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10.3389/fimmu.2018.00608

http://scihub22266oqcxt.onion/10.3389/fimmu.2018.00608
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C5879147!5879147!29632539
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suck abstract from ncbi


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pmid29632539      Front+Immunol 2018 ; 9 (ä): ä
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  • Factors Influencing the Differentiation of Human Monocytic Myeloid-Derived Suppressor Cells Into Inflammatory Macrophages #MMPMID29632539
  • Bayik D; Tross D; Klinman DM
  • Front Immunol 2018[]; 9 (ä): ä PMID29632539show ga
  • Monocytic myeloid-derived suppressor cells (mMDSC) accumulate within tumors where they create an immunosuppressive milieu that inhibits the activity of cytotoxic T and NK cells thereby allowing cancers to evade immune elimination. The toll-like receptors 7/8 agonist R848 induces human mMDSC to mature into inflammatory macrophage (MACinflam). This work demonstrates that TNF?, IL-6, and IL-10 produced by maturing mMDSC are critical to the generation of MACinflam. Neutralizing any one of these cytokines significantly inhibits R848-dependent mMDSC differentiation. mMDSC cultured in pro-inflammatory cytokine IFN? or the combination of TNF? plus IL-6 differentiate into MACinflam more efficiently than those treated with R848. These mMDSC-derived macrophages exert anti-tumor activity by killing cancer cells. RNA-Seq analysis of the genes expressed when mMDSC differentiate into MACinflam indicates that TNF? and the transcription factors NF-?B and STAT4 are major hubs regulating this process. These findings support the clinical evaluation of R848, IFN?, and/or TNF? plus IL-6 for intratumoral therapy of established cancers.
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