Analyze Diet
Journal of veterinary internal medicine2011; 26(1); 153-161; doi: 10.1111/j.1939-1676.2011.00847.x

Comparison of cytokine mRNA expression in the bronchoalveolar lavage fluid of horses with inflammatory airway disease and bronchoalveolar lavage mastocytosis or neutrophilia using REST software analysis.

Abstract: The pathophysiology of inflammatory airway disease (IAD) is unknown, but in some cases involves the accumulation of mast cells, neutrophils, or both in the bronchoalveolar lavage fluid (BALF). The objective of this study was to characterize cytokine gene expression in the BALF cells of horses with IAD, including a comparison of cytokine gene expression between IAD horses with increased BALF mast cells (IAD-Mast) or neutrophils (IAD-Neutro). Methods: The mRNA expression of IL-4, IFN-γ, IL-17, IL-8, IL-1β, IL-5, IL-6, IL-10, IL-12p35, and eotaxin-2 was studied by quantitative polymerase chain reaction (QPCR) with efficiency correction in BALF samples of 17 horses with IAD (IAD-total), also subcategorized as 8 IAD-Mast and 9 IAD-Neutro, and 10 controls. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used as a reference gene. Relative expression software tool (REST) analysis provided ratios of expression, statistical analysis, and confidence intervals for the results. Results: Compared with the control group, IL-5, IL-1β, IL-6, IL-8, and IL-10 mRNA expression was upregulated 3.5-, 3.4-, 2.8-, 2.2-, and 1.9-fold, respectively, in the IAD-total group. The IAD-Neutro group showed increased expression of IL-17, IL-8, and IL-5 (4.7-, 2.5-, and 2.9-fold, respectively) and a decreased expression of IL-4 (3.4-fold) compared with the IAD-Mast group. Conclusions: Cytokines from the Th2 family plays a key role in IAD and a different pathophysiology may be involved in mast cell versus neutrophil BALF accumulation in IAD horses.
Publication Date: 2011-12-14 PubMed ID: 22168153DOI: 10.1111/j.1939-1676.2011.00847.xGoogle Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research article investigates the genetic expression of cytokines—a type of protein involved in cell signaling—in the bronchoalveolar lavage fluid (BALF) of horses suffering from inflammatory airway disease (IAD). The main focus of the study is to compare the cytokine expressions in IAD horses showing an increased number of mast cells or neutrophils in their BALF.

Research Objective

  • Due to the unclear pathogenesis of IAD, this study aims to understand the illness by looking at cytokine gene expression in the BALF cells of horses affected by IAD. Particularly, researchers compared cytokine gene expressions between horses exhibiting increased BALF mast cells (IAD-Mast) and those having increased BALF neutrophils (IAD-Neutro).

Methods

  • The research involved studying mRNA expression of several cytokines (IL-4, IFN-γ, IL-17, IL-8, IL-1β, IL-5, IL-6, IL-10, IL-12p35, and eotaxin-2) via quantitative polymerase chain reaction (QPCR), with efficiency correction done in BALF samples of 17 horses with IAD.
  • These horses were also categorised into two groups, consisting of 8 IAD-Mast and 9 IAD-Neutro subjects.
  • 10 normal horses served as controls. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used as a reference gene.
  • Relative expression software tool (REST) was used in the analysis, providing ratios of expression, statistical analysis, and confidence intervals on the results.

Results

  • When compared to the control group, expressions of IL-5, IL-1β, IL-6, IL-8, and IL-10 mRNA were upregulated 3.5-, 3.4-, 2.8-, 2.2-, and 1.9-fold, respectively, in horses with IAD.
  • In IAD-Neutro horses, researchers observed increased expression of IL-17, IL-8, and IL-5 up to 4.7-, 2.5-, and 2.9-fold, respectively, and decreased expression of IL-4 by 3.4-fold when compared with the IAD-Mast group.

Conclusions

  • Findings from the research suggest that Th2 family cytokines serve a crucial function in IAD.
  • Differring pathophysiology may be implicated in the accumulation of mast cells versus neutrophils in BALF within the horses battling IAD.

Cite This Article

APA
Beekman L, Tohver T, Léguillette R. (2011). Comparison of cytokine mRNA expression in the bronchoalveolar lavage fluid of horses with inflammatory airway disease and bronchoalveolar lavage mastocytosis or neutrophilia using REST software analysis. J Vet Intern Med, 26(1), 153-161. https://doi.org/10.1111/j.1939-1676.2011.00847.x

Publication

ISSN: 1939-1676
NlmUniqueID: 8708660
Country: United States
Language: English
Volume: 26
Issue: 1
Pages: 153-161

Researcher Affiliations

Beekman, L
  • Department of Veterinary Clinical and Diagnostic Sciences, University of Calgary, Calgary, Alberta, Canada.
Tohver, T
    Léguillette, R

      MeSH Terms

      • Animals
      • Bronchoalveolar Lavage Fluid / cytology
      • Bronchoalveolar Lavage Fluid / immunology
      • Chemokine CCL11 / biosynthesis
      • Chemokine CCL11 / genetics
      • Chemokine CCL11 / immunology
      • Cytokines / biosynthesis
      • Cytokines / genetics
      • Cytokines / immunology
      • Female
      • Gene Expression Regulation
      • Horse Diseases / genetics
      • Horse Diseases / immunology
      • Horses
      • Interleukins / biosynthesis
      • Interleukins / genetics
      • Interleukins / immunology
      • Male
      • Mast Cells / immunology
      • Mastocytosis / genetics
      • Mastocytosis / immunology
      • Mastocytosis / veterinary
      • Neutrophils / immunology
      • RNA, Messenger / biosynthesis
      • RNA, Messenger / chemistry
      • RNA, Messenger / genetics
      • Real-Time Polymerase Chain Reaction / veterinary
      • Respiratory Tract Diseases / genetics
      • Respiratory Tract Diseases / immunology
      • Respiratory Tract Diseases / veterinary
      • Statistics, Nonparametric

      Citations

      This article has been cited 31 times.
      1. Morini M, Gobbo F, Rinnovati R, Romagnoli N, Peli A, Massarenti C, Spadari A, Pietra M. Bronchoalveolar Lavage Cytology in Severe Equine Asthma: Cytocentrifugated versus Sediment Smear Preparations. Vet Sci 2023 Aug 16;10(8).
        doi: 10.3390/vetsci10080527pubmed: 37624314google scholar: lookup
      2. Lee DH, Lee EB, Seo JP, Ko EJ. In vitro effects of monophosphoryl lipid A and Poly I:C combination on equine cells. J Vet Sci 2023 May;24(3):e37.
        doi: 10.4142/jvs.23007pubmed: 37271505google scholar: lookup
      3. Woodrow JS, Sheats MK, Cooper B, Bayless R. Asthma: The Use of Animal Models and Their Translational Utility. Cells 2023 Apr 5;12(7).
        doi: 10.3390/cells12071091pubmed: 37048164google scholar: lookup
      4. Woodrow JS, Hines M, Sommardahl C, Flatland B, Lo Y, Wang Z, Sheats MK, Lennon EM. Initial investigation of molecular phenotypes of airway mast cells and cytokine profiles in equine asthma. Front Vet Sci 2022;9:997139.
        doi: 10.3389/fvets.2022.997139pubmed: 36713876google scholar: lookup
      5. Padoan E, Ferraresso S, Pegolo S, Barnini C, Castagnaro M, Bargelloni L. Gene Expression Profiles of the Immuno-Transcriptome in Equine Asthma. Animals (Basel) 2022 Dec 20;13(1).
        doi: 10.3390/ani13010004pubmed: 36611613google scholar: lookup
      6. Sage SE, Nicholson P, Peters LM, Leeb T, Jagannathan V, Gerber V. Single-cell gene expression analysis of cryopreserved equine bronchoalveolar cells. Front Immunol 2022;13:929922.
        doi: 10.3389/fimmu.2022.929922pubmed: 36105804google scholar: lookup
      7. Janssen P, Tosi I, Hego A, Maréchal P, Marichal T, Radermecker C. Neutrophil Extracellular Traps Are Found in Bronchoalveolar Lavage Fluids of Horses With Severe Asthma and Correlate With Asthma Severity. Front Immunol 2022;13:921077.
        doi: 10.3389/fimmu.2022.921077pubmed: 35911691google scholar: lookup
      8. Lee DH, Lee EB, Seo JP, Ko EJ. Evaluation of concurrent vaccinations with recombinant canarypox equine influenza virus and inactivated equine herpesvirus vaccines. J Anim Sci Technol 2022 May;64(3):588-598.
        doi: 10.5187/jast.2022.e30pubmed: 35709134google scholar: lookup
      9. Di Pietro R, Dubuc V, Manguin E, Giroux-Lafond R, Bédard C, Boivin R, Lavoie JP, Vesper SJ, Leclere M. Characterization of fungal exposure and dectin-1 expression in healthy horses and horses with severe asthma. Am J Vet Res 2022 May 8;83(6).
        doi: 10.2460/ajvr.21.09.0143pubmed: 35524958google scholar: lookup
      10. Karagianni AE, Kurian D, Cillán-Garcia E, Eaton SL, Wishart TM, Pirie RS. Training associated alterations in equine respiratory immunity using a multiomics comparative approach. Sci Rep 2022 Jan 10;12(1):427.
        doi: 10.1038/s41598-021-04137-3pubmed: 35013475google scholar: lookup
      11. Kang H, Bienzle D, Lee GKC, Piché É, Viel L, Odemuyiwa SO, Beeler-Marfisi J. Flow cytometric analysis of equine bronchoalveolar lavage fluid cells in horses with and without severe equine asthma. Vet Pathol 2022 Jan;59(1):91-99.
        doi: 10.1177/03009858211042588pubmed: 34521286google scholar: lookup
      12. Karagianni AE, Eaton SL, Kurian D, Cillán-Garcia E, Twynam-Perkins J, Raper A, Wishart TM, Pirie RS. Application across species of a one health approach to liquid sample handling for respiratory based -omics analysis. Sci Rep 2021 Jul 12;11(1):14292.
        doi: 10.1038/s41598-021-93839-9pubmed: 34253818google scholar: lookup
      13. Davis KU, Sheats MK. Differential gene expression and Ingenuity Pathway Analysis of bronchoalveolar lavage cells from horses with mild/moderate neutrophilic or mastocytic inflammation on BAL cytology. Vet Immunol Immunopathol 2021 Apr;234:110195.
        doi: 10.1016/j.vetimm.2021.110195pubmed: 33588285google scholar: lookup
      14. Hellman S, Tydén E, Hjertner B, Nilsfors F, Hu K, Morein B, Fossum C. Cytokine responses to various larval stages of equine strongyles and modulatory effects of the adjuvant G3 in vitro. Parasite Immunol 2021 Jan;43(1):e12794.
        doi: 10.1111/pim.12794pubmed: 32969532google scholar: lookup
      15. Hue E, Orard M, Toquet MP, Depecker M, Couroucé A, Pronost S, Paillot R, Richard EA. Asymmetrical Pulmonary Cytokine Profiles Are Linked to Bronchoalveolar Lavage Fluid Cytology of Horses With Mild Airway Neutrophilia. Front Vet Sci 2020;7:226.
        doi: 10.3389/fvets.2020.00226pubmed: 32391392google scholar: lookup
      16. Bond SL, Hundt J, Léguillette R. Effect of injected dexamethasone on relative cytokine mRNA expression in bronchoalveolar lavage fluid in horses with mild asthma. BMC Vet Res 2019 Nov 6;15(1):397.
        doi: 10.1186/s12917-019-2144-xpubmed: 31694631google scholar: lookup
      17. Gao Y, Sang FF, Meng L, Wang Y, Ma WT, Chen K. Preparation of a novel monoclonal antibody against caprine interleukin-17A and its applications in immunofluorescence and immunohistochemistry assays. BMC Biotechnol 2019 Jul 17;19(1):47.
        doi: 10.1186/s12896-019-0543-5pubmed: 31315680google scholar: lookup
      18. Davis KU, Sheats MK. Bronchoalveolar Lavage Cytology Characteristics and Seasonal Changes in a Herd of Pastured Teaching Horses. Front Vet Sci 2019;6:74.
        doi: 10.3389/fvets.2019.00074pubmed: 30923711google scholar: lookup
      19. Dauvillier J, Ter Woort F, van Erck-Westergren E. Fungi in respiratory samples of horses with inflammatory airway disease. J Vet Intern Med 2019 Mar;33(2):968-975.
        doi: 10.1111/jvim.15397pubmed: 30576012google scholar: lookup
      20. Bond S, Léguillette R, Richard EA, Couetil L, Lavoie JP, Martin JG, Pirie RS. Equine asthma: Integrative biologic relevance of a recently proposed nomenclature. J Vet Intern Med 2018 Nov;32(6):2088-2098.
        doi: 10.1111/jvim.15302pubmed: 30294851google scholar: lookup
      21. Ivester KM, Couëtil LL, Moore GE. An observational study of environmental exposures, airway cytology, and performance in racing thoroughbreds. J Vet Intern Med 2018 Sep;32(5):1754-1762.
        doi: 10.1111/jvim.15226pubmed: 30222207google scholar: lookup
      22. Barton AK, Pelli A, Rieger M, Gehlen H. Procalcitonin as a biomarker in equine chronic pneumopathies. BMC Vet Res 2016 Dec 9;12(1):281.
        doi: 10.1186/s12917-016-0912-4pubmed: 27938364google scholar: lookup
      23. Couëtil LL, Cardwell JM, Gerber V, Lavoie JP, Léguillette R, Richard EA. Inflammatory Airway Disease of Horses--Revised Consensus Statement. J Vet Intern Med 2016 Mar-Apr;30(2):503-15.
        doi: 10.1111/jvim.13824pubmed: 26806374google scholar: lookup
      24. Houtsma A, Bedenice D, Pusterla N, Pugliese B, Mapes S, Hoffman AM, Paxson J, Rozanski E, Mukherjee J, Wigley M, Mazan MR. Association between inflammatory airway disease of horses and exposure to respiratory viruses: a case control study. Multidiscip Respir Med 2015;10:33.
        doi: 10.1186/s40248-015-0030-3pubmed: 26535117google scholar: lookup
      25. Ivester KM, Couëtil LL, Zimmerman NJ. Investigating the link between particulate exposure and airway inflammation in the horse. J Vet Intern Med 2014 Nov-Dec;28(6):1653-65.
        doi: 10.1111/jvim.12458pubmed: 25273818google scholar: lookup
      26. Richard EA, Depecker M, Defontis M, Leleu C, Fortier G, Pitel PH, Couroucé-Malblanc A. Cytokine concentrations in bronchoalveolar lavage fluid from horses with neutrophilic inflammatory airway disease. J Vet Intern Med 2014 Nov-Dec;28(6):1838-44.
        doi: 10.1111/jvim.12464pubmed: 25269933google scholar: lookup
      27. Bartenschlager F, Kuropka B, Schmitz P, Dumke F, Landmann K, Gruber AD, Weise C, Schnabel CL, Gehlen H, Mundhenk L. Proteomic profiling of equine airway mucus reveals compositional changes in asthmatic phenotypes. Sci Rep 2026 Feb 10;16(1):5880.
        doi: 10.1038/s41598-026-38766-3pubmed: 41667845google scholar: lookup
      28. Sanz MG, Jellen G, Cody L, Bergsma J, Cha M, Kogan C, Kordas G, Bayly WM, Leguillette R. Use of inhaled ciclesonide for treatment of moderate asthma in Thoroughbred racehorses. J Vet Intern Med 2025 Mar-Apr;39(2):e17267.
        doi: 10.1111/jvim.17267pubmed: 39945569google scholar: lookup
      29. Karagianni AE, Richard EA, Toquet MP, Hue ES, Courouce-Malblanc A, McGorum B, Kurian D, Aguilar J, Mazeri S, Wishart TM, Pirie RS. Distinct Molecular Profiles Underpin Mild-To-Moderate Equine Asthma Cytological Profiles. Cells 2024 Nov 20;13(22).
        doi: 10.3390/cells13221926pubmed: 39594673google scholar: lookup
      30. Wjst VF, Lübke S, Wagner B, Rhyner C, Jentsch MC, Arnold C, Lohmann KL, Schnabel CL. Aspergillus fumigatus antigen-reactive Th17 cells are enriched in bronchoalveolar lavage fluid in severe equine asthma. Front Immunol 2024;15:1367971.
        doi: 10.3389/fimmu.2024.1367971pubmed: 39229267google scholar: lookup
      31. Bond S, Léguillette R. A CONSORT-guided, randomized controlled clinical trial of nebulized administration of dexamethasone and saline on lower airway cytokine mRNA expression in horses with moderate asthma. J Vet Intern Med 2024 Mar-Apr;38(2):1214-1223.
        doi: 10.1111/jvim.16983pubmed: 38205666google scholar: lookup