Exploring immunological specificity using synthetic peptide combinatorial libraries

被引:84
作者
Pinilla, C
Martin, R
Gran, B
Appel, JR
Boggiano, C
Wilson, DB
Houghten, RA
机构
[1] Torrey Pines Inst Mol Studies, San Diego, CA 92121 USA
[2] NINDS, Cellular Immunol Sect, Neuroimmunol Branch, Natl Inst Hlth, Bethesda, MD 20892 USA
关键词
D O I
10.1016/S0952-7915(99)80033-8
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 definition of epitopes for human B and T cells is fundamental for the understanding of the immune response mechanism and its role in the prevention and cause of human disease. This understanding can be applied to the design of diagnostics and synthetic vaccines. In recent years, the understanding of the specificity of B and T cells has been advanced significantly by the development and use of combinatorial libraries made up of thousands to millions of synthetic peptides. The use of this approach has had four major effects: first, the definition of high affinity ligands both for T cells and antibodies; second, the application of alternative means for identifying immunologically relevant peptides for use as potential preventive and therapeutic vacc nes; third, a new appreciation of the requirements for TCR interactions with peptide-MHC complexes in immunogenicity; fourth, the establishment of new principles regarding the level of cross-reactivity in immunological recognition.
引用
收藏
页码:193 / 202
页数:10
相关论文
共 65 条
[1]   Exploring antibody polyspecificity using synthetic combinatorial libraries [J].
Appel, JR ;
Buencamino, J ;
Houghten, RA ;
Pinilla, C .
MOLECULAR DIVERSITY, 1996, 2 (1-2) :29-34
[2]  
Appel JR, 1996, PEPTIDE RES, V9, P174
[3]  
Appel JR, 1998, J PEPT RES, V52, P346
[4]  
APPEL JR, 1992, IMMUNOMETHODS, V1, P17
[5]   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
[6]   A peptide mimic of a protective epitope of respiratory syncytial virus selected from a combinatorial library induces virus-neutralizing antibodies and reduces viral load in vivo [J].
Chargelegue, D ;
Obeid, OE ;
Hsu, SC ;
Shaw, MD ;
Denbury, AN ;
Taylor, G ;
Steward, MW .
JOURNAL OF VIROLOGY, 1998, 72 (03) :2040-2046
[7]   A basis for alloreactivity: MHC helical residues broaden peptide recognition by the TCR [J].
Daniel, C ;
Horvath, S ;
Allen, PM .
IMMUNITY, 1998, 8 (05) :543-552
[8]   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
[9]   Ligand recognition by αβ T cell receptors [J].
Davis, MM ;
Boniface, JJ ;
Reich, Z ;
Lyons, D ;
Hampl, J ;
Arden, B ;
Chien, YH .
ANNUAL REVIEW OF IMMUNOLOGY, 1998, 16 :523-+
[10]   Two human T cell receptors bind in a similar diagonal mode to the HLA-A2/Tax peptide complex using different TCR amino acids [J].
Ding, YH ;
Smith, KJ ;
Garboczi, DN ;
Utz, U ;
Biddison, WE ;
Wiley, DC .
IMMUNITY, 1998, 8 (04) :403-411