T cell lines generated with type II collagen proliferate in an autologous mixed lymphocyte response

被引:3
作者
Catchpole, B
Hamblin, AS
Staines, NA
机构
[1] Univ London, Univ London Royal Vet Coll, Dept Pathol & Infect Dis, London NW1 0TU, England
[2] Kings Coll London, Infect & Immun Res Grp, London WC2R 2LS, England
基金
英国惠康基金;
关键词
antigen presentation; arthritis; autoreactive T cell; type II collagen;
D O I
10.1006/jaut.2001.0537
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Collagen-induced arthritis (CIA) is a T cell-dependent disease induced in susceptible rodents by immunizing with bovine type II collagen (bCII). In order to study T cell responses, a programme to generate bCII-specific T cell lines from arthritic rats was initiated. Lymph node cells from bCII-immune WA/KIR/kcl rats were cultured with bCII in vitro, and the T cells were isolated and restimulated with bCII-pulsed antigen presenting cells (APC) (thymus cells or splenic low density cells). However, T cells, generated initially to bCII, subsequently proliferated upon co-culture with syngeneic APC even in the absence of bCII This suggests that exposure to bCII resulted in the activation of a population of self-reactive T cells which proliferate in an autologous mixed lymphocyte response. In contrast, short-term T cell lines generated to ovalbumin, heat-denatured bCII and the collagen peptide bCII(184-198) proliferated in response to specific anti-en-pulsed APC without demonstrating self-reactivity. Since denatured bCII and bCII(184-198) peptide are not arthritogenic and failed to generate self reactivity in vitro, this suggests that the native triple helical conformation of bCII is required for stimulating autoreactive T cell responses. (C) 2001 Academic Press.
引用
收藏
页码:181 / 189
页数:9
相关论文
共 30 条
[1]   Molecular mimicry in the MHC. Hidden clues to autoimmunity? [J].
Baum, H ;
Davies, H ;
Peakman, M .
IMMUNOLOGY TODAY, 1996, 17 (02) :64-70
[2]   MONOCLONAL-ANTIBODIES AND ARTHRITIS [J].
BILLINGHAM, MEJ ;
HICKS, C ;
CARNEY, S .
AGENTS AND ACTIONS, 1990, 29 (1-2) :77-87
[3]   ATTENUATION OF COLLAGEN ARTHRITIS AND MODULATION OF DELAYED-TYPE HYPERSENSITIVITY BY TYPE-II COLLAGEN REACTIVE T-CELL LINES [J].
BRAHN, E ;
TRENTHAM, DE .
CELLULAR IMMUNOLOGY, 1987, 109 (01) :139-147
[4]   THE MRC OX-62 ANTIGEN - A USEFUL MARKER IN THE PURIFICATION OF RAT VEILED CELLS WITH THE BIOCHEMICAL-PROPERTIES OF AN INTEGRIN [J].
BRENAN, M ;
PUKLAVEC, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (06) :1457-1465
[5]   Antigen presentation of Type II collagen in rats [J].
Catchpole, B ;
Staines, NA ;
Hamblin, AS .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2001, 125 (03) :478-484
[6]  
DOSREIS GA, 1981, J IMMUNOL, V127, P2456
[7]   THYMUS INDEPENDENCE OF A COLLAGEN-LIKE SYNTHETIC POLYPEPTIDE AND OF COLLAGEN, AND NEED FOR THYMUS AND BONE MARROW-CELL COOPERATION IN IMMUNE-RESPONSE TO GELATIN [J].
FUCHS, S ;
MOZES, E ;
MAOZ, A ;
SELA, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1974, 139 (01) :148-158
[8]   Generation of autoreactive CD4 T cells in Lewis rats after immunisation and culture with bovine type II collagen. [J].
Gibson, K ;
Lanchbury, JS ;
Staines, NA .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1997, 25 (02) :S239-S239
[9]  
GRIFFITHS MM, 1984, J IMMUNOL, V132, P2830
[10]   Identical expression of CD45R isoforms by CD45RC(+) 'revertant' memory and CD45RC(+) naive CD4 T cells [J].
Hargreaves, M ;
Bell, EB .
IMMUNOLOGY, 1997, 91 (03) :323-330