV-neutralising antibody response in adult horses and also provides indirect protection for humans. Maternally derived HeV-G specific antibodies could interfere with subsequent foal vaccination, although other factors such as foal age and the suitability of vaccination protocols that have been optimised for adult horses may also be important. The aim of this study was to measure the HeV-G specific antibody levels of previously unvaccinated mares and their foals at key time points during the preliminary HeV vaccination schedule of three vaccinations. Previously unvaccinated mares and their foals were vaccinated according to the manufacturers recommendations and serum samples were tested for HeV-G specific antibodies using a microsphere-based immunoassay. There was no difference in the humoral response to vaccination between the mares and foals, and both mare and foal groups demonstrated a strong HeV-G specific antibody response after completion of the preliminary vaccination schedule. This study highlights the importance of the third vaccination in eliciting a strong antibody response in foals, as has been demonstrated previously for adult horses. However, the absence of passively acquired immunity and the limited response of foals to the initial two vaccinations does leave foals vulnerable to infection during the majority of the first year of life.
Publication Date: 2025-09-15 PubMed ID: 40961579DOI: 10.1016/j.vetmic.2025.110732Google Scholar: Lookup
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  • Journal Article

Summary

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Overview

  • This study evaluates the effectiveness of the Hendra virus vaccination schedule in previously unvaccinated mares and their foals, specifically focusing on the antibody response they develop following the recommended prime and boost vaccination regimen.
  • The findings show that both mares and foals develop strong Hendra virus-specific antibody responses after completing the vaccination schedule, confirming the effectiveness of the protocol for foals as well as adult horses.

Background

  • Hendra virus (HeV) is a highly dangerous virus causing severe respiratory and neurological symptoms in horses and humans, often resulting in high mortality.
  • The Equivac® HeV vaccine is designed for horses and is based on a recombinant soluble form of the virus’s G glycoprotein (HeV-sG), which triggers the immune system to produce neutralizing antibodies against HeV.
  • Vaccinating horses not only protects the animals but also helps reduce the risk of transmission to humans.
  • Foals typically acquire maternal antibodies passively from their vaccinated mothers, which might interfere or modify the effectiveness of their own vaccination responses.
  • Current vaccination protocols are optimized mainly for adult horses, and their suitability for foals has been unclear.

Objectives

  • To measure HeV-G specific antibody levels in previously unvaccinated mares and their foals at specific time points during the foals’ vaccination schedule.
  • To assess whether the existing vaccination protocol used for adult horses is effective in foals.
  • To identify the importance of each vaccination dose (especially the third boosting dose) in developing strong immunity in foals.

Methodology

  • Selection of previously unvaccinated mares and their foals for the study.
  • Administration of the Equivac® HeV vaccine following the manufacturer’s recommended preliminary schedule of three vaccinations (prime and two booster doses).
  • Collection of serum samples at key stages of the vaccination process to monitor antibody levels.
  • Use of a microsphere-based immunoassay to precisely measure HeV-G specific antibody concentrations in the serum samples.

Findings

  • No significant difference was found in the antibody response between mares and foals after vaccination, indicating that foals respond similarly to unvaccinated adult horses.
  • Strong HeV-G specific antibody responses were observed in both groups after the completion of all three vaccine doses.
  • The third vaccination was critical in eliciting a robust antibody response in foals, confirming the importance of the full prime-boost-boost schedule rather than just the initial doses.
  • Foals had little to no passively derived immunity from their mothers since the mares were previously unvaccinated, resulting in limited protection during early life stages.
  • This limited early immunity and response to the first two vaccinations potentially leaves foals vulnerable to Hendra virus infection for most of their first year.

Implications

  • Vaccination schedules optimized for adult horses are also effective for foals if completed fully.
  • It is crucial for foals to complete all three initial vaccine doses to develop adequate protection against Hendra virus.
  • There is a window of vulnerability to infection in foals due to the absence of maternal antibodies and initial low vaccine response, highlighting the need for careful management during their first year.
  • Ensuring timely vaccination of mares prior to foaling might help provide passive immunity to foals in future settings, which could influence foal vaccination strategies.

Cite This Article

APA
Carey KJ, Smith I, Hartley CA, Bailey KE, McIntosh K, Broder CC, Gilkerson JR. (2025). Vaccination against Hendra virus of previously unvaccinated mares and their foals demonstrates the effectiveness of the current prime and boost vaccination schedule for foals. Vet Microbiol, 310, 110732. https://doi.org/10.1016/j.vetmic.2025.110732

Publication

ISSN: 1873-2542
NlmUniqueID: 7705469
Country: Netherlands
Language: English
Volume: 310
Pages: 110732
PII: S0378-1135(25)00368-2

Researcher Affiliations

Carey, Kimberley J
  • Centre for Equine Infectious Disease, Melbourne Veterinary School, Faculty of Science, The University of Melbourne, Corner Park Drive and Flemington Road, Parkville, VIC 3010, Australia. Electronic address: careyk@student.unimelb.edu.au.
Smith, Ina
  • CSIRO Health and Biosecurity, Black Mountain Laboratories, Clunies Ross Street, Black Mountain ACT 2601, Australia. Electronic address: ina.smith@csiro.au.
Hartley, Carol A
  • Centre for Equine Infectious Disease, Melbourne Veterinary School, Faculty of Science, The University of Melbourne, Corner Park Drive and Flemington Road, Parkville, VIC 3010, Australia. Electronic address: carolah@unimelb.edu.au.
Bailey, Kirsten E
  • Centre for Equine Infectious Disease, Melbourne Veterinary School, Faculty of Science, The University of Melbourne, Corner Park Drive and Flemington Road, Parkville, VIC 3010, Australia. Electronic address: baileyk@unimelb.edu.au.
McIntosh, Kath
  • Northern Rivers Equine, 78 Gray Road, Kyabram, VIC 3620, Australia. Electronic address: kath@nrequine.com.au.
Broder, Christopher C
  • Department of Microbiology and Immunology, Uniformed Services University, 4301 Jones Bridge Road, Bethesda, MD 20814, United States. Electronic address: christopher.broder@usuhs.edu.
Gilkerson, James R
  • Centre for Equine Infectious Disease, Melbourne Veterinary School, Faculty of Science, The University of Melbourne, Corner Park Drive and Flemington Road, Parkville, VIC 3010, Australia. Electronic address: jrgilk@unimelb.edu.au.

MeSH Terms

  • Animals
  • Horses
  • Hendra Virus / immunology
  • Horse Diseases / prevention & control
  • Horse Diseases / virology
  • Horse Diseases / immunology
  • Henipavirus Infections / veterinary
  • Henipavirus Infections / prevention & control
  • Henipavirus Infections / virology
  • Henipavirus Infections / immunology
  • Female
  • Antibodies, Viral / blood
  • Viral Vaccines / immunology
  • Viral Vaccines / administration & dosage
  • Vaccination / veterinary
  • Immunization Schedule
  • Immunization, Secondary / veterinary
  • Antibodies, Neutralizing / blood

Conflict of Interest Statement

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: C.C.B. is a United States federal employee and co-inventor on US and foreign patents pertaining to soluble forms of the Hendra virus and Nipah virus G glycoproteins whose assignee is the United States as represented by the Henry M. Jackson Foundation for the Advancement of Military Medicine (Bethesda, Maryland). Soluble forms of the Hendra virus and Nipah virus G glycoproteins are licensed to Zoetis Inc. The remaining authors declare no competing interests.

Citations

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