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Targeting Insulin Resistance in Type 2 Diabetes Via Immune Modulation of Cord Blood-derived Multipotent Stem Cells (CB-SCs) in Stem Cell Educator Therapy: Phase I/II Clinical Trial

Abstract

Background: The prevalence of type 2 diabetes (T2D) is increasing worldwide and creating a significant burden on health systems, highlighting the need for the development of innovative therapeutic approaches to overcome immune dysfunction, which is likely a key factor in the development of insulin resistance in T2D. It suggests that immune modulation may be a useful tool in treating the disease.

Methods: In an open-label, phase 1/phase 2 study, patients (N=36) with long-standing T2D were divided into three groups (Group A, oral medications, n=18; Group B, oral medications+insulin injections, n=11; Group C having impaired β-cell function with oral medications+insulin injections, n=7). All patients received one treatment with the Stem Cell Educator therapy in which a patient's blood is circulated through a closed-loop system that separates mononuclear cells from the whole blood, briefly co-cultures them with adherent cord blood-derived multipotent stem cells (CB-SCs), and returns the educated autologous cells to the patient's circulation.

Results: Clinical findings indicate that T2D patients achieve improved metabolic control and reduced inflammation markers after receiving Stem Cell Educator therapy. Median glycated hemoglobin (HbA1C) in Group A and B was significantly reduced from 8.61%±1.12 at baseline to 7.25%±0.58 at 12 weeks (P=2.62E-06), and 7.33%±1.02 at one year post-treatment (P=0.0002). Homeostasis model assessment (HOMA) of insulin resistance (HOMA-IR) demonstrated that insulin sensitivity was improved post-treatment. Notably, the islet beta-cell function in Group C subjects was markedly recovered, as demonstrated by the restoration of C-peptide levels. Mechanistic studies revealed that Stem Cell Educator therapy reverses immune dysfunctions through immune modulation on monocytes and balancing Th1/Th2/Th3 cytokine production.

Conclusions: Clinical data from the current phase 1/phase 2 study demonstrate that Stem Cell Educator therapy is a safe approach that produces lasting improvement in metabolic control for individuals with moderate or severe T2D who receive a single treatment. In addition, this approach does not appear to have the safety and ethical concerns associated with conventional stem cell-based approaches.

Trial Registration: ClinicalTrials.gov number, NCT01415726.

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References
1.
Radaelli T, Farrell K, Huston-Presley L, Amini S, Kirwan J, McIntyre H . Estimates of insulin sensitivity using glucose and C-Peptide from the hyperglycemia and adverse pregnancy outcome glucose tolerance test. Diabetes Care. 2009; 33(3):490-4. PMC: 2827494. DOI: 10.2337/dc09-1463. View

2.
Kohn L, Wallace B, Schwartz F, McCall K . Is type 2 diabetes an autoimmune-inflammatory disorder of the innate immune system?. Endocrinology. 2005; 146(10):4189-91. DOI: 10.1210/en.2005-0920. View

3.
Sell H, Habich C, Eckel J . Adaptive immunity in obesity and insulin resistance. Nat Rev Endocrinol. 2012; 8(12):709-16. DOI: 10.1038/nrendo.2012.114. View

4.
Winer S, Paltser G, Chan Y, Tsui H, Engleman E, Winer D . Obesity predisposes to Th17 bias. Eur J Immunol. 2009; 39(9):2629-35. DOI: 10.1002/eji.200838893. View

5.
Chatzigeorgiou A, Karalis K, Bornstein S, Chavakis T . Lymphocytes in obesity-related adipose tissue inflammation. Diabetologia. 2012; 55(10):2583-2592. DOI: 10.1007/s00125-012-2607-0. View