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. Author manuscript; available in PMC: 2016 Apr 15.
Published in final edited form as: Cancer Res. 2015 Feb 26;75(8):1635–1644. doi: 10.1158/0008-5472.CAN-14-3016

Figure 6.

Figure 6

IL-10R is highly upregulated by PD-1+ CD8+ TILs. A and B, Dot plots from one representative patient (A) and summary data (B) showing ex vivo IL-10R expression by NY-ESO-1 tet- CD8+ T cells from PBMCs of healthy donors (n=9) and by CD8+ TILs from melanoma patients (n=9). C and D, Dot plots from one representative patient (C) and summary data for all nine patients with advanced melanoma (D) showing ex vivo IL-10R expression by PD-1high, PD-1int and PD-1low subsets of CD8+ TILs. E, Flow cytometry analysis from one melanoma patient showing the percentages of CFSElo CD8+ TILs among total CD8+ TILs. CFSE-labeled CD8+ TILs were incubated with anti-CD3-pulsed non-T cell fraction of one melanoma tumor single cell suspension in the presence of anti-IL-10R and/or anti-PD-1 or IgG control antibodies before the evaluation of the CD8+ T cells proliferation by flow cytometry. * P < 0.05 and ** P < 0.01. Horizontal bars depict the mean percentage or MFI of IL-10R expression by NY-ESO-1 tet- CD8+ T cells or CD8+ TILs. Data shown are representative of two independent experiments performed in duplicate.