Antigen arrays in T cell immunology

被引:19
作者
Hiemstra, HS [1 ]
Drijfhout, JW [1 ]
Roep, BO [1 ]
机构
[1] Leiden Univ, Ctr Med, Dept Immunochem & Blood Bank, NL-2300 RC Leiden, Netherlands
关键词
D O I
10.1016/S0952-7915(99)00054-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The screening of compound arrays in in vitro bioassays has developed into a powerful tool for the identification of biologically active substances. In the past decade, this technology has increasingly been applied to immunology. As the specificity of the immune system is determined by antigen detection via receptors on B and T cells, targeting the specificity of these immune receptors with random arrays is unique in its ability to generate general and quantitative information on cellular (cross-)reactivity. Synthetic array studies have been useful for identification of epitopes and antigens from databases by defining recognition patterns, isolation of synthetic peptides capable of modulating T cell responsiveness, characterisation of TCR promiscuity, and identification of functionally cross-reacting peptides that are potentially involved in molecular mimicry.
引用
收藏
页码:80 / 84
页数:5
相关论文
共 47 条
[1]   CELLULAR-IMMUNITY TO A DETERMINANT COMMON TO GLUTAMATE-DECARBOXYLASE AND COXSACKIE-VIRUS IN INSULIN-DEPENDENT DIABETES [J].
ATKINSON, MA ;
BOWMAN, MA ;
CAMPBELL, L ;
DARROW, BL ;
KAUFMAN, DL ;
MACLAREN, NK .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (05) :2125-2129
[2]  
Bach JM, 1998, EUR J IMMUNOL, V28, P1902
[3]   Use of combinatorial peptide libraries to construct functional mimics of tumor epitopes recognized by MHC class I-restricted cytolytic T lymphocytes [J].
Blake, J ;
Johnston, JV ;
Hellstrom, KE ;
Marquardt, H ;
Chen, LP .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (01) :121-130
[4]  
BOON T, 1994, ANNU REV IMMUNOL, V12, P337, DOI 10.1146/annurev.iy.12.040194.002005
[5]   Treatment of experimental encephalomyelitis with a peptide analogue of myelin basic protein [J].
Brocke, S ;
Gijbels, K ;
Allegretta, M ;
Ferber, I ;
Piercy, C ;
Blankenstein, T ;
Martin, R ;
Utz, U ;
Karin, N ;
Mitchell, D ;
Veromaa, T ;
Waisman, A ;
Gaur, A ;
Conlon, P ;
Ling, N ;
Fairchild, PJ ;
Wraith, DC ;
OGarra, A ;
Fathman, CG ;
Steinman, L .
NATURE, 1996, 379 (6563) :343-346
[6]   Selection of biologically active peptides by phage display of random peptide libraries [J].
Cortese, R ;
Monaci, P ;
Luzzago, A ;
Santini, C ;
Bartoli, F ;
Cortese, I ;
Fortugno, P ;
Galfre, G ;
Nicosia, A ;
Felici, F .
CURRENT OPINION IN BIOTECHNOLOGY, 1996, 7 (06) :616-621
[7]   HLA class I binding motifs derived from random peptide libraries differ at the COOH terminus from those of eluted peptides [J].
Davenport, MP ;
Smith, KJ ;
Barouch, D ;
Reid, SW ;
Bodnar, WM ;
Willis, AC ;
Hunt, DF ;
Hill, AVS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (02) :367-371
[8]   Definition of agonists and design of antagonists for alloreactive T cell clones using synthetic peptide libraries [J].
de Koster, HS ;
Vermeulen, CJ ;
Hiemstra, HS ;
Amons, R ;
Drijfhout, JW ;
Koning, F .
INTERNATIONAL IMMUNOLOGY, 1999, 11 (04) :585-591
[9]  
FALK K, 1994, IMMUNOGENETICS, V39, P230
[10]   New ligands binding to the human leukocyte antigen class II molecule DRB1(*)0101 based on the activity pattern of an undecapeptide library [J].
Fleckenstein, B ;
Kalbacher, H ;
Muller, CP ;
Stoll, D ;
Halder, T ;
Jung, G ;
Wiesmuller, KH .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 240 (01) :71-77