Author/Authors :
TOOTEE, Ali Diabetes Research Center - Endocrinology and Metabolism Clinical Sciences Institute - Tehran University of Medical Sciences, Tehran, Iran , NASLI ESFAHANI, Ensieh Diabetes Research Center - Endocrinology and Metabolism Clinical Sciences Institute - Tehran University of Medical Sciences, Tehran, Iran , GHODSI, Maryam Diabetes Research Center - Endocrinology and Metabolism Clinical Sciences Institute - Tehran University of Medical Sciences, Tehran, Iran , RAZI, Farideh Diabetes Research Center - Endocrinology and Metabolism Clinical Sciences Institute - Tehran University of Medical Sciences, Tehran, Iran , ADIBI, Hossein Endocrinology and Metabolism Research Center - Endocrinology and Metabolism Clinical Sciences Institute - Tehran University of Medical Sciences, Tehran, Iran , HESHMAT, Ramin Chronic Diseases Research Center - Endocrinology and Metabolism Population Sciences Institute - Tehran University of Medical Sciences, Tehran, Iran , LARIJANI, Bagher Endocrinology and Metabolism Research Center - Endocrinology and Metabolism Clinical Sciences Institute - Tehran University of Medical Sciences, Tehran, Iran
Abstract :
Background: Although the pathogenesis of diabetes type 1 (T1D) is not fully elucidated. Different clusters of lym-phocytes such as CD4+ and CD8+ T cells are involved in it. Moreover, the mechanism of how stem-cell therapy re-sults in significant therapeutic outcomes in diabetes remains obscure. In the current study, we aimed to analyze lym-phocyte subsets in patients with T1D before and after treatment with Liver-derived Fetal Stem-cells, and investigated the potential underlying immunological mechanism of therapeutic effects of stem-cell therapy.
Methods: Seventy-two patients with T1D were selected for our study and underwent allotransplantation of liver-derived fetal stem-cells. Relative counts of peripheral blood T and B lymphocyte subsets were detected by the means of flow cytometry analysis.
Results: Our results demonstrated that administration of fetal liver-derived fetal stem-cells resulted in significant changes in the subpopulations of lymphocytes of the patients, more specifically, levels of CD4+, CD8+, CD16+, and CD19+ lymphocytes.
Conclusion: The findings of this study demonstrated that different subsets of lymphocytes significantly change fol-lowing stem-cell therapy for diabetes. As it is demonstrated that immunological mechanisms are involved in pathogen-esis of diabetes, these changes can suggest that therapeutic effect of stem-cell therapy for diabetes may be exerted via alternations in different lymphocyte subsets.
Keywords :
Diabetes , Fetal stem-cell , Flow cytometry , Lymphocyte