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CD28 expression in sentinel node biopsies from breast cancer patients in comparison with CD3-ζ chain expression

BACKGROUND: Immunosuppression is documented in several malignant diseases, including breast cancer. Subsequently, future therapeutic concepts might include immunological approaches. However, detailed knowledge about tumor immunogenicity and host immunoreactivity, and how to assess these adequately,...

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Autores principales: Schüle, Jana M, Bergkvist, Leif, Håkansson, Leif, Gustafsson, Bertil, Håkansson, Annika
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC545070/
https://www.ncbi.nlm.nih.gov/pubmed/15613231
http://dx.doi.org/10.1186/1479-5876-2-45
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author Schüle, Jana M
Bergkvist, Leif
Håkansson, Leif
Gustafsson, Bertil
Håkansson, Annika
author_facet Schüle, Jana M
Bergkvist, Leif
Håkansson, Leif
Gustafsson, Bertil
Håkansson, Annika
author_sort Schüle, Jana M
collection PubMed
description BACKGROUND: Immunosuppression is documented in several malignant diseases, including breast cancer. Subsequently, future therapeutic concepts might include immunological approaches. However, detailed knowledge about tumor immunogenicity and host immunoreactivity, and how to assess these adequately, is still limited. We studied CD28 and CD3-ζ expression in sentinel node biopsies (SNB) from breast cancer patients to analyze tumor-related changes in T cell activity. METHOD: 25 women underwent surgery for primary breast cancer, including SNB. Frozen sections from 21 sentinel nodes could be analyzed with a double-staining technique. CD28 expression was studied in CD4+ and CD8+ T-lymphocyte subsets and compared with CD3-ζ expression in three specified nodal regions. RESULTS: The degree of CD28 expression varied between the different lymph node areas. The lowest degree of CD28 expression was observed in CD4+ T-lymphocytes in the paracortex and germinal centers. Here, a good agreement with CD3-ζ expression was found. A higher CD28 expression was noted in CD4+ T-cells in the primary follicles, where concordance with CD3-ζ expression was weaker. The CD8+ T-lymphocyte subset displayed generally a higher degree of CD28 expression than the CD4+ subset. CONCLUSION: Sentinel lymph nodes from breast cancer patients displayed local immunosuppression of varying extent. In the areas with the lowest degree of CD28 expression an accordingly low CD3-ζ expression was found. The SNB might prove an important diagnostic tool for the evaluation of interactions between tumor and the host immune system, helping to select patients who might benefit from adjuvant immunotherapy.
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spelling pubmed-5450702005-01-23 CD28 expression in sentinel node biopsies from breast cancer patients in comparison with CD3-ζ chain expression Schüle, Jana M Bergkvist, Leif Håkansson, Leif Gustafsson, Bertil Håkansson, Annika J Transl Med Research BACKGROUND: Immunosuppression is documented in several malignant diseases, including breast cancer. Subsequently, future therapeutic concepts might include immunological approaches. However, detailed knowledge about tumor immunogenicity and host immunoreactivity, and how to assess these adequately, is still limited. We studied CD28 and CD3-ζ expression in sentinel node biopsies (SNB) from breast cancer patients to analyze tumor-related changes in T cell activity. METHOD: 25 women underwent surgery for primary breast cancer, including SNB. Frozen sections from 21 sentinel nodes could be analyzed with a double-staining technique. CD28 expression was studied in CD4+ and CD8+ T-lymphocyte subsets and compared with CD3-ζ expression in three specified nodal regions. RESULTS: The degree of CD28 expression varied between the different lymph node areas. The lowest degree of CD28 expression was observed in CD4+ T-lymphocytes in the paracortex and germinal centers. Here, a good agreement with CD3-ζ expression was found. A higher CD28 expression was noted in CD4+ T-cells in the primary follicles, where concordance with CD3-ζ expression was weaker. The CD8+ T-lymphocyte subset displayed generally a higher degree of CD28 expression than the CD4+ subset. CONCLUSION: Sentinel lymph nodes from breast cancer patients displayed local immunosuppression of varying extent. In the areas with the lowest degree of CD28 expression an accordingly low CD3-ζ expression was found. The SNB might prove an important diagnostic tool for the evaluation of interactions between tumor and the host immune system, helping to select patients who might benefit from adjuvant immunotherapy. BioMed Central 2004-12-21 /pmc/articles/PMC545070/ /pubmed/15613231 http://dx.doi.org/10.1186/1479-5876-2-45 Text en Copyright © 2004 Schüle et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Schüle, Jana M
Bergkvist, Leif
Håkansson, Leif
Gustafsson, Bertil
Håkansson, Annika
CD28 expression in sentinel node biopsies from breast cancer patients in comparison with CD3-ζ chain expression
title CD28 expression in sentinel node biopsies from breast cancer patients in comparison with CD3-ζ chain expression
title_full CD28 expression in sentinel node biopsies from breast cancer patients in comparison with CD3-ζ chain expression
title_fullStr CD28 expression in sentinel node biopsies from breast cancer patients in comparison with CD3-ζ chain expression
title_full_unstemmed CD28 expression in sentinel node biopsies from breast cancer patients in comparison with CD3-ζ chain expression
title_short CD28 expression in sentinel node biopsies from breast cancer patients in comparison with CD3-ζ chain expression
title_sort cd28 expression in sentinel node biopsies from breast cancer patients in comparison with cd3-ζ chain expression
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC545070/
https://www.ncbi.nlm.nih.gov/pubmed/15613231
http://dx.doi.org/10.1186/1479-5876-2-45
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