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Predictive Immune Modeling of Solid Tumors
Published on: February 25, 2020
Cancer immunotherapy: special issue of BMB Reports in 2021
1Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Korea.
Abstract:
Basically, cancer is a disease initiated by mutations in the genome. However, cancer is regarded not only as a genetical disease but also an immunological disease because cancer cells can be targeted by the immune system. The immune system recognizes mutated proteins as non-self, foreign antigens, so-called neoantigens, and exerts diverse effector functions to eliminate tumor cells. Anti-tumor immune responses resemble immune responses against viruses. In anti-tumor immune responses, CD8+ and CD4+ T cells are the main effector cells. In addition, dendritic cells (DCs) play a crucial role in the priming of CD8+ and CD4+ T cells, and natural killer (NK) cells also contribute to the anti-tumor immune responses. Recently, immune checkpoint inhibitors (ICIs), including antibodies against cytotoxic T-lymphocyte-associated protein 4 (CTLA- 4), programmed cell death 1 (PD-1), and programmed cell death ligand 1 (PD-L1), became available for the treatment of various types of cancer. Moreover, chimeric antigenic receptor (CAR)-T cells have been successfully used to treat hematologic malignancies. However, current cancer immunotherapy has some limitations. ICIs fail to control tumors in a considerable proportion of cancer patients and CAR-T cell therapy does not effectively control solid tumors. To overcome these limitations, further research and development are required. In the current issue of BMB Reports, seven review articles in the field of cancer immunotherapy were published. [BMB Reports 2021; 54(1): 1-1].
Insights
Cancer immunotherapy harnesses the immune system to fight tumors by targeting mutated neoantigens. While effective, limitations in immune checkpoint inhibitors and CAR-T cell therapies necessitate further research for broader cancer treatment.
Area of Science:
- Immunology
- Oncology
- Genetics
Background:
- Cancer arises from genomic mutations, but is also an immunological disease where the immune system targets cancer cells.
- The immune system recognizes tumor-specific neoantigens, activating effector cells like CD8+ and CD4+ T cells, dendritic cells (DCs), and natural killer (NK) cells.
Discussion:
- Immune checkpoint inhibitors (ICIs) targeting CTLA-4, PD-1, and PD-L1, and chimeric antigen receptor (CAR)-T cell therapies have shown success in treating certain cancers.
- Current immunotherapies face limitations, with ICIs ineffective in many patients and CAR-T cell therapy struggling with solid tumors.
Key Insights:
- Cancer immunotherapy leverages the immune system's ability to identify and eliminate tumor cells via neoantigen recognition.
- T cells (CD8+ and CD4+) are key effectors, supported by DCs and NK cells in anti-tumor responses.
Outlook:
- Overcoming current limitations in cancer immunotherapy requires continued research and development.
- This collection of reviews in BMB Reports highlights advancements and future directions in the field of cancer immunotherapy.
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