Tertiary lymphoid structures and associated plasma cells play an important role in the biology of triple-negative breast cancers

三阴性乳腺癌 CD38 等离子体电池 CD20 病理 乳腺癌 间质细胞 免疫组织化学 B细胞 生物 癌症 医学 抗体 内科学 癌症研究 免疫学 川地34 骨髓 细胞生物学 干细胞
作者
Dominique Yuan Bin Seow,Joe Yeong,Johnathan Xiande Lim,Noel Chia,Jeffrey Chun Tatt Lim,Clara Chong Hui Ong,Puay Hoon Tan,Jabed Iqbal
出处
期刊:Breast Cancer Research and Treatment [Springer Science+Business Media]
卷期号:180 (2): 369-377 被引量:52
标识
DOI:10.1007/s10549-020-05548-y
摘要

Triple-negative breast cancers (TNBC) are aggressive tumours that exhibit abundant lymphoid infiltrates which modulate tumour behaviour. Recent findings suggest that TNBC with higher densities of plasma cells are associated with a favourable prognosis, and tertiary lymphoid structures (TLS) have prognostic significance. Here, we studied the phenotype and function of plasma cells in TNBCs by assessing their association with IgG Kappa light chain expression, B cells, and TLS. A retrospective analysis of 269 TNBC cases was performed. Tumour-infiltrating CD38+ plasma cells, CD20+ B cells, and TLS were evaluated on conventional haematoxylin–eosin-stained and immunohistochemical-stained sections of TNBC. We then selected TNBC cases demonstrating the highest and lowest densities of plasma cells, and examined their association with TLS, B cells, as well as immunoglobulin expression using Opal-Vectra multiplex immunofluorescence (IF). TNBC with high density of plasma cells showed significantly higher numbers of IgG Kappa+ CD38+ cells (p = 0.0089, p < 0.0001), and higher numbers of TLS (p < 0.0001), compared to TNBC with low density of plasma cells. TNBC with high density of plasma cells also showed higher numbers of CD20+ B cells in the tumour core (p < 0.0001), invasive margin (p < 0.0001), as well as stromal (p = 0.015) compartments. TNBC with high density of plasma cells are associated with higher numbers of IgG Kappa+ CD38+ cells, CD20+ B cells, and TLS. Further studies to characterize the function of plasma cell infiltrates and how they may interact with other tumour-infiltrating lymphocytes and TLS in TNBC may help improve existing immunotherapy strategies.
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