BACKGROUND: Hepatocellular carcinoma (HCC) is the sixth most common malignancy worldwide with a high mortality. The available treatment options are limited, thus the development of new therapeutic approaches is of a high clinical significance. KEY MESSAGES: The immune system plays a central role in the pathogenesis of HCC by supporting tumor growth, tumor survival, angiogenesis and the development of vascular infiltration and metastasis. In contrast, the immune system also exhibits a protective role in tumor surveillance, and specific CD8+ T-cells can be detected for various tumor-associated antigens. However, antitumoral potential of the immune system is limited by various inhibitory mechanisms, for example, an impaired priming and activation of CD8+ T-cells, inhibitory cells (e.g., regulatory T-cells) or the expression of inhibitory receptors (e.g., programmed cell death-1 and cytotoxic T-lymphocyte antigen-4). Immunotherapeutic strategies addressing these inhibitory mechanisms, for example, by providing a source of tumor antigens, depleting immunosuppressive cells or blocking inhibitory receptors, aim to induce and boost naturally occurring antitumoral immune responses. CONCLUSION: HCC is a tumor with a high incidence and mortality in developing countries as well as in the Western world. Due to the immune system's central role in the pathogenesis and surveillance of HCC, immunotherapy is a new treatment option that has yielded first promising results.
BACKGROUND:Hepatocellular carcinoma (HCC) is the sixth most common malignancy worldwide with a high mortality. The available treatment options are limited, thus the development of new therapeutic approaches is of a high clinical significance. KEY MESSAGES: The immune system plays a central role in the pathogenesis of HCC by supporting tumor growth, tumor survival, angiogenesis and the development of vascular infiltration and metastasis. In contrast, the immune system also exhibits a protective role in tumor surveillance, and specific CD8+ T-cells can be detected for various tumor-associated antigens. However, antitumoral potential of the immune system is limited by various inhibitory mechanisms, for example, an impaired priming and activation of CD8+ T-cells, inhibitory cells (e.g., regulatory T-cells) or the expression of inhibitory receptors (e.g., programmed cell death-1 and cytotoxic T-lymphocyte antigen-4). Immunotherapeutic strategies addressing these inhibitory mechanisms, for example, by providing a source of tumor antigens, depleting immunosuppressive cells or blocking inhibitory receptors, aim to induce and boost naturally occurring antitumoral immune responses. CONCLUSION: HCC is a tumor with a high incidence and mortality in developing countries as well as in the Western world. Due to the immune system's central role in the pathogenesis and surveillance of HCC, immunotherapy is a new treatment option that has yielded first promising results.
Authors: Luzie A Doemel; Jessica G Santana; Lynn J Savic; Fabian M Laage Gaupp; Tabea Borde; Alexandra Petukhova-Greenstein; Ahmet S Kucukkaya; Isabel T Schobert; Charlie A Hamm; Bernhard Gebauer; John J Walsh; Irvin Rexha; Fahmeed Hyder; MingDe Lin; David C Madoff; Todd Schlachter; Julius Chapiro; Daniel Coman Journal: Eur Radiol Date: 2021-10-31 Impact factor: 7.034
Authors: Itziar Otano; David Escors; Anna Schurich; Harsimran Singh; Francis Robertson; Brian R Davidson; Giuseppe Fusai; Frederick A Vargas; Zhi M D Tan; Jia Y J Aw; Navjyot Hansi; Patrick T F Kennedy; Shao-An Xue; Hans J Stauss; Antonio Bertoletti; Andrea Pavesi; Mala K Maini Journal: Mol Ther Date: 2018-08-16 Impact factor: 11.454
Authors: Nicholas J W Easom; Kerstin A Stegmann; Leo Swadling; Laura J Pallett; Alice R Burton; Dennis Odera; Nathalie Schmidt; Wei-Chen Huang; Giuseppe Fusai; Brian Davidson; Mala K Maini Journal: Front Immunol Date: 2018-05-09 Impact factor: 8.786