Healthy myeloid-derived suppressor cells express the surface ectoenzyme Vanin-2 (VNN2)
Molecular Immunology, ISSN: 0161-5890, Vol: 142, Page: 1-10
2022
- 6Citations
- 5Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations6
- Citation Indexes6
- CrossRef3
- Captures5
- Readers5
Article Description
Study of human monocytic Myeloid-Derived Suppressor cells Mo-MDSC (CD14 + HLA-DR neg/low ) has been hampered by the lack of positive cell-surface markers. In order to identify positive markers for Mo-MDSC, we performed microarray analysis comparing Mo-MDSC cells from healthy subjects versus CD14 + HLA-DR high monocytes. We have identified the surface ectoenzyme Vanin-2(VNN2) protein as a novel biomarker highly-enriched in healthy subjects Mo-MDSC. Indeed, healthy subjects Mo-MDSC cells expressed 68 % VNN2, whereas only 9% VNN2 expression was observed on CD14 + HLA-DR high cells (n = 4 p < 0.01). The top 10 percent positive VNN2 monocytes expressed CD33 and CD11b while being negative for HLA-DR, CD3, CD15, CD19 and CD56, consistent with a Mo-MDSC phenotype. CD14 + VNN2 high monocytes were able to inhibit CD8 T cell proliferation comparably to traditional Mo-MDSC at 51 % and 48 % respectively. However, VNN2 expression on CD14 + monocytes from glioma patients was inversely correlated to their grade. CD14 + VNN2 high monocytes thus appear to mark a monocytic population similar to Mo-MDSC only in healthy subjects, which may be useful for tumor diagnoses.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0161589021003503; http://dx.doi.org/10.1016/j.molimm.2021.12.011; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85121481765&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/34953280; https://linkinghub.elsevier.com/retrieve/pii/S0161589021003503; https://dx.doi.org/10.1016/j.molimm.2021.12.011
Elsevier BV
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