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Circulating regulatory T cells from breast cancer patients in response to neoadjuvant chemotherapy

BACKGROUND: Immune escape of tumor cells is a new hallmark of cancer in general, and breast cancer, in particular. Previous studies have demonstrated that the immunological profile in peripheral blood may be a prognostic and/or predictive biomarker in breast cancer. Thus, higher number of regulatory...

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Autores principales: Sánchez-Margalet, Víctor, Barco-Sánchez, Antonio, Vilariño-García, Teresa, Jiménez-Cortegana, Carlos, Pérez-Pérez, Antonio, Henao-Carrasco, Fernando, Virizuela-Echaburu, Juan A., Nogales-Fernández, Esteban, Álamo-de la Gala, María C., Lobo-Acosta, María A., Palazón-Carrión, Natalia, Nieto, Adoración, de la Cruz-Merino, Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798280/
https://www.ncbi.nlm.nih.gov/pubmed/35116734
http://dx.doi.org/10.21037/tcr.2018.12.30
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author Sánchez-Margalet, Víctor
Barco-Sánchez, Antonio
Vilariño-García, Teresa
Jiménez-Cortegana, Carlos
Pérez-Pérez, Antonio
Henao-Carrasco, Fernando
Virizuela-Echaburu, Juan A.
Nogales-Fernández, Esteban
Álamo-de la Gala, María C.
Lobo-Acosta, María A.
Palazón-Carrión, Natalia
Nieto, Adoración
de la Cruz-Merino, Luis
author_facet Sánchez-Margalet, Víctor
Barco-Sánchez, Antonio
Vilariño-García, Teresa
Jiménez-Cortegana, Carlos
Pérez-Pérez, Antonio
Henao-Carrasco, Fernando
Virizuela-Echaburu, Juan A.
Nogales-Fernández, Esteban
Álamo-de la Gala, María C.
Lobo-Acosta, María A.
Palazón-Carrión, Natalia
Nieto, Adoración
de la Cruz-Merino, Luis
author_sort Sánchez-Margalet, Víctor
collection PubMed
description BACKGROUND: Immune escape of tumor cells is a new hallmark of cancer in general, and breast cancer, in particular. Previous studies have demonstrated that the immunological profile in peripheral blood may be a prognostic and/or predictive biomarker in breast cancer. Thus, higher number of regulatory T cells (Tregs) in blood from patients with breast cancer has been reported in relation to normal donors. In the present study, we planned to evaluate the changes in different cell populations in peripheral blood: neutrophils, monocytes and lymphocytes, as well as lymphocyte subpopulations [natural killer (NK), B lymphocytes, T lymphocytes, both CD4(+) and CD8(+), and Tregs] from patients with local breast cancer (both Her2(+) and Her2(−)), before, during and after neoadjuvant chemotherapy. METHODS: We have employed flow cytometry for the cell analysis of fresh samples obtained before and whilst the neoadjuvant treatment was accomplished. We have studied 50 successive patients from the Breast Cancer Unit of the Virgen Macarena University Hospital during 2 years. RESULTS: Neoadjuvant chemotherapy induced a significant reduction in B cells, especially in Her2(−) patients, and a reduction in NK cells. CD4(+) T cells decreased, whereas CD8(+) cells only decreased in Her2(−) patients. Tregs were also diminished, especially in Her2(+) patients, in response to treatment. Thus, higher CD8/Treg ratio was observed in Her2(+) patients. A higher percentage of Her2(+) patients (66.6%) achieved complete response than Her2(−) patients (27.5%). Monocytes and neutrophils were not changed in peripheral blood. CONCLUSIONS: Even though the decrease in B cells and NK cells in response to chemotherapy may be deleterious in the neoadjuvant treatment of breast cancer, the decrease in Tregs and CD4 T cells, but not CD8 T cells, increasing the CD8/Treg ratio, especially in Her2(+) patients, may reveal a new tool to monitor the immune response in breast cancer treated with chemotherapy in the neoadjuvant setting.
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spelling pubmed-87982802022-02-02 Circulating regulatory T cells from breast cancer patients in response to neoadjuvant chemotherapy Sánchez-Margalet, Víctor Barco-Sánchez, Antonio Vilariño-García, Teresa Jiménez-Cortegana, Carlos Pérez-Pérez, Antonio Henao-Carrasco, Fernando Virizuela-Echaburu, Juan A. Nogales-Fernández, Esteban Álamo-de la Gala, María C. Lobo-Acosta, María A. Palazón-Carrión, Natalia Nieto, Adoración de la Cruz-Merino, Luis Transl Cancer Res Original Article BACKGROUND: Immune escape of tumor cells is a new hallmark of cancer in general, and breast cancer, in particular. Previous studies have demonstrated that the immunological profile in peripheral blood may be a prognostic and/or predictive biomarker in breast cancer. Thus, higher number of regulatory T cells (Tregs) in blood from patients with breast cancer has been reported in relation to normal donors. In the present study, we planned to evaluate the changes in different cell populations in peripheral blood: neutrophils, monocytes and lymphocytes, as well as lymphocyte subpopulations [natural killer (NK), B lymphocytes, T lymphocytes, both CD4(+) and CD8(+), and Tregs] from patients with local breast cancer (both Her2(+) and Her2(−)), before, during and after neoadjuvant chemotherapy. METHODS: We have employed flow cytometry for the cell analysis of fresh samples obtained before and whilst the neoadjuvant treatment was accomplished. We have studied 50 successive patients from the Breast Cancer Unit of the Virgen Macarena University Hospital during 2 years. RESULTS: Neoadjuvant chemotherapy induced a significant reduction in B cells, especially in Her2(−) patients, and a reduction in NK cells. CD4(+) T cells decreased, whereas CD8(+) cells only decreased in Her2(−) patients. Tregs were also diminished, especially in Her2(+) patients, in response to treatment. Thus, higher CD8/Treg ratio was observed in Her2(+) patients. A higher percentage of Her2(+) patients (66.6%) achieved complete response than Her2(−) patients (27.5%). Monocytes and neutrophils were not changed in peripheral blood. CONCLUSIONS: Even though the decrease in B cells and NK cells in response to chemotherapy may be deleterious in the neoadjuvant treatment of breast cancer, the decrease in Tregs and CD4 T cells, but not CD8 T cells, increasing the CD8/Treg ratio, especially in Her2(+) patients, may reveal a new tool to monitor the immune response in breast cancer treated with chemotherapy in the neoadjuvant setting. AME Publishing Company 2019-02 /pmc/articles/PMC8798280/ /pubmed/35116734 http://dx.doi.org/10.21037/tcr.2018.12.30 Text en 2019 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
Sánchez-Margalet, Víctor
Barco-Sánchez, Antonio
Vilariño-García, Teresa
Jiménez-Cortegana, Carlos
Pérez-Pérez, Antonio
Henao-Carrasco, Fernando
Virizuela-Echaburu, Juan A.
Nogales-Fernández, Esteban
Álamo-de la Gala, María C.
Lobo-Acosta, María A.
Palazón-Carrión, Natalia
Nieto, Adoración
de la Cruz-Merino, Luis
Circulating regulatory T cells from breast cancer patients in response to neoadjuvant chemotherapy
title Circulating regulatory T cells from breast cancer patients in response to neoadjuvant chemotherapy
title_full Circulating regulatory T cells from breast cancer patients in response to neoadjuvant chemotherapy
title_fullStr Circulating regulatory T cells from breast cancer patients in response to neoadjuvant chemotherapy
title_full_unstemmed Circulating regulatory T cells from breast cancer patients in response to neoadjuvant chemotherapy
title_short Circulating regulatory T cells from breast cancer patients in response to neoadjuvant chemotherapy
title_sort circulating regulatory t cells from breast cancer patients in response to neoadjuvant chemotherapy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798280/
https://www.ncbi.nlm.nih.gov/pubmed/35116734
http://dx.doi.org/10.21037/tcr.2018.12.30
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