| Literature DB >> 33800301 |
Timo Burster1, Fabian Gärtner2, Christiane Bulach2, Anuar Zhanapiya1, Adrian Gihring2, Uwe Knippschild2.
Abstract
Immunotherapy has been established as an important area in the therapy of malignant diseases. Immunogenicity sufficient for immune recognition and subsequent elimination can be bypassed by tumors through altered and/or reduced expression levels of major histocompatibility complex class I (MHC I) molecules. Natural killer (NK) cells can eliminate tumor cells in a MHC I antigen presentation-independent manner by an array of activating and inhibitory receptors, which are promising candidates for immunotherapy. Here we summarize the latest findings in recognizing and regulating MHC I molecules that affect NK cell surveillance of glioblastoma cells.Entities:
Keywords: MHC; NK cells; cathepsin G; immunotherapy; proteases
Year: 2021 PMID: 33800301 PMCID: PMC7998501 DOI: 10.3390/ph14030236
Source DB: PubMed Journal: Pharmaceuticals (Basel) ISSN: 1424-8247