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Equine veterinary journal2007; 39(5); 414-416; doi: 10.2746/042516407x204573

Antibodies to elastin peptides in sera of Warmblood horses at different ages.

Abstract: Early diagnosis and monitoring progression of chronic diseases in elastin-rich tissues, such as chronic progressive lymphoedema in draught horses and chronic obstructive pulmonary disease (COPD) is still a real challenge in the horse. Use of an enzyme-linked immunosorbent assay (ELISA) to detect anti-elastin antibody (AEAb) levels might be useful to assess the status of such diseases. Baseline levels, representing physiological breakdown of elastin in normal horses, are not available at present. Objective: Levels of AEAb in healthy horses are generally low and follow the same age-related pattern as found in man. Therefore, elevation of AEAb levels in serum can be used to evaluate pathological elastin breakdown in elastin-rich tissues. Methods: Sera of 84 clinically healthy Warmblood horses were evaluated for the presence of AEAbs by means of a modified version of an ELISA technique used in man. The horses were divided in 5 age groups: A) 11 years. Results: Antibodies to elastin were found in all equine serum samples tested. Their levels were lowest in Group A, low in Groups B and E and highest in animals age 2-10 years. Conclusions: Measuring AEAbs in serum of horses by an ELISA technique proved to be possible and levels were stable during well-defined life stages. Conclusions: Changes in AEAb levels are expected to be useful for early diagnosis and for monitoring progression of diseases that affect elastin-rich tissues, such as chronic progressive lymphoedema and COPD.
Publication Date: 2007-10-04 PubMed ID: 17910265DOI: 10.2746/042516407x204573Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This study outlines a method for early detection and monitoring of chronic diseases in horses, such as chronic progressive lymphoedema and chronic obstructive pulmonary disease (COPD), targeting elastin-rich tissues. Researchers utilized an enzyme-linked immunosorbent assay (ELISA) to detect anti-elastin antibody levels in the surmised horses and arrived at an age-related pattern correlation.

Research Context

  • Chronic diseases in elastin-rich tissues like chronic progressive lymphoedema and COPD pose significant threats to horse health. Early diagnosis and effective monitoring of these diseases remain a challenge.
  • Horses, alike humans, contain anti-elastin antibodies (AEAbs). The researchers speculated that studying these levels could facilitate the evaluation of pathological elastin breakdown in elastin-rich tissues, thereby, helping in the diagnosis and screening of chronic diseases.

Research Methodology

  • The study involved testing the sera of 84 clinically healthy Warmblood horses to detect the presence of AEAbs.
  • A modified version of an ELISA technique, commonly used in human testing, was employed to detect the antibodies.
  • The test subjects were divided into five groups based on their age: less than 4 months, 4 to 23 months, 2 to 3 years, 4 to 10 years, and over 11 years.

Findings

  • The test showed the presence of antibodies to elastin in all tested equine serum samples.
  • The detected levels of the antibodies varied across the different age groups with the lowest in horses less than four months old, low in those aged between 4 to 23 months and over 11 years, and highest in horses aged between 2 to 10 years.

Conclusions and Implications

  • The use of the ELISA technique in measuring AEAbs in the serum of horses proved feasible and provided stable readings across different life stages.
  • Changes in AEAb levels can provide important signals for early diagnosis and tracking the progression of diseases affecting elastin-rich tissues.
  • The study provides groundwork for further investigations into the potential utility of this approach in veterinary disease management.

Cite This Article

APA
van Brantegem L, de Cock HE, Affolter VK, Duchateau L, Govaere J, Ferraro GL, Ducatelle R. (2007). Antibodies to elastin peptides in sera of Warmblood horses at different ages. Equine Vet J, 39(5), 414-416. https://doi.org/10.2746/042516407x204573

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 39
Issue: 5
Pages: 414-416

Researcher Affiliations

van Brantegem, L
  • Laboratory of Pathology, Department of Veterinary Medicine, Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, University of Antwerp, Wilrijk, Belgium.
de Cock, H E V
    Affolter, V K
      Duchateau, L
        Govaere, J
          Ferraro, G L
            Ducatelle, R

              MeSH Terms

              • Aging / metabolism
              • Aging / physiology
              • Animals
              • Autoantibodies / blood
              • Chronic Disease
              • Diagnosis, Differential
              • Disease Progression
              • Elastin / blood
              • Elastin / immunology
              • Elastin / metabolism
              • Enzyme-Linked Immunosorbent Assay / methods
              • Enzyme-Linked Immunosorbent Assay / standards
              • Enzyme-Linked Immunosorbent Assay / veterinary
              • Horse Diseases / blood
              • Horse Diseases / diagnosis
              • Horses
              • Lung Diseases, Obstructive / blood
              • Lung Diseases, Obstructive / diagnosis
              • Lung Diseases, Obstructive / veterinary
              • Lymphedema / blood
              • Lymphedema / diagnosis
              • Lymphedema / veterinary
              • Peptides / blood
              • Peptides / immunology
              • Peptides / metabolism
              • Reference Values
              • Sensitivity and Specificity
              • Severity of Illness Index

              Citations

              This article has been cited 1 times.
              1. Brys M, Claerebout E, Chiers K. Chronic Progressive Lymphedema in Belgian Draft Horses: Understanding and Managing a Challenging Disease. Vet Sci 2023 May 12;10(5).
                doi: 10.3390/vetsci10050347pubmed: 37235431google scholar: lookup