» Articles » PMID: 38638377

Treatment Options for Hepatocellular Carcinoma Using Immunotherapy: Present and Future

Overview
Specialty Gastroenterology
Date 2024 Apr 19
PMID 38638377
Authors
Affiliations
Soon will be listed here.
Abstract

Hepatocellular carcinoma (HCC) is a common cancer, and the body's immune responses greatly affect its progression and the prognosis of patients. Immunological suppression and the maintenance of self-tolerance in the tumor microenvironment are essential responses, and these form part of the theoretical foundations of immunotherapy. In this review, we first discuss the tumor microenvironment of HCC, describe immunosuppression in HCC, and review the major biomarkers used to track HCC progression and response to treatment. We then examine antibody-based therapies, with a focus on immune checkpoint inhibitors (ICIs), monoclonal antibodies that target key proteins in the immune response (programmed cell death protein 1, anti-cytotoxic T-lymphocyte associated protein 4, and programmed death-ligand 1) which have transformed the treatment of HCC and other cancers. ICIs may be used alone or in conjunction with various targeted therapies for patients with advanced HCC who are receiving first-line treatments or subsequent treatments. We also discuss the use of different cellular immunotherapies, including T cell receptor (TCR) T cell therapy and chimeric antigen receptor (CAR) T cell therapy. We then review the use of HCC vaccines, adjuvant immunotherapy, and oncolytic virotherapy, and describe the goals of future research in the development of treatments for HCC.

Citing Articles

Advancements in Immunotherapeutic Treatments for Hepatocellular Carcinoma: Potential of Combination Therapies.

Zarlashat Y, Mushtaq H, Pham L, Abbas W, Sato K Int J Mol Sci. 2024; 25(13).

PMID: 38999940 PMC: 11241106. DOI: 10.3390/ijms25136830.

References
1.
Buonaguro F, Buonaguro L . Cancer vaccines for hepatocellular carcinoma: future directions. Immunotherapy. 2016; 8(4):391-3. DOI: 10.2217/imt-2015-0018. View

2.
Schirrmacher V . Oncolytic Newcastle disease virus as a prospective anti-cancer therapy. A biologic agent with potential to break therapy resistance. Expert Opin Biol Ther. 2015; 15(12):1757-71. DOI: 10.1517/14712598.2015.1088000. View

3.
Takakura K, Kajihara M, Ito Z, Ohkusa T, Gong J, Koido S . Dendritic-tumor fusion cells in cancer immunotherapy. Discov Med. 2015; 19(104):169-74. View

4.
Prieto J, Melero I, Sangro B . Immunological landscape and immunotherapy of hepatocellular carcinoma. Nat Rev Gastroenterol Hepatol. 2015; 12(12):681-700. DOI: 10.1038/nrgastro.2015.173. View

5.
Du X, Tang F, Liu M, Su J, Zhang Y, Wu W . A reappraisal of CTLA-4 checkpoint blockade in cancer immunotherapy. Cell Res. 2018; 28(4):416-432. PMC: 5939050. DOI: 10.1038/s41422-018-0011-0. View