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• W2968140570 abstract "Immunotherapy has emerged as a potent alternative for cancer treatment, unfortunately, the clinical benefit remains limited to few patients and immunotherapy resistance due to immunosuppressive tumor microenvironment represents the major reason of such a failure. Arginase-1 is one of the enzymes contributing to the establishment of such immunosuppression. Among the human immune cells, polymorphonuclear cells (PMNs) represent the major source of arginase-1, while myeloid-derived suppressor cells (MDSCs) are the main arginase-1 producing cells in mice. Due to arginase-1 potential impact in dampening the immune response, there is a growing interest in assaying arginase-1 levels and functions. Thus, in this chapter we propose how to evaluate the expression and activity of arginase in human peripheral blood-derived PMNs and in MDSCs isolated from tumor-bearing mice." @default.
• W2968140570 created "2019-08-22" @default.
• W2968140570 creator A5052489243 @default.
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• W2968140570 date "2020-01-01" @default.
• W2968140570 modified "2023-10-18" @default.
• W2968140570 title "Detection and functional evaluation of arginase-1 isolated from human PMNs and murine MDSC" @default.
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• W2968140570 doi "https://doi.org/10.1016/bs.mie.2019.07.022" @default.
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