Nalazite se na CroRIS probnoj okolini. Ovdje evidentirani podaci neće biti pohranjeni u Informacijskom sustavu znanosti RH. Ako je ovo greška, CroRIS produkcijskoj okolini moguće je pristupi putem poveznice www.croris.hr
izvor podataka: crosbi

A summary of current NKG2D-based CAR clinical trials (CROSBI ID 300804)

Prilog u časopisu | pregledni rad (znanstveni) | međunarodna recenzija

(young European Federation of Immunological Societies (yEFIS)) Curio, Sophie ; Jonsson, Gustav ; Marinović, Sonja A summary of current NKG2D-based CAR clinical trials // Immunotherapy advances, 1 (2021), 1; ltab018, 8. doi: 10.1093/immadv/ltab018

Podaci o odgovornosti

Curio, Sophie ; Jonsson, Gustav ; Marinović, Sonja

young European Federation of Immunological Societies (yEFIS)

engleski

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. 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.

NKG2D ; CAR T cells ; immunotherapy ; adoptive cell transfer

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o izdanju

1 (1)

2021.

ltab018

8

objavljeno

2732-4303

10.1093/immadv/ltab018

Povezanost rada

Biologija

Poveznice