Detection of vimentin-specific autoreactive CD8+ T cells in cardiac transplant patients

被引:48
作者
Barber, LD
Whitelegg, A
Madrigal, JA
Banner, NR
Rose, ML
机构
[1] Royal Free Hosp, Antholy Nolan Res Inst, London NW3 2QG, England
[2] Royal Brompton & Harefield NHS Trust, Harefield, Middx, England
[3] Univ London Imperial Coll Sci Technol & Med, Harefield Hosp, Sch Med, Heart Sci Ctr, Harefield UB9 6JH, Middx, England
关键词
D O I
10.1097/01.tp.0000129068.03900.25
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Evidence is emerging that autoimmunity can play a role in allograft rejection. Reports have described the presence of autoantibodies in transplant patients and CD4(+) autoreactive T cells in rodent models of allograft rejection. The objective of this study was to seek evidence of CD8(+) T-cell-mediated autoimmunity in the transplant setting. The authors have previously observed autoimmunity to the non-polymorphic cytoskeletal protein vimentin in cardiac transplant patients. In this study, vimentin antibody-positive patients were screened for the presence of vimentin-specific self-major histocompatibility complex class I-restricted CD8(+) T cells. Methods. Two peptide sequences from vimentin that bound HIA-A*0201 were identified and fluorochromelabeled A*0201 tetramers with each peptide were constructed to screen for vimentin-specific T cells. Results. Tetramer-binding CD8(+) T cells were detected in peripheral blood lymphocytes from two of six patients after expansion by in vitro stimulation with peptide. Tetramer-binding T cells produced interferon-gamma in an antigen-specific fashion. No autoreactive T cells specific for vimentin were detected after peptide stimulation of T cells from eight healthy A*0201-positive volunteers. Conclusions. This finding is the first evidence of CD8(+) T-cell-mediated autoimmunity in human transplant patients.
引用
收藏
页码:1604 / 1609
页数:6
相关论文
共 31 条
[11]   A new enzyme-linked immunosorbent assay to measure anti-endothelial antibodies after cardiac transplantation demonstrates greater inhibition of antibody formation by tacrolimus compared with cyclosporine [J].
Jurcevic, S ;
Dunn, MJ ;
Crisp, S ;
Busing, K ;
Rinaldi, M ;
Pellegrini, C ;
Yacoub, MH ;
Vigano, M ;
Banner, NL ;
Rose, ML .
TRANSPLANTATION, 1998, 65 (09) :1197-1202
[12]   Tracking T cells with tetramers: New tales from new tools [J].
Klenerman, P ;
Cerundolo, V ;
Dunbar, RR .
NATURE REVIEWS IMMUNOLOGY, 2002, 2 (04) :263-272
[13]   Anti-skeletal muscle glycolipid antibodies in human heart transplantation as markers of acute rejection - Correlation with endomyocardial biopsy [J].
Laguens, RP ;
Argel, MI ;
Chambo, JG ;
Vigliano, CA ;
SanMartino, JA ;
Perrone, SV ;
Favaloro, RR .
TRANSPLANTATION, 1996, 62 (02) :211-216
[14]  
Miller Leslie W., 2001, Cardiology Clinics, V19, P141, DOI 10.1016/S0733-8651(05)70200-9
[15]   Targeted T-cell therapy for human leukemia: Cytotoxic T lymphocytes specific for a peptide derived from proteinase 3 preferentially lyse human myeloid leukemia cells [J].
Molldrem, J ;
Dermime, S ;
Parker, K ;
Jiang, YZ ;
Mavroudis, D ;
Hensel, N ;
Fukushima, P ;
Barrett, AJ .
BLOOD, 1996, 88 (07) :2450-2457
[16]   Vimentin is secreted by activated macrophages [J].
Mor-Vaknin, N ;
Punturieri, A ;
Sitwala, K ;
Markovitz, DM .
NATURE CELL BIOLOGY, 2003, 5 (01) :59-63
[17]  
NAIR S, UNPUB MICE IMMUNIZED
[18]   PARTIAL-PURIFICATION AND SOME PROPERTIES OF BB7.2 - A CYTO-TOXIC MONOCLONAL-ANTIBODY WITH SPECIFICITY FOR HLA-A2 AND A VARIANT OF HLA-A28 [J].
PARHAM, P ;
BRODSKY, FM .
HUMAN IMMUNOLOGY, 1981, 3 (04) :277-299
[19]  
PARKER KC, 1994, J IMMUNOL, V152, P163
[20]   Heat shock proteins, anti-heat shock protein reactivity and allograft rejection [J].
Pockley, AG .
TRANSPLANTATION, 2001, 71 (11) :1503-1507