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Frontiers in veterinary science2025; 12; 1625431; doi: 10.3389/fvets.2025.1625431

Safety study of leucoreduced allogeneic pooled freeze-dried platelet-rich plasma in healthy equine joints.

Abstract: Clinical use of blood-derived intra-articular therapies, such as platelet-rich plasma (PRP), have increased in equine athletes due to their proposed disease-modifying effects. Need for a shelf-stable, allogeneic PRP product with known composition for standardized treatment exists. The objective of this study was to compare systemic and local effects of a single intra-articular injection of equine leucoreduced allogeneic pooled freeze-dried PRP (alloPRP) to a placebo control (saline) in normal, healthy equine joints. Unassigned: Twelve healthy horses were randomly assigned to either control (saline) or treatment (alloPRP) ( = 6 horses per group). The study used a blinded 2-period, 2-treatment, 2-joint non-crossover experimental design. Each study period was defined as 1 week, followed by a 2-week washout between study periods. One joint (radiocarpal or tarsocrural joint) was treated and evaluated per study period. Treatment sequence and limbs chosen for treatment were randomized for each horse. Systemic effects were measured at different time points by physical examination, bloodwork (complete blood count and serum biochemistry), and lameness examination (subjective and objective). Local effects to the joint measured at different time points included heat, swelling, joint circumference, and response to passive flexion as well as synovial fluid analysis. Data was analyzed using linear mixed models with significance set at  < 0.05. Unassigned: There were no differences between groups for joint swelling ( = 0.40), joint circumference ( = 0.55), heat scores ( = 0.09), or passive flexion ( 0.70) following intra-articular injections. Both subjective and objective lameness scores were no different on any study day for both treatment ( 0.47) and control groups ( 0.31). There were no differences in complete blood count or serum biochemistry values between groups. No difference in synovial fluid TNCC ( = 0.80), TP ( = 0.94), or synovial fluid concentrations of TNFα ( 0.45) and IL-1raP ( 0.18) were observed between groups for each sampled time point (T0 and T7d). Unassigned: The alloPRP formulation was demonstrated to be safe for use in equine joints. Further investigation is necessary for evaluation of clinical efficacy.
Publication Date: 2025-07-14 PubMed ID: 40727274PubMed Central: PMC12301550DOI: 10.3389/fvets.2025.1625431Google Scholar: Lookup
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  • Journal Article

Summary

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The research examines the safety of using leucoreduced allogeneic pooled freeze-dried platelet-rich plasma (alloPRP) in horse joints, comparing its effects with saline as a control. The results indicate that the alloPRP formulation is safe for use, but its clinical effectiveness needs further exploration.

Study Objective and Methodology

  • The primary objective of this research was to assess the systemic and local effects of an injection of equine leucoreduced allogeneic pooled freeze-dried PRP (alloPRP) compared to a placebo control (saline) in healthy horse joints.
  • The researchers used a double-blind non-crossover experimental design involving a total of 12 healthy horses. These animals were randomly split into two groups (6 per group) with the first group receiving the alloPRP treatment and the other being administered a control saline solution.
  • The study was carried out over two periods of one week each, segregated by a two-week ‘washout’ period. In each period, a joint (either the radiocarpal or tarsocrural joint) was treated and evaluated.

Measurements and Data Analysis

  • Both systemic and local effects were measured at various time points, using physical examination, complete blood count, serum biochemistry, and both subjective and objective lameness examinations.
  • Local effects on the joint were also measured, which included heat, swelling, joint circumference, synovial fluid analysis, and the response to passive flexion.
  • The gathered data was analyzed using linear mixed models and the level of significance set at <0.05.

Results

  • Results demonstrated no significant differences between the alloPRP treatment group and the control group in terms of joint swelling, joint circumference, heat scores, passive flexion, or lameness scores on any study day.
  • Additionally, there were no observed differences in complete blood count or serum biochemistry values between the groups.
  • Even synovial fluid analyses—specifically TNCC, TP, TNFα, and IL-1raP concentrations—showed no distinction between the groups at sampled time points.

Conclusion

  • The study concluded that the use of alloPRP was safe in equine joints, despite not showing significant differences when compared to a saline solution.
  • However, the team juxtaposed this result with an acknowledgment that further study is needed to evaluate the clinical efficacy of alloPRP treatments.

Cite This Article

APA
Kooy S, Constant J, Cole R, Boone L. (2025). Safety study of leucoreduced allogeneic pooled freeze-dried platelet-rich plasma in healthy equine joints. Front Vet Sci, 12, 1625431. https://doi.org/10.3389/fvets.2025.1625431

Publication

ISSN: 2297-1769
NlmUniqueID: 101666658
Country: Switzerland
Language: English
Volume: 12
Pages: 1625431
PII: 1625431

Researcher Affiliations

Kooy, Sarah
  • Department of Clinical Sciences, College of Veterinary Medicine, Auburn University, Auburn, AL, United States.
Constant, Jemma
  • College of Veterinary Medicine, Auburn University, Auburn, AL, United States.
Cole, Robert
  • Department of Clinical Sciences, College of Veterinary Medicine, Auburn University, Auburn, AL, United States.
Boone, Lindsey
  • Department of Clinical Sciences, College of Veterinary Medicine, Auburn University, Auburn, AL, United States.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

This article includes 25 references
  1. Ireland JL, Clegg PD, McGowan CM, McKane SA, Chandler KJ, Pinchbeck GL. Disease prevalence in geriatric horses in the United Kingdom: veterinary clinical assessment of 200 cases.. Equine Vet J (2012) 44:101–6.
  2. Caron JP, Genovese RL. Principles and practices of joint disease treatment. In: Diagnosis and management of lameness in the horse. eds. Ross, M and Sue Dyson, S USA: Elsevier science. (2003). 746–64.
  3. Bogers SH. Cell-based therapies for joint disease in veterinary medicine: what we have learned and what we need to know.. Front Vet Sci (2018) 5:70.
    doi: 10.3389/fvets.2018.00070pmc: PMC5911772pubmed: 29713634google scholar: lookup
  4. Peng C, Yang L, Labens R, Gao Y, Zhu Y, Li J. A systematic review and Meta-analysis of the efficacy of platelet-rich plasma products for treatment of equine joint disease.. Equine Vet J (2024) 56:858–69.
    doi: 10.1111/evj.14042pubmed: 38185481google scholar: lookup
  5. Tokawa PKA, Baccarin RYA, Zanotto GM. Intra-articular corticosteroids: systematic review of effects on osteoarthritis and joint health.. Equine Vet Educ (2025) 37:371–81.
    doi: 10.1111/eve.14097google scholar: lookup
  6. Ríos DL, López C, Carmona JU. Platelet-rich gel supernatants stimulate the release of anti-inflammatory proteins on culture Media of Normal Equine Synovial Membrane Explants.. Vet Med Int (2015) 2015:547052: 1–9.
    doi: 10.1155/2015/547052pmc: PMC4451761pubmed: 26090267google scholar: lookup
  7. Carmona JU, Ríos DL, López C, Álvarez ME, Pérez JE, Bohórquez ME. effects of platelet-rich gel supernatants on histology and chondrocyte apoptosis scores, hyaluronan release and gene expression of equine cartilage explants challenged with lipopolysaccharide.. BMC Vet Res (2016) 12:135.
    doi: 10.1186/s12917-016-0759-8pmc: PMC4929746pubmed: 27369779google scholar: lookup
  8. Hosseini S, Soltani-Zangbar MS, Zamani M, Yaghoubi Y, Rikhtegar Ghiasi R, Motavalli R. Comparative evaluation of autologous platelet-rich plasma and platelet lysate in patients with knee osteoarthritis.. Growth Factors (2023) 41:165–77.
    doi: 10.1080/08977194.2023.2227273pubmed: 37351894google scholar: lookup
  9. Peña AN, Sommerfeld SD, Anderson AE, Han J, Maestas DR, Mejias JC. Autologous protein solution processing alters lymphoid and myeloid cell populations and modulates gene expression dependent on cell type.. Arthritis Res Ther (2022) 24:221.
    doi: 10.1186/s13075-022-02875-xpmc: PMC9465964pubmed: 36096945google scholar: lookup
  10. Tyrnenopoulou P, Diakakis N, Karayannopoulou M, Savvas I, Koliakos G. Evaluation of intra-articular injection of autologous platelet lysate (Pl) in horses with osteoarthritis of the distal interphalangeal joint.. Vet Q (2016) 36:56–62.
    doi: 10.1080/01652176.2016.1141257pubmed: 26828234google scholar: lookup
  11. Garbin LC, Contino EK, Olver CS, Frisbie DD. A safety evaluation of allogeneic freeze-dried platelet-rich plasma or conditioned serum compared to autologous frozen products equivalents in equine healthy joints.. BMC Vet Res (2022) 18:141.
    doi: 10.1186/s12917-022-03225-4pmc: PMC9014566pubmed: 35436878google scholar: lookup
  12. Camargo Garbin L, McIlwraith CW, Frisbie DD. Evaluation of allogeneic freeze-dried platelet lysate in cartilage exposed to interleukin 1-Β .. BMC Vet Res (2019) 15:386.
    doi: 10.1186/s12917-019-2118-zpmc: PMC6824121pubmed: 31675958google scholar: lookup
  13. Pietramaggiori G, Scherer SS, Mathews JC, Alperovich M, Yang HJ, Neuwalder J. Healing modulation induced by freeze-dried platelet-rich plasma and micronized allogeneic dermis in a diabetic wound model.. Wound Repair Regen (2008) 16:218–25.
  14. McCarrel T, Fortier L. Temporal growth factor release from platelet-rich plasma, Trehalose lyophilized platelets, and bone marrow aspirate and their effect on tendon and ligament gene expression.. J Orthop Res (2009) 27:1033–42.
    doi: 10.1002/jor.20853pubmed: 19170097google scholar: lookup
  15. Hassan NH, Ahmad RE, Kamarul T, Looi QHD, Chong PP. Allogenic platelet-rich plasma for treating cartilage injury: a systematic review of the evidence on the basic sciences for potential future applications.. Cells Tissues Organs (2024) 213:338–55.
    doi: 10.1159/000535018pubmed: 37944499google scholar: lookup
  16. Zhang ZY, Huang AW, Fan JJ, Wei K, Jin D, Chen B. The potential use of allogeneic platelet-rich plasma for large bone defect treatment: immunogenicity and defect healing efficacy.. Cell Transplant (2013) 22:175–87.
    doi: 10.3727/096368912x653183pubmed: 22863146google scholar: lookup
  17. Jo CH, Lee SY, Yoon KS, Oh S, Shin S. Allogenic pure platelet-rich plasma therapy for rotator cuff disease: a bench and bed study.. Am J Sports Med (2018) 46:3142–54.
    doi: 10.1177/0363546518800268pubmed: 30311796google scholar: lookup
  18. Textor JA, Tablin F. Intra-articular use of a platelet-rich product in Normal horses: clinical signs and Cytologic responses.. Vet Surg (2013) 42:499–510.
  19. Moreira JJ, Moraes APL, Brossi PM, Machado TS, Michelacci YM, Massoco CO. Autologous processed plasma: cytokine profile and effects upon injection into healthy equine joints.. J Vet Sci (2015) 16:47.
    doi: 10.4142/jvs.2015.16.1.47pmc: PMC4367149pubmed: 25269714google scholar: lookup
  20. Smit Y, Thompson PN, Mahne AT, Marais HJ, Goddard A. Clinical findings, synovial fluid cytology and growth factor concentrations after intra-articular use of a platelet-rich product in horses with osteoarthritis.. J S Afr Vet Assoc (2019) 90:1–9.
    doi: 10.4102/jsava.v90i0.1721pmc: PMC6556911pubmed: 31170778google scholar: lookup
  21. Velloso Alvarez A, Boone LH, Braim AP, Taintor JS, Caldwell F, Wright JC. A survey of clinical usage of non-steroidal intra-articular therapeutics by equine practitioners.. Front Vet Sci (2020) 7:579967.
    doi: 10.3389/fvets.2020.579967pmc: PMC7642446pubmed: 33195592google scholar: lookup
  22. Owens SD, Kol A, Walker NJ, Borjesson DL. Allogeneic mesenchymal stem cell treatment induces specific alloantibodies in horses.. Stem Cells Int (2016) 2016:1–8.
    doi: 10.1155/2016/5830103pmc: PMC5018342pubmed: 27648075google scholar: lookup
  23. Colbath AC, Dow SW, Hopkins LS, Phillips JN, McIlwraith CW, Goodrich LR. Allogeneic vs. autologous intra-articular mesenchymal stem cell injection within normal horses: clinical and cytological comparisons suggest safety.. Equine Vet J (2020) 52:144–51.
    doi: 10.1111/evj.13136pubmed: 31120574google scholar: lookup
  24. Colbath AC, Dow SW, Hopkins LS, Phillips JN, McIlwraith CW, Goodrich LR. Induction of synovitis using interleukin-1 beta: are there differences in the response of middle carpal joint compared to the tibiotarsal joint?. Front Vet Sci (2018) 5:208.
    doi: 10.3389/fvets.2018.00208pmc: PMC6127273pubmed: 30234134google scholar: lookup
  25. Moraes APL, Moreira JJ, Brossi PM, Machado TS, Michelacci YM, Baccarin RY. Short- and long-term effects of platelet-rich plasma upon healthy equine joints: clinical and laboratory aspects.. Can Vet J (2015) 56:831.
    pmc: PMC4502851pubmed: 26246629

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