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Features of Immunosenescence in Women Newly Diagnosed With Breast Cancer

Adults exposed to childhood maltreatment have increased stress reactivity. This profile is associated with dysregulation of the immune system, including enhanced inflammatory reactions and accelerated senescence. Subjects exposed to ear stress have increased risk for several age-related diseases, in...

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Autores principales: Trintinaglia, Lauren, Bandinelli, Lucas Poitevin, Grassi-Oliveira, Rodrigo, Petersen, Laura Esteves, Anzolin, Marcelo, Correa, Bruna Luz, Schuch, Jaqueline Bohrer, Bauer, Moisés Evandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055359/
https://www.ncbi.nlm.nih.gov/pubmed/30061900
http://dx.doi.org/10.3389/fimmu.2018.01651
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author Trintinaglia, Lauren
Bandinelli, Lucas Poitevin
Grassi-Oliveira, Rodrigo
Petersen, Laura Esteves
Anzolin, Marcelo
Correa, Bruna Luz
Schuch, Jaqueline Bohrer
Bauer, Moisés Evandro
author_facet Trintinaglia, Lauren
Bandinelli, Lucas Poitevin
Grassi-Oliveira, Rodrigo
Petersen, Laura Esteves
Anzolin, Marcelo
Correa, Bruna Luz
Schuch, Jaqueline Bohrer
Bauer, Moisés Evandro
author_sort Trintinaglia, Lauren
collection PubMed
description Adults exposed to childhood maltreatment have increased stress reactivity. This profile is associated with dysregulation of the immune system, including enhanced inflammatory reactions and accelerated senescence. Subjects exposed to ear stress have increased risk for several age-related diseases, including cardiovascular disease, type II diabetes, and cancer. Although previous studies have reported immune changes in advanced cancer, very little information is available regarding early stage breast cancer. Here, 29 patients with breast cancer were recruited: 15 with history of childhood maltreatment (CM+) and 14 without history (CM−). Twenty-seven healthy women without CM were selected as the control group. Peripheral blood was collected and lymphocyte subsets phenotyped by multi-color flow cytometry (B cells, CD4+ T, CD8+ T, natural killer cells, activated T cells, regulatory T cells, and senescence-associated T cells). Because human cytomegalovirus (CMV) was associated with signatures of early senescence, the CMV serology was determined by ELISA. None of the subjects had IgM reactivity to CMV, excluding acute viral infection. There was a higher proportion of patients with increased CMV IgG levels in the CM+ group as compared to CM− or controls. Different stages of T-cell differentiation can be determined based on the cell-surface expression of the costimulatory molecules CD27 and CD28: ear (CD27+CD28+), intermediate-differentiated (CD27−CD28+), and late-differentiated or senescent T cells (CD27−CD28−). After adjusting for age and education, ear T cells (CD27+CD28+) were found reduced in CM+ and CM− patients (p < 0.0001). In contrast, intermediate-differentiated T cells (CD27−CD28+; p < 0.0001), senescent T cells (CD27−CD28−; p < 0.0001), and exhausted T cells (CD8+CD27−CD28−PD1+; p < 0.0001) were found expanded in both CM+ and CM− groups. Our data suggest that features of immunosenescence are associated with newly diagnosed breast cancer, regardless of the CM history.
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spelling pubmed-60553592018-07-30 Features of Immunosenescence in Women Newly Diagnosed With Breast Cancer Trintinaglia, Lauren Bandinelli, Lucas Poitevin Grassi-Oliveira, Rodrigo Petersen, Laura Esteves Anzolin, Marcelo Correa, Bruna Luz Schuch, Jaqueline Bohrer Bauer, Moisés Evandro Front Immunol Immunology Adults exposed to childhood maltreatment have increased stress reactivity. This profile is associated with dysregulation of the immune system, including enhanced inflammatory reactions and accelerated senescence. Subjects exposed to ear stress have increased risk for several age-related diseases, including cardiovascular disease, type II diabetes, and cancer. Although previous studies have reported immune changes in advanced cancer, very little information is available regarding early stage breast cancer. Here, 29 patients with breast cancer were recruited: 15 with history of childhood maltreatment (CM+) and 14 without history (CM−). Twenty-seven healthy women without CM were selected as the control group. Peripheral blood was collected and lymphocyte subsets phenotyped by multi-color flow cytometry (B cells, CD4+ T, CD8+ T, natural killer cells, activated T cells, regulatory T cells, and senescence-associated T cells). Because human cytomegalovirus (CMV) was associated with signatures of early senescence, the CMV serology was determined by ELISA. None of the subjects had IgM reactivity to CMV, excluding acute viral infection. There was a higher proportion of patients with increased CMV IgG levels in the CM+ group as compared to CM− or controls. Different stages of T-cell differentiation can be determined based on the cell-surface expression of the costimulatory molecules CD27 and CD28: ear (CD27+CD28+), intermediate-differentiated (CD27−CD28+), and late-differentiated or senescent T cells (CD27−CD28−). After adjusting for age and education, ear T cells (CD27+CD28+) were found reduced in CM+ and CM− patients (p < 0.0001). In contrast, intermediate-differentiated T cells (CD27−CD28+; p < 0.0001), senescent T cells (CD27−CD28−; p < 0.0001), and exhausted T cells (CD8+CD27−CD28−PD1+; p < 0.0001) were found expanded in both CM+ and CM− groups. Our data suggest that features of immunosenescence are associated with newly diagnosed breast cancer, regardless of the CM history. Frontiers Media S.A. 2018-07-16 /pmc/articles/PMC6055359/ /pubmed/30061900 http://dx.doi.org/10.3389/fimmu.2018.01651 Text en Copyright © 2018 Trintinaglia, Bandinelli, Grassi-Oliveira, Petersen, Anzolin, Correa, Schuch and Bauer. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Trintinaglia, Lauren
Bandinelli, Lucas Poitevin
Grassi-Oliveira, Rodrigo
Petersen, Laura Esteves
Anzolin, Marcelo
Correa, Bruna Luz
Schuch, Jaqueline Bohrer
Bauer, Moisés Evandro
Features of Immunosenescence in Women Newly Diagnosed With Breast Cancer
title Features of Immunosenescence in Women Newly Diagnosed With Breast Cancer
title_full Features of Immunosenescence in Women Newly Diagnosed With Breast Cancer
title_fullStr Features of Immunosenescence in Women Newly Diagnosed With Breast Cancer
title_full_unstemmed Features of Immunosenescence in Women Newly Diagnosed With Breast Cancer
title_short Features of Immunosenescence in Women Newly Diagnosed With Breast Cancer
title_sort features of immunosenescence in women newly diagnosed with breast cancer
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6055359/
https://www.ncbi.nlm.nih.gov/pubmed/30061900
http://dx.doi.org/10.3389/fimmu.2018.01651
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