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Defective thymocyte maturation in horses with severe combined immunodeficiency.

Abstract: Six monoclonal antibodies, designated EqT2, EqT3, EqT6, EqT7, EqT12, and EqT13, which identify T lymphocyte antigens present at different stages of T cell maturation were used to examine T lymphocyte development in foals with severe combined immunodeficiency (SCID). Flow microfluorimetry demonstrated the presence of EqT12+ and EqT13+ prothymocytes and a few phenotypically mature EqT2+ and EqT3+ thymocytes within the thymic remnants of SCID foals. However, very few EqT6+ and EqT7+ resident cortical thymocytes were detected. The near absence of EqT6+ and EqT7+ cortical thymocytes was confirmed by immunofluorescence analysis of thymic tissue from SCID foals. Those cells present were larger than normal cortical thymocytes. Furthermore, their activities of adenosine deaminase, adenosine monophosphate-deaminase, and 5' nucleotidase differed from those of normal cortical thymocytes. The combined evidence of monoclonal antibody analysis, size parameters, and purine enzyme activities demonstrate the near absence of cortical thymocytes in horses with this genetically defined immunodeficiency disorder.
Publication Date: 1987-12-15 PubMed ID: 3500980
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't
  • Research Support
  • U.S. Gov't
  • P.H.S.

Summary

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The research article focuses on learning about the development of T lymphocytes, a type of white blood cell, in horse foals suffering from severe combined immunodeficiency (SCID) through the use of six monoclonal antibodies. It showed that the immunodeficient foals had different levels of these cells compared to normal, indicating a lack of thymocyte maturation.

Use of Monoclonal Antibodies in Determining Thymocyte Development

  • The study utilized six monoclonal antibodies. These are specifically designed proteins that can identify and bind to certain antigens on cells. In this study, they were used to pinpoint T lymphocyte antigens, which are present in different stages of T cell maturation.
  • The antibodies were named as EqT2, EqT3, EqT6, EqT7, EqT12, and EqT13 and were used to observe T lymphocyte development in SCID-affected foals.

Flow Microfluorimetry to Detect Thymocyte Levels

  • Flow microfluorimetry, a methodology used to measure physical and chemical characteristics of particles present in a fluid as it passes through a laser, revealed the presence of certain types of prothymocytes and thymocytes (EqT12+, EqT13+, EqT2+, and EqT3+) within the thymic remnants of SCID foals.
  • However, the method also demonstrated that very few EqT6+ and EqT7+ resident cortical thymocytes were present.

Immunofluorescence Analysis Confirmed Findings

  • The results from flow microfluorimetry were further confirmed by conducting immunofluorescence analysis. This technique applies antibodies marked with fluorescent dyes to tissue samples in order to visualize the distribution of the target molecule.
  • It confirmed the near absence of EqT6+ and EqT7+ cortical thymocytes in SCID foals. In addition, the remaining cells were found to be larger than normal thymocytes.

Differences in Enzyme Activities

  • The researchers also noticed differences in enzyme activities. The cells from SCID foals showed varied activities of adenosine deaminase, adenosine monophosphate-deaminase, and 5′ nucleotidase compared to normal cortical thymocytes.
  • These findings, together with those obtained from monoclonal antibody analysis and size parameters, demonstrated the near absence of mature T cells in horses affected by this immunodeficiency disorder.

In conclusion, the research hinted at defective thymocyte maturation as a probable factor in horses suffering from SCID, emphasizing the need for further investigations in this area to develop potential treatments.

Cite This Article

APA
Wyatt CR, Magnuson NS, Perryman LE. (1987). Defective thymocyte maturation in horses with severe combined immunodeficiency. J Immunol, 139(12), 4072-4076.

Publication

ISSN: 0022-1767
NlmUniqueID: 2985117R
Country: United States
Language: English
Volume: 139
Issue: 12
Pages: 4072-4076

Researcher Affiliations

Wyatt, C R
  • Department of Veterinary Microbiology and Pathology, Washington State University, Pullman 99164.
Magnuson, N S
    Perryman, L E

      MeSH Terms

      • Animals
      • Antibodies, Monoclonal / immunology
      • Antigens, Surface / analysis
      • Cell Differentiation
      • Horse Diseases / immunology
      • Horse Diseases / pathology
      • Horses / immunology
      • Immunologic Deficiency Syndromes / immunology
      • Immunologic Deficiency Syndromes / pathology
      • Immunologic Deficiency Syndromes / veterinary
      • T-Lymphocytes / enzymology
      • T-Lymphocytes / immunology
      • T-Lymphocytes / pathology
      • Thymus Gland / pathology

      Grant Funding

      • HD 08886 / NICHD NIH HHS

      Citations

      This article has been cited 8 times.
      1. McCLURE JT, Lunn DP, McGUIRK SM. Combined immunodeficiency in 3 foals.. Equine Vet Educ 1993 Feb;5(1):14-18.
      2. 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
      3. Perryman LE, Mason PH, Chrisp CE. Effect of spleen cell populations on resolution of Cryptosporidium parvum infection in SCID mice.. Infect Immun 1994 Apr;62(4):1474-7.
      4. Lunn DP, McClure JT, Schobert CS, Holmes MA. Abnormal patterns of equine leucocyte differentiation antigen expression in severe combined immunodeficiency foals suggests the phenotype of normal equine natural killer cells.. Immunology 1995 Mar;84(3):495-9.
        pubmed: 7751035
      5. Perryman LE, O'Rourke KI, McGuire TC. Immune responses are required to terminate viremia in equine infectious anemia lentivirus infection.. J Virol 1988 Aug;62(8):3073-6.
      6. Perryman LE, Riggs MW, Mason PH, Fayer R. Kinetics of Cryptosporidium parvum sporozoite neutralization by monoclonal antibodies, immune bovine serum, and immune bovine colostrum.. Infect Immun 1990 Jan;58(1):257-9.
        doi: 10.1128/iai.58.1.257-259.1990pubmed: 2294054google scholar: lookup
      7. Lunn DP, Holmes MA, Duffus WP. Three monoclonal antibodies identifying antigens on all equine T lymphocytes, and two mutually exclusive T-lymphocyte subsets.. Immunology 1991 Oct;74(2):251-7.
        pubmed: 1748472
      8. Perryman LE, O'Rourke KI, Mason PH, McGuire TC. Equine monoclonal antibodies recognize common epitopes on variants of equine infectious anaemia virus.. Immunology 1990 Dec;71(4):592-4.
        pubmed: 1703988