Analyze Diet
Veterinary immunology and immunopathology1999; 71(1); 17-28; doi: 10.1016/s0165-2427(99)00082-3

Characterization of T-lymphocytes in the anterior uvea of eyes with chronic equine recurrent uveitis.

Abstract: Equine recurrent uveitis (ERU), a chronic, recurrent inflammation primarily of the anterior uveal tract, is the most common cause of blindness in horses. Recently, T-lymphocytes have been found to be the most numerous cell type to infiltrate the anterior uveal of horses with ERU. In the present study, we characterized the T-lymphocyte population in the anterior uveal tract of eyes of horses with chronic ERU by evaluating the microscopic appearance (histopathologic features), the T-lymphocyte subsets, and the relative levels and amounts of T-lymphocyte cytokine mRNA in the anterior uvea. Seven inflamed eyes (from six horses with chronic ERU) and 5 normal eyes (from five horses with nonocular problems) were studied. After clinical examination, the eyes were removed, ocular fluids were aspirated, and anterior uveal tissues (iris and ciliary body) were processed for histologic and molecular (RNA isolation) analyses. Histologic examination by hematoxylin and eosin (H and E) staining and immunohistochemistry evaluating T-lymphocyte subsets (anti-CD4, CD8, CD5) were performed for each sample. RNA samples were analyzed for levels of messenger (m) RNA specific for interleukin (IL)-2, 4, and interferon-gamma (IFNgamma) by quantitative reverse transcriptase polymerase chain reaction (QRT-PCR). Eyes with ERU exhibited characteristic clinical signs, including corneal edema, aqueous flare, posterior synechia, corpora nigra degeneration, and cataract formation. Histologically, infiltration of the uveal tract with lymphocytes, plasma cells, and macrophages was most evident in the ciliary body and base of the iris. Loss of tissue structure (destruction) was most evident in the ciliary processes. Infiltrating lymphocytes were predominantly CD4+ T-cells (e.g. 48% CD4+ and 18% CD8+ in the ciliary body stroma), as determined by immunohistochemistry. Few inflammatory cells were observed in the normal eyes. The QRT-PCR results revealed increased transcription of IL-2 and IFNgamma and low IL-4 mRNA expression in eyes with chronic ERU compared to normal eyes, demonstrating a Thelper (Th) 1-like inflammatory response in eyes with ERU.
Publication Date: 1999-10-16 PubMed ID: 10522783DOI: 10.1016/s0165-2427(99)00082-3Google 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.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't
  • Research Support
  • U.S. Gov't
  • P.H.S.

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.

The study focuses on examining T-lymphocytes, a type of white blood cell, present in the anterior uvea of the eyes of horses suffering from equine recurrent uveitis (ERU), a common cause of blindness in horses.

Research Context

  • Equine recurrent uveitis (ERU) is a chronic, recurring inflammation condition that primarily affects the anterior uveal tract of horses.
  • The anterior uveal tract consists of the iris and the ciliary body.
  • ERU is the most frequent cause of blindness in horses, and it has been recently discovered that T-lymphocytes are the most common cellular type infiltrating the anterior uveal tract in ERU instances.

Research Methodology

  • In the study, the T-lymphocyte population in the anterior uvea of horses with chronic ERU was characterized.
  • A total of seven inflamed eyes (from six horses with chronic ERU) and 5 normal eyes (from five horses with no ocular issues) were studied.
  • Post clinical examination, the eyes were removed for further analysis.
  • Anterior uveal tissues (iris and ciliary body) were processed for histologic and molecular (RNA isolation) analyses.
  • Immunohistochemistry was used to assess T-lymphocyte subsets (anti-CD4, CD8, CD5) while quantitative reverse transcriptase polymerase chain reaction (QRT-PCR) was used to analyze the levels of specific messenger (m) RNA (interleukin (IL)-2, 4, and interferon-gamma (IFNgamma)).

Findings

  • ERU-affected eyes exhibited specific clinical signs such as corneal edema, aqueous flare, posterior synechia, corpora nigra degeneration, and cataract formation.
  • There was notable infiltration of the anterior uvea (particularly the ciliary body and base of the iris) by lymphocytes, plasma cells, and macrophages.
  • The ciliary process experienced maximum tissue structure loss due to this infiltration.
  • Immunohistochemistry revealed that infiltrating lymphocytes were primarily CD4+ T-cells.
  • Injection of lymphocytes, plasma cells, and macrophages was very rare in normal eyes.
  • Using QRT-PCR, it was discovered that the transcription of IL-2 and IFNgamma were higher, while IL-4 mRNA expression was lower, in ERU-affected eyes as compared to normal eyes. This indicated a Thelper (Th) 1-like inflammatory response in ERU-affected eyes.

Cite This Article

APA
Gilger BC, Malok E, Cutter KV, Stewart T, Horohov DW, Allen JB. (1999). Characterization of T-lymphocytes in the anterior uvea of eyes with chronic equine recurrent uveitis. Vet Immunol Immunopathol, 71(1), 17-28. https://doi.org/10.1016/s0165-2427(99)00082-3

Publication

ISSN: 0165-2427
NlmUniqueID: 8002006
Country: Netherlands
Language: English
Volume: 71
Issue: 1
Pages: 17-28

Researcher Affiliations

Gilger, B C
  • Department of Companion Animal and Special Species Medicine, College of Veterinary Medicine, North Carolina State University, Raleigh 27606, USA. brian_gilger@ncsu.edu
Malok, E
    Cutter, K V
      Stewart, T
        Horohov, D W
          Allen, J B

            MeSH Terms

            • Animals
            • Chronic Disease
            • Ciliary Body / immunology
            • Ciliary Body / pathology
            • Cytokines / biosynthesis
            • Cytokines / genetics
            • Horse Diseases / immunology
            • Horse Diseases / pathology
            • Horses
            • Immunoenzyme Techniques / veterinary
            • Iris / immunology
            • Iris / pathology
            • RNA, Messenger / metabolism
            • Recurrence
            • Reverse Transcriptase Polymerase Chain Reaction / veterinary
            • T-Lymphocyte Subsets / immunology
            • T-Lymphocytes / immunology
            • Uveitis, Anterior / immunology
            • Uveitis, Anterior / pathology
            • Uveitis, Anterior / veterinary

            Grant Funding

            • EY11364 / NEI NIH HHS

            Citations

            This article has been cited 22 times.
            1. Sprenzel CJ, Amann B, Deeg CA, Degroote RL. Glycan Signatures on Neutrophils in an Equine Model for Autoimmune Uveitis. Biomolecules 2025 Oct 12;15(10).
              doi: 10.3390/biom15101444pubmed: 41154673google scholar: lookup
            2. Fleischer AB, Amann B, von Toerne C, Degroote RL, Schmalen A, Weißer T, Hauck SM, Deeg CA. Differential Expression of ARG1 and MRC2 in Retinal Müller Glial Cells During Autoimmune Uveitis. Biomolecules 2025 Feb 14;15(2).
              doi: 10.3390/biom15020288pubmed: 40001591google scholar: lookup
            3. Stafford LS, Plummer CE, Smith WC, Gibson DJ, Sharma J, Vicuna V, Diakite S, Larkin J 3rd. A peptide mimic of SOCS1 modulates equine peripheral immune cells in vitro and ocular effector functions in vivo: implications for recurrent uveitis. Front Immunol 2024;15:1513157.
              doi: 10.3389/fimmu.2024.1513157pubmed: 39867889google scholar: lookup
            4. Plummer CE, Polk T, Sharma J, Bae SS, Barr O, Jones A, Kitchen H, Wilhelmy M, Devin K, Clay Smith W, Kolaczkowski BD, Larkin J 3rd. Open label safety and efficacy pilot to study mitigation of equine recurrent uveitis through topical suppressor of cytokine signaling-1 mimetic peptide. Sci Rep 2022 May 3;12(1):7177.
              doi: 10.1038/s41598-022-11338-xpubmed: 35505065google scholar: lookup
            5. Fingerhut L, Yücel L, Strutzberg-Minder K, von Köckritz-Blickwede M, Ohnesorge B, de Buhr N. Ex Vivo and In Vitro Analysis Identify a Detrimental Impact of Neutrophil Extracellular Traps on Eye Structures in Equine Recurrent Uveitis. Front Immunol 2022;13:830871.
              doi: 10.3389/fimmu.2022.830871pubmed: 35251020google scholar: lookup
            6. Wollanke B, Gerhards H, Ackermann K. Infectious Uveitis in Horses and New Insights in Its Leptospiral Biofilm-Related Pathogenesis. Microorganisms 2022 Feb 7;10(2).
            7. Xiao J, Zhao C, Zhang Y, Qu Y, Liang A, Zhang M, Cheng G. Results of modified CO(2) laser-assisted sclerectomy monotherapy versus trabeculectomy combination therapy in the eyes with uveitic glaucoma. Lasers Med Sci 2022 Mar;37(2):949-959.
              doi: 10.1007/s10103-021-03339-5pubmed: 34003406google scholar: lookup
            8. Martin de Bustamante M, Gomez D, MacNicol J, Hamor R, Plummer C. The Fecal Bacterial Microbiota in Horses with Equine Recurrent Uveitis. Animals (Basel) 2021 Mar 9;11(3).
              doi: 10.3390/ani11030745pubmed: 33803123google scholar: lookup
            9. Degroote RL, Deeg CA. Immunological Insights in Equine Recurrent Uveitis. Front Immunol 2020;11:609855.
              doi: 10.3389/fimmu.2020.609855pubmed: 33488614google scholar: lookup
            10. Wiedemann C, Amann B, Degroote RL, Witte T, Deeg CA. Aberrant Migratory Behavior of Immune Cells in Recurrent Autoimmune Uveitis in Horses. Front Cell Dev Biol 2020;8:101.
              doi: 10.3389/fcell.2020.00101pubmed: 32211402google scholar: lookup
            11. MacDonald ES, Barrett JG. The Potential of Mesenchymal Stem Cells to Treat Systemic Inflammation in Horses. Front Vet Sci 2019;6:507.
              doi: 10.3389/fvets.2019.00507pubmed: 32039250google scholar: lookup
            12. Fingerhut L, Ohnesorge B, von Borstel M, Schumski A, Strutzberg-Minder K, Mörgelin M, Deeg CA, Haagsman HP, Beineke A, von Köckritz-Blickwede M, de Buhr N. Neutrophil Extracellular Traps in the Pathogenesis of Equine Recurrent Uveitis (ERU). Cells 2019 Nov 27;8(12).
              doi: 10.3390/cells8121528pubmed: 31783639google scholar: lookup
            13. Saldinger LK, Nelson SG, Bellone RR, Lassaline M, Mack M, Walker NJ, Borjesson DL. Horses with equine recurrent uveitis have an activated CD4+ T-cell phenotype that can be modulated by mesenchymal stem cells in vitro. Vet Ophthalmol 2020 Jan;23(1):160-170.
              doi: 10.1111/vop.12704pubmed: 31441218google scholar: lookup
            14. Sharma J, Larkin J 3rd. Therapeutic Implication of SOCS1 Modulation in the Treatment of Autoimmunity and Cancer. Front Pharmacol 2019;10:324.
              doi: 10.3389/fphar.2019.00324pubmed: 31105556google scholar: lookup
            15. Schauer M, Kleinwort KJH, Degroote RL, Wiedemann C, Kremmer E, Hauck SM, Deeg CA. Interaction of septin 7 and DOCK8 in equine lymphocytes reveals novel insights into signaling pathways associated with autoimmunity. Sci Rep 2018 Aug 17;8(1):12332.
              doi: 10.1038/s41598-018-30753-7pubmed: 30120291google scholar: lookup
            16. Sandmeyer LS, Bauer BS, Feng CX, Grahn BH. Equine recurrent uveitis in western Canadian prairie provinces: A retrospective study (2002-2015). Can Vet J 2017 Jul;58(7):717-722.
              pubmed: 28698690
            17. Smith JR, Stempel AJ, Bharadwaj A, Appukuttan B. Involvement of B cells in non-infectious uveitis. Clin Transl Immunology 2016 Feb;5(2):e63.
              doi: 10.1038/cti.2016.2pubmed: 26962453google scholar: lookup
            18. Degroote RL, Hauck SM, Amann B, Hirmer S, Ueffing M, Deeg CA. Unraveling the equine lymphocyte proteome: differential septin 7 expression associates with immune cells in equine recurrent uveitis. PLoS One 2014;9(3):e91684.
              doi: 10.1371/journal.pone.0091684pubmed: 24614191google scholar: lookup
            19. Kulbrock M, Lehner S, Metzger J, Ohnesorge B, Distl O. A genome-wide association study identifies risk loci to equine recurrent uveitis in German warmblood horses. PLoS One 2013;8(8):e71619.
              doi: 10.1371/journal.pone.0071619pubmed: 23977091google scholar: lookup
            20. Verma A, Matsunaga J, Artiushin S, Pinne M, Houwers DJ, Haake DA, Stevenson B, Timoney JF. Antibodies to a novel leptospiral protein, LruC, in the eye fluids and sera of horses with Leptospira-associated uveitis. Clin Vaccine Immunol 2012 Mar;19(3):452-6.
              doi: 10.1128/CVI.05524-11pubmed: 22237897google scholar: lookup
            21. Verma A, Kumar P, Babb K, Timoney JF, Stevenson B. Cross-reactivity of antibodies against leptospiral recurrent uveitis-associated proteins A and B (LruA and LruB) with eye proteins. PLoS Negl Trop Dis 2010 Aug 3;4(8):e778.
              doi: 10.1371/journal.pntd.0000778pubmed: 20689825google scholar: lookup
            22. Verma A, Artiushin S, Matsunaga J, Haake DA, Timoney JF. LruA and LruB, novel lipoproteins of pathogenic Leptospira interrogans associated with equine recurrent uveitis. Infect Immun 2005 Nov;73(11):7259-66.