| Literature DB >> 33322408 |
Piamsiri Sawaisorn1, Korakot Atjanasuppat1, Usanarat Anurathapan1, Somchai Chutipongtanate2,3,4, Suradej Hongeng1.
Abstract
Chimeric antigen receptors (CARs) are among the curative immunotherapeutic approaches that exploit the antigen specificity and cytotoxicity function of potent immune cells against cancers. Neuroblastomas, the most common extracranial pediatric solid tumors with diverse characteristics, could be a promising candidate for using CAR therapies. Several methods harness CAR-modified cells in neuroblastoma to increase therapeutic efficiency, although the assessment has been less successful. Regarding the improvement of CARs, various trials have been launched to overcome insufficient capacity. However, the reasons behind the inadequate response against neuroblastoma of CAR-modified cells are still not well understood. It is essential to update the present state of comprehension of CARs to improve the efficiency of CAR therapies. This review summarizes the crucial features of CARs and their design for neuroblastoma, discusses challenges that impact the outcomes of the immunotherapeutic competence, and focuses on devising strategies currently being investigated to improve the efficacy of CARs for neuroblastoma immunotherapy.Entities:
Keywords: CAR T cells; immunotherapy; pediatric neuroblastoma; strategy
Year: 2020 PMID: 33322408 PMCID: PMC7768386 DOI: 10.3390/vaccines8040753
Source DB: PubMed Journal: Vaccines (Basel) ISSN: 2076-393X