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Chimeric antigen receptor (CAR)-T cell therapy is a revolutionary new pillar in cancer treatment. Although treatment with CAR-T cells has produced remarkable clinical responses with certain subsets of B cell leukemia or lymphoma, many challenges limit the therapeutic efficacy of CAR-T cells in solid tumors and hematological malignancies. Barriers to effective CAR-T cell therapy include severe life-threatening toxicities, modest anti-tumor activity, antigen escape, restricted trafficking, and limited tumor infiltration. In addition, the host and tumor microenvironment interactions with CAR-T cells critically alter CAR-T cell function. Furthermore, a complex workforce is required to develop and implement these treatments. In order to overcome these significant challenges, innovative strategies and approaches to engineer more powerful CAR-T cells with improved anti-tumor activity and decreased toxicity are necessary. In this review, we discuss recent innovations in CAR-T cell engineering to improve clinical efficacy in both hematological malignancy and solid tumors and strategies to overcome limitations of CAR-T cell therapy in both hematological malignancy and solid tumors.
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Robert C. Sterner
University of Wisconsin–Madison
Rosalie M. Sterner
Mayo Clinic
SHILAP Revista de lepidopterología
Blood Cancer Journal
University of Wisconsin–Madison
Mayo Clinic
Mayo Clinic in Arizona
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Sterner et al. (Tue,) studied this question.
synapsesocial.com/papers/69d71ae5ef370a38abf508b4 — DOI: https://doi.org/10.1038/s41408-021-00459-7
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