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Myeloid-derived suppressor cells (MDSCs) in patients with solid tumors: considerations for granulocyte colony-stimulating factor treatment

. 2018 Dec ; 67 (12) : 1919-1929. [epub] 20180510

Language English Country Germany Media print-electronic

Document type Journal Article, Review

Grant support
AZV 16-31966A Ministerstvo Zdravotnictví Ceské Republiky (CZ)
DRO 00209805 Ministerstvo Zdravotnictví Ceské Republiky
LO1413 Ministerstvo Školství, Mládeže a Tělovýchovy (CZ)
LM15089 Ministerstvo Školství, Mládeže a Tělovýchovy (CZ)
LM2015090 Ministerstvo Školství, Mládeže a Tělovýchovy (CZ)

Links

PubMed 29748897
PubMed Central PMC11028306
DOI 10.1007/s00262-018-2166-4
PII: 10.1007/s00262-018-2166-4
Knihovny.cz E-resources

Myeloid-derived suppressor cells (MDSCs) have been shown to contribute to tumor escape from host immune surveillance and to cancer progression by production of tumor-promoting soluble factors. Granulocyte colony-stimulating factor (G-CSF) is a principle cytokine controlling granulocyte number. Recombinant human G-CSF (rhG-CSF) has become the main therapeutic agent for the treatment of neutropenia and prophylaxis of febrile neutropenia in cancer patients. However, we show here that rhG-CSF triggers accumulation of granulocytic and monocytic subsets. Consequently, we discuss the pharmacological use of granulopoiesis stimulating factors not only in the context of febrile neutropenia but also from the perspective of MDSC-dependent and MDSC-independent mechanisms of immunosuppression and cancer angiogenesis.

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