Equine immunity to viruses.
Abstract: The identification of some of the adaptive immune responses to infection with equine viruses has been the first step toward rational immunoprophylactic design. Sufficient knowledge of infection-induced immunity and informed estimates of the requirements for long-term immunity for EIV have now been obtained. Thus, the future for inactivated EIV vaccines is promising now that new adjuvants have been applied to induce cellular immunity and safe methods have been designed to stimulate virus-neutralizing (VN) antibody at mucosal surfaces. Adenoviruses induce circulating VN antibody, the presence of which appears to correlate with protection from reinfection. Therefore, the potential of vaccines to induce VN antibody and protect from challenge is an important next step with this virus. With persistent viruses such as EHV-1, antibody-mediated protection from infection can be achieved only at the site of initial infection, that is, the nasopharynx and upper respiratory tract. Systemic dissemination is very rapid and consequently VN antibody is unlikely to play a major role in prevention of disease once the initial infection event has occurred. Cellular immune responses, particularly CTLs, play a dominant role in protection and recovery and are important in immune surveillance and determination of the outcome of reactivation of latent virus. Therefore, the key to future EHV-1 vaccine design is to focus on stimulation of CTL responses, and this requires the successful presentation of vaccine-derived antigenic peptides to MHC class I molecules that are recognized by specific receptors on CTL. There is some evidence that stimulation of EHV-1-specific CTL precursors may correlate with immunity to this virus. By analogy with gamma herpesviruses in humans, CTL precursor frequency may also function as an immune correlate for EHV-2. Although EAV infection induces strong immunity in females and geldings, persistent infection of the genital tract is an important route of dissemination from stallions. Although inactivated vaccines induce strong immunity (which depends upon VN activity of serum antibody) to first infection, the immunologic control of persistent infection is currently poorly understood; however, analogy with other persistent viruses suggests that CTLs are also likely to play an important role in the control of persistent EAV infections.
Publication Date: 2000-04-07 PubMed ID: 10752138
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Summary
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The research article explores the progress in understanding how horses’ immune systems respond to certain viral infections, and how this knowledge can inform the development of more efficient vaccines. It focuses mainly on three specific viruses: Equine Influenza Virus (EIV), Equine Herpes Virus-1 (EHV-1), and Equine Arteritis Virus (EAV).
Immunity to Equine Influenza Virus (EIV)
- The researchers have made strides in understanding the immune responses triggered by a horse’s body when infected with EIV. Such knowledge is essential in designing immunoprophylactic efforts – such as vaccines – against the virus.
- Once infected, a horse’s immune system can remember the virus, leading to long-term immunity. Scientists can use this knowledge to design vaccines that mimic this natural immune defense mechanism.
- Additionally, new adjuvants (substances that enhance the body’s immune response to an antigen) have been introduced that can stimulate cellular immunity — this means that they can spur the body’s cells to defend against the virus.
- Different methods have also been developed to promote the creation of virus-neutralizing (VN) antibodies at the mucosal surfaces of a horse’s body – these are areas like the nose and mouth, which are often the first point of contact with the virus.
Adenovirus Immunity and Vaccine Development
- The presence of VN antibodies, induced by adenoviruses, appears to protect against reinfection.
- The development of vaccines that can stimulate the production of these antibodies and provide protection from the virus is a crucial next step in this research.
Immunity to Equine Herpes Virus-1 (EHV-1)
- Unlike with EIV and adenoviruses, VN antibodies’ role in preventing EHV-1 is limited, as this virus spreads very swiftly through the body.
- However, antibody-mediated protection can be successful at the initial site of infection — typically the nasopharynx (back of the nose) and upper respiratory tract — indicating that vaccines targeting these areas may be effective.
- The researchers found that cellular immune responses, especially from cytotoxic T lymphocytes (CTLs), are essential not only in initial protection but also in recovery and immune surveillance.
- EHV-1-specific CTL precursors may correlate with immunity to this virus, suggesting that the future EHV-1 vaccine design should focus on how to stimulate CTL responses that recognize the virus.
Persistent Infection and Immunity to Equine Arteritis Virus (EAV)
- EAV infection induces strong immunity in horses, but stallions can continue to carry and spread the virus through the genital tract even after recovery.
- Although inactivated vaccines have been able to induce a potent immunity (which depends upon VN activity of serum antibody) to a first EAV infection, the control of these persistent infections is not yet fully understood.
- Like with EHV-1, CTLs are likely to play a crucial role in controlling persistent EAV infections, providing a possible area for future vaccine development.
Cite This Article
APA
Slater J, Hannant D.
(2000).
Equine immunity to viruses.
Vet Clin North Am Equine Pract, 16(1), 49-68.
Publication
Researcher Affiliations
- Department of Clinical Veterinary Medicine, University of Cambridge, United Kingdom. jds1001@cam.ac.uk
MeSH Terms
- Acute-Phase Proteins / analysis
- Adaptation, Physiological
- Animals
- Antibodies, Viral / biosynthesis
- Horses / immunology
- Immunity, Innate
- Influenza A virus / immunology
- Surface Properties
- T-Lymphocytes / immunology
- Viruses / immunology
References
This article includes 51 references
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