Gene therapy in autoimmune diseases: Challenges and opportunities

被引:18
作者
Leung, Patrick S. C. [1 ]
Dhirapong, Amy [1 ]
Wu, Ping-Yi [1 ,2 ]
Tao, Mi-Hua [1 ,2 ]
机构
[1] Univ Calif Davis, Sch Med, Div Rheumatol Allergy & Clin Immunol, Davis, CA 95616 USA
[2] Acad Sinica, Inst Biomed Sci, Taipei 11529, Taiwan
关键词
Gene therapy; Immunomodulation; Clinical trials; Multiple sclerosis; Rheumatoid arthritis; MYELIN BASIC-PROTEIN; T-CELL VACCINATION; RHEUMATOID-ARTHRITIS; MULTIPLE-SCLEROSIS; INTRAARTICULAR INJECTION; IMMUNE-SYSTEM; MURINE MODEL; DNA; ENCEPHALOMYELITIS; TOLERANCE;
D O I
10.1016/j.autrev.2009.10.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Clinical treatment of autoimmune disorders presents a special challenge. For decades, most clinical regimens in autoimmunity has been largely symptomatic and non-disease specific. Although data from vigorous research has lead to accumulating knowledge on the pathogenic and immunological mechanisms of many autoimmune diseases, their direct clinical applications have been sparse. Advances in biotechnology have laid the groundwork for potent and specific molecular targeting therapies by gene therapy, and have just begun to be investigated in the treatment of autoimmune disorders. Such work has been largely based on the availability of well-established animal models of common autoimmune disorders, and the efficacy of strategic approaches initially investigated and validated in these models. Although these preclinical animal model studies have provided the proof-of-concept for multiple potential applications, human clinical trials on gene therapy in autoimmunity are still at its infancy. The recent success of Phase I/II clinical trials of gene therapy in rheumatoid arthritis and multiple sclerosis, development of cutting edge technology in target identification, as well as gene delivery systems have now set the stage for a more thorough and vigorous pace in the near future to advance this exciting field. (C) 2009 Elsevier B.V. All rights reserved
引用
收藏
页码:170 / 174
页数:5
相关论文
共 87 条
[11]   Therapeutic Effect of Exosomes From Indoleamine 2,3-Dioxygenase-Positive Dendritic Cells in Collagen-Induced Arthritis and Delayed-Type Hypersensitivity Disease Models [J].
Bianco, Nicole R. ;
Kim, Seon Hee ;
Ruffner, Melanie A. ;
Robbins, Paul D. .
ARTHRITIS AND RHEUMATISM, 2009, 60 (02) :380-389
[12]   Sialic acid-binding Ig-like lectin I expression in inflammatory and resident monocytes is a potential biomarker for monitoring disease activity and success of therapy in systemic lupus erythematosus [J].
Biesen, Robert ;
Demir, Cemal ;
Barkhudarova, Fidan ;
Gruen, Joachim R. ;
Steinbrich-Zoellner, Marta ;
Backhaus, Marina ;
Haeupl, Thomas ;
Rudwaleit, Martin ;
Riemekasten, Gabriela ;
Radbruch, Andreas ;
Hiepe, Falk ;
Burmester, Gerd-Ruediger ;
Gruetzkau, Andreas .
ARTHRITIS AND RHEUMATISM, 2008, 58 (04) :1136-1145
[13]   Animal Models for Target Diseases in Gene Therapy - using DNA and siRNA Delivery Strategies [J].
Blagbrough, Ian S. ;
Zara, Chiara .
PHARMACEUTICAL RESEARCH, 2009, 26 (01) :1-18
[14]   A randomized, controlled study of a single intra-articular injection of etanercept or glucocorticosteroids in patients with rheumatoid arthritis [J].
Bliddal, H. ;
Terslev, L. ;
Qvistgaard, E. ;
Konig, M. ;
Holm, C. C. ;
Rogind, H. ;
Boesen, M. ;
Danneskiold-Samsoe, B. ;
Torp-Pedersen, S. .
SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, 2006, 35 (05) :341-345
[15]  
Boissier M C, 2004, Reumatismo, V56, P51
[16]   Autologous bone marrow-derived rat mesenchymal stem cells promote PDX-1 and insulin expression in the islets, alter T cell cytokine pattern and preserve regulatory T cells in the periphery and induce sustained normoglycemia [J].
Boumaza, Imene ;
Srinivasan, Suganya ;
Witt, William T. ;
Feghali-Bostwick, Carol ;
Dai, Yifan ;
Garcia-Ocana, Adolfo ;
Feili-Hariri, Maryam .
JOURNAL OF AUTOIMMUNITY, 2009, 32 (01) :33-42
[17]   Intraarticular gene transfer of TNFR:Fc suppresses experimental arthritis with reduced systemic distribution of the gene product [J].
Chan, JMK ;
Villarreal, G ;
Jin, WW ;
Stepan, T ;
Burstein, H ;
Wahl, SM .
MOLECULAR THERAPY, 2002, 6 (06) :727-736
[18]   In vivo administration of plasmid DNA encoding recombinant immunotoxin DT390-IP-10 attenuates experimental autoimmune encephalomyelitis [J].
Chen, Wenjie ;
Li, Hong ;
Jia, Yi ;
Lv, Meili ;
Li, Mingyuan ;
Feng, Ping ;
Hu, Huaizhong ;
Zhang, Lin .
JOURNAL OF AUTOIMMUNITY, 2007, 28 (01) :30-40
[19]   Pain and Rheumatology: Thinking Outside the Joint [J].
Clauw, Daniel J. ;
Witter, James .
ARTHRITIS AND RHEUMATISM, 2009, 60 (02) :321-324
[20]  
CLEMENT N, 2009, HUM GENE THER