4.8 Review

Natural Killer Cells and Regulatory T Cells Cross Talk in Hepatocellular Carcinoma: Exploring Therapeutic Options for the Next Decade

Journal

FRONTIERS IN IMMUNOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.643310

Keywords

liver; NK cells; regulatory T cells; hepatocellular carcinoma; tumour microenvironment; GMP cell therapy

Categories

Funding

  1. Sir Jules Thorn Trust Biomedical Research Grant
  2. Transbioline Innovative Medicine Initiative Research Grant
  3. Medical Research Foundation from the The Medical Research Council [M019829, S009338]
  4. CRUK (HUNTER accelerator award) the NIHR Birmingham BRC
  5. NIHR Southampton BRC
  6. Queen Elizabeth Hospital Birmingham Charity

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Despite advancements in immunotherapy, treating HCC remains challenging. Research is needed to develop novel NK cell-targeted immunotherapy and control Treg frequency and function in HCC. Combining GMP-NK cell immunotherapy with CPI targeting NK and CD8 T cells may offer a promising therapeutic option.
Despite major advances in immunotherapy, hepatocellular carcinoma (HCC) remains a challenging target. Natural Killer (NK) cells are crucial components of the anti-HCC immune response, which can be manipulated for immunotherapeutic benefit as primary targets, modulators of the tumour microenvironment and in synchronising with tumour antigen specific effector CD8 cells for tumour clearance. Regulatory T cells shape the anti-tumour response from effector T cells via multiple suppressive mechanisms. Future research is needed to address the development of novel NK cell-targeted immunotherapy and on restraining Treg frequency and function in HCC. We have now entered a new era of anti-cancer treatment using checkpoint inhibitor (CPI)-based strategies. Combining GMP-NK cell immunotherapy to enhance the frequency of NK cells with CPI targeting both NK and CD8 T cells to release co-inhibitory receptors and enhance the cells anti-tumour immunity of HCC would be an attractive therapeutic option in the treatment of HCC. These therapeutic approaches should now be complemented by the application of genomic, proteomic and metabolomic approaches to understanding the microenvironment of HCC which, together with deep immune profiling of peripheral blood and HCC tissue before and during treatment, will provide the much-needed personalised medicine approach required to improve clinical outcomes for patients with HCC.

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