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Research in veterinary science1999; 66(3); 277-279; doi: 10.1053/rvsc.1998.0256

Characterisation of equine T helper cells: demonstration of Th1- and Th2-like cells in long-term equine T-cell cultures.

Abstract: The aim of this study was to characterise CD4+T-cells in equines, as these cells are pivotal in establishing immune responses or regulating established ones. Peripheral blood mononuclear cells from a pony immunised with ovalbumin were cultured in vitro in the presence of the specific antigen and autologous antigen presenting cells. During the antigen starvation phase, cells were maintained on recombinant equine IL-2. After 35 days of culture, most of the cells were CD4+, CD8-and sIg-. Cells proliferated specifically in the presence of antigen, as tested on day 42 of culture. These cells were analysed by in-situ hybridisation to detect m RNA for IL-2 and IL-4, the presence of which suggested the existence of of Th1- and Th2-like cells.
Publication Date: 1999-05-20 PubMed ID: 10333472DOI: 10.1053/rvsc.1998.0256Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research focuses on the identification and study of two types of T helper cells (Th1 and Th2) present in horses. These cells are crucial for initiating and controlling immune reactions.

Objective of Research

  • The main aim of the research was to identify and characterise CD4+T-cells in horses. These cells are of utmost importance in triggering immune responses or managing established ones.

Research Methodology

  • Peripheral blood mononuclear cells from a pony immunised with ovalbumin (a protein found in egg white) were cultured in vitro (outside the body, in a controlled environment).
  • This culture was done in the presence of the specific antigen (substance that triggers an immune response) and autologous antigen-presenting cells (cells from the same individual that process and present antigens for the T-cells).
  • In the absence of the antigen (starvation phase), cells were maintained on recombinant equine IL-2 (a type of protein that regulates immune responses).

Observations and Findings

  • After 35 days of culture, the majority of the cells were CD4+, CD8- (markers for T helper cells) and sIg- (surface Ig- indicating absence of B-cells).
  • These cells showed specific growth in the presence of the antigen. This was tested on day 42 of the culture.
  • Further inspection of these cells was done by in-situ hybridisation (a technique that allows observing gene expression at a specific location) to detect mRNA for IL-2 and IL-4. mRNA (messenger RNA) are molecules that carry coding information for the synthesis of proteins from the DNA.
  • The presence of IL-2 and IL-4 suggested the existence of Th1- and Th2-like cells respectively. These cells are subsets of T helper cells and have distinct roles in immune response. While Th1 cells are involved in cell-mediated immunity, Th2 cells are crucial for humoral or antibody-mediated immunity.

Cite This Article

APA
Aggarwal N, Holmes MA. (1999). Characterisation of equine T helper cells: demonstration of Th1- and Th2-like cells in long-term equine T-cell cultures. Res Vet Sci, 66(3), 277-279. https://doi.org/10.1053/rvsc.1998.0256

Publication

ISSN: 0034-5288
NlmUniqueID: 0401300
Country: England
Language: English
Volume: 66
Issue: 3
Pages: 277-279

Researcher Affiliations

Aggarwal, N
  • Department of Clinical Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge, CB3 0ES, UK. neeraj@vet.purdue.edu
Holmes, M A

    MeSH Terms

    • Animals
    • CD4 Antigens / analysis
    • Cells, Cultured
    • Horses / immunology
    • In Situ Hybridization / veterinary
    • Interleukin-2 / analysis
    • Interleukin-4 / analysis
    • RNA, Messenger / analysis
    • Th1 Cells / immunology
    • Th2 Cells / immunology
    • Time Factors

    Citations

    This article has been cited 1 times.
    1. Szabó MP, Castagnolli KC, Santana DA, de Castro MB, Romano MA. Amblyomma cajennense ticks induce immediate hypersensitivity in horses and donkeys.. Exp Appl Acarol 2004;33(1-2):109-17.