Analyze Diet
Veterinary immunology and immunopathology2007; 118(1-2); 30-39; doi: 10.1016/j.vetimm.2007.04.009

Immune parameters in mares resistant and susceptible to persistent post-breeding endometritis: effects of immunomodulation.

Abstract: Our objective was to characterize immune parameters in susceptible (SM) and resistant (RM) mares, with and without artificial insemination (AI) and immunomodulation. Eight RM and eight SM were selected based on their reproductive history and functional tests. Both groups of mares were evaluated during three consecutive cycles: Cycle 1, untreated cycle (control); Cycle 2, AI with dead semen; Cycle 3, AI with dead semen and immunomodulation. Endometrial biopsies were taken during the three cycles as follows: Cycle 1--at estrus, when follicles > or =35mm and at diestrus (7+/-1 days after ovulation); Cycle 2--at estrus 24h post-AI, and at diestrus; Cycle 3--at estrus 24h after treatment with a Mycobacterium phlei cell-wall extract (MCWE) and AI, and at diestrus. The mRNA transcription (mRNAT) of IL-8 and IL-10 were determined by real-time PCR. Image analysis of immunohistochemistry slides was performed using digital software (Image-Pro Plus v 5.0; Media Cybernetics); the percentage of stained area was determined for Major Histocompatibility Complex II (MHC-II), polymorphonuclear leukocytes (PMN) and T lymphocytes (TL) on each tissue section. In Cycle 1, SM had significantly higher MHC-II, TL, PMN and IL-8 than RM during estrus (P<0.006, P<0.0005, P<0.05, respectively), while transcription of IL-10 was significantly lower than in RM (P<0.0001). During diestrus, SM had higher levels of TL, PMN and IL-8 than RM (P<0.0001). After AI (Cycle 2), SM had higher levels of IL-8 and lower levels of IL-10 than RM at estrus and no differences were detected for MHC-II, TL and PMN positive cells. During diestrus in the same cycle, all the immune parameters were higher in SM mares (P<0.005, P<0.0004, P<0.0001, P<0.02, respectively). When MCWE was applied at the time of AI (Cycle 3), SM expressed significant higher levels of IL-10 24h after treatment (P<0.005), which were also higher than in the control Cycle 2 or after AI (Cycle 2). However, no significant differences were detected for MHC-II, lymphocytes-PMN or IL-8 between SM and RM during diestrus in Cycle 3. This study showed that SM had higher levels of all immune parameters except IL-10 than RM during Cycle 1. After AI (Cycle 2), the inflammatory condition persisted in SM but not RM mares until day 7 post-ovulation. Following treatment with MCWE at the time of AI (Cycle 3) uterine immunological changes in SM resulted in an endometrial immune environment similar to that found in normal RM.
Publication Date: 2007-05-03 PubMed ID: 17559943DOI: 10.1016/j.vetimm.2007.04.009Google 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.
  • Controlled Clinical Trial
  • Journal Article

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 research paper focuses on assessing immune deviations in mares susceptible to a condition called persistent post-breeding endometritis (PPBE). The immune responses were gauged over three cycles: an untreated cycle, AI with dead semen, and AI with dead semen and immunomodulation. The study concluded that susceptible mares exhibited higher inflammatory conditions than resistant mares; however, immune conditions normalized post immunomodulation with MCWE.

Study Design and Procedure

  • Eight susceptible mares (SM) and eight resistant mares (RM) were chosen for the study based on their reproductive history and functionality.
  • The mares underwent evaluation over three consecutive cycles: during Cycle 1(untreated), Cycle 2(dead semen AI), and Cycle 3(dead semen AI plus immunomodulation with Mycobacterium phlei cell-wall extract or MCWE).
  • Biopsies were performed at estrus and diestrus during all cycles to evaluate immune responses.
  • The estimation of IL-8 and IL-10 mRNA transcription was done via real-time PCR.
  • Digital image analysis of immunohistochemistry slides was done to evaluate the percentage of stained area for Major Histocompatibility Complex II (MHC-II), polymorphonuclear leukocytes (PMN), and T lymphocytes (TL).

Findings

  • In Cycle 1, SM mares showed higher MHC-II, TL, PMN, IL-8, and lower IL-10 mRNA transcription than RM.
  • During diestrus in Cycle 1, SM had higher levels of TL, PMN, IL-8, and lower IL-10 than RM.
  • Post AI (Cycle 2), SM mares demonstrated higher levels of IL-8, lower IL-10, and similar levels of MHC-II, TL, and PMN at estrus and diestrus when compared to RM mares.
  • Post MCWE application during AI (Cycle 3), SM mares showed higher levels of IL-10 at estrus but similar levels of MHC-II, TL, PMN, and IL-8 at diestrus as RM mares.

Conclusion

  • During a natural cycle, susceptible mares exhibit an elevated immune response characterized by high levels of IL-8 and lower IL-10, compared to resistant mares.
  • Artificial insemination accentuates the inflammatory condition in susceptible mares up until the 7th day post-ovulation, whereas this doesn’t occur in resistant mares.
  • Notably, with the use of MCWE at the time of AI, immunological conditions in susceptible mares normalize and become similar to the endometrial immune environment of resistant mares.

The results of this study aid in understanding the immune response in mares towards PPBE and offer avenues for its management especially through immunomodulation.

Cite This Article

APA
Fumuso EA, Aguilar J, Giguère S, Rivulgo M, Wade J, Rogan D. (2007). Immune parameters in mares resistant and susceptible to persistent post-breeding endometritis: effects of immunomodulation. Vet Immunol Immunopathol, 118(1-2), 30-39. https://doi.org/10.1016/j.vetimm.2007.04.009

Publication

ISSN: 0165-2427
NlmUniqueID: 8002006
Country: Netherlands
Language: English
Volume: 118
Issue: 1-2
Pages: 30-39

Researcher Affiliations

Fumuso, Elida Ana
  • UNICEN, Facultad de Ciencias Veterinarias, Pinto 399, Tandil 7000, Argentina. efumuso@vet.unicen.edu.ar
Aguilar, Javier
    Giguère, Steeve
      Rivulgo, Margarita
        Wade, José
          Rogan, Dragan

            MeSH Terms

            • Animals
            • Cell Wall
            • Disease Susceptibility
            • Endometritis / immunology
            • Endometritis / prevention & control
            • Endometritis / veterinary
            • Estrous Cycle
            • Female
            • Genes, MHC Class II
            • Horse Diseases / immunology
            • Horse Diseases / prevention & control
            • Horses
            • Immunologic Factors / pharmacology
            • Insemination, Artificial / adverse effects
            • Interleukin-10 / genetics
            • Interleukin-10 / metabolism
            • Interleukin-8 / genetics
            • Interleukin-8 / metabolism
            • Lymphocytes / metabolism
            • Mycobacterium phlei
            • Uterus / cytology

            Citations

            This article has been cited 16 times.
            1. Scholtz M, Guthrie AJ, Newton R, Schulman ML. Review of Pseudomonas aeruginosa and Klebsiella pneumoniae as venereal pathogens in horses. Equine Vet J 2025 May;57(3):587-597.
              doi: 10.1111/evj.14201pubmed: 39103748google scholar: lookup
            2. Novello G, Souza FF, Canisso IF. Platelet-Rich Plasma Proteome of Mares Susceptible to Persistent-Breeding-Induced Endometritis Differs from Resistant Mares. Animals (Basel) 2024 Jul 18;14(14).
              doi: 10.3390/ani14142100pubmed: 39061562google scholar: lookup
            3. Ignácio FS, Garcia LV, de Souza GG, Amatti LZ, de Barros LD, Bergfelt DR, Camargo GS, de Meira C, de Almeida BFM. Hematological and Biochemical Effects Associated with Prolonged Administration of the NSAID Firocoxib in Adult Healthy Horses. Vet Sci 2024 Jun 5;11(6).
              doi: 10.3390/vetsci11060256pubmed: 38922003google scholar: lookup
            4. Lange-Consiglio A, Gaspari G, Funghi F, Capra E, Cretich M, Frigerio R, Bosi G, Cremonesi F. Amniotic Mesenchymal-Derived Extracellular Vesicles and Their Role in the Prevention of Persistent Post-Breeding Induced Endometritis. Int J Mol Sci 2023 Mar 8;24(6).
              doi: 10.3390/ijms24065166pubmed: 36982240google scholar: lookup
            5. Katila T, Ferreira-Dias G. Evolution of the Concepts of Endometrosis, Post Breeding Endometritis, and Susceptibility of Mares. Animals (Basel) 2022 Mar 19;12(6).
              doi: 10.3390/ani12060779pubmed: 35327176google scholar: lookup
            6. Solano-Suárez G, Caixeta LS, Masic A, Manríquez D, Hatamoto-Zervoudakis L, Paudyal S, Velasquez-Munoz A, Velez J, Pinedo PJ. Effect of peripartal administration of mycobacterium cell wall fraction on health and fertility of Holstein cows under organic-certified management. J Anim Sci 2021 Sep 1;99(9).
              doi: 10.1093/jas/skab191pubmed: 34468760google scholar: lookup
            7. Wojtysiak K, Ryszka W, Stefaniak T, Król J, Kozdrowski R. Changes in the Secretion of Anti-Inflammatory Cytokines and Acute-Phase Proteins in the Uterus after Artificial Insemination in the Mare. Animals (Basel) 2020 Dec 19;10(12).
              doi: 10.3390/ani10122438pubmed: 33352707google scholar: lookup
            8. Schöniger S, Schoon HA. The Healthy and Diseased Equine Endometrium: A Review of Morphological Features and Molecular Analyses. Animals (Basel) 2020 Apr 5;10(4).
              doi: 10.3390/ani10040625pubmed: 32260515google scholar: lookup
            9. Canisso IF, Segabinazzi LGTM, Fedorka CE. Persistent Breeding-Induced Endometritis in Mares - a Multifaceted Challenge: From Clinical Aspects to Immunopathogenesis and Pathobiology. Int J Mol Sci 2020 Feb 20;21(4).
              doi: 10.3390/ijms21041432pubmed: 32093296google scholar: lookup
            10. Nash DM, Paddison J, Davies Morel MCG, Barnea ER. Preimplantation factor modulates acute inflammatory responses of equine endometrium. Vet Med Sci 2018 Nov;4(4):351-356.
              doi: 10.1002/vms3.126pubmed: 30273998google scholar: lookup
            11. Krakowski L, Bartoszek P, Krakowska I, Stachurska A, Piech T, Brodzki P, Wrona Z. Changes in Blood Lymphocyte Subpopulations and Expression of MHC-II Molecules in Wild Mares Before and After Parturition. J Vet Res 2017 Jun;61(2):217-221.
              doi: 10.1515/jvetres-2017-0028pubmed: 29978076google scholar: lookup
            12. Marth CD, Firestone SM, Glenton LY, Browning GF, Young ND, Krekeler N. Oestrous cycle-dependent equine uterine immune response to induced infectious endometritis. Vet Res 2016 Nov 8;47(1):110.
              doi: 10.1186/s13567-016-0398-xpubmed: 27825391google scholar: lookup
            13. Falomo ME, Ferroni L, Tocco I, Gardin C, Zavan B. Immunomodulatory Role of Adipose-Derived Stem Cells on Equine Endometriosis. Biomed Res Int 2015;2015:141485.
              doi: 10.1155/2015/141485pubmed: 26180781google scholar: lookup
            14. Liang XJ, Yuan L, Hu J, Yu HH, Li T, Lin SF, Tang SB. Phosphomannopentaose sulfate (PI-88) suppresses angiogenesis by downregulating heparanase and vascular endothelial growth factor in an oxygen-induced retinal neovascularization animal model. Mol Vis 2012;18:1649-57.
              pubmed: 22773903
            15. Christoffersen M, Woodward E, Bojesen AM, Jacobsen S, Petersen MR, Troedsson MH, Lehn-Jensen H. Inflammatory responses to induced infectious endometritis in mares resistant or susceptible to persistent endometritis. BMC Vet Res 2012 Mar 29;8:41.
              doi: 10.1186/1746-6148-8-41pubmed: 22458733google scholar: lookup
            16. Kalpokas I, Perdigón F, Rivero R, Talmon M, Sartore I, Viñoles C. Effect of a povidone-iodine intrauterine infusion on progesterone levels and endometrial steroid receptor expression in mares. Acta Vet Scand 2010 Dec 16;52(1):66.
              doi: 10.1186/1751-0147-52-66pubmed: 21162724google scholar: lookup