The Possible Future Roles for iPSC-Derived Therapy for Autoimmune Diseases

被引:14
作者
Hew, Meilyn [1 ]
O'Connor, Kevin [2 ]
Edel, Michael J. [3 ,4 ,5 ]
Lucas, Michaela [1 ,6 ,7 ,8 ]
机构
[1] Queen Elizabeth II Med Ctr, Dept Clin Immunol, Pathwest Lab Med, Perth, WA 6009, Australia
[2] Royal Perth Hosp, Dept Clin Immunol, Perth, WA 6000, Australia
[3] Univ Barcelona, Hosp Clin, Dept Physiol Sci 1, Control Pluripotency Lab,Fac Med, E-08036 Barcelona, Spain
[4] Victor Chang Cardiac Res Inst, Sydney, NSW 2010, Australia
[5] Univ Western Australia, CCTRM, Sch Med & Pharmacol Anat Physiol & Human Biol, Perth, WA 6009, Australia
[6] Univ Western Australia, Harry Perkins Inst Med Res, Sch Med & Pharmacol, Perth, WA 6009, Australia
[7] Univ Western Australia, Harry Perkins Inst Med Res, Sch Pathol & Lab Med, Perth, WA 6009, Australia
[8] Murdoch Univ, Inst Immunol & Infect Dis, Perth, WA 6150, Australia
关键词
inducible; pluripotent; stem cells; autoimmunity; therapy; lupus; diabetes; multiple sclerosis; PLURIPOTENT STEM-CELLS; REGULATORY T-CELLS; ANTIGEN-SPECIFIC SUPPRESSION; MULTIPLE-SCLEROSIS; DENDRITIC CELLS; RHEUMATOID-ARTHRITIS; RISK-FACTORS; IN-VIVO; GENERATION; DIFFERENTIATION;
D O I
10.3390/jcm4061193
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The ability to generate inducible pluripotent stem cells (iPSCs) and the potential for their use in treatment of human disease is of immense interest. Autoimmune diseases, with their limited treatment choices are a potential target for the clinical application of stem cell and iPSC technology. IPSCs provide three potential ways of treating autoimmune disease; (i) providing pure replacement of lost cells (immuno-reconstitution); (ii) through immune-modulation of the disease process in vivo; and (iii) for the purposes of disease modeling in vitro. In this review, we will use examples of systemic, system-specific and organ-specific autoimmunity to explore the potential applications of iPSCs for treatment of autoimmune diseases and review the evidence of iPSC technology in auto-immunity to date.
引用
收藏
页码:1193 / 1206
页数:14
相关论文
共 65 条
[1]   Negligible immunogenicity of terminally differentiated cells derived from induced pluripotent or embryonic stem cells [J].
Araki, Ryoko ;
Uda, Masahiro ;
Hoki, Yuko ;
Sunayama, Misato ;
Nakamura, Miki ;
Ando, Shunsuke ;
Sugiura, Mayumi ;
Ideno, Hisashi ;
Shimada, Akemi ;
Nifuji, Akira ;
Abe, Masumi .
NATURE, 2013, 494 (7435) :100-104
[2]   GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region [J].
Armstrong, D. L. ;
Zidovetzki, R. ;
Alarcon-Riquelme, M. E. ;
Tsaos, B. P. ;
Criswell, L. A. ;
Kimberly, R. P. ;
Harley, J. B. ;
Sivils, K. L. ;
Vyse, T. J. ;
Gaffney, P. M. ;
Langefeld, C. D. ;
Jacob, C. O. .
GENES AND IMMUNITY, 2014, 15 (06) :347-354
[3]   Environmental risk factors for multiple sclerosis. Part I: The role of infection [J].
Ascherio, Alberto ;
Munger, Kassandra L. .
ANNALS OF NEUROLOGY, 2007, 61 (04) :288-299
[4]   Immunobiology of dendritic cells [J].
Banchereau, J ;
Briere, F ;
Caux, C ;
Davoust, J ;
Lebecque, S ;
Liu, YT ;
Pulendran, B ;
Palucka, K .
ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 :767-+
[5]   The functional and molecular characterisation of human embryonic stem cell-derived insulin-positive cells compared with adult pancreatic beta cells [J].
Basford, C. L. ;
Prentice, K. J. ;
Hardy, A. B. ;
Sarangi, F. ;
Micallef, S. J. ;
Li, X. ;
Guo, Q. ;
Elefanty, A. G. ;
Stanley, E. G. ;
Keller, G. ;
Allister, E. M. ;
Nostro, M. C. ;
Wheeler, M. B. .
DIABETOLOGIA, 2012, 55 (02) :358-371
[6]   Activation of the type I interferon system in primary Sjogren's syndrome -: A possible etiopathogenic mechanism [J].
Båve, U ;
Nordmark, G ;
Lövgren, T ;
Rönnelid, J ;
Cajander, S ;
Eloranta, ML ;
Alm, GV ;
Rönnblom, L .
ARTHRITIS AND RHEUMATISM, 2005, 52 (04) :1185-1195
[7]   Therapeutic vaccination using CD4+ CD25+ antigen-specific regulatory T cells [J].
Bluestone, JA ;
Tang, QZ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 :14622-14626
[8]   Human regulatory T cells: role in autoimmune disease and therapeutic opportunities [J].
Brusko, Todd M. ;
Putnam, Amy L. ;
Bluestone, Jeffrey A. .
IMMUNOLOGICAL REVIEWS, 2008, 223 :371-390
[9]   Leukemia Inhibitory Factor Inhibits T Helper 17 Cell Differentiation and Confers Treatment Effects of Neural Progenitor Cell Therapy in Autoimmune Disease [J].
Cao, Wei ;
Yang, Yiqing ;
Wang, Zhengyi ;
Liu, Ailian ;
Fang, Lei ;
Wu, Fenglan ;
Hong, Jian ;
Shi, Yufang ;
Leung, Stewart ;
Dong, Chen ;
Zhang, Jingwu Z. .
IMMUNITY, 2011, 35 (02) :273-284
[10]   Generation of systemic lupus erythematosus-specific induced pluripotent stem cells from urine [J].
Chen, Yuyu ;
Luo, Rongping ;
Xu, Yong ;
Cai, Xiujuan ;
Li, Wuxian ;
Tan, Kuibi ;
Huang, Jianrong ;
Dai, Yong .
RHEUMATOLOGY INTERNATIONAL, 2013, 33 (08) :2127-2134