Intratumoural immune heterogeneity as a hallmark of tumour evolution and progression in hepatocellular carcinoma

Author:

Nguyen Phuong H. D.,Ma SimingORCID,Phua Cheryl Z. J.,Kaya Neslihan A.ORCID,Lai Hannah L. H.,Lim Chun Jye,Lim Jia Qi,Wasser Martin,Lai Liyun,Tam Wai LeongORCID,Lim Tony K. H.,Wan Wei Keat,Loh Tracy,Leow Wei Qiang,Pang Yin Huei,Chan Chung Yip,Lee Ser Yee,Cheow Peng Chung,Toh Han Chong,Ginhoux FlorentORCID,Iyer Shridhar,Kow Alfred W. C.,Young Dan Yock,Chung Alexander,Bonney Glen K.,Goh Brian K. P.,Albani SalvatoreORCID,Chow Pierce K. H.ORCID,Zhai Weiwei,Chew ValerieORCID

Abstract

AbstractThe clinical relevance of immune landscape intratumoural heterogeneity (immune-ITH) and its role in tumour evolution remain largely unexplored. Here, we uncover significant spatial and phenotypic immune-ITH from multiple tumour sectors and decipher its relationship with tumour evolution and disease progression in hepatocellular carcinomas (HCC). Immune-ITH is associated with tumour transcriptomic-ITH, mutational burden and distinct immune microenvironments. Tumours with low immune-ITH experience higher immunoselective pressure and escape via loss of heterozygosity in human leukocyte antigens and immunoediting. Instead, the tumours with high immune-ITH evolve to a more immunosuppressive/exhausted microenvironment. This gradient of immune pressure along with immune-ITH represents a hallmark of tumour evolution, which is closely linked to the transcriptome-immune networks contributing to disease progression and immune inactivation. Remarkably, high immune-ITH and its transcriptomic signature are predictive for worse clinical outcome in HCC patients. This in-depth investigation of ITH provides evidence on tumour-immune co-evolution along HCC progression.

Funder

MOH | National Medical Research Council

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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