4.7 Article

Allogeneic mesenchymal stem cell treatment alleviates experimental and clinical Sjogren syndrome

Journal

BLOOD
Volume 120, Issue 15, Pages 3142-3151

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2011-11-391144

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Funding

  1. National Nature Science Foundation of China [30430690, 30972736]
  2. National Basic Research Program of China [2007CB947304, 2010CB944801]
  3. Funding Project for Academic Human Resources Development in Institutions of Higher Learning Under the Jurisdiction of Beijing Municipality [PHR20090510]
  4. Funding Project to Science Facility in Institutions of Higher Learning Under the jurisdiction of Beijing Municipality [PXM 2009-014226-074691, PXM2011-014226-07-000066]
  5. Major International (Regional) Joint Research Project [81120108021]
  6. Jiangsu Province Natural Science Foundation [BK2009034]
  7. Jiangsu Province Kejiao Xingwei Program
  8. National Institutes of Health, National Institute of Dental and Craniofacial Research

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Sjogren syndrome (SS) is a systemic autoimmune disease characterized by dry mouth and eyes, and the cellular and molecular mechanisms for its pathogenesis are complex. Here we reveal, for the first time, that bone marrow mesenchymal stem cells in SS-like NOD/Ltj mice and human patients were defective in immunoregulatory functions. Importantly, treatment with mesenchymal stem cells (MSCs) suppressed autoimmunity and restored salivary gland secretory function in both mouse models and SS patients. MSC treatment directed T cells toward Treg and Th2, while suppressing Th17 and Tfh responses, and alleviated disease symptoms. Infused MSCs migrated toward the inflammatory regions in a stromal cell-derived factor-1-dependent manner, as neutralization of stromal cell-derived factor-1 ligand CXCR4 abolished the effectiveness of bone marrow mesenchymal stem cell treatment. Collectively, our study suggests that immunologic regulatory functions of MSCs play an important role in SS pathogenesis, and allogeneic MSC treatment may provide a novel, effective, and safe therapy for patients with SS. This study was registered atwww.clinicaltrials.gov as NCT00953485. (Blood. 2012; 120(15): 3142-3151)

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