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The Journal of general virology2000; 81(Pt 11); 2735-2739; doi: 10.1099/0022-1317-81-11-2735

Equine infectious anaemia virus proteins with epitopes most frequently recognized by cytotoxic T lymphocytes from infected horses.

Abstract: Efficacious lentiviral vaccines designed to induce cytotoxic T lymphocytes (CTL) in outbred populations with a diverse repertoire of MHC class I molecules should contain or express multiple viral proteins. To determine the equine infectious anaemia virus (EIAV) proteins with epitopes most frequently recognized by CTL from seven horses infected for 0.5 to 7 years, retroviral vector-transduced target cells expressing viral proteins were used in CTL assays. Gag p15 was recognized by CTL from 100% of these infected horses. p26 was recognized by CTL from 86%, SU and the middle third of Pol protein were each recognized by 43%, TM by 29%, and S2 by 14%. Based on these results, it is likely that a construct expressing the 359 amino acids constituting p15 and p26 would contain epitopes capable of stimulating CTL in most horses.
Publication Date: 2000-10-20 PubMed ID: 11038386DOI: 10.1099/0022-1317-81-11-2735Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • U.S. Gov't
  • P.H.S.

Summary

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This study investigates the key proteins of the equine infectious anaemia virus (EIAV) that are recognized by cytotoxic T lymphocytes (CTLs) in the horses. The researchers believe that a vaccine construct containing the p15 and p26 proteins could potentially stimulate CTLs in most horses.

Introduction to the Study

  • The study aims to identify key proteins in the Equine Infectious Anaemia Virus (EIAV) that are most commonly recognized by cytotoxic T lymphocytes (CTLs) in infected horses.
  • The goal of the research is to provide insights that could contribute to the development of vaccines that effectively stimulate an immune response.

Methodology

  • Researchers studied seven horses that had been infected with EIAV for periods ranging from 0.5 to 7 years.
  • They utilized target cells that were transduced (introduced) with the retroviral vector to express viral proteins, and used these cells in the CTL assays.
  • Through this process, they examined how CTL recognized various EIAV proteins such as Gag p15, p26, SU, Pol, TM, and S2.

Results

  • Results revealed that all the infected horses (100%) recognized the Gag p15 protein.
  • Similarly, 86% of the infected horses recognized the p26 protein.
  • However, other proteins were recognized less frequently with SU and the middle third of Pol protein recognized by 43%, TM by 29%, and S2 by 14% of infected horses.

Implications

  • Based on the high recognition rate of the p15 and p26 proteins by the CTLs in the infected horses, the researchers suggest that a vaccine construct expressing these two proteins could potentially stimulate an immune response in most horses.
  • This research provides valuable insights that may guide the development of more effective lentiviral vaccines for horses by targeting these key viral proteins.

Cite This Article

APA
McGuire TC, Leib SR, Lonning SM, Zhang W, Byrne KM, Mealey RH. (2000). Equine infectious anaemia virus proteins with epitopes most frequently recognized by cytotoxic T lymphocytes from infected horses. J Gen Virol, 81(Pt 11), 2735-2739. https://doi.org/10.1099/0022-1317-81-11-2735

Publication

ISSN: 0022-1317
NlmUniqueID: 0077340
Country: England
Language: English
Volume: 81
Issue: Pt 11
Pages: 2735-2739

Researcher Affiliations

McGuire, Travis C
  • Department of Veterinary Microbiology and Pathology1 and Department of Animal Sciences2, Washington State University, Pullman, WA 99164-7040, USA.
Leib, Steven R
  • Department of Veterinary Microbiology and Pathology1 and Department of Animal Sciences2, Washington State University, Pullman, WA 99164-7040, USA.
Lonning, Scott M
  • Department of Veterinary Microbiology and Pathology1 and Department of Animal Sciences2, Washington State University, Pullman, WA 99164-7040, USA.
Zhang, Wei
  • Department of Veterinary Microbiology and Pathology1 and Department of Animal Sciences2, Washington State University, Pullman, WA 99164-7040, USA.
Byrne, Katherine M
  • Department of Veterinary Microbiology and Pathology1 and Department of Animal Sciences2, Washington State University, Pullman, WA 99164-7040, USA.
Mealey, Robert H
  • Department of Veterinary Microbiology and Pathology1 and Department of Animal Sciences2, Washington State University, Pullman, WA 99164-7040, USA.

MeSH Terms

  • Animals
  • Antigens, Viral / immunology
  • Cytotoxicity, Immunologic
  • Epitopes / immunology
  • Equine Infectious Anemia / immunology
  • Horses / immunology
  • Horses / virology
  • Infectious Anemia Virus, Equine / immunology
  • T-Lymphocytes, Cytotoxic / immunology

Grant Funding

  • AI24291 / NIAID NIH HHS

Citations

This article has been cited 11 times.
  1. Liu C, Cook SJ, Craigo JK, Cook FR, Issel CJ, Montelaro RC, Horohov DW. Epitope shifting of gp90-specific cellular immune responses in EIAV-infected ponies.. Vet Immunol Immunopathol 2014 Oct 15;161(3-4):161-9.
    doi: 10.1016/j.vetimm.2014.08.001pubmed: 25176006google scholar: lookup
  2. Taylor SD, Leib SR, Carpenter S, Mealey RH. Selection of a rare neutralization-resistant variant following passive transfer of convalescent immune plasma in equine infectious anemia virus-challenged SCID horses.. J Virol 2010 Jul;84(13):6536-48.
    doi: 10.1128/JVI.00218-10pubmed: 20392850google scholar: lookup
  3. Mealey RH, Leib SR, Littke MH, Wagner B, Horohov DW, McGuire TC. Viral load and clinical disease enhancement associated with a lentivirus cytotoxic T lymphocyte vaccine regimen.. Vaccine 2009 Apr 21;27(18):2453-68.
    doi: 10.1016/j.vaccine.2009.02.048pubmed: 19368787google scholar: lookup
  4. Mealey RH, Littke MH, Leib SR, Davis WC, McGuire TC. Failure of low-dose recombinant human IL-2 to support the survival of virus-specific CTL clones infused into severe combined immunodeficient foals: lack of correlation between in vitro activity and in vivo efficacy.. Vet Immunol Immunopathol 2008 Jan 15;121(1-2):8-22.
    doi: 10.1016/j.vetimm.2007.07.011pubmed: 17727961google scholar: lookup
  5. Mealey RH, Littke MH, Leib SR, Davis WC, McGuire TC. Cloning and large-scale expansion of epitope-specific equine cytotoxic T lymphocytes using an anti-equine CD3 monoclonal antibody and human recombinant IL-2.. Vet Immunol Immunopathol 2007 Jul 15;118(1-2):121-8.
    doi: 10.1016/j.vetimm.2007.04.001pubmed: 17498813google scholar: lookup
  6. Mealey RH, Lee JH, Leib SR, Littke MH, McGuire TC. A single amino acid difference within the alpha-2 domain of two naturally occurring equine MHC class I molecules alters the recognition of Gag and Rev epitopes by equine infectious anemia virus-specific CTL.. J Immunol 2006 Nov 15;177(10):7377-90.
    doi: 10.4049/jimmunol.177.10.7377pubmed: 17082657google scholar: lookup
  7. Chung C, Mealey RH, McGuire TC. Evaluation of high functional avidity CTL to Gag epitope clusters in EIAV carrier horses.. Virology 2005 Nov 25;342(2):228-39.
    doi: 10.1016/j.virol.2005.07.033pubmed: 16139857google scholar: lookup
  8. Mealey RH, Sharif A, Ellis SA, Littke MH, Leib SR, McGuire TC. Early detection of dominant Env-specific and subdominant Gag-specific CD8+ lymphocytes in equine infectious anemia virus-infected horses using major histocompatibility complex class I/peptide tetrameric complexes.. Virology 2005 Aug 15;339(1):110-26.
    doi: 10.1016/j.virol.2005.05.025pubmed: 15979679google scholar: lookup
  9. Chung C, Mealey RH, McGuire TC. CTL from EIAV carrier horses with diverse MHC class I alleles recognize epitope clusters in Gag matrix and capsid proteins.. Virology 2004 Sep 15;327(1):144-54.
    doi: 10.1016/j.virol.2004.06.035pubmed: 15327905google scholar: lookup
  10. Mealey RH, Zhang B, Leib SR, Littke MH, McGuire TC. Epitope specificity is critical for high and moderate avidity cytotoxic T lymphocytes associated with control of viral load and clinical disease in horses with equine infectious anemia virus.. Virology 2003 Sep 1;313(2):537-52.
    doi: 10.1016/s0042-6822(03)00344-1pubmed: 12954220google scholar: lookup
  11. Mealey RH, Fraser DG, Oaks JL, Cantor GH, McGuire TC. Immune reconstitution prevents continuous equine infectious anemia virus replication in an Arabian foal with severe combined immunodeficiency: lessons for control of lentiviruses.. Clin Immunol 2001 Nov;101(2):237-47.
    doi: 10.1006/clim.2001.5109pubmed: 11683583google scholar: lookup