Changes in airway inflammatory cell populations in standardbred racehorses after interferon-alpha administration.
Abstract: Natural human interferon-alpha (nHuIFN alpha) was administered to actively training Standardbred racehorses with inflammatory airway disease (IAD). Inflammatory airway disease was characterized by poor exercise performance and inflammation and exudate in the upper and lower airway. Placebo, 50, 150, or 450 units(U) of nHuIFN alpha was administered orally for 5 consecutive days to eight horses per treatment group in a double-blind, randomized block design. Response to nHuIFN alpha was monitored by semiquantitative endoscopic examination score and cytologic examination of bronchoalveolar lavage fluid (BALF) performed at baseline (Day 1), Day 8 and Day 15 after initiation of nHuIFN alpha administration. Neutrophil, macrophage, lymphocyte, and nucleated cell counts in BALF were lower (P < 0.05), compared with BALF cell counts in placebo-treated horses 8 days after administration of 50 U and 150 U nHuIFN alpha, and 15 days after administration of 50 U nHuIFN alpha. Neutrophil, lymphocyte and nucleated cell counts were lower than cell counts from placebo-treated horses, 8 days following administration of 450 U nHuIFN alpha. The proportion CD4-, CD5-, and CD8-positive lymphocytes in BALF was not affected by administration of nHuIFN alpha. Oral administration of low-dose nHuIFN alpha reduced inflammation of the lowest respiratory tract in Standardbred racehorses with IAD.
Publication Date: 1996-01-01 PubMed ID: 8677636DOI: 10.1016/0165-2427(95)05480-4Google Scholar: Lookup
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- Clinical Trial
- Journal Article
- Randomized Controlled Trial
- Research Support
- Non-U.S. Gov't
Summary
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The study examines the impact of natural human interferon-alpha (nHuIFN alpha) on Standardbred racehorses experiencing inflammatory airway disease. The findings indicate that nHuIFN alpha, administered orally, significantly reduced inflammation in the horses’ respiratory tract.
Study Overview
- The research was conducted on Standardbred racehorses actively undergoing training, all of whom were suffering from inflammatory airway disease (IAD). IAD is marked by poor exercise performance along with inflammation and exudate in the upper and lower airway.
- The test was performed as a double-blind, randomized block design where the horses were given either a placebo or doses of 50 units (U), 150 U, or 450 U of nHuIFN alpha. The doses were given orally for five consecutive days with eight horses in each treatment group.
Observation and Evaluation
- The reaction to nHuIFN alpha was monitored by performing a semiquantitative endoscopic examination score and cytologic examination of bronchoalveolar lavage fluid (BALF), which was used to measure changes in inflammation. These were conducted at three stages: at baseline (Day 1), then on Day 8 and Day 15 after starting the nHuIFN alpha treatment.
- In comparison to the placebo, the BALF cell counts were lower eight days after administering 50 U and 150 U nHuIFN alpha, and 15 days after administering 50 U nHuIFN alpha. Specifically, there were fewer neutrophils, macrophages, lymphocytes, and nucleated cells (all components of the immune system involved in inflammation).
- The number of neutrophils, lymphocytes, and nucleated cells also showed a decrease eight days after administrating 450 U nHuIFN alpha.
- The treatments however, did not affect the proportion of CD4-, CD5-, and CD8-positive lymphocytes in the BALF.
Conclusion
- The main find from this study is that oral administration of low-dose nHuIFN alpha significantly reduced inflammation in the lowest respiratory tract of Standardbred racehorses experiencing IAD. This suggests that nHuIFN alpha may be a potential therapeutic agent for managing IAD in racehorses.
Cite This Article
APA
Moore BR, Krakowka S, Cummins JM, Robertson JT.
(1996).
Changes in airway inflammatory cell populations in standardbred racehorses after interferon-alpha administration.
Vet Immunol Immunopathol, 49(4), 347-358.
https://doi.org/10.1016/0165-2427(95)05480-4 Publication
Researcher Affiliations
- Department of Clinical Sciences, College of Veterinary Medicine, Ohio State University, Columbus 43210-1089, USA. Moore.B@vet.ksu.edu
MeSH Terms
- Administration, Oral
- Animals
- Bronchoalveolar Lavage Fluid / cytology
- Bronchoalveolar Lavage Fluid / immunology
- Cell Count
- Double-Blind Method
- Female
- Horse Diseases / immunology
- Horse Diseases / pathology
- Horse Diseases / therapy
- Horses
- Humans
- Inflammation / pathology
- Inflammation / therapy
- Inflammation / veterinary
- Interferon-alpha / administration & dosage
- Interferon-alpha / therapeutic use
- Male
- Respiratory Tract Diseases / pathology
- Respiratory Tract Diseases / therapy
- Respiratory Tract Diseases / veterinary
Citations
This article has been cited 7 times.- Frazzini S, Riva F, Amadori M. Therapeutic and Prophylactic Use of Oral, Low-Dose IFNs in Species of Veterinary Interest: Back to the Future. Vet Sci 2021 Jun 11;8(6).
- Wu W, Metcalf JP. The Role of Type I IFNs in Influenza: Antiviral Superheroes or Immunopathogenic Villains?. J Innate Immun 2020;12(6):437-447.
- Mamber SW, Lins J, Gurel V, Hutcheson DP, Pinedo P, Bechtol D, Krakowka S, Fields-Henderson R, Cummins JM. Low-dose oral interferon modulates expression of inflammatory and autoimmune genes in cattle. Vet Immunol Immunopathol 2016 Apr;172:64-71.
- 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.
- Akai M, Hobo S, Wada S. Effect of Low-Dose Human Interferon-alpha on Shipping Fever of Thoroughbred Racehorses. J Equine Sci 2008;19(4):91-5.
- Koo H, Ryu SH, Ahn HJ, Jung WK, Park YK, Kwon NH, Kim SH, Kim JM, Yoo BW, Choi SI, Davis WC, Park YH. Immunostimulatory effects of the anionic alkali mineral complex Barodon on equine lymphocytes. Clin Vaccine Immunol 2006 Nov;13(11):1255-66.
- Moore I, Horney B, Day K, Lofstedt J, Cribb AE. Treatment of inflammatory airway disease in young standardbreds with interferon alpha. Can Vet J 2004 Jul;45(7):594-601.
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