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...

Full description

Saved in:
Bibliographic Details
Main Authors: Groth, Christopher (Author) , Bitsch, Rebekka (Author) , Lasser, Samantha (Author) , Özbay Kurt, Feyza Gül (Author) , Kurzay, Annina (Author) , Petrova, Vera (Author) , Altevogt, Peter (Author) , Utikal, Jochen (Author) , Umansky, Viktor (Author)
Format: Article (Journal)
Language:English
Published: 2021
In: International journal of cancer
Year: 2021, Volume: 149, Issue: 9, Pages: 1628-1638
ISSN:1097-0215
DOI:10.1002/ijc.33731
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1002/ijc.33731
Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ijc.33731
Get full text
Author Notes:Christopher Groth, Rebekka Weber, Samantha Lasser, Feyza Gül Özbay, Annina Kurzay, Vera Petrova, Peter Altevogt, Jochen Utikal, Viktor Umansky
Description
Summary: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.
Item Description:Gesehen am 30.03.2023
Physical Description:Online Resource
ISSN:1097-0215
DOI:10.1002/ijc.33731