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Production of LacZ Inducible T Cell Hybridoma Specific for Human and Mouse gp100(25–33) Peptides

Identification and quantification of immunogenic peptides and tumor-derived epitopes presented on MHC-I molecules are essential for basic studies and vaccines generation. Although lymphocytes derived from transgenic mice can serve as sensitive detectors of processes of antigen presentation and recog...

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Detalles Bibliográficos
Autores principales: Cafri, Gal, Sharbi-Yunger, Adi, Tzehoval, Esther, Eisenbach, Lea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3562179/
https://www.ncbi.nlm.nih.gov/pubmed/23383339
http://dx.doi.org/10.1371/journal.pone.0055583
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author Cafri, Gal
Sharbi-Yunger, Adi
Tzehoval, Esther
Eisenbach, Lea
author_facet Cafri, Gal
Sharbi-Yunger, Adi
Tzehoval, Esther
Eisenbach, Lea
author_sort Cafri, Gal
collection PubMed
description Identification and quantification of immunogenic peptides and tumor-derived epitopes presented on MHC-I molecules are essential for basic studies and vaccines generation. Although lymphocytes derived from transgenic mice can serve as sensitive detectors of processes of antigen presentation and recognition, they are not always available. The use of cell lines might be extremely useful. In this study, we generated a lacZ inducible CD8(+) hybridoma (BUSA14) capable of recognizing both human and mouse gp100(25–33) melanoma antigens presented on dendritic and tumor cell lines. This hybridoma expresses a variety of membranal T cell markers and secretes IL-2 and TNFα. Thus, BUSA14 offers a quantifiable, cheap and straightforward tool for studying peptide presentation by MHC-I molecules on the cell surface.
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spelling pubmed-35621792013-02-04 Production of LacZ Inducible T Cell Hybridoma Specific for Human and Mouse gp100(25–33) Peptides Cafri, Gal Sharbi-Yunger, Adi Tzehoval, Esther Eisenbach, Lea PLoS One Research Article Identification and quantification of immunogenic peptides and tumor-derived epitopes presented on MHC-I molecules are essential for basic studies and vaccines generation. Although lymphocytes derived from transgenic mice can serve as sensitive detectors of processes of antigen presentation and recognition, they are not always available. The use of cell lines might be extremely useful. In this study, we generated a lacZ inducible CD8(+) hybridoma (BUSA14) capable of recognizing both human and mouse gp100(25–33) melanoma antigens presented on dendritic and tumor cell lines. This hybridoma expresses a variety of membranal T cell markers and secretes IL-2 and TNFα. Thus, BUSA14 offers a quantifiable, cheap and straightforward tool for studying peptide presentation by MHC-I molecules on the cell surface. Public Library of Science 2013-02-01 /pmc/articles/PMC3562179/ /pubmed/23383339 http://dx.doi.org/10.1371/journal.pone.0055583 Text en © 2013 Cafri et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cafri, Gal
Sharbi-Yunger, Adi
Tzehoval, Esther
Eisenbach, Lea
Production of LacZ Inducible T Cell Hybridoma Specific for Human and Mouse gp100(25–33) Peptides
title Production of LacZ Inducible T Cell Hybridoma Specific for Human and Mouse gp100(25–33) Peptides
title_full Production of LacZ Inducible T Cell Hybridoma Specific for Human and Mouse gp100(25–33) Peptides
title_fullStr Production of LacZ Inducible T Cell Hybridoma Specific for Human and Mouse gp100(25–33) Peptides
title_full_unstemmed Production of LacZ Inducible T Cell Hybridoma Specific for Human and Mouse gp100(25–33) Peptides
title_short Production of LacZ Inducible T Cell Hybridoma Specific for Human and Mouse gp100(25–33) Peptides
title_sort production of lacz inducible t cell hybridoma specific for human and mouse gp100(25–33) peptides
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3562179/
https://www.ncbi.nlm.nih.gov/pubmed/23383339
http://dx.doi.org/10.1371/journal.pone.0055583
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