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Review
. 2018 Sep;1(2):65-74.
doi: 10.1093/pcmedi/pby011. Epub 2018 Sep 6.

Recent updates on cancer immunotherapy

Affiliations
Review

Recent updates on cancer immunotherapy

Ming Liu et al. Precis Clin Med. 2018 Sep.

Abstract

Traditional cancer therapies include surgery, radiation, and chemotherapy, all of which are typically non-specific approaches. Cancer immunotherapy is a type of cancer treatment that helps the immune system fight cancer. Cancer immunotherapy represents a standing example of precision medicine: immune checkpoint inhibitors precisely target the checkpoints; tumor infiltrating lymphocytes, TCR T cells, and CAR T cells precisely kill cancer cells through tumor antigen recognition; and cancer vaccines are made from patient-derived dendritic cells, tumor cell DNA, or RNA, or oncolytic viruses, thus offering a type of personalized medicine. This review will highlight up-to-date advancement in most, if not all, of the immunotherapy strategies.

Keywords: cancer; immune evasion; immunotherapy.

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Figures

Figure 1.
Figure 1.
Diagram of mechanisms of tumor immune evasion. Tumor cells evade immune responses through a variety of mechanisms: (i) downregulation of antigen processing and presentation machinery and thus antigen presentation (see ↓), (ii) upregulation of PD-L1 on tumor cells and PD-1 on effector T cells (see ↑) and facilitation of binding of PD-L1 and B7-1/2 to PD-1 and CTLA-4, respectively, (iii) secretion of immune suppressive modulators (TGF-β, IL-8, IL-10, IL-18, CSF1, VEGF, gangliosides, ROS, Kynurenines, K+) and metabolites (adenosine, PGE, lactate) into TME, (iv) deprivation of immune activating metabolites (glucose, arginine, glutamine, tryptophan) from TME, (v) recruitment and/or activation of Treg, MDSC and TAM, and (vi) inhibition of effector T cell infiltration.

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References

    1. Gros A, Parkhurst MR, Tran E, et al. . Prospective identification of neoantigen-specific lymphocytes in the peripheral blood of melanoma patients. Nat Med 2016;22:433–8. - PMC - PubMed
    1. Finn OJ. A Believer’s Overview of Cancer Immunosurveillance and Immunotherapy. J Immunol 2018;200:385–91. - PMC - PubMed
    1. Vinay DS, Ryan EP, Pawelec G, et al. . Immune evasion in cancer: Mechanistic basis and therapeutic strategies. Semin Cancer Biol 2015;35:S185–98. - PubMed
    1. Manguso RT, Pope HW, Zimmer MD, et al. . In vivo CRISPR screening identifies Ptpn2 as a cancer immunotherapy target. Nature 2017;547:413–8. - PMC - PubMed
    1. Goel S, DeCristo MJ, Watt AC, et al. . CDK4/6 inhibition triggers anti-tumour immunity. Nature 2017;548:471–5. - PMC - PubMed

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