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Advances in CAR-NK cell therapy for lung cancer: is it a better choice in the future?
Liu, Fengqin; Miao, Xia; Han, Lu; Song, Xiao.
Afiliação
  • Liu F; The Third Department of Geriatrics, Weifang People's Hospital, Weifang, Shandong, China.
  • Miao X; Central Supply Service Department (CSSD), Weifang People's Hospital, Weifang, Shandong, China.
  • Han L; The Third Department of Geriatrics, Weifang People's Hospital, Weifang, Shandong, China.
  • Song X; Department of Gastroenterology, Weifang People's Hospital, Weifang, Shandong, China.
Front Oncol ; 14: 1390006, 2024.
Article em En | MEDLINE | ID: mdl-38863635
ABSTRACT
Lung cancer remains one of the leading causes of cancer-related mortality worldwide necessitating the development of innovative therapeutic strategies. Chimeric antigen receptor (CAR) natural killer (NK) cell therapy represents a promising advancement in the field of oncology offering a novel approach to target and eliminate tumor cells with high specificity and reduced risk of immune-related adverse effects. This paper reviews the mechanism, potential targets, and recent advances in CAR-NK cell therapy for lung cancer, including the design and engineering of CAR-NK cells, preclinical studies, and the outcomes of early-phase clinical trials. We highlight the unique advantages of using NK cells, such as their innate ability to recognize and kill cancer cells and their reduced potential for inducing graft-versus-host disease (GvHD) and cytokine release syndrome (CRS) compared to CAR T-cell therapies. Results from recent studies demonstrate significant antitumor activity in lung cancer models with improved targeting and persistence of CAR-NK cells observed in vitro and in vivo. Finally, we discuss the challenges in optimizing CAR-NK cell therapies, including the potential resistance mechanisms. The paper concludes with an outlook on the future directions of CAR-NK cell research and its implications for lung cancer treatment emphasizing the importance of continued innovation and collaboration in the field.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article