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Split T Cell Tolerance against a Self/Tumor Antigen: Spontaneous CD4(+) but Not CD8(+) T Cell Responses against p53 in Cancer Patients and Healthy Donors

Analyses of NY-ESO-1-specific spontaneous immune responses in cancer patients revealed that antibody and both CD4(+) and CD8(+) T cell responses were induced together in cancer patients. To explore whether such integrated immune responses are also spontaneously induced for other tumor antigens, we h...

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Autores principales: Tsuji, Takemasa, Matsuzaki, Junko, Ritter, Erika, Miliotto, Anthony, Ritter, Gerd, Odunsi, Kunle, Old, Lloyd J., Gnjatic, Sacha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3155555/
https://www.ncbi.nlm.nih.gov/pubmed/21858191
http://dx.doi.org/10.1371/journal.pone.0023651
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author Tsuji, Takemasa
Matsuzaki, Junko
Ritter, Erika
Miliotto, Anthony
Ritter, Gerd
Odunsi, Kunle
Old, Lloyd J.
Gnjatic, Sacha
author_facet Tsuji, Takemasa
Matsuzaki, Junko
Ritter, Erika
Miliotto, Anthony
Ritter, Gerd
Odunsi, Kunle
Old, Lloyd J.
Gnjatic, Sacha
author_sort Tsuji, Takemasa
collection PubMed
description Analyses of NY-ESO-1-specific spontaneous immune responses in cancer patients revealed that antibody and both CD4(+) and CD8(+) T cell responses were induced together in cancer patients. To explore whether such integrated immune responses are also spontaneously induced for other tumor antigens, we have evaluated antibody and T cell responses against self/tumor antigen p53 in ovarian cancer patients and healthy individuals. We found that 21% (64/298) of ovarian cancer patients but no healthy donors showed specific IgG responses against wild-type p53 protein. While none of 12 patients with high titer p53 antibody showed spontaneous p53-specific CD8(+) T cell responses following a single in vitro sensitization, significant p53-specific IFN-γ producing CD4(+) T cells were detected in 6 patients. Surprisingly, similar levels of p53-specific CD4(+) T cells but not CD8(+) T cells were also detected in 5/10 seronegative cancer patients and 9/12 healthy donors. Importantly, p53-specific CD4(+) T cells in healthy donors originated from a CD45RA(−) antigen-experienced T cell population and recognized naturally processed wild-type p53 protein. These results raise the possibility that p53-specific CD4(+) T cells reflect abnormalities in p53 occurring in normal individuals and that they may play a role in processes of immunosurveillance or immunoregulation of p53-related neoplastic events.
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spelling pubmed-31555552011-08-19 Split T Cell Tolerance against a Self/Tumor Antigen: Spontaneous CD4(+) but Not CD8(+) T Cell Responses against p53 in Cancer Patients and Healthy Donors Tsuji, Takemasa Matsuzaki, Junko Ritter, Erika Miliotto, Anthony Ritter, Gerd Odunsi, Kunle Old, Lloyd J. Gnjatic, Sacha PLoS One Research Article Analyses of NY-ESO-1-specific spontaneous immune responses in cancer patients revealed that antibody and both CD4(+) and CD8(+) T cell responses were induced together in cancer patients. To explore whether such integrated immune responses are also spontaneously induced for other tumor antigens, we have evaluated antibody and T cell responses against self/tumor antigen p53 in ovarian cancer patients and healthy individuals. We found that 21% (64/298) of ovarian cancer patients but no healthy donors showed specific IgG responses against wild-type p53 protein. While none of 12 patients with high titer p53 antibody showed spontaneous p53-specific CD8(+) T cell responses following a single in vitro sensitization, significant p53-specific IFN-γ producing CD4(+) T cells were detected in 6 patients. Surprisingly, similar levels of p53-specific CD4(+) T cells but not CD8(+) T cells were also detected in 5/10 seronegative cancer patients and 9/12 healthy donors. Importantly, p53-specific CD4(+) T cells in healthy donors originated from a CD45RA(−) antigen-experienced T cell population and recognized naturally processed wild-type p53 protein. These results raise the possibility that p53-specific CD4(+) T cells reflect abnormalities in p53 occurring in normal individuals and that they may play a role in processes of immunosurveillance or immunoregulation of p53-related neoplastic events. Public Library of Science 2011-08-12 /pmc/articles/PMC3155555/ /pubmed/21858191 http://dx.doi.org/10.1371/journal.pone.0023651 Text en Tsuji 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
Tsuji, Takemasa
Matsuzaki, Junko
Ritter, Erika
Miliotto, Anthony
Ritter, Gerd
Odunsi, Kunle
Old, Lloyd J.
Gnjatic, Sacha
Split T Cell Tolerance against a Self/Tumor Antigen: Spontaneous CD4(+) but Not CD8(+) T Cell Responses against p53 in Cancer Patients and Healthy Donors
title Split T Cell Tolerance against a Self/Tumor Antigen: Spontaneous CD4(+) but Not CD8(+) T Cell Responses against p53 in Cancer Patients and Healthy Donors
title_full Split T Cell Tolerance against a Self/Tumor Antigen: Spontaneous CD4(+) but Not CD8(+) T Cell Responses against p53 in Cancer Patients and Healthy Donors
title_fullStr Split T Cell Tolerance against a Self/Tumor Antigen: Spontaneous CD4(+) but Not CD8(+) T Cell Responses against p53 in Cancer Patients and Healthy Donors
title_full_unstemmed Split T Cell Tolerance against a Self/Tumor Antigen: Spontaneous CD4(+) but Not CD8(+) T Cell Responses against p53 in Cancer Patients and Healthy Donors
title_short Split T Cell Tolerance against a Self/Tumor Antigen: Spontaneous CD4(+) but Not CD8(+) T Cell Responses against p53 in Cancer Patients and Healthy Donors
title_sort split t cell tolerance against a self/tumor antigen: spontaneous cd4(+) but not cd8(+) t cell responses against p53 in cancer patients and healthy donors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3155555/
https://www.ncbi.nlm.nih.gov/pubmed/21858191
http://dx.doi.org/10.1371/journal.pone.0023651
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