CD14型
髓源性抑制细胞
CD33
CD19
免疫学
单核细胞
CD8型
癌症研究
人口
免疫系统
CD3型
分化群
髓样
医学
生物
细胞
抑制器
细胞生物学
内科学
癌症
干细胞
遗传学
环境卫生
川地34
作者
David Soler,Amber Kerstetter-Fogle,A. B. Young,Pat Rayman,James H. Finke,Sarah M. Debanne,Kevin D. Cooper,Jill S. Barnholtz‐Sloan,Andrew E. Sloan,Thomas S. McCormick
标识
DOI:10.1016/j.molimm.2021.12.011
摘要
Study of human monocytic Myeloid-Derived Suppressor cells Mo-MDSC (CD14+ HLA-DRneg/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-DRhigh 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-DRhigh 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+VNN2high 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+VNN2high monocytes thus appear to mark a monocytic population similar to Mo-MDSC only in healthy subjects, which may be useful for tumor diagnoses.
科研通智能强力驱动
Strongly Powered by AbleSci AI