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Dadun > Depósito Académico > CIMA (Centro de Investigación Médica Aplicada) > Área de Terapia génica y Hepatología > Inmunología hepatitis virales > DA - CIMA - Terapia génica y Hepatología - Inmunología hepatitis virales - Artículos de revista >

Identification and characterization of a T-helper peptide from carcinoembryonic antigen
Authors: Ruiz, M. (Marta)
Kobayashi, H. (Hiroya)
Lasarte, J.J. (Juan José)
Prieto, J. (Jesús)
Borras-Cuesta, F. (Francisco)
Celis, E. (Esteban)
Sarobe, P. (Pablo)
Keywords: Carcinoembryonic Antigen/chemistry
Carcinoembryonic Antigen/immunology
Peptides/chemistry
T-Lymphocytes, Helper-Inducer/chemistry
Issue Date: 2004
Publisher: American association for cancer research
Publisher version: http://dx.doi.org/10.1158/1078-0432.CCR-03-0476
ISSN: 1078-0432
Citation: Ruiz M, Kobayashi H, Lasarte JJ, Prieto J, Borras-Cuesta F, Celis E, at al. Identification and characterization of a T-helper peptide from carcinoembryonic antigen. Clin Cancer Res 2004 Apr 15;10(8):2860-2867.
Abstract
PURPOSE: The purpose of this research was to identify promiscuous T-helper cell determinants (THd) from carcinoembryonic antigen (CEA) to be used to prime T-cell help for cancer therapy. CEA was selected because this antigen is expressed in an important variety of carcinomas. EXPERIMENTAL DESIGN: Potential promiscuous THd from CEA were predicted using available computer algorithms. Predicted peptides were synthesized and tested in binding experiments to different HLA-DR molecules. Binder peptides were then used to prime T-cell responses both in vitro and in vivo. RESULTS: Twenty 15-mer peptides from CEA were predicted to bind to different HLA-DR molecules. The promiscuous character of these peptides was demonstrated in binding experiments. Fifteen of 20 peptides tested were able to bind to HLA-DR4, but only CEA (625-639) was shown to be presented after processing of recombinant CEA. CEA (625-639) was also found to be presented by HLA-DR53. Moreover, immunization of HLA-DR4 transgenic mice with CEA (625-639) in conjunction with class I epitope OVA (257-264), induced a CTL response specific of OVA (257-264). CONCLUSIONS: CEA (625-639) might be a relevant promiscuous THd peptide for cancer therapy.
Permanent link: http://hdl.handle.net/10171/20434
Appears in Collections:DA - Medicina - Medicina Interna - Artículos de revista
DA - CIMA - Terapia génica y Hepatología - Inmunología experimental - Artículos de revista
DA - CIMA - Terapia génica y Hepatología - Inmunología hepatitis virales - Artículos de revista

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