Evaluation of Stem Cell Therapy Effects on the Immune Response in Rheumatoid Arthritis Patients

Refractory rheumatoid arthritis patients who met the inclusion/exclusion criteria have been selected. After signing informed consent form, autologous stem cells were obtained by bone marrow aspiration. Isolation and culture (3 to 4 weeks in MEM-alpha medium) of mesenchymal stem cells (MSCs) were performed in accredited good manufacturing practices (GMP) clean room. A panel of cluster of differentiation (CD) markers including CD105, CD166, CD44, CD45, CD90, and CD34 were checked for making sure about differentiation of cells into MSCs after 3-4 weeks of cell culture. Viability of MSCs was checked by Trypan blue testing and all of the cultivations were negative for bacterial contamination. A single dose of 1000000 to 2000000 mesenchymal stem cells/kg infused into patients intravenously. To prevent anaphylactic reactions, a single intravenous dose of hydrocortison (100 ml) and oral dimenhydrinate (10 ml) were administered before MSCs infusion into patients. The effects of mesenchymal stem cells on the cellular and humoral immune responses and also the role of chemokines in homing of immune cells were studied at time points 1, 6 and 12 months after intravenous administration of MSCs in refractory rheumatoid arthritis.

Inclusion criteria

• Resistant RA patients to non-biological DMARDs;
• Treated RA patients by non-biological drugs;
• Treated RA patients by Prednisolone, Hydroxychloroquine, Sulfasalazine and Methotrexate;
• Patients age between 35-60 years;
• Refractory RA patients with no other rheumatologic disorders and inflammatory diseases.

Exclusion criteria

• Non-resistant RA patients to non-biological DMARDs.