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- W4361931305 abstract "<p>Gating strategy for quantification of subsets of T cells and regulatory T cells (Tregs), monocytes and myeloid-derived suppressor cells (MDSCs). Total cells were selected by gating on Time vs. SSC-A. Duplicates were removed via progressive gating on FSC-H vs. FSC-A and SSC-H vs. SSC-A. Dead cells were excluded by considering only EMA-negative cells. (A) A morphological gate was used to identify the population of lymphocytes. Next, CD3+ cells were selected and further separated into CD4+ and CD8+ cells. Ki67 expression was investigated on CD4+ and CD8+ cells. CD8+ T cells with suppressive potential were defined as CD103+. Previously described phenotypes of Tregs were defined as CD4+CD25+FoxP3+ and CD4+CD127lowCD25+FoxP3+. These were further subdivided into proliferating (Ki67+CD45RA-) and non-proliferating Tregs (Ki67-CD45RA+). (B) A lineage cocktail (CD3, CD19, CD56) was used to avoid cross-contamination. Previously described MDSC populations were identified as Lin-CD14+HLA-DRlow and Lin-CD14-CD15+CD11b+ within the all-cell gate. Overall monocytes were defined as CD14+, while subsets were separated into classical monocytes (Lin-CD14+CD16-HLA-DR+), non-classical monocytes (Lin-CD14-CD16+HLA-DR+) and Lin- CD14-CD16dimHLA-DR+ monocytes within the all-cell gate.</p>" @default.
- W4361931305 created "2023-04-05" @default.
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- W4361931305 date "2023-03-31" @default.
- W4361931305 modified "2023-10-16" @default.
- W4361931305 title "Supplementary Figure 1 from Increases in Absolute Lymphocytes and Circulating CD4<sup>+</sup> and CD8<sup>+</sup> T Cells Are Associated with Positive Clinical Outcome of Melanoma Patients Treated with Ipilimumab" @default.
- W4361931305 doi "https://doi.org/10.1158/1078-0432.22467413.v1" @default.
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