Abstract 216P
Background
A previous pan-cancer single-cell study on the tumor microenvironment (TME), particularly tumor-infiltrating lymphocytes (TILs), highlighted both the heterogeneity and dynamics of various T cell subtypes. However, the spatial heterogeneity of TILs in breast cancer has not been extensively studied. We aimed to investigate the spatial heterogeneity of the TME using spatial transcriptomics.
Methods
We retrospectively collected FFPE samples from five breast cancer cases (2 triple-negative breast cancer [TNBC] with high TILs, 2 TNBC with low TILs, 1 hormone receptor-positive[HR+] breast cancer with TIL high TILs) and performed the Visium Spatial Gene Expression method (10x Genomics). Subsequently, using public TILs single-cell data from a pan-cancer study, we predicted and annotated cell types in each Visium spot (single cell deconvolution). We studied the distribution of T cell subtypes across three layers at 3mm intervals from the most peripheral to the central direction of the tumor.
Results
The distribution of 24 CD4+ subtypes and 17 CD8+ subtypes was examined. In all five cases, the CD8.c.12.Tex.CXCL13 subtype showed a statistically significant increase in cell numbers at the tumor center compared to the periphery. The CD4.c20.Treg.TNFRSF9 subtype displayed a similar trend, with higher cell counts in the tumor center and lower counts in the periphery. Conversely, the CD8.c10.Trm.ZNF683 subtype, a key subtype in the previous pan-cancer study, exhibited varying distribution patterns between cases.
Conclusions
TILs in breast cancer consist of diverse subtypes. Numerical heterogeneity was observed among T cell subtypes, along with spatial heterogeneity between the tumor’s central and peripheral regions. Furthermore, heterogeneity was evident between individual tumors. However, some consistent distribution patterns, such as the CD8.c.12.Tex.CXCL13 population, were also observed across cases. Further studies are needed to determine the clinical significance of this spatial heterogeneity.
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
215P - Differential spatial gene expression and clinicopathologic characteristics are associated with exceptional response to immune checkpoint inhibition in recurrent/metastatic head and neck cancer
Presenter: Niki Gavrielatou
Session: Poster Display session
217P - Tumor-derived CCL15 regulates RNA m6A methylation in cancer-associated fibroblasts to promote hepatocellular carcinoma growth
Presenter: Yueguo Li
Session: Poster Display session
Resources:
Abstract
218P - A novel tumor adenosine signature to guide indication selection for adenosine pathway inhibitors
Presenter: Sophie Dekoninck
Session: Poster Display session
220P - Correlation research between oral flora diversity and radiation-induced stomatitis after postoperative radiotherapy for oral squamous cell carcinoma
Presenter: Qin Zheng
Session: Poster Display session
221P - Chemoradiotherapy induced adaptive anti-tumor T cell immunity in patients with non-small cell lung cancer
Presenter: Yaoyao Xie
Session: Poster Display session
222P - Features of epithelial-to-mesenchymal transition (EMT) and humoral immune response in ulcerated acral melanoma: A transcriptomic and spatial proteomic analysis.
Presenter: Estefania Vazquez
Session: Poster Display session
223P - Frequency of the number of myeloid-derived suppressor cells in patients with lung cancer according to T stage
Presenter: Jelena Vukovic
Session: Poster Display session
224P - Immunological Dynamics in Triple-Negative Breast Cancer: Peripheral Immune Responses to Neoadjuvant Therapy
Presenter: Rita Santos
Session: Poster Display session
225P - Assessment of immune cell populations in the peripheral blood of metastatic prostate cancer
Presenter: Vanessa Patel
Session: Poster Display session