| Literature DB >> 34224592 |
Christopher Groth1,2,3,4,5, Rebekka Weber1,2,3, Samantha Lasser1,2,3,6, Feyza Gül Özbay1,2,3,6, Annina Kurzay1,2,6, Vera Petrova1,2,3, Peter Altevogt1,2,3, Jochen Utikal1,2, Viktor Umansky1,2,3.
Abstract
Myeloid-derived suppressor cells (MDSC) represent a highly immunosuppressive population that expands in tumor bearing hosts and inhibits both T and NK cell anti-tumor 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. This article is protected by copyright. All rights reserved. This article is protected by copyright. All rights reserved.Entities:
Keywords: PMN-MDSC; immunosuppression; immunotherapy; metastasis; neutrophils
Year: 2021 PMID: 34224592 DOI: 10.1002/ijc.33731
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396