TY - JOUR
T1 - Comparative analysis of monocytic and granulocytic myeloid-derived suppressor cell subsets in patients with gastrointestinal malignancies
AU - Duffy, Austin
AU - Zhao, Fei
AU - Haile, Lydia
AU - Gamrekelashvili, Jaba
AU - Fioravanti, Suzanne
AU - Ma, Chi
AU - Kapanadze, Tamar
AU - Compton, Kathryn
AU - Figg, William D.
AU - Greten, Tim F.
N1 - Funding Information:
Acknowledgments This research was supported by the Intramural Research Program of the NIH, National Cancer Institute, Center for Cancer Research.
PY - 2013/2
Y1 - 2013/2
N2 - Myeloid-derived suppressor cells (MDSC) are a heterogenous population of cells comprising myeloid progenitor cells and immature myeloid cells, which have the ability to suppress the effector immune response. In humans, MDSC have not been well characterized owing to the lack of specific markers, although it is possible to broadly classify the MDSC phenotypes described in the literature as being predominantly granulocytic (expressing markers such as CD15, CD66, CD33) or monocytic (expressing CD14). In this study, we set out to perform a direct comparative analysis across both granulocytic and monocytic MDSC subsets in terms of their frequency, absolute number, and function in the peripheral blood of patients with advanced GI cancer. We also set out to determine the optimal method of sample processing given that this is an additional source of heterogeneity. Our findings demonstrate consistent changes across sample processing methods for monocytic MDSC, suggesting that reliance upon cryopreserved PBMC is acceptable. Although we did not see an increase in the population of granulocytic MDSC, these cells were found to be more suppressive than their monocytic counterparts.
AB - Myeloid-derived suppressor cells (MDSC) are a heterogenous population of cells comprising myeloid progenitor cells and immature myeloid cells, which have the ability to suppress the effector immune response. In humans, MDSC have not been well characterized owing to the lack of specific markers, although it is possible to broadly classify the MDSC phenotypes described in the literature as being predominantly granulocytic (expressing markers such as CD15, CD66, CD33) or monocytic (expressing CD14). In this study, we set out to perform a direct comparative analysis across both granulocytic and monocytic MDSC subsets in terms of their frequency, absolute number, and function in the peripheral blood of patients with advanced GI cancer. We also set out to determine the optimal method of sample processing given that this is an additional source of heterogeneity. Our findings demonstrate consistent changes across sample processing methods for monocytic MDSC, suggesting that reliance upon cryopreserved PBMC is acceptable. Although we did not see an increase in the population of granulocytic MDSC, these cells were found to be more suppressive than their monocytic counterparts.
KW - Cancer
KW - Immune
KW - Myeloid-derived suppressor cells
KW - Suppressor
UR - http://www.scopus.com/inward/record.url?scp=84874117271&partnerID=8YFLogxK
U2 - 10.1007/s00262-012-1332-3
DO - 10.1007/s00262-012-1332-3
M3 - Article
C2 - 23011590
AN - SCOPUS:84874117271
SN - 0340-7004
VL - 62
SP - 299
EP - 307
JO - Cancer Immunology Immunotherapy
JF - Cancer Immunology Immunotherapy
IS - 2
ER -