Literature DB >> 23572052

Stem cell therapy to cure type 1 diabetes: from hype to hope.

Preeti Chhabra1, Kenneth L Brayman.   

Abstract

Type 1 diabetes mellitus (T1D) is a chronic, multifactorial autoimmune disease that involves the progressive destruction of pancreatic β-cells, ultimately resulting in the loss of insulin production and secretion. The goal of clinical intervention is to prevent or arrest the onset and progression of autoimmunity, reverse β-cell destruction, and restore glycometabolic and immune homeostasis. Despite promising outcomes observed with islet transplantation and advancements in immunomodulatory therapies, the need for an effective cell replacement strategy for curing T1D still persists. Stem cell therapy offers a solution to the cited challenges of islet transplantation. While the regenerative potential of stem cells can be harnessed to make available a self-replenishing supply of glucose-responsive insulin-producing cells, their immunomodulatory properties may potentially be used to prevent, arrest, or reverse autoimmunity, ameliorate innate/alloimmune graft rejection, and prevent recurrence of the disease. Herein, we discuss the therapeutic potential of stem cells derived from a variety of sources for the cure of T1D, for example, embryonic stem cells, induced pluripotent stem cells, bone marrow-derived hematopoietic stem cells, and multipotent mesenchymal stromal cells derived from bone marrow, umbilical cord blood, and adipose tissue. The benefits of combinatorial approaches designed to ensure the successful clinical translation of stem cell therapeutic strategies, such as approaches combining effective stem cell strategies with islet transplantation, immunomodulatory drug regimens, and/or novel bioengineering techniques, are also discussed. To conclude, the application of stem cell therapy in the cure for T1D appears extremely promising.

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Year:  2013        PMID: 23572052      PMCID: PMC3667565          DOI: 10.5966/sctm.2012-0116

Source DB:  PubMed          Journal:  Stem Cells Transl Med        ISSN: 2157-6564            Impact factor:   6.940


  119 in total

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Review 2.  iPS cells in type 1 diabetes research and treatment.

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Review 3.  New and future immunomodulatory therapy in type 1 diabetes.

Authors:  James E Tooley; Frank Waldron-Lynch; Kevan C Herold
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Review 4.  Long-term outcome after pancreas transplantation.

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Journal:  Curr Opin Organ Transplant       Date:  2012-02       Impact factor: 2.640

5.  Independence of exogenous insulin following immunoablation and stem cell reconstitution in newly diagnosed diabetes type I.

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Journal:  Bone Marrow Transplant       Date:  2010-06-28       Impact factor: 5.483

6.  Co-transplantation of mesenchymal stem cells maintains islet organisation and morphology in mice.

Authors:  C L Rackham; P C Chagastelles; N B Nardi; A C Hauge-Evans; P M Jones; A J F King
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7.  Highly efficient miRNA-mediated reprogramming of mouse and human somatic cells to pluripotency.

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Journal:  Cell Stem Cell       Date:  2011-04-08       Impact factor: 24.633

8.  Induced pluripotent stem cells generated without viral integration.

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  46 in total

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Review 4.  Immune Mechanisms and Pathways Targeted in Type 1 Diabetes.

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Review 5.  Benefits of healthy adipose tissue in the treatment of diabetes.

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Journal:  World J Diabetes       Date:  2014-08-15

Review 6.  Mesenchymal stem cells help pancreatic islet transplantation to control type 1 diabetes.

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7.  Type 1 Diabetes Mellitus Donor Mesenchymal Stromal Cells Exhibit Comparable Potency to Healthy Controls In Vitro.

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Journal:  Stem Cells Transl Med       Date:  2016-07-13       Impact factor: 6.940

Review 8.  Current progress of human trials using stem cell therapy as a treatment for diabetes mellitus.

Authors:  Shuk Kei Cheng; Elisse Y Park; Andjela Pehar; Alexandra C Rooney; G Ian Gallicano
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Review 9.  Therapeutic potential of mesenchymal stem cells in treating both types of diabetes mellitus and associated diseases.

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10.  Investigating the route of administration and efficacy of adipose tissue-derived mesenchymal stem cells and conditioned medium in type 1 diabetic mice.

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