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      Adipose Mesenchymal Stromal Cell-Based Therapy for Severe Osteoarthritis of the Knee: A Phase I Dose-Escalation Trial

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          Abstract

          This phase I clinical trial evaluated the safety and clinical efficacy of adipose-derived stromal cells (ASCs) in osteoarthritis. Eighteen patients with severe knee osteoarthritis were treated with a single intra-articular injection of autologous ASCs at low (2 × 10 6 cells), medium (10 × 10 6), or high (50 × 10 6) doses ( n = 6 each). After 6 months, no serious adverse events were reported, and patients treated with low-dose ASCs significantly improved in pain and function.

          Abstract

          Osteoarthritis (OA) is the most widespread musculoskeletal disorder in adults. It leads to cartilage damage associated with subchondral bone changes and synovial inflammation, causing pain and disability. The present study aimed at evaluating the safety of a dose-escalation protocol of intra-articular injected adipose-derived stromal cells (ASCs) in patients with knee OA, as well as clinical efficacy as secondary endpoint. A bicentric, uncontrolled, open phase I clinical trial was conducted in France and Germany with regulatory agency approval for ASC expansion procedure in both countries. From April 2012 to December 2013, 18 consecutive patients with symptomatic and severe knee OA were treated with a single intra-articular injection of autologous ASCs. The study design consisted of three consecutive cohorts (six patients each) with dose escalation: low dose (2 × 10 6 cells), medium dose (10 × 10 6), and high dose (50 × 10 6). The primary outcome parameter was safety evaluated by recording adverse events throughout the trial, and secondary parameters were pain and function subscales of the Western Ontario and McMaster Universities Arthritis Index. After 6 months of follow-up, the procedure was found to be safe, and no serious adverse events were reported. Four patients experienced transient knee joint pain and swelling after local injection. Interestingly, patients treated with low-dose ASCs experienced significant improvements in pain levels and function compared with baseline. Our data suggest that the intra-articular injection of ASCs is a safe therapeutic alternative to treat severe knee OA patients. A placebo-controlled double-blind phase IIb study is being initiated to assess clinical and structural efficacy.

          Significance

          Although this phase I study included a limited number of patients without a placebo arm, it showed that local injection of autologous adipose-derived stem cells was safe and well tolerated in patients with knee osteoarthritis. This study also provides encouraging preliminary evidence of efficacy. Larger and controlled long-term studies are now mandatory to confirm whether this new strategy of cell therapy can improve pain and induce structural benefit in osteoarthritis.

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          Most cited references12

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          Osteoarthritis cartilage histopathology: grading and staging.

          Current osteoarthritis (OA) histopathology assessment methods have difficulties in their utility for early disease, as well as their reproducibility and validity. Our objective was to devise a more useful method to assess OA histopathology that would have wide application for clinical and experimental OA assessment and would become recognized as the standard method. An OARSI Working Group deliberated on principles, standards and features for an OA cartilage pathology assessment system. Using current knowledge of the pathophysiology of OA morphologic features, a proposed system was presented at OARSI 2000. Subsequently, this was widely circulated for comments amongst experts in OA pathology. An OA cartilage pathology assessment system based on six grades, which reflect depth of the lesion and four stages reflecting extent of OA over the joint surface was developed. The OARSI cartilage OA histopathology grading system appears consistent and simple to apply. Further studies are required to confirm the system's utility.
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            Is Open Access

            Comparing the Immunomodulatory Properties of Bone Marrow, Adipose Tissue, and Birth-Associated Tissue Mesenchymal Stromal Cells

            Mesenchymal stromal cells (MSC) have gained immense attraction in regenerative medicine, tissue engineering, and immunotherapy. This is based on their differentiation potential and the supply of pro-regenerative and immunomodulatory signals. MSC can be isolated from a multitude of tissue sources, but mainly bone marrow, adipose tissue, and birth-associated tissues (e.g., umbilical cord, cord blood, placenta) appear to be relevant for clinical translation in immune-mediated disorders. However, only a few studies directly compared the immunomodulatory potency of MSC from different tissue sources. This review compiles the current literature regarding the similarities and differences between these three sources for MSCs with a special focus on their immunomodulatory effects on T-lymphocyte subsets and monocytes, macrophages, and dendritic cells.
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              • Article: not found

              Dose-dependent immunomodulatory effect of human stem cells from amniotic membrane: a comparison with human mesenchymal stem cells from adipose tissue.

              Bone marrow-derived mesenchymal stem cells (BMSCs) have been used for allogeneic application in tissue engineering but have certain drawbacks. Therefore, stem cells (SC)s derived from other adult tissue sources have been considered as an alternative. However, there is only limited knowledge on their immunomodulatory properties. The aim of our study was to compare the immunomodulatory potential of human amniotic mesenchymal and human amniotic epithelial cells with that of human adipose-derived SCs under identical experimental conditions. We have demonstrated a dose-dependent inhibition of peripheral blood mononuclear cell (PBMC) immune responses in mixed lymphocyte reactions (up to 66-93% inhibition) and phytohemagglutinin activation assays (up to 67-96% inhibition). The lowest SC-to-PBMC ratio able to inhibit PBMC proliferation significantly was 1:8. Subcultivation (passage 2-6) did not alter immunoinhibitory properties, whereas cryopreservation significantly reduced the immunomodulatory potential. Using transwell systems, we have demonstrated an inhibition mechanism that is dependent on cell contact. Additionally, in coculture with allogeneic PBMCs, SCs were well tolerated and at most provoked mild alloreactions in singular cases. This study demonstrates, for the first time, contact- and dose-dependent immunosuppression of mesenchymal and epithelial amniotic SC populations, as well as of adipose tissue-derived SCs. All three cell types may be considered as possible alternatives to BMSCs for allogeneic application in tissue engineering.
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                Author and article information

                Journal
                Stem Cells Transl Med
                Stem Cells Transl Med
                Stem Cells Translational Medicine
                sctm
                Stem Cells Translational Medicine
                Stem Cells Translational Medicine
                AlphaMed Press (Durham, NC, USA )
                2157-6564
                2157-6580
                July 2016
                23 May 2016
                1 July 2017
                : 5
                : 7
                : 847-856
                Affiliations
                [ a ]Clinical Immunology and Osteoarticular Diseases Therapeutic Unit, Lapeyronie University Hospital, Montpellier, France
                [ b ]INSERM, U1183, Saint-Eloi Hospital, Montpellier, France
                [ c ]Department of Orthopaedic Surgery, König-Ludwig-Haus, University of Würzburg, Würzburg, Germany
                [ d ]Fraunhofer Institute for Interfacial Engineering and Biotechnology IGB, Translational Center “Regenerative Therapies for Oncology and Musculoskeletal Diseases,” Würzburg, Germany
                [ e ]Department for Cell and Tissue Pathobiology of Tumor, Hospital Saint Eloi, Montpellier, France
                [ f ]Regenerative Medicine Institute, Galway University, Galway, Ireland
                [ g ]Etablissement Français du Sang, Toulouse, France
                [ h ]INSERM U1031 STROMAlab, Toulouse, France
                [ i ]CNRS, Université Toulouse III, UPS UMR5273 F-31 432 STROMAlab, Toulouse, France
                [ j ]Univercell Biosolutions, Toulouse, France
                [ k ]Department of Orthopaedic Surgery, Lapeyronie University Hospital, Montpellier, France
                [ l ]Department of Radiology, Lapeyronie Hospital, Montpellier, France
                [ m ]Laboratory of Immunorheumatology and Tissue Regeneration, Istituto Ortopedico Rizzoli, Bologna, Italy
                [ n ]MRB Research Center Magnetic Resonance Bavaria, Würzburg, Germany
                [ o ]Maxillofacial, Plastic Reconstructive, and Aesthetic Surgery Department, Gui de Chauliac Hospital, Montpellier, France
                Author notes
                Correspondence: Christian Jorgensen, M.D., Ph.D., Clinical Immunology and Osteoarticular Diseases Therapeutic Unit, CHRU Lapeyronie, 371, avenue du doyen Gaston Giraud, 34295 Montpellier, France; INSERM U1183, IFR3, Université Montpellier I, Hopital Saint Eloi Batiment INM, 80 rue Augustin Fliche BP, 74103-34091 Montpellier cedex 5, France. Telephone: (33) 4 67 33 77 98; E-Mail: christian.jorgensen@ 123456inserm.fr
                Article
                PMC4922848 PMC4922848 4922848 20150245
                10.5966/sctm.2015-0245
                4922848
                27217345
                6b185393-01d0-4e64-b20a-934c547c9fcd
                ©AlphaMed Press
                History
                : 12 September 2015
                : 13 January 2016
                Page count
                Pages: 10
                Categories
                48
                47
                Human Clinical Article
                Custom metadata
                v1

                Phase I clinical trial,Osteoarthritis,Adipose mesenchymal stromal cells,Intra-articular injection,Therapeutic potential,Regenerative medicine

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