Gene therapy for arthritis

被引:77
作者
Robbins, PD
Evans, CH
Chernajovsky, Y
机构
[1] Univ Pittsburgh, Sch Med, Dept Mol Genet & Biochem, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Sch Med, Dept Orthopaed Surg, Pittsburgh, PA USA
[3] Univ Pittsburgh, Sch Med, Dept Mol Med, Pittsburgh, PA USA
[4] Harvard Univ, Sch Med, Dept Mol Orthopaed, Boston, MA USA
[5] Queen Mary Univ, St Bartholomews & Royal London Sch Med & Dent, Bone & Joint Res Unit, London, England
关键词
D O I
10.1038/sj.gt.3302040
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Rheumatoid arthritis is an autoimmune disease with intra-articular inflammation and synovial hyperplasia that results in progressive degradation of cartilage and bone, in severe cases it causes systemic complications. Recently, biological agents that suppress the activities of proinflammatory cytokines have shown efficacy as antiarthritic drugs, but require frequent administration. Thus, gene transfer approaches are being developed as an alternative approach for targeted, more efficient and sustained delivery of inhibitors of inflammatory cytokines as well as other therapeutic agents. Indeed, the efficacy of gene transfer for the treatment of arthritis has been demonstrated in mouse, rat, rabbit, and horse models of disease whereas the feasibility of the approach has been demonstrated in Phase I clinical trials. In this review, the current status of both preclinical and clinical arthritis gene therapy is presented. In addition, the advantages and disadvantages of different types of vectors, target cells and therapeutic genes being developed for the treatment of arthritis are summarized. Finally, the future directions of the rapidly developed field of arthritis gene therapy are outlined.
引用
收藏
页码:902 / 911
页数:10
相关论文
共 124 条
  • [21] Pathogenic lymphoid cells engineered to express TGF beta 1 ameliorate disease in a collagen-induced arthritis model
    Chernajovsky, Y
    Adams, G
    Triantaphyllopoulos, K
    Ledda, MF
    Podhajcer, OL
    [J]. GENE THERAPY, 1997, 4 (06) : 553 - 559
  • [22] Systemic gene therapy for arthritis
    Chernajovsky, Y
    [J]. DRUGS OF TODAY, 1999, 35 (4-5) : 361 - 377
  • [23] GENE-THERAPY OF RHEUMATOID-ARTHRITIS VIA CYTOKINE REGULATION - FUTURE PERSPECTIVES
    CHERNAJOVSKY, Y
    FELDMANN, M
    MAINI, RN
    [J]. BRITISH MEDICAL BULLETIN, 1995, 51 (02) : 503 - 516
  • [24] CHERNAJOVSKY Y, 2003, AM J PHARMACOGENOMIC, V2, P223
  • [25] DAI L, IN PRESS GENE THERAP
  • [26] Vasoactive intestinal peptide prevents experimental arthritis by downregulating both autoimmune and inflammatory components of the disease
    Delgado, M
    Abad, C
    Martinez, C
    Laceta, J
    Gomariz, RP
    [J]. NATURE MEDICINE, 2001, 7 (05) : 563 - 568
  • [27] Dreja H, 2000, ARTHRITIS RHEUM-US, V43, P1698, DOI 10.1002/1529-0131(200008)43:8<1698::AID-ANR5>3.0.CO
  • [28] 2-8
  • [29] RANDOMIZED DOUBLE-BLIND COMPARISON OF CHIMERIC MONOCLONAL-ANTIBODY TO TUMOR-NECROSIS-FACTOR-ALPHA (CA2) VERSUS PLACEBO IN RHEUMATOID-ARTHRITIS
    ELLIOTT, MJ
    MAINI, RN
    FELDMANN, M
    KALDEN, JR
    ANTONI, C
    SMOLEN, JS
    LEEB, B
    BREEDVELD, FC
    MACFARLANE, JD
    BIJL, H
    WOODY, JN
    [J]. LANCET, 1994, 344 (8930) : 1105 - 1110
  • [30] Evans CH, 1997, J RHEUMATOL, V24, P2061