Emerging approaches for the therapy of autoimmune and chronic inflammatory disease

被引:32
作者
Cope, AP [1 ]
Feldmann, M [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Fac Med, Kennedy Inst Rheumatol Div, London W6 8LH, England
关键词
D O I
10.1016/j.coi.2004.09.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Progress in defining protein and gene signatures that characterize autoimmune-mediated inflammatory diseases has uncovered a large number of potential therapeutic targets. Preclinical data from rodent models can be generated rapidly, as can data from the genetic crosses of gene-deficient mice on autoimmune-susceptible backgrounds. But humans are not the same as mice, and however robust preclinical data might appear, therapeutic intervention in patients with autoimmune disease remains the definitive experiment. Several studies published in the past year have tested paradigms of autoimmune disease in clinical trials. Recent therapeutic approaches for targeting B-cell subsets and co-stimulatory pathways are described here in detail. It is our belief that the future of immunotherapy in the clinic will depend to some extent upon the availability of biomarkers for defining biological signatures of immune function in vivo.
引用
收藏
页码:780 / 786
页数:7
相关论文
共 40 条
[11]   Sustained improvement in rheumatoid arthritis following a protocol designed to deplete B lymphocytes [J].
Edwards, JCW ;
Cambridge, G .
RHEUMATOLOGY, 2001, 40 (02) :205-211
[12]   Efficacy of B-cell-targeted therapy with rituximab in patients with rheumatoid arthritis [J].
Edwards, JCW ;
Szczepanski, L ;
Szechinski, J ;
Filipowicz-Sosnowska, A ;
Emery, P ;
Close, DR ;
Stevens, RM ;
Shaw, T .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (25) :2572-2581
[13]   Compromised function of regulatory T cells in rheumatoid arthritis and reversal by anti-TNFα therapy [J].
Ehrenstein, MR ;
Evans, JG ;
Singh, A ;
Moore, S ;
Warnes, G ;
Isenberg, DA ;
Mauri, C .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 200 (03) :277-285
[14]  
Furie R, 2003, ARTHRITIS RHEUM, V48, pS377
[15]   Cutting edge: BAFF regulates CD21/35 and CD23 expression independent of its B cell survival function [J].
Gorelik, L ;
Cutler, AH ;
Thill, G ;
Miklasz, SD ;
Shea, DE ;
Ambrose, C ;
Bixler, SA ;
Su, LH ;
Scott, ML ;
Kalled, SL .
JOURNAL OF IMMUNOLOGY, 2004, 172 (02) :762-766
[16]   Rituximab:: An insider's historical perspective [J].
Grillo-López, AJ .
SEMINARS IN ONCOLOGY, 2000, 27 (06) :9-16
[17]   TACI and BCMA are receptors for a TNF homologue implicated in B-cell autoimmune disease [J].
Gross, JA ;
Johnston, J ;
Mudri, S ;
Enselman, R ;
Dillon, SR ;
Madden, K ;
Xu, WF ;
Parrish-Novak, J ;
Foster, D ;
Lofton-Day, C ;
Moore, M ;
Littau, A ;
Grossman, A ;
Haugen, H ;
Foley, K ;
Blumberg, H ;
Harrison, K ;
Kindsvogel, W ;
Clegg, CH .
NATURE, 2000, 404 (6781) :995-999
[18]   TACI-Ig neutralizes molecules critical for B cell development and autoimmune disease: Impaired B cell maturation in mice lacking BLyS [J].
Gross, JA ;
Dillon, SR ;
Mudri, S ;
Johnston, J ;
Littau, A ;
Roque, R ;
Rixon, M ;
Schou, O ;
Foley, KP ;
Haugen, H ;
McMillen, S ;
Waggie, K ;
Schreckhise, RW ;
Shoemaker, K ;
Vu, T ;
Moore, M ;
Grossman, A ;
Clegg, CH .
IMMUNITY, 2001, 15 (02) :289-302
[19]   BAFF/BLyS can potentiate B-cell selection with the B-cell coreceptor complex [J].
Hase, H ;
Kanno, Y ;
Kojima, M ;
Hasegawa, K ;
Sakurai, D ;
Kojima, H ;
Tsuchiya, N ;
Tokunaga, K ;
Masawa, N ;
Azuma, M ;
Okumura, K ;
Kobata, T .
BLOOD, 2004, 103 (06) :2257-2265
[20]   Activation of human T cells by FcR nonbinding anti-CD3 mAb, hOKT3γ1(Ala-Ala) [J].
Herold, KC ;
Burton, JB ;
Francois, F ;
Poumian-Ruiz, E ;
Glandt, M ;
Bluestone, JA .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (03) :409-418