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. 2017 Jan 20;66(4):503–513. doi: 10.1007/s00262-016-1953-z

Table 2.

MDSCs isolated from the spleens of both cancer patients and those with benign cysts suppress T cell activation and proliferation

Patient tumor type Stage % Suppressiona
CD15+ CD14+
Benign p. cyst n/a 55.0 n/a
Benign p. cyst n/a 89.7 n/a
Benign p. cyst n/a 47.8 17.5
P. adenocarcinoma I 40.6 n/a
P. adenocarcinoma I 13.9 n/a
P. neuroendocrine tumor I 21.8 28.9
P. neuroendocrine tumor I 33.3 9.75
P. neuroendocrine tumor Ib 40.6 n/a
P. neuroendocrine tumor IIb 8.63 n/a
P. neuroendocrine tumor IV 33.3 9.75
P. neuroendocrine tumor IV 85.9 n/a
Ovarian cancer IV 21.8 28.9
Melanoma IV 35.6 41.1
Colon adenocarcinoma IIIb 47.3 n/a

aCFSE-labeled T cells were stimulated with allogenic dendritic cells in the presence of HLA-DR+ control cells or MDSCs. After 4 days, cells were stained with antibodies specific for CD3, CD8, and CD25 and the frequency of divided (CFSE low) CDS T cells was determined by flow cytometry. The percent suppression of proliferation was determined for each sample relative to HLA-DR+ cells