Tumor promoting capacity of polymorphonuclear myeloid-derived suppressor cells and their neutralization

Myeloid-derived suppressor cells (MDSC) represent a highly immunosuppressive population that expands in tumor bearing hosts and inhibits both T and NK cell antitumor effector functions. Among MDSC subpopulations, the polymorphonuclear (PMN) one is gaining increasing interest since it is a predominan...

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Hauptverfasser: Groth, Christopher (VerfasserIn) , Bitsch, Rebekka (VerfasserIn) , Lasser, Samantha (VerfasserIn) , Özbay Kurt, Feyza Gül (VerfasserIn) , Kurzay, Annina (VerfasserIn) , Petrova, Vera (VerfasserIn) , Altevogt, Peter (VerfasserIn) , Utikal, Jochen (VerfasserIn) , Umansky, Viktor (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2021
In: International journal of cancer
Year: 2021, Jahrgang: 149, Heft: 9, Pages: 1628-1638
ISSN:1097-0215
DOI:10.1002/ijc.33731
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.1002/ijc.33731
Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ijc.33731
Volltext
Verfasserangaben:Christopher Groth, Rebekka Weber, Samantha Lasser, Feyza Gül Özbay, Annina Kurzay, Vera Petrova, Peter Altevogt, Jochen Utikal, Viktor Umansky

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520 |a Myeloid-derived suppressor cells (MDSC) represent a highly immunosuppressive population that expands in tumor bearing hosts and inhibits both T and NK cell antitumor effector functions. Among MDSC subpopulations, the polymorphonuclear (PMN) one is gaining increasing interest since it is a predominant MDSC subset in most cancer entities and inherits unique properties to facilitate metastatic spread. In addition, further improvement in distinguishing PMN-MDSC from neutrophils has contributed to the design of novel therapeutic approaches. In this review, we summarize the current view on the origin of PMN-MDSC and their relation to classical neutrophils. Furthermore, we outline the metastasis promoting features of these cells and promising strategies of their targeting to improve the efficacy of cancer immunotherapy. 
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