| Literature DB >> 31176617 |
Hany E Marei1, Asma Althani2, Thomas Caceci3, Roberto Arriga4, Tommaso Sconocchia5, Alessio Ottaviani6, Giulia Lanzilli6, Mario Roselli4, Sara Caratelli6, Carlo Cenciarelli6, Giuseppe Sconocchia6.
Abstract
The chimeric antigen receptor T cell (CAR-T cell) immunotherapy currently represents a hot research trend and it is expected to revolutionize the field of cancer therapy. Promising outcomes have been achieved using CAR-T cell therapy for haematological malignancies. Despite encouraging results, several challenges still pose eminent hurdles before being fully recognized. Directing CAR-T cells to target a single tumour associated antigen (TAA) as the case in haematological malignancies might be much simpler than targeting the extensive inhibitory microenvironments associated with solid tumours. This review focuses on the basic principles involved in development of CAR-T cells, emphasizing the differences between humoral IgG, T-cell receptors, CAR and Fcγ-CR constructs. It also highlights the complex inhibitory network that is usually associated with solid tumours, and tackles recent advances in the clinical studies that have provided great hope for the future use of CAR-T cell immunotherapy. While current Fcγ-CR T cell immunotherapy is in pre-clinical stage, is expected to provide a sound therapeutic approach to add to existing classical chemo- and radio-therapeutic modalities.Entities:
Keywords: CAR T cells; Fcγ-CR T cell; Hematological malignancies; Immunotherapy; Solid cancers
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Year: 2019 PMID: 31176617 DOI: 10.1016/j.bcp.2019.06.002
Source DB: PubMed Journal: Biochem Pharmacol ISSN: 0006-2952 Impact factor: 5.858