Heat shock proteins (HSP) for immunotherapy of rheumatoid arthritis (RA)

被引:22
作者
Yung, GLP
Le, TD
Roord, S
Prakken, B
Albani, S
机构
[1] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Pediat, La Jolla, CA 92093 USA
[3] Androclus Therapeut, San Diego, CA 92121 USA
[4] IACOPO Inst Translat Med, San Diego, CA USA
[5] Univ Chile Independencia 1027, Fac Med Norte, ICBM, Santiago, Chile
[6] Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, NL-3508 Utrecht, Netherlands
关键词
D O I
10.1007/s00011-003-1204-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Rheumatoid arthritis (RA) is an inflammatory disease that primarily involves the joints and has a worldwide prevalence of about one percent, with a female to male ratio of 3:1. This chapter summarizes some of the recent progress in molecular immunology, and discusses the application of this new knowledge for therapeutic purposes. We focus on our recent experiences and that of others in modulation of antigen specific responses as a tool for manipulating autoimmune inflammation. Particular emphasis is given to the concept of exploiting for therapeutic purposes a natural mechanism of immune regulation. This mechanism is based on sequential cross recognition of bacterial and human derived heat shock protein peptides.
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收藏
页码:443 / 451
页数:9
相关论文
共 71 条
[1]   Preventive administration of Mycobacterium tuberculosis 10-kDa heat shock protein (hsp 10) suppresses adjuvant arthritis in Lewis rats [J].
Agnello, D ;
Scanziani, E ;
Di Giancamillo, M ;
Leoni, F ;
Modena, D ;
Mascagni, P ;
Introna, M ;
Ghezzi, P ;
Villa, P .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2002, 2 (04) :463-474
[2]   IMMUNE-RESPONSES TO THE ESCHERICHIA-COLI DNAJ HEAT-SHOCK PROTEIN IN JUVENILE RHEUMATOID-ARTHRITIS AND THEIR CORRELATION WITH DISEASE-ACTIVITY [J].
ALBANI, S ;
RAVELLI, A ;
MASSA, M ;
DEBENEDETTI, F ;
ANDREE, G ;
ROUDIER, J ;
MARTINI, A ;
CARSON, AD .
JOURNAL OF PEDIATRICS, 1994, 124 (04) :561-565
[3]   A multistep molecular mimicry hypothesis for the pathogenesis of rheumatoid arthritis [J].
Albani, S ;
Carson, DA .
IMMUNOLOGY TODAY, 1996, 17 (10) :466-470
[4]   POSITIVE SELECTION IN AUTOIMMUNITY - ABNORMAL IMMUNE-RESPONSES TO A BACTERIAL DNAJ ANTIGENIC DETERMINANT IN PATIENTS WITH EARLY RHEUMATOID-ARTHRITIS [J].
ALBANI, S ;
KEYSTONE, E ;
NELSON, JL ;
OLLIER, WER ;
LACAVA, A ;
MONTEMAYOR, AC ;
WEBER, DA ;
MONTECUCCO, C ;
MARTINI, A ;
CARSON, DA .
NATURE MEDICINE, 1995, 1 (05) :448-452
[5]   THE SUSCEPTIBILITY SEQUENCE TO RHEUMATOID-ARTHRITIS IS A CROSS-REACTIVE B-CELL EPITOPE SHARED BY THE ESCHERICHIA-COLI HEAT-SHOCK PROTEIN DNAJ AND THE HISTOCOMPATIBILITY LEUKOCYTE ANTIGEN DRB10401 MOLECULE [J].
ALBANI, S ;
TUCKWELL, JE ;
ESPARZA, L ;
CARSON, DA ;
ROUDIER, J .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (01) :327-331
[6]   Mechanisms of disease: Molecular mimicry and autoimmunity. [J].
Albert, LJ ;
Inman, RD .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (27) :2068-2074
[7]   HLA-DR4 and HLA-DR10 motifs that carry susceptibility to rheumatoid arthritis bind 70-kD heat shock proteins [J].
Auger, I ;
Escola, JM ;
Gorvel, JP ;
Roudier, J .
NATURE MEDICINE, 1996, 2 (03) :306-310
[8]   A function for the QKRAA amino acid motif: Mediating binding of DnaJ to DnaK - Implications for the association of rheumatoid arthritis with HLA-DR4 [J].
Auger, I ;
Roudier, J .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (08) :1818-1822
[9]   Molecular mimicry in the MHC. Hidden clues to autoimmunity? [J].
Baum, H ;
Davies, H ;
Peakman, M .
IMMUNOLOGY TODAY, 1996, 17 (02) :64-70
[10]   MHC MOLECULAR MIMICRY IN DIABETES [J].
BAUM, H ;
BRUSIC, V ;
CHOUDHURI, K ;
CUNNINGHAM, P ;
VERGANI, D ;
PEAKMAN, M .
NATURE MEDICINE, 1995, 1 (05) :388-388