Equine IgE responses to non-viral vaccine components.
Abstract: Vaccination of horses is performed annually or semi-annually with multiple viral antigens, either in a combination vaccine or as separate injections. While this practice undoubtedly prevents infection from such diseases as rabies, equine influenza, West Nile virus, and equine herpes virus, the procedure is not without repercussions. Hypersensitivity reactions, including fatal anaphylactic shock, after vaccination, although uncommon, have increased in incidence in recent years. Studies reported herein document the development of IgE antibodies against non-target antigen components of equine viral vaccines. We hypothesize that viral vaccines can induce an IgE response to non-target antigens, which could elicit an adverse response after vaccination with another viral vaccine containing the same component. In one study IgE responses to components of West Nile virus vaccine were evaluated by ELISA before and after vaccination in 30 horses. In a second five-year study 77 horses were similarly tested for IgE antibodies against bovine serum albumin (BSA), a component of most viral vaccines. Mast cell sensitization was evaluated in horses with high, moderate, and negative serum BSA specific IgE using an intradermal skin test with BSA. Over the five-year period high IgE responder horses showed gradually increasing BSA specific serum IgE levels and positive skin test reactivity, yet none had an adverse event. Sera from horses that had developed adverse vaccine reactions were also tested for IgE antibodies. Several of these horses had extremely high levels of BSA-specific IgE. These data suggest that non-essential protein components of vaccines may sensitize horses for future adverse responses to vaccination.
Copyright © 2012 Elsevier Ltd. All rights reserved.
Publication Date: 2012-10-23 PubMed ID: 23088888DOI: 10.1016/j.vaccine.2012.10.029Google Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research article discusses the potential link between equine viral vaccines and hypersensitivity reactions in horses, particularly due to the development of IgE antibodies against non-target antigens in these vaccines. The study finds that horses may develop an increasing sensitivity to certain vaccines over time without immediate adverse effects, however those showing adverse reactions had high levels of specific IgE antibodies.
Understanding the Research
- The research primarily focused on the adverse reactions observed in horses after vaccination. Although vaccines prevent horses from severe ailments like rabies, West Nile virus, equine influenza, and equine herpes virus, there are increasing incidences of hypersensitivity reactions including fatal anaphylactic shock.
- The authors proposed that these adverse reactions might be due to the development of Immunoglobulin E (IgE) antibodies against non-target components of these viral vaccines. This means that the horse’s immune system might maladaptively respond to components of the vaccine that are not the virus itself, causing a harmful overreaction.
Study Design and Methodology
- Two studies were conducted to test the authors’ hypothesis. The first evaluated the IgE responses to components of West Nile virus vaccine in 30 horses before and after vaccination. The second study was a lengthier process conducted over five years, testing 77 horses for IgE antibodies against bovine serum albumin (BSA), a common component of most viral vaccines.
- Mast cell sensitization, which indicates the immune system’s readiness to react against an allergen, was evaluated in horses showing high, moderate, and negative BSA-specific IgE levels using a skin test.
Findings and Significance
- The results showed high responder horses gradually increasing in their BSA-specific IgE levels over the five years. They also exhibited positive skin test reactivity, indicating an increasing sensitivity to the non-viral vaccine component. Despite this growing sensitization, no adverse events were recorded in these horses. However, horses that did present adverse reactions to vaccines displayed extremely high levels of BSA-specific IgE.
- This indicates that the non-essential protein components of vaccines may sensitize some horses for potential future adverse responses to vaccination. That is, certain horses may become more prone to hypersensitivity reactions with successive vaccinations due to the development of IgE antibodies against components of the vaccine that aren’t the target virus itself.
- The implication of this research could be significant in understanding and preventing adverse vaccine reactions and in improving the formulation of equine vaccines. The study basically suggests caution and further research into the potential sensitizing effects of non-viral vaccine components.
Cite This Article
APA
Gershwin LJ, Netherwood KA, Norris MS, Behrens NE, Shao MX.
(2012).
Equine IgE responses to non-viral vaccine components.
Vaccine, 30(52), 7615-7620.
https://doi.org/10.1016/j.vaccine.2012.10.029 Publication
Researcher Affiliations
- Department of Pathology, Microbiology, and Immunology, School of Veterinary Medicine, University of California, Davis, United States. ljgershwin@ucdavis.edu
MeSH Terms
- Animals
- Enzyme-Linked Immunosorbent Assay
- Excipients / administration & dosage
- Excipients / adverse effects
- Horses
- Immunoglobulin E / blood
- Serum Albumin, Bovine / administration & dosage
- Serum Albumin, Bovine / adverse effects
- Serum Albumin, Bovine / immunology
- West Nile Virus Vaccines / administration & dosage
- West Nile Virus Vaccines / adverse effects
- West Nile Virus Vaccines / immunology
Citations
This article has been cited 11 times.- Punzón E, García-Castillo M, Rico MA, Padilla L, Pradera A. Local, systemic and immunologic safety comparison between xenogeneic equine umbilical cord mesenchymal stem cells, allogeneic canine adipose mesenchymal stem cells and placebo: a randomized controlled trial. Front Vet Sci 2023;10:1098029.
- Depuydt E, Broeckx SY, Chiers K, Patruno M, Da Dalt L, Duchateau L, Saunders J, Pille F, Martens A, Van Hecke L, Spaas JH. Cellular and Humoral Immunogenicity Investigation of Single and Repeated Allogeneic Tenogenic Primed Mesenchymal Stem Cell Treatments in Horses Suffering From Tendon Injuries. Front Vet Sci 2021;8:789293.
- Rowland AL, Burns ME, Levine GJ, Watts AE. Preparation Technique Affects Recipient Immune Targeting of Autologous Mesenchymal Stem Cells. Front Vet Sci 2021;8:724041.
- Entenfellner J, Gahan J, Garvey M, Walsh C, Venner M, Cullinane A. Response of Sport Horses to Different Formulations of Equine Influenza Vaccine. Vaccines (Basel) 2020 Jul 10;8(3).
- Cullinane A, Gahan J, Walsh C, Nemoto M, Entenfellner J, Olguin-Perglione C, Garvey M, Huang Fu TQ, Venner M, Yamanaka T, Barrandeguy M, Fernandez CJ. Evaluation of Current Equine Influenza Vaccination Protocols Prior to Shipment, Guided by OIE Standards. Vaccines (Basel) 2020 Feb 29;8(1).
- Barberini DJ, Aleman M, Aristizabal F, Spriet M, Clark KC, Walker NJ, Galuppo LD, Amorim RM, Woolard KD, Borjesson DL. Safety and tracking of intrathecal allogeneic mesenchymal stem cell transplantation in healthy and diseased horses. Stem Cell Res Ther 2018 Apr 10;9(1):96.
- Gershwin LJ. Adverse Reactions to Vaccination: From Anaphylaxis to Autoimmunity. Vet Clin North Am Small Anim Pract 2018 Mar;48(2):279-290.
- Owens SD, Kol A, Walker NJ, Borjesson DL. Allogeneic Mesenchymal Stem Cell Treatment Induces Specific Alloantibodies in Horses. Stem Cells Int 2016;2016:5830103.
- Arzi B, Mills-Ko E, Verstraete FJ, Kol A, Walker NJ, Badgley MR, Fazel N, Murphy WJ, Vapniarsky N, Borjesson DL. Therapeutic Efficacy of Fresh, Autologous Mesenchymal Stem Cells for Severe Refractory Gingivostomatitis in Cats. Stem Cells Transl Med 2016 Jan;5(1):75-86.
- Paillot R. A Systematic Review of Recent Advances in Equine Influenza Vaccination. Vaccines (Basel) 2014 Nov 14;2(4):797-831.
- Shin YS, Suh DH, Yang EM, Ye YM, Park HS. Serum Specific IgE to Thyroid Peroxidase Activates Basophils in Aspirin Intolerant Urticaria. J Korean Med Sci 2015 Jun;30(6):705-9.
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