Single-cell RNA sequencing shows the immunosuppressive landscape and tumor heterogeneity of HBV-associated hepatocellular carcinoma

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作者
Daniel Wai-Hung Ho
Yu-Man Tsui
Lo-Kong Chan
Karen Man-Fong Sze
Xin Zhang
Jacinth Wing-Sum Cheu
Yung-Tuen Chiu
Joyce Man-Fong Lee
Albert Chi-Yan Chan
Elaine Tin-Yan Cheung
Derek Tsz-Wai Yau
Nam-Hung Chia
Irene Lai-Oi Lo
Pak-Chung Sham
Tan-To Cheung
Carmen Chak-Lui Wong
Irene Oi-Lin Ng
机构
[1] The University of Hong Kong,Department of Pathology
[2] The University of Hong Kong,State Key Laboratory of Liver Research
[3] The University of Hong Kong,Department of Surgery
[4] Queen Elizabeth Hospital,Department of Pathology
[5] Queen Elizabeth Hospital,Department of Surgery
[6] The University of Hong Kong,Department of Psychiatry
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Interaction between tumor cells and immune cells in the tumor microenvironment is important in cancer development. Immune cells interact with the tumor cells to shape this process. Here, we use single-cell RNA sequencing analysis to delineate the immune landscape and tumor heterogeneity in a cohort of patients with HBV-associated human hepatocellular carcinoma (HCC). We found that tumor-associated macrophages suppress tumor T cell infiltration and TIGIT-NECTIN2 interaction regulates the immunosuppressive environment. The cell state transition of immune cells towards a more immunosuppressive and exhaustive status exemplifies the overall cancer-promoting immunocellular landscape. Furthermore, the heterogeneity of global molecular profiles reveals co-existence of intra-tumoral and inter-tumoral heterogeneity, but is more apparent in the latter. This analysis of the immunosuppressive landscape and intercellular interactions provides mechanistic information for the design of efficacious immune-oncology treatments in hepatocellular carcinoma.
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