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A novel category of antigens enabling CTL immunity to tumor escape variants: Cinderella antigens
Deficiencies in MHC class I antigen presentation are a common feature of tumors and allows escape from cytotoxic T lymphocyte (CTL)-mediated killing. It is crucial to take this capacity of tumors into account for the development of T-cell-based immunotherapy, as it may strongly impair their effectiv...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249164/ https://www.ncbi.nlm.nih.gov/pubmed/22116347 http://dx.doi.org/10.1007/s00262-011-1160-x |
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author | Seidel, Ursula J. E. Oliveira, Claudia C. Lampen, Margit H. van Hall, Thorbald |
author_facet | Seidel, Ursula J. E. Oliveira, Claudia C. Lampen, Margit H. van Hall, Thorbald |
author_sort | Seidel, Ursula J. E. |
collection | PubMed |
description | Deficiencies in MHC class I antigen presentation are a common feature of tumors and allows escape from cytotoxic T lymphocyte (CTL)-mediated killing. It is crucial to take this capacity of tumors into account for the development of T-cell-based immunotherapy, as it may strongly impair their effectiveness. A variety of escape mechanisms has been described thus far, but progress in counteracting them is poor. Here we review a novel strategy to target malignancies with defects in the antigenic processing machinery (APM). The concept is based on a unique category of CD8(+) T-cell epitopes that is associated with impaired peptide processing, which we named TEIPP. We characterized this alternative peptide repertoire emerging in MHC-I on tumors lacking classical antigen processing due to defects in the peptide transporter TAP (transporter associated with peptide processing). These TEIPPs exemplify interesting parallels with the folktale figure Cinderella: they are oppressed and neglected by a stepmother (like functional TAP prevents TEIPP presentation), until the suppression is released and Cinderella/TEIPP achieves unexpected recognition. TEIPP-specific CTLs and their cognate peptide-epitopes provide a new strategy to counteract immune evasion by APM defects and bear potential to targeting escape variants observed in a wide range of cancers. |
format | Online Article Text |
id | pubmed-3249164 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-32491642012-01-11 A novel category of antigens enabling CTL immunity to tumor escape variants: Cinderella antigens Seidel, Ursula J. E. Oliveira, Claudia C. Lampen, Margit H. van Hall, Thorbald Cancer Immunol Immunother Focussed Research Review Deficiencies in MHC class I antigen presentation are a common feature of tumors and allows escape from cytotoxic T lymphocyte (CTL)-mediated killing. It is crucial to take this capacity of tumors into account for the development of T-cell-based immunotherapy, as it may strongly impair their effectiveness. A variety of escape mechanisms has been described thus far, but progress in counteracting them is poor. Here we review a novel strategy to target malignancies with defects in the antigenic processing machinery (APM). The concept is based on a unique category of CD8(+) T-cell epitopes that is associated with impaired peptide processing, which we named TEIPP. We characterized this alternative peptide repertoire emerging in MHC-I on tumors lacking classical antigen processing due to defects in the peptide transporter TAP (transporter associated with peptide processing). These TEIPPs exemplify interesting parallels with the folktale figure Cinderella: they are oppressed and neglected by a stepmother (like functional TAP prevents TEIPP presentation), until the suppression is released and Cinderella/TEIPP achieves unexpected recognition. TEIPP-specific CTLs and their cognate peptide-epitopes provide a new strategy to counteract immune evasion by APM defects and bear potential to targeting escape variants observed in a wide range of cancers. Springer-Verlag 2011-11-25 2012 /pmc/articles/PMC3249164/ /pubmed/22116347 http://dx.doi.org/10.1007/s00262-011-1160-x Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Focussed Research Review Seidel, Ursula J. E. Oliveira, Claudia C. Lampen, Margit H. van Hall, Thorbald A novel category of antigens enabling CTL immunity to tumor escape variants: Cinderella antigens |
title | A novel category of antigens enabling CTL immunity to tumor escape variants: Cinderella antigens |
title_full | A novel category of antigens enabling CTL immunity to tumor escape variants: Cinderella antigens |
title_fullStr | A novel category of antigens enabling CTL immunity to tumor escape variants: Cinderella antigens |
title_full_unstemmed | A novel category of antigens enabling CTL immunity to tumor escape variants: Cinderella antigens |
title_short | A novel category of antigens enabling CTL immunity to tumor escape variants: Cinderella antigens |
title_sort | novel category of antigens enabling ctl immunity to tumor escape variants: cinderella antigens |
topic | Focussed Research Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249164/ https://www.ncbi.nlm.nih.gov/pubmed/22116347 http://dx.doi.org/10.1007/s00262-011-1160-x |
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