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Analysis of dendritic cells in tumor-free and tumor-containing sentinel lymph nodes from patients with breast cancer
INTRODUCTION: Sentinel lymph node (SLN) biopsy allows identification of the first lymph node into which a primary tumor drains. In breast cancer, identification of tumor cells in the SLNs is a predictor of the tumor's metastatic potential. In the present article, we tested the hypotheses that a...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2004
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC468660/ https://www.ncbi.nlm.nih.gov/pubmed/15217509 http://dx.doi.org/10.1186/bcr808 |
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author | Poindexter, Nancy J Sahin, Aysegul Hunt, Kelly K Grimm, Elizabeth A |
author_facet | Poindexter, Nancy J Sahin, Aysegul Hunt, Kelly K Grimm, Elizabeth A |
author_sort | Poindexter, Nancy J |
collection | PubMed |
description | INTRODUCTION: Sentinel lymph node (SLN) biopsy allows identification of the first lymph node into which a primary tumor drains. In breast cancer, identification of tumor cells in the SLNs is a predictor of the tumor's metastatic potential. In the present article, we tested the hypotheses that a positive immune response can occur in tumor-free SLNs and that the activation state of dendritic cells (DCs), the major antigen presenting cells within SLNs, predicts the immune status and metastatic potential of the tumor. METHODS: Fifty paraffin-embedded SLN sections, 25 tumor-free and 25 tumor-containing, from patients with breast cancer were analyzed by immunohistochemistry to determine the immune maturation state of their DCs. In addition, 12 lymph nodes from noncancer-containing breasts were analyzed. Tissues were stained with antibodies against CD3, MHC class II, CD1a, CD83, IL-10, and IL-12. Mature DCs were defined by CD83 expression and immature DCs by CD1a expression. RESULTS: We found a trend toward higher numbers of mature CD83-positive DCs in tumor-free SLNs than in tumor-containing SLNs (P = 0.07). In addition, tumor-free SLNs were more likely to contain cells expressing IL-10 (P = 0.02) and, to a lesser extent, IL-12 (P = 0.12). In contrast, when all SLNs, both tumor-free and tumor-containing, were compared with uninvolved lymph nodes, the numbers of mature and immature DCs were similar. CONCLUSIONS: Our results suggest tumor-free SLNs are immunologically competent and potentially a site of tumor-specific T-cell activation, as evidenced by the presence of greater numbers of mature DCs and cytokine-producing cells in tumor-free SLNs. |
format | Text |
id | pubmed-468660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-4686602004-07-16 Analysis of dendritic cells in tumor-free and tumor-containing sentinel lymph nodes from patients with breast cancer Poindexter, Nancy J Sahin, Aysegul Hunt, Kelly K Grimm, Elizabeth A Breast Cancer Res Research Article INTRODUCTION: Sentinel lymph node (SLN) biopsy allows identification of the first lymph node into which a primary tumor drains. In breast cancer, identification of tumor cells in the SLNs is a predictor of the tumor's metastatic potential. In the present article, we tested the hypotheses that a positive immune response can occur in tumor-free SLNs and that the activation state of dendritic cells (DCs), the major antigen presenting cells within SLNs, predicts the immune status and metastatic potential of the tumor. METHODS: Fifty paraffin-embedded SLN sections, 25 tumor-free and 25 tumor-containing, from patients with breast cancer were analyzed by immunohistochemistry to determine the immune maturation state of their DCs. In addition, 12 lymph nodes from noncancer-containing breasts were analyzed. Tissues were stained with antibodies against CD3, MHC class II, CD1a, CD83, IL-10, and IL-12. Mature DCs were defined by CD83 expression and immature DCs by CD1a expression. RESULTS: We found a trend toward higher numbers of mature CD83-positive DCs in tumor-free SLNs than in tumor-containing SLNs (P = 0.07). In addition, tumor-free SLNs were more likely to contain cells expressing IL-10 (P = 0.02) and, to a lesser extent, IL-12 (P = 0.12). In contrast, when all SLNs, both tumor-free and tumor-containing, were compared with uninvolved lymph nodes, the numbers of mature and immature DCs were similar. CONCLUSIONS: Our results suggest tumor-free SLNs are immunologically competent and potentially a site of tumor-specific T-cell activation, as evidenced by the presence of greater numbers of mature DCs and cytokine-producing cells in tumor-free SLNs. BioMed Central 2004 2004-06-04 /pmc/articles/PMC468660/ /pubmed/15217509 http://dx.doi.org/10.1186/bcr808 Text en Copyright © 2004 Poindexter et al.; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research Article Poindexter, Nancy J Sahin, Aysegul Hunt, Kelly K Grimm, Elizabeth A Analysis of dendritic cells in tumor-free and tumor-containing sentinel lymph nodes from patients with breast cancer |
title | Analysis of dendritic cells in tumor-free and tumor-containing sentinel lymph nodes from patients with breast cancer |
title_full | Analysis of dendritic cells in tumor-free and tumor-containing sentinel lymph nodes from patients with breast cancer |
title_fullStr | Analysis of dendritic cells in tumor-free and tumor-containing sentinel lymph nodes from patients with breast cancer |
title_full_unstemmed | Analysis of dendritic cells in tumor-free and tumor-containing sentinel lymph nodes from patients with breast cancer |
title_short | Analysis of dendritic cells in tumor-free and tumor-containing sentinel lymph nodes from patients with breast cancer |
title_sort | analysis of dendritic cells in tumor-free and tumor-containing sentinel lymph nodes from patients with breast cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC468660/ https://www.ncbi.nlm.nih.gov/pubmed/15217509 http://dx.doi.org/10.1186/bcr808 |
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