Literature DB >> 26582538

Human embryonic and induced pluripotent stem cells in clinical trials.

Dusko Ilic1, Liani Devito2, Cristian Miere2, Stefano Codognotto3.   

Abstract

BACKGROUND: Human embryonic and induced pluripotent stem cells (hESC and hiPSC) have tremendous potential for clinical implementation. In spite of all hurdles and controversy, clinical trials in treatment of spinal cord injury, macular degeneration of retina, type 1 diabetes and heart failure are already ongoing. SOURCES OF DATA: ClinicalTrials.gov database, International Clinical Trials Registry Platform, PubMed and press releases and websites of companies and institutions working on hESC- and iPSC-based cellular therapy. AREAS OF AGREEMENT: The initial results from multiple clinical trials demonstrate that hESC-based therapies are safe and promising. AREAS OF CONTROVERSY: Are iPSC cells safe in the clinical application? Is there a room for both hESC and iPSC in the future clinical applications? GROWING POINTS: Increasing number of new clinical trials. AREAS TIMELY FOR DEVELOPING RESEARCH: Development of hESC- and/or iPSC-based cellular therapy for other diseases.
© The Author 2015. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  diabetes; heart repair; human embryonic stem cells (hESC); human induced pluripotent stem cells (hiPSC); macular degeneration; spinal cord injury

Mesh:

Year:  2015        PMID: 26582538     DOI: 10.1093/bmb/ldv045

Source DB:  PubMed          Journal:  Br Med Bull        ISSN: 0007-1420            Impact factor:   4.291


  26 in total

Review 1.  Response to: Dittrich et al.: Non-Embryo-Destructive Extraction of Pluripotent Embryonic Stem Cells - Overlooked Legal Prohibitions, Professional Legal Consequences and Inconsistencies in Patent Law.

Authors:  T Faltus; U Storz
Journal:  Geburtshilfe Frauenheilkd       Date:  2016-12       Impact factor: 2.915

2.  Non-fibro-adipogenic pericytes from human embryonic stem cells attenuate degeneration of the chronically injured mouse muscle.

Authors:  Gina M Mosich; Regina Husman; Paras Shah; Abhinav Sharma; Kevin Rezzadeh; Temidayo Aderibigbe; Vivian J Hu; Daniel J McClintick; Genbin Wu; Jonathan D Gatto; Haibin Xi; April D Pyle; Bruno Péault; Frank A Petrigliano; Ayelet Dar
Journal:  JCI Insight       Date:  2019-12-19

Review 3.  Derivation of Human Induced Pluripotent Stem Cell (iPSC) Lines and Mechanism of Pluripotency: Historical Perspective and Recent Advances.

Authors:  Arvind Chhabra
Journal:  Stem Cell Rev Rep       Date:  2017-12       Impact factor: 5.739

Review 4.  Concise Review: Human Pluripotent Stem Cells to Produce Cell-Based Cancer Immunotherapy.

Authors:  Huang Zhu; Yi-Shin Lai; Ye Li; Robert H Blum; Dan S Kaufman
Journal:  Stem Cells       Date:  2018-01-03       Impact factor: 6.277

5.  Addressing Manufacturing Challenges for Commercialization of iPSC-Based Therapies.

Authors:  Mehdi Dashtban; Krishna Morgan Panchalingam; Mehdi Shafa; Behnam Ahmadian Baghbaderani
Journal:  Methods Mol Biol       Date:  2021

Review 6.  Stem Cell-Derived Exosomes, Autophagy, Extracellular Matrix Turnover, and miRNAs in Cardiac Regeneration during Stem Cell Therapy.

Authors:  Priyanka Prathipati; Shyam Sundar Nandi; Paras Kumar Mishra
Journal:  Stem Cell Rev Rep       Date:  2017-02       Impact factor: 5.739

Review 7.  Nonhuman Primate Studies to Advance Vision Science and Prevent Blindness.

Authors:  Michael J Mustari
Journal:  ILAR J       Date:  2017-12-01

Review 8.  A Broad Overview and Review of CRISPR-Cas Technology and Stem Cells.

Authors:  Simon N Waddington; Riccardo Privolizzi; Rajvinder Karda; Helen C O'Neill
Journal:  Curr Stem Cell Rep       Date:  2016-02-11

9.  31P NMR 2D Mapping of Creatine Kinase Forward Flux Rate in Hearts with Postinfarction Left Ventricular Remodeling in Response to Cell Therapy.

Authors:  Ling Gao; Weina Cui; Pengyuan Zhang; Albert Jang; Wuqiang Zhu; Jianyi Zhang
Journal:  PLoS One       Date:  2016-09-08       Impact factor: 3.240

10.  Efficient Killing of Murine Pluripotent Stem Cells by Natural Killer (NK) Cells Requires Activation by Cytokines and Partly Depends on the Activating NK Receptor NKG2D.

Authors:  Carina Gröschel; Daniela Hübscher; Jessica Nolte; Sebastian Monecke; André Sasse; Leslie Elsner; Walter Paulus; Claudia Trenkwalder; Bojan Polić; Ahmed Mansouri; Kaomei Guan; Ralf Dressel
Journal:  Front Immunol       Date:  2017-07-26       Impact factor: 7.561

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