T-cell recognition of differentially tolerated epitopes of cartilage proteoglycan aggrecan in arthritis

被引:34
作者
Buzás, EI
Végvári, A
Murad, YM
Finnegan, A
Mikecz, K
Glant, TT [1 ]
机构
[1] Rush Univ, Med Ctr, Sect Biochem & Mol Biol, Dept Orthopaed Surg, Chicago, IL 60612 USA
[2] Rush Univ, Med Ctr, Dept Biochem, Chicago, IL 60612 USA
[3] Rush Univ, Med Ctr, Dept Immunol Microbiol, Chicago, IL 60612 USA
[4] Rush Univ, Med Ctr, Dept Internal Med, Rheumatol Sect, Chicago, IL 60612 USA
基金
美国国家卫生研究院;
关键词
T-cell epitopes; T-cell responses; arthritis; proteoglycan-induced arthritis; cryptic epitopes; full activator; partial activation; conditionally immunogenic;
D O I
10.1016/j.cellimm.2004.08.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Proteoglycan (PG) aggrecan, a major macromolecular component of cartilage, is highly immunogenic; it induces arthritis in genetically susceptible BALB/c mice. The present study maps the T-cell epitope repertoire of cartilage PG by identifying a total of 27 distinct T-cell epitopes. An epitope hierarchy, accounting for the different effector functions of PG-specific T cells, and determinant spreading, has been found. T-cell responses to four epitopes were associated with arthritis induction. Some of the T-cell epitopes were full T-cell activators, whereas a number of subdominant and cryptic epitopes proved to be partial activators in vitro, inducing either cytokine secretion or T-cell proliferation, but not both. A few T-cell epitopes of the core protein of cartilage PG were clearly recognized by T cells in PG-immunized arthritic animals, but the corresponding peptides did not induce T-cell responses when injected into naive BALB/c mice; thus these T-cell epitopes were designated as "conditionally immunogenic." (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:98 / 108
页数:11
相关论文
共 55 条
[1]   A multistep molecular mimicry hypothesis for the pathogenesis of rheumatoid arthritis [J].
Albani, S ;
Carson, DA .
IMMUNOLOGY TODAY, 1996, 17 (10) :466-470
[2]  
AMETANI A, 1989, COLD SH Q B, V54, P505
[3]   T and B cell recovery in arthritis adoptively transferred to SCID mice:: Antigen-specific activation is required for restoration of autopathogenic CD4+ Th1 cells in a syngeneic system [J].
Bárdos, T ;
Mikecz, K ;
Finnegan, A ;
Zhang, J ;
Glant, TT .
JOURNAL OF IMMUNOLOGY, 2002, 168 (12) :6013-6021
[4]   ARTHRITOGENICITY OF MINOR CARTILAGE COLLAGENS (TYPE-IX AND TYPE-XI) IN MICE [J].
BOISSIER, MC ;
CHIOCCHIA, G ;
RONZIERE, MC ;
HERBAGE, D ;
FOURNIER, C .
ARTHRITIS AND RHEUMATISM, 1990, 33 (01) :1-8
[5]   Selection of self-reactive peptides within human aggrecan by use of a HLA-DRB1*0401 peptide binding motif [J].
Boots, AMH ;
Verheijden, GFM ;
Schoningh, R ;
van Staveren, CJ ;
Bos, E ;
Elewaut, D ;
de Keyser, F ;
Veys, E ;
Joosten, I ;
Rijnders, AWM .
JOURNAL OF AUTOIMMUNITY, 1997, 10 (06) :569-578
[6]   THE SPECIFICITY OF RECOGNITION OF A CYTOTOXIC LYMPHOCYTE-T EPITOPE [J].
BURROWS, SR ;
RODDA, SJ ;
SUHRBIER, A ;
GEYSEN, HM ;
MOSS, DJ .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (01) :191-195
[7]  
BUZAS EI, 1995, J IMMUNOL, V155, P2679
[8]  
Buzas EI, 1998, ARTHRITIS RHEUM-US, V41, pS215
[9]  
DOEGE KJ, 1991, J BIOL CHEM, V266, P894
[10]   SEPARATION OF IL-4 PRODUCTION FROM TH-CELL PROLIFERATION BY AN ALTERED T-CELL RECEPTOR LIGAND [J].
EVAVOLD, BD ;
ALLEN, PM .
SCIENCE, 1991, 252 (5010) :1308-1310