| Literature DB >> 35202772 |
Parvin Akbari1, Afroditi Katsarou1, Roxanna Daghighian1, Lotte W H G van Mil1, Elisabeth J M Huijbers1, Arjan W Griffioen2, Judy R van Beijnum3.
Abstract
For successful application of chimeric antigen receptor (CAR) T cell therapy in solid tumors, major hurdles have to be overcome. CAR T cells have to cross the vascular barrier, which is hampered by the anergic state of the tumor vasculature, characterized by suppressed levels of leukocyte adhesion molecules on the endothelium. Additional immunosuppressive mechanisms in the solid tumor microenvironment can affect infiltration, activity and persistence of CAR T cells. Redirecting CAR T cells towards the tumor vasculature poses a possible solution, as molecular targets of tumor endothelial cells can be directly engaged from within the blood. In this review, we discuss recent advances in CAR T cell therapy against solid tumors, with a focus on targeting the tumor vasculature. Furthermore, we discuss opportunities to overcome challenges and barriers through engineering of CAR T cells to enhance trafficking, safety and efficacy.Entities:
Keywords: Angiogenesis; CAR T cell; Cancer; Immune suppression; Tumor microenvironment
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Year: 2022 PMID: 35202772 DOI: 10.1016/j.bbcan.2022.188701
Source DB: PubMed Journal: Biochim Biophys Acta Rev Cancer ISSN: 0304-419X Impact factor: 11.414