| Literature DB >> 36167831 |
Duc Huynh1, Pia Winter1, Florian Märkl1, Stefan Endres1,2,3, Sebastian Kobold4,5,6.
Abstract
The clinical use of cellular immunotherapies is gaining momentum and the number of approved indications is steadily increasing. One class of cellular therapies-chimeric antigen receptor (CAR)-modified T cells-has achieved impressive results in distinct blood cancer indications. These existing cellular therapies treating blood cancers face significant relapse rates, and their application beyond hematology has been underwhelming, especially in solid oncology. Major reasons for resistance source largely in the tumor microenvironment (TME). The TME in fact functionally suppresses, restricts, and excludes adoptive immune cells, which limits the efficacy of cellular immunotherapies from the onset. Many promising efforts are ongoing to adapt cellular immunotherapies to address these obstacles, with the aim of reshaping the tumor microenvironment to ameliorate function and to achieve superior efficacy against both hematological and solid malignancies.Entities:
Keywords: CAR-T cells; Cellular immunotherapy; Cytokine; Inflammation; Stroma; Tumor microenvironment
Year: 2022 PMID: 36167831 DOI: 10.1007/s00281-022-00962-4
Source DB: PubMed Journal: Semin Immunopathol ISSN: 1863-2297 Impact factor: 11.759