趋化因子受体
头颈部鳞状细胞癌
免疫系统
生物
C-C趋化因子受体6型
CCL21型
CXCR3型
趋化因子
CXCR5型
癌症研究
受体
细胞生物学
免疫学
癌症
头颈部癌
遗传学
生物化学
作者
Boxin Zhang,Hao Li,Yuan‐Tong Liu,Dian Xiong,Lu Zhang,Zhi‐Jun Sun
出处
期刊:Cancer Letters
[Elsevier]
日期:2023-02-24
卷期号:558: 216105-216105
被引量:13
标识
DOI:10.1016/j.canlet.2023.216105
摘要
Tertiary lymphoid structures (TLSs) are organized aggregates of immune cells associated with favourable prognosis and response to immunotherapy in cancer, but the immune architecture of TLSs remains poorly elucidated. Here, we hypothesize that the spatial architecture of leukocytes in TLSs can be reconstructed de novo, at least partially, by cell-inherent chemokine receptors profiles. Single-cell RNA-sequencing (scRNA-seq) revealed 47 subpopulations of leukocytes in head and neck squamous cell carcinoma (HNSC). Combined with bulk RNA-seq, we observed that CXCR3, CCR7, CCR6, CXCR5, and CCR1 are TLS-associated chemokine receptors. According to the spatial reference, the cellular atlas with TLS-associated chemokine receptors in HNSC TLSs was elaborately portrayed by multiplex immunohistochemistry (mIHC). Subsequently, we explored the functions and evolutionary trajectory of cells distributed in TLSs. Our investigation presents an approach to reconstructing the immune architecture of TLSs, which would help boost the antitumor immune response by inducing neogenesis TLSs in HNSC.
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