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Veterinary research2004; 34(6); 791-801; doi: 10.1051/vetres:2003033

Cross-species reactivity of seven monoclonal antibodies with equine lymphocytes by flow cytometry.

Abstract: The recognition of equine lymphocyte antigens by monoclonal antibodies (mAbs) directed against human CD11a, CD18, CD21, CD23, CD29 and DR, as well as mouse CD23 was studied by flow cytometry. Unlike anti-CD11a, -CD21, -CD23 and DR mAbs, anti-CD18 and CD29 mAbs labelled the same percentage of horse peripheral blood lymphocytes (PBL) as human PBL. Double-staining with anti-horse immunoglobulin antibodies showed that anti-CD21 and -CD23 mAbs are mainly bound to peripheral blood B lymphocytes. The seven mAbs were also tested on the lymph node and thymus cells. The molecular targets of anti-CD11a, CD18 and CD29 mAbs were confirmed by immunoprecipitation of the membrane proteins. Our results suggest that anti-CD18, -CD29 and -DR mAbs recognise similarly expressed molecular homologues on equine cells, but that anti-CD11a, -CD21 and -CD23 mAbs recognise either different molecules or homologues that are expressed at different levels on horse cells.
Publication Date: 2004-01-30 PubMed ID: 14746773DOI: 10.1051/vetres:2003033Google Scholar: Lookup
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  • Journal Article

Summary

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The research paper studies how seven monoclonal antibodies react with horse lymphocytes, discovering that three of them behave similarly to how they act with human cells, while the remaining four show different reactions or levels of expression.

Overview of the Study

  • The researchers looked into the behaviour of seven different monoclonal antibodies (mAbs). These were monoclonal antibodies against human CD11a, CD18, CD21, CD23, CD29, DR, and mouse CD23. The medium of analysis was flow cytometry, a technique used to measure physical and chemical characteristics of cells or particles.
  • The mAbs were applied to equine (horse) lymphocytes, which are white blood cells in the immune system. These were compared to their recognized behaviour on human lymphocytes.
  • Interestingly, two different sets of results were found: one group of mAbs (against CD18, CD29, and DR) demonstrated a similar level of reaction with horse peripheral blood lymphocytes (PBL) as with human PBL, while the group formed by anti-CD11a, anti-CD21, and anti-CD23 mAbs either interacted with different molecules entirely or showed a distinct level of expression on horse PBL as compared to human PBL.

High Complexity in Immunochemistry

  • Continuous double-staining experiments with anti-horse immunoglobulin antibodies demonstrated that anti-CD21 and anti-CD23 mAbs mostly bind to peripheral blood B lymphocytes. In simpler terms: a secondary round of staining using particular antibodies showed that two of the monoclonal antibodies mostly connected with a specific type of lymphocyte.
  • All seven mAbs were also tested on lymph node and thymus cells to further evaluate their behaviour.
  • Immunoprecipitation of membrane proteins was used to confirm the molecular targets of anti-CD11a, CD18, and CD29 mAbs.
  • The findings from the study underscore the complexity and specificity involved in immunochemistry, and pave the way for further work in understanding how these specific monoclonal antibodies act at different levels of the equine immune system.

Cite This Article

APA
Mérant C, Bonnefont C, Desbos A, Greenland T, Cadoré JL, Monier JC. (2004). Cross-species reactivity of seven monoclonal antibodies with equine lymphocytes by flow cytometry. Vet Res, 34(6), 791-801. https://doi.org/10.1051/vetres:2003033

Publication

ISSN: 0928-4249
NlmUniqueID: 9309551
Country: England
Language: English
Volume: 34
Issue: 6
Pages: 791-801

Researcher Affiliations

Mérant, Catherine
  • Laboratoire d'Immunopathologie, Service de Médecine, Département des Animaux de Compagnie, Ecole Vétérinaire de Lyon, BP 83, 1 avenue Bourgelat, 69280 Marcy-l'Etoile, France. c.merant@ploufragan.afssa.fr
Bonnefont, Catherine
    Desbos, Agnès
      Greenland, Timothy
        Cadoré, Jean-Luc
          Monier, Jean-Claude

            MeSH Terms

            • Animals
            • Antibodies, Monoclonal / immunology
            • Antibody Specificity
            • Antigens, CD / immunology
            • Cross Reactions
            • Electrophoresis, Polyacrylamide Gel / veterinary
            • Flow Cytometry / methods
            • Flow Cytometry / veterinary
            • Horses / blood
            • Horses / immunology
            • Humans
            • Integrins / immunology
            • Lymph Nodes / cytology
            • Lymph Nodes / immunology
            • Lymphocytes / immunology
            • Mice
            • Precipitin Tests / veterinary
            • Species Specificity
            • Thymus Gland / cytology
            • Thymus Gland / immunology

            Citations

            This article has been cited 2 times.
            1. Carossino M, Loynachan AT, Canisso IF, Cook RF, Campos JR, Nam B, Go YY, Squires EL, Troedsson MHT, Swerczek T, Del Piero F, Bailey E, Timoney PJ, Balasuriya UBR. Equine Arteritis Virus Has Specific Tropism for Stromal Cells and CD8(+) T and CD21(+) B Lymphocytes but Not for Glandular Epithelium at the Primary Site of Persistent Infection in the Stallion Reproductive Tract.. J Virol 2017 Jul 1;91(13).
              doi: 10.1128/JVI.00418-17pubmed: 28424285google scholar: lookup
            2. Delcambre GH, Liu J, Herrington JM, Vallario K, Long MT. Immunohistochemistry for the detection of neural and inflammatory cells in equine brain tissue.. PeerJ 2016;4:e1601.
              doi: 10.7717/peerj.1601pubmed: 26855862google scholar: lookup