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Selective immunoglobulin M deficiency in foals.

Abstract: Selective immunoglobulin M deficiency was diagnosed in 5 foals, on the basis of reduced serum immunoglobulin M concentrations (more than 2 standard deviations below the normal mean). All 5 foals had clinical signs or lesions involving the respiratory tract. Lkebsiella sp was isolated from joint fluids, bronchial lymph nodes, or tracheal washings from the 3 foals in which such samples were available for microbiologic evaluation.
Publication Date: 1977-01-15 PubMed ID: 833046
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Summary

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This research focuses on the detection of selective immunoglobulin M deficiency in 5 foals which was diagnosed based on lower serum immunoglobulin M concentrations and clinical signs involving respiratory issues.

Study Overview

  • The study revolves around a novel discovery made amidst the medical examination of foals (young horses) in which a deficiency was found in their Immunoglobulin M (IgM) levels. IgM is the first antibody made by the body to fight any new infection. It provides the initial defense against infections.
  • This deficiency was noticed to be ‘selective’, implying it was only the IgM levels that were compromised, potentially leaving the foals more vulnerable to infections. Five foals were part of this finding.

Diagnosis

  • These deficiencies were diagnosed through blood tests which demonstrated a significant reduction in the foals’ serum immunoglobulin M concentrations, with values exceeding 2 standard deviations below the mean value for healthy equine subjects.
  • This shortfall has crucial implications as it signifies the horses’ weakened immune response, which informs their ability to combat infections effectively on first exposure.

Clinical Significance

  • Interestingly, all the foals diagnosed with this IgM deficit also exhibited clinical symptoms or lesions associated with their respiratory tract.
  • This finding indicates a likely link between this deficiency and respiratory problems, making it a potentially significant marker for preliminary diagnostics in such cases.

Microbiological Evaluation

  • In three of the five foals, additional samples from joint fluids, bronchial lymph nodes, or tracheal washings were available for further microbiological evaluation.
  • A bacterial species called Klebsiella was found in these samples. Klebsiella is known to cause various infections including pneumonia, bloodstream infections, wound or surgical site infections, and meningitis.
  • The emergence of this bacteria in the foals’ bodily fluids offers a potential explanation for the respiratory afflictions noted amongst these subjects.

Cite This Article

APA
Perryman LE, McGuire TC, Hilbert BJ. (1977). Selective immunoglobulin M deficiency in foals. J Am Vet Med Assoc, 170(2), 212-215.

Publication

ISSN: 0003-1488
NlmUniqueID: 7503067
Country: United States
Language: English
Volume: 170
Issue: 2
Pages: 212-215

Researcher Affiliations

Perryman, L E
    McGuire, T C
      Hilbert, B J

        MeSH Terms

        • Animals
        • Bronchopneumonia / veterinary
        • Complement C3 / analysis
        • Dysgammaglobulinemia / immunology
        • Dysgammaglobulinemia / veterinary
        • Female
        • Horse Diseases / immunology
        • Horses
        • Immunoglobulin A / analysis
        • Immunoglobulin G / analysis
        • Immunoglobulin M / analysis
        • Immunologic Deficiency Syndromes / veterinary
        • Leukocyte Count
        • Lymphocyte Activation
        • Male
        • Pneumonia / veterinary

        Citations

        This article has been cited 2 times.
        1. Flaminio MJ, Tallmadge RL, Salles-Gomes CO, Matychak MB. Common variable immunodeficiency in horses is characterized by B cell depletion in primary and secondary lymphoid tissues. J Clin Immunol 2009 Jan;29(1):107-16.
          doi: 10.1007/s10875-008-9221-4pubmed: 18677444google scholar: lookup
        2. Magnuson NS, Perryman LE. In vitro of adenosine on lymphocytes and erythrocytes from horses with combined immunodeficiency. J Clin Invest 1979 Jul;64(1):89-101.
          doi: 10.1172/JCI109468pubmed: 447864google scholar: lookup