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- W3148442950 endingPage "104347" @default.
- W3148442950 startingPage "104347" @default.
- W3148442950 abstract "Myeloid-derived suppressor cells (MDSC) are important immune-regulatory cells but their identification remains difficult. Here, we provide a critical view on selected surface markers, transcriptional and translational pathways commonly used to identify MDSC by specific, their developmental origin and new possibilities by transcriptional or proteomic profiling. Discrimination of MDSC from their non-suppressive counterparts is a prerequisite for the development of successful therapies. Understanding the switch mechanisms that direct granulocytic and monocytic development into a pro-inflammatory or anti-inflammatory direction will be crucial for therapeutic strategies. Manipulation of these myeloid checkpoints are exploited by tumors and pathogens, such as M. tuberculosis (Mtb), HIV or SARS-CoV-2, that induce MDSC for immune evasion. Thus, specific markers for MDSC identification may reveal also novel molecular candidates for therapeutic intervention at the level of MDSC." @default.
- W3148442950 created "2021-04-13" @default.
- W3148442950 creator A5013841622 @default.
- W3148442950 creator A5048588973 @default.
- W3148442950 date "2021-06-01" @default.
- W3148442950 modified "2023-10-14" @default.
- W3148442950 title "Comments on the ambiguity of selected surface markers, signaling pathways and omics profiles hampering the identification of myeloid-derived suppressor cells" @default.
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