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A summary of current NKG2D-based CAR clinical trials
Author(s) -
Sophie Curio,
Gustav Jonsson,
Sonja Marinović
Publication year - 2021
Publication title -
immunotherapy advances
Language(s) - English
Resource type - Journals
ISSN - 2732-4303
DOI - 10.1093/immadv/ltab018
Subject(s) - nkg2d , chimeric antigen receptor , immune system , immunotherapy , clinical trial , cancer immunotherapy , tumor cells , antigen , cancer , medicine , cancer research , immunology , immunity , biology , bioinformatics , cytotoxic t cell , in vitro , biochemistry
Summary Cancer immunotherapies have significantly improved patient survival and treatment options in recent years. Nonetheless, the success of immunotherapy is limited to certain cancer types and specific subgroups of patients, making the development of new therapeutic approaches a topic of ongoing research. Chimeric antigen receptor (CAR) cells are engineered immune cells that are programmed to specifically eliminate cancer cells. Ideally, a CAR recognizes antigens that are restricted to tumor cells to avoid off-target effects. NKG2D is an activating immunoreceptor and an important player in anti-tumor immunity due to its ability to recognize tumor cells and initiate an anti-tumor immune response. Ligands for NKG2D are expressed on malignant or stressed cells and typically absent from healthy tissue, making it a promising CAR candidate. Here, we provide a summary of past and ongoing NKG2D-based CAR clinical trials and comment on potential pitfalls.

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