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Lymphocytes from ponies experimentally infected with equine herpesvirus 1: subpopulation dynamics and their response to mitogens.

Abstract: Six pony foals, free of detectable serum neutralization (SN) antibody against equine herpesvirus type 1 by the standard virus-neutralization (VN) test, were inoculated with equine herpesvirus type 1. The ponies showed typical clinical signs of respiratory tract disease and developed a transient leukopenia, involving lymphocytes as well as neutrophils. The leukopenia reached its lowest point on postinoculation days (PID) 3 to 5 and then returned to base-line values by PID 8 to 10. On quantitation of lymphocyte subpopulations, T and B lymphocytes were decreased during the onset of leukopenia and then recouped during the recovery from leukopenia. However, the proportions of the T and B lymphocytes remained constant during the lymphopenia, ranging from 70% to 80% and 20% to 30%, respectively. The lymphocyte blastogenic response to mitogens increased to peak by PID 2 to 5 and then decreased to base line values or below by PID 7. Mitogen responses of T lymphocyte and mixed lymphocyte preparations were nearly similar. However, the responses of 2 ponies wee somewhat different from the responses of others in that there was an increase in the B lymphocytes in the range of 40% to 50% during the recovery phase of lymphopenia. Also, the 2 ponies' mixed lymphocyte response to mitogens was considerably higher and the T lymphocyte response to mitogen was lower as compared with that of mixed lymphocyte preparation. The importance of these 2 types of responses is discussed.
Publication Date: 1982-07-01 PubMed ID: 6285778
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  • Journal Article
  • Research Support
  • U.S. Gov't
  • Non-P.H.S.

Summary

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The research puts six pony foals, that have no existing immunity against equine herpesvirus type 1, under study to observe the changes in their lymphocyte populations post inoculation with the virus. The study discovers the occurrence of transient leukopenia and identifies differences in the behavior of T and B lymphocyte subpopulations during different stages of the disease.

Methodology

  • The study involves six pony foals free from any detectable serum neutralization antibody against equine herpesvirus type 1. This prerequisite ensures that the ponies’ immune system has not been exposed to this virus before.
  • The ponies are inoculated with the virus, and their immune response is closely monitored.

Observations Post Inoculation

  • After infection, the ponies displayed typical signs of respiratory tract disease, indicating the successful transmission of the virus.
  • A transient leukopenia, a temporary decrease in the count of white blood cells, was observed, affecting lymphocytes and neutrophils.
  • The lowest leukocyte count was reached between the third and fifth day post-inoculation, but it returned to normal between the eighth and tenth day.

Dynamics of Lymphocyte Subpopulations

  • Detailed examination of white blood cells revealed that both T and B lymphocytes decreased during leukopenic onset but recovered as the leukopenic phase ended.
  • Interestingly, during the period of leukopenia, the ratio of T to B lymphocytes remained stable, with T lymphocytes accounting for 70% to 80% and B lymphocytes accounting for 20% to 30% of the total count.

Response to Mitogens

  • The lymphocyte blastogenic response to mitogens, substances that encourage cell division, peaked between the second and fifth day, then decreased to baseline or below by the seventh day.
  • Responses from T lymphocytes and mixed lymphocyte preparations were nearly identical. However, two ponies showed an increase in B lymphocytes up to 40%-50% during the recovery phase, as well as an unusually high mixed lymphocyte response to mitogens and a lower T lymphocyte response.

The research concludes by discussing the significance of the varying responses noted in the two subpopulations of lymphocytes during the different stages of the disease.

Cite This Article

APA
Bumgardner MK, Dutta SK, Campbell DL, Myrup AC. (1982). Lymphocytes from ponies experimentally infected with equine herpesvirus 1: subpopulation dynamics and their response to mitogens. Am J Vet Res, 43(7), 1308-1310.

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 43
Issue: 7
Pages: 1308-1310

Researcher Affiliations

Bumgardner, M K
    Dutta, S K
      Campbell, D L
        Myrup, A C

          MeSH Terms

          • Acute Disease
          • Animals
          • Antibodies, Viral / analysis
          • B-Lymphocytes / drug effects
          • Concanavalin A / pharmacology
          • Herpesviridae Infections / immunology
          • Herpesviridae Infections / veterinary
          • Herpesvirus 1, Equid / immunology
          • Horse Diseases / immunology
          • Horses
          • Leukocyte Count / veterinary
          • Lymphopenia / immunology
          • Lymphopenia / veterinary
          • Neutralization Tests
          • Phytohemagglutinins / pharmacology
          • Pokeweed Mitogens / pharmacology
          • Respiratory Tract Infections / immunology
          • Respiratory Tract Infections / veterinary
          • T-Lymphocytes / drug effects

          Citations

          This article has been cited 3 times.
          1. Molinková D, Celer V Jr, Jahn P. Isolation and partial characterization of equine herpesvirus type 1 in Czechia. Folia Microbiol (Praha) 2004;49(5):605-11.
            doi: 10.1007/BF02931542pubmed: 15702554google scholar: lookup
          2. Smith D, Hamblin A, Edington N. Equid herpesvirus 1 infection of endothelial cells requires activation of putative adhesion molecules: an in vitro model. Clin Exp Immunol 2002 Aug;129(2):281-7.
          3. de la Cuesta-Torrado M, Velloso Alvarez A, Cárdenas-Rebollo JM, Neira-Egea P, Vitale V, Cuervo-Arango J. Comparison of clinical variables and outcome of 2 natural equine herpesvirus myeloencephalopathy outbreaks induced by equine herpesvirus-1 A2254/N752 strain in sport horses. J Vet Intern Med 2025 Jan-Feb;39(1):e17287.
            doi: 10.1111/jvim.17287pubmed: 39778904google scholar: lookup