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The Veterinary clinics of North America. Equine practice2000; 16(1); 1-14; doi: 10.1016/s0749-0739(17)30115-3

Equine T-cell cytokines. Protection and pathology.

Abstract: The ultimate reason for better characterizing the immune response to infectious agents is the hope that this knowledge may lead to the development of better preventative or therapeutic measures. As more information becomes available, it becomes possible to incorporate these findings into the design of better vaccines and treatments. Likewise, attempts to either enhance or suppress specific helper T-cell responses may be required to control immunopathologic reactions. Although cytokine intervention in the clinical setting remains theoretic at this time, future manipulation based on the TH1/TH2 paradigm is probable.
Publication Date: 2000-04-07 PubMed ID: 10752135DOI: 10.1016/s0749-0739(17)30115-3Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't
  • Research Support
  • U.S. Gov't
  • Non-P.H.S.
  • Review

Summary

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The research paper delves into the understanding of the equine immune response to infectious agents to aid the development of improved preventative or therapeutic solutions. It discusses the potential use of the TH1/TH2 paradigm for better control of immunopathologic reactions.

Understanding Equine Immunity

The primary motivation for this research was to better characterize the immune response of horses to infectious agents. This was done with the hope of acquiring knowledge that could assist development of effective preventative or therapeutic measures. The immune response in this context refers to:

  • How the horse’s immune system responds to infections.
  • The kinds of cells that are activated during these responses.
  • How these cells interact with one another and with the pathogen in question.

Improving Vaccines and Treatments

This research is important as it informs the design of better vaccines and treatments. These would incorporate findings and data gained through a deeper understanding of the horse’s immune response. Improvements could include:

  • Finding more effective antigens to include in vaccines.
  • Designing treatments that leverage the horse’s immune system more effectively.
  • Identifying new targets for drug development.

Manipulating Helper T-Cell Responses

Another significant aspect of the study involves attempts to control immunopathologic reactions. Immunopathologic reactions occur when the immune response to infection causes harm to the organism’s own body. The researchers suggest that being able to either amplify or suppress specific helper T-cell responses could be key to controlling these harmful reactions.

Cytokine Intervention

Currently, the idea of cytokine intervention, or manipulating the messenger molecules of the immune system, is theoretical. However, the study posits that future manipulation based on the TH1/TH2 paradigm is probable. This paradigm differentiates immune responses into two types, TH1, which promotes cell-mediated immunity, and TH2, which stimulates humoral immunity. Effective manipulation could potentially allow for more controlled and targeted immune responses.

Cite This Article

APA
Horohov DW. (2000). Equine T-cell cytokines. Protection and pathology. Vet Clin North Am Equine Pract, 16(1), 1-14. https://doi.org/10.1016/s0749-0739(17)30115-3

Publication

ISSN: 0749-0739
NlmUniqueID: 8511904
Country: United States
Language: English
Volume: 16
Issue: 1
Pages: 1-14

Researcher Affiliations

Horohov, D W
  • Department of Veterinary Microbiology and Parasitology, School of Veterinary Medicine, Louisiana State University, Baton Rouge, USA.

MeSH Terms

  • Animals
  • Antibody Formation
  • Cytokines / physiology
  • Horses / immunology
  • Models, Immunological
  • T-Lymphocyte Subsets / immunology

Citations

This article has been cited 1 times.
  1. MacDonald ES, Barrett JG. The Potential of Mesenchymal Stem Cells to Treat Systemic Inflammation in Horses.. Front Vet Sci 2019;6:507.
    doi: 10.3389/fvets.2019.00507pubmed: 32039250google scholar: lookup