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Harnessing NK cells for cancer immunotherapy: immune checkpoint receptors and chimeric antigen receptors
Authors:Nayoung Kim  Dong-Hee Lee  Woo Seon Choi  Eunbi Yi  HyoJeong Kim  Jung Min Kim  Hyung-Seung Jin  Hun Sik Kim
Institution:1.Department of Convergence Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea;2.Asan Institute for Life Sciences, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea;3.Department of Biomedical Sciences, Seoul 05505, Korea;4.Stem Cell Immunomodulation Research Center (SCIRC), Seoul 05505, Korea;5.Department of Microbiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea
Abstract:Natural killer (NK) cells, key antitumor effectors of the innate immune system, are endowed with the unique ability to spontaneously eliminate cells undergoing a neoplastic transformation. Given their broad reactivity against diverse types of cancer and close association with cancer prognosis, NK cells have gained considerable attention as a promising therapeutic target for cancer immunotherapy. NK cell-based therapies have demonstrated favorable clinical efficacies in several hematological malignancies but limited success in solid tumors, thus highlighting the need to develop new therapeutic strategies to restore and optimize antitumor activity while preventing tumor immune escape. The current therapeutic modalities yielding encouraging results in clinical trials include the blockade of immune checkpoint receptors to overcome the immune-evasion mechanism used by tumors and the incorporation of tumor-directed chimeric antigen receptors to enhance NK cell antitumor specificity and activity. These observations, together with recent advances in the understanding of NK cell activation within the tumor microenvironment, will facilitate the optimal design of NK cell-based therapy against a broad range of cancers and, more desirably, refractory cancers.
Keywords:Cancer immunotherapy  Chimeric antigen receptors  Im-mune checkpoint receptors  Immune escape  Natural killer cells
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