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A summary of current NKG2D-based CAR clinical trials

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...

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Detalles Bibliográficos
Autores principales: Curio, Sophie, Jonsson, Gustav, Marinović, Sonja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8480431/
https://www.ncbi.nlm.nih.gov/pubmed/34604863
http://dx.doi.org/10.1093/immadv/ltab018
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author Curio, Sophie
Jonsson, Gustav
Marinović, Sonja
author_facet Curio, Sophie
Jonsson, Gustav
Marinović, Sonja
author_sort Curio, Sophie
collection PubMed
description 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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spelling pubmed-84804312021-09-30 A summary of current NKG2D-based CAR clinical trials Curio, Sophie Jonsson, Gustav Marinović, Sonja Immunother Adv TrialsWatch 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. Oxford University Press 2021-08-13 /pmc/articles/PMC8480431/ /pubmed/34604863 http://dx.doi.org/10.1093/immadv/ltab018 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Immunology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle TrialsWatch
Curio, Sophie
Jonsson, Gustav
Marinović, Sonja
A summary of current NKG2D-based CAR clinical trials
title A summary of current NKG2D-based CAR clinical trials
title_full A summary of current NKG2D-based CAR clinical trials
title_fullStr A summary of current NKG2D-based CAR clinical trials
title_full_unstemmed A summary of current NKG2D-based CAR clinical trials
title_short A summary of current NKG2D-based CAR clinical trials
title_sort summary of current nkg2d-based car clinical trials
topic TrialsWatch
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8480431/
https://www.ncbi.nlm.nih.gov/pubmed/34604863
http://dx.doi.org/10.1093/immadv/ltab018
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