Tumor-infiltrating B cells and T cells correlate with postoperative prognosis in triple-negative carcinoma of the breast

Abstract Background In this study, we investigated CD20+ TILs in triple-negative breast cancer (TNBC) and their relationship with T lymphocyte subsets (CD4+, CD8+, CD25+, and FOXP3+), including their combined prognostic value using an immunohistochemical staining method. Methods We investigated 107...

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Main Authors: Hajime Kuroda, Tsengelmaa Jamiyan, Rin Yamaguchi, Akinari Kakumoto, Akihito Abe, Oi Harada, Atsuko Masunaga
Format: Article
Language:English
Published: BMC 2021-03-01
Series:BMC Cancer
Subjects:
Online Access:https://doi.org/10.1186/s12885-021-08009-x
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author Hajime Kuroda
Tsengelmaa Jamiyan
Rin Yamaguchi
Akinari Kakumoto
Akihito Abe
Oi Harada
Atsuko Masunaga
author_facet Hajime Kuroda
Tsengelmaa Jamiyan
Rin Yamaguchi
Akinari Kakumoto
Akihito Abe
Oi Harada
Atsuko Masunaga
author_sort Hajime Kuroda
collection DOAJ
description Abstract Background In this study, we investigated CD20+ TILs in triple-negative breast cancer (TNBC) and their relationship with T lymphocyte subsets (CD4+, CD8+, CD25+, and FOXP3+), including their combined prognostic value using an immunohistochemical staining method. Methods We investigated 107 patients with TNBC for whom a full-face section stained by hematoxylin and eosin between 2006 and 2018 at Dokkyo Medical University Hospital was available. Results The strongest association of infiltrating CD20+ TILs was with CD4+ TILs. There was a significant relationship between CD20+ and CD4+ TILs (r = 0.177; p < 0.001), CD8+ TILs (r = 0.085; p = 0.002), and FOXP3+ TILs (r = 0.0043; p = 0.032). No significant relationships were observed between the CD20+ and CD25+ TILs (r = 0.012; p = 0.264). Multivariate analysis revealed that only the CD20+/FOXP3 ratio was an independent factor for relapse-free survival (p < 0.001) and overall survival (p < 0.001). Patients with tumors highly infiltrated by CD4+, CD8+, and CD20+ TILs had a good prognosis. In contrast, those with tumors weakly infiltrated by CD20+ TILs but highly infiltrated by CD25+ and FOXP3+ TILs had a poor prognosis. Conclusions CD20+ TILs may support an increase in CD4+ and CD8+ TILs, which altered the anti-tumor response, resulting in a positive prognosis. CD20+ TILs correlated with FOXP3+ Treg lymphocytes, which were reported to be correlated with a poor prognosis. Our study suggested that TIL-B cells have dual and conflicting roles in TIL-T immune reactions in TNBC.
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spelling doaj.art-162ca5d5a81a4077be0deae2afc3dc992022-12-21T21:30:06ZengBMCBMC Cancer1471-24072021-03-0121111010.1186/s12885-021-08009-xTumor-infiltrating B cells and T cells correlate with postoperative prognosis in triple-negative carcinoma of the breastHajime Kuroda0Tsengelmaa Jamiyan1Rin Yamaguchi2Akinari Kakumoto3Akihito Abe4Oi Harada5Atsuko Masunaga6Department of Diagnostic Pathology, Tokyo Women’s Medical University, Medical Center EastDepartment of Diagnostic Pathology, Dokkyo Medical UniversityDepartment of Pathology & Laboratory Medicine, Kurume University Medical CenterDepartment of Diagnostic Pathology, Tokyo Women’s Medical University, Medical Center EastBreast Center, Dokkyo Medical UniversityBreast center, Showa UniversityDepartment of Diagnostic Pathology, Tokyo Women’s Medical University, Medical Center EastAbstract Background In this study, we investigated CD20+ TILs in triple-negative breast cancer (TNBC) and their relationship with T lymphocyte subsets (CD4+, CD8+, CD25+, and FOXP3+), including their combined prognostic value using an immunohistochemical staining method. Methods We investigated 107 patients with TNBC for whom a full-face section stained by hematoxylin and eosin between 2006 and 2018 at Dokkyo Medical University Hospital was available. Results The strongest association of infiltrating CD20+ TILs was with CD4+ TILs. There was a significant relationship between CD20+ and CD4+ TILs (r = 0.177; p < 0.001), CD8+ TILs (r = 0.085; p = 0.002), and FOXP3+ TILs (r = 0.0043; p = 0.032). No significant relationships were observed between the CD20+ and CD25+ TILs (r = 0.012; p = 0.264). Multivariate analysis revealed that only the CD20+/FOXP3 ratio was an independent factor for relapse-free survival (p < 0.001) and overall survival (p < 0.001). Patients with tumors highly infiltrated by CD4+, CD8+, and CD20+ TILs had a good prognosis. In contrast, those with tumors weakly infiltrated by CD20+ TILs but highly infiltrated by CD25+ and FOXP3+ TILs had a poor prognosis. Conclusions CD20+ TILs may support an increase in CD4+ and CD8+ TILs, which altered the anti-tumor response, resulting in a positive prognosis. CD20+ TILs correlated with FOXP3+ Treg lymphocytes, which were reported to be correlated with a poor prognosis. Our study suggested that TIL-B cells have dual and conflicting roles in TIL-T immune reactions in TNBC.https://doi.org/10.1186/s12885-021-08009-xBreastTriple-negative cancerTumor-infiltrating B lymphocytesTumor-infiltrating T lymphocytes
spellingShingle Hajime Kuroda
Tsengelmaa Jamiyan
Rin Yamaguchi
Akinari Kakumoto
Akihito Abe
Oi Harada
Atsuko Masunaga
Tumor-infiltrating B cells and T cells correlate with postoperative prognosis in triple-negative carcinoma of the breast
BMC Cancer
Breast
Triple-negative cancer
Tumor-infiltrating B lymphocytes
Tumor-infiltrating T lymphocytes
title Tumor-infiltrating B cells and T cells correlate with postoperative prognosis in triple-negative carcinoma of the breast
title_full Tumor-infiltrating B cells and T cells correlate with postoperative prognosis in triple-negative carcinoma of the breast
title_fullStr Tumor-infiltrating B cells and T cells correlate with postoperative prognosis in triple-negative carcinoma of the breast
title_full_unstemmed Tumor-infiltrating B cells and T cells correlate with postoperative prognosis in triple-negative carcinoma of the breast
title_short Tumor-infiltrating B cells and T cells correlate with postoperative prognosis in triple-negative carcinoma of the breast
title_sort tumor infiltrating b cells and t cells correlate with postoperative prognosis in triple negative carcinoma of the breast
topic Breast
Triple-negative cancer
Tumor-infiltrating B lymphocytes
Tumor-infiltrating T lymphocytes
url https://doi.org/10.1186/s12885-021-08009-x
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