Allogeneic vs. autologous intra‐articular mesenchymal stem cell injection within normal horses: Clinical and cytological comparisons suggest safety
Autor: | Leone S. Hopkins, Aimee C. Colbath, Laurie R. Goodrich, Jennifer N Phillips, Steven W. Dow, C. W. McILWRAITH |
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Rok vydání: | 2019 |
Předmět: |
medicine.medical_specialty
040301 veterinary sciences medicine.medical_treatment Bone Marrow Cells Mesenchymal Stem Cell Transplantation Transplantation Autologous Cryopreservation Injections Intra-Articular 0403 veterinary science Synovial Fluid medicine Animals Transplantation Homologous Synovial fluid Horses business.industry Mesenchymal stem cell 0402 animal and dairy science Arthrocentesis Horse Mesenchymal Stem Cells 04 agricultural and veterinary sciences General Medicine Joint effusion 040201 dairy & animal science Surgery medicine.anatomical_structure Lameness Bone marrow medicine.symptom business Biomarkers |
Zdroj: | Equine Veterinary Journal. 52:144-151 |
ISSN: | 2042-3306 0425-1644 |
DOI: | 10.1111/evj.13136 |
Popis: | Background Allogeneic bone marrow-derived mesenchymal stem cells (BMDMSCs) could provide multiple advantages over autologous BMDMSCs, including creating an 'off-the-shelf' treatment together with the ability to control for donor variation. Objectives The objective of the study was to compare the clinical and synovial fluid response of the normal equine joint to autologous and pooled-allogeneic BMDMSCs while controlling for individual variation and joint variations in response to intra-articular injections. We hypothesised that, by controlling for individual animal and joint variation, we could identify differences between allogeneic vs. autologous BMDMSCs in noninflamed joints. Study design Randomised-controlled experiment. Methods Bone marrow was harvested from eight horses. Autologous BMDMSCs were culture expanded, cryopreserved and thawed immediately prior to administration. For allogeneic BMDMSC treatments, four horses' BMDMSCs were culture expanded, pooled, cryopreserved and thawed immediately prior to use. Ten million (autologous or pooled-allogeneic) BMDMSCs were administered into contralateral forelimb metacarpophalangeal joints so that every autologous and allogeneic injection could be compared within the same animal. Clinical parameters included subjective lameness, objective lameness (Lameness Locator™), response to flexion, joint circumference and joint effusion. Arthrocentesis was performed for assessment of the nucleated cell count, differential cell count, total protein, and synovial concentrations of prostaglandin E2 (PGE2) and c-reactive protein (CRP). All parameters were measured at baseline, 6, 12, 24, 72, 168 and 336 h post-injection. Results No difference was detected in any parameters between forelimb metacarpophalangeal joints administered autologous or pooled-allogeneic BMDMSCs. Main limitations This study did not attempt to measure efficacy of BMDMSCs for musculoskeletal disease and should be followed by properly controlled efficacy trials. Conclusions The study did not identify any clinical or cytological differences in the normal joint response to allogeneic or autologous BMDMSCs. A larger study to prove equivalence is warranted as allogeneic BMDMSCs may be a feasible alternative to autologous BMDMSCs. |
Databáze: | OpenAIRE |
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