Gene therapy in rheumatic diseases

被引:10
作者
Vervoordeldonk, MJBM [1 ]
Tak, PP [1 ]
机构
[1] Univ Amsterdam, Div Clin Immunol & Rheumatol, Dept Med, Acad Med Ctr, NL-1100 DD Amsterdam, Netherlands
来源
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY | 2001年 / 15卷 / 05期
关键词
gene therapy; rheumatoid arthritis; vectors; animal models; human trial;
D O I
10.1053/berh.2001.0193
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rheumatoid arthritis (RA) is a chronic inflammatory disease characterized by joint inflammation as well as progressive cartilage and bone destruction. Advances in the understanding of the pathophysiology of RA have led to the development of new therapeutic strategies, including gene therapy. Gene therapy offers a new approach to deliver therapeutic proteins to the joints of arthritis patients. Local as well as systemic gene therapy can be envisaged for the treatment of arthritis. Several viral and non-viral vectors have been used in animal models for rheumatoid arthritis for ex vivo and in vivo delivery of therapeutic genes. Promising pre-clinical data have resulted from the application of these strategies. Using ex vivo gene delivery, successful and safe gene transfer has been demonstrated in the joints of RA patients. Although new insights into the role of cytokines and other mediators of chronic inflammation have provided novel targets for therapeutic intervention, the development of vectors that induce long-term and regulated gene expression remains a challenge.
引用
收藏
页码:771 / 788
页数:18
相关论文
共 72 条
[1]  
Apparailly F, 1998, J IMMUNOL, V160, P5213
[2]   INHIBITION OF THE PRODUCTION AND EFFECTS OF INTERLEUKIN-1 AND TUMOR-NECROSIS-FACTOR-ALPHA IN RHEUMATOID-ARTHRITIS [J].
AREND, WP ;
DAYER, JM .
ARTHRITIS AND RHEUMATISM, 1995, 38 (02) :151-160
[3]   Mechanisms of action of interferon-beta in multiple sclerosis [J].
Arnason, BGW ;
Dayal, A ;
Qu, ZX ;
Jensen, MA ;
Genc, K ;
Reder, AT .
SPRINGER SEMINARS IN IMMUNOPATHOLOGY, 1996, 18 (01) :125-148
[4]   Prevention of murine collagen-induced arthritis in the knee and ipsilateral paw by local expression of human interleukin-1 receptor antagonist protein in the knee [J].
Bakker, AC ;
Joosten, LAB ;
Arntz, OJ ;
Helsen, MMA ;
Bendele, AM ;
vandeLoo, FAJ ;
vandenBerg, WB .
ARTHRITIS AND RHEUMATISM, 1997, 40 (05) :893-900
[5]   INTRAARTICULAR EXPRESSION OF BIOLOGICALLY-ACTIVE INTERLEUKIN-1 RECEPTOR-ANTAGONIST PROTEIN BY EX-VIVO GENE-TRANSFER [J].
BANDARA, G ;
MUELLER, GM ;
GALEALAURI, J ;
TINDAL, MH ;
GEORGESCU, HI ;
SUCHANEK, MK ;
HUNG, GL ;
GLORIOSO, JC ;
ROBBINS, PD ;
EVANS, CH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (22) :10764-10768
[6]   Transplantation of adenovirally transduced allogeneic chondrocytes into articular cartilage defects in vivo [J].
Baragi, VM ;
Renkiewicz, RR ;
Qiu, LP ;
Brammer, D ;
Riley, JM ;
Sigler, RE ;
Frenkel, SR ;
Amin, A ;
Abramson, SB ;
Roessler, BJ .
OSTEOARTHRITIS AND CARTILAGE, 1997, 5 (04) :275-282
[7]  
BLANCO FJ, 1995, AM J PATHOL, V146, P75
[8]   Intra-articular IL-4 gene therapy in arthritis: anti-inflammatory effect and enhanced Th2 activity [J].
Boyle, DL ;
Nguyen, KHY ;
Zhuang, S ;
Shi, Y ;
McCormack, JE ;
Chada, S ;
Firestein, GS .
GENE THERAPY, 1999, 6 (12) :1911-1918
[9]   Direct adenovirus-mediated insulin-like growth factor I gene transfer enhances transplant chondrocyte function [J].
Brower-Toland, BD ;
Saxer, RA ;
Goodrich, LR ;
Mi, ZB ;
Robbins, PD ;
Evans, CH ;
Nixon, AJ .
HUMAN GENE THERAPY, 2001, 12 (02) :117-129
[10]   Deficient Fas ligand expression by synovial lymphocytes from patients with rheumatoid arthritis [J].
Cantwell, MJ ;
Hua, T ;
Zvaifler, NJ ;
Kipps, TJ .
ARTHRITIS AND RHEUMATISM, 1997, 40 (09) :1644-1652