| Literature DB >> 28351852 |
Jilu Zhang1, Sunny Mai1, Hui-Ming Chen1, Kyeongah Kang1, Xian Chang Li2,3, Shu-Hsia Chen1,4,5, Ping-Ying Pan6,4.
Abstract
Myeloid-derived suppressor cells (MDSCs), a population of immature myeloid cells expanded and accumulated in tumor-bearing mice and in patients with cancer, have been shown to mediate immune suppression and to promote tumor progression, thereby, posing a major hurdle to the success of immune-activating cancer therapies. MDSCs, like their healthy counterparts, such as monocytes/macrophages and granulocytes, express an array of costimulatory and coinhibitory molecules as well as myeloid activators and inhibitory receptors, such as leukocyte immunoglobulin-like receptors (LILR) A and B. This review summarizes current findings on the LILR family members in various diseases, their potential roles in the pathogenesis, and possible strategies to revert or enhance the suppressive function of MDSCs for the benefit of patients by targeting LILRs. © Society for Leukocyte Biology.Entities:
Keywords: MDSCs; autoimmunity; cancer; infection; transplant tolerance
Mesh:
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Year: 2017 PMID: 28351852 PMCID: PMC5505746 DOI: 10.1189/jlb.5MR1216-534R
Source DB: PubMed Journal: J Leukoc Biol ISSN: 0741-5400 Impact factor: 4.962