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. 2018 Jan 4;8:1895. doi: 10.3389/fimmu.2017.01895

Table 1.

Impact of monocytic myeloid-derived suppressor cells (M-MDSC) on infectious disease outcome and their immunosuppressive effects.

Microbial organism Context of M-MDSC investigation Major outcome; immunosuppressive effect Reference
Viruses
Immunodeficiency virus [human immunodeficiency viruse (HIV), simian immunodeficiency virus, LP-BM5] M-MDSC and total MDSC Host detrimental; suppress T-cell and B-cell responses, express inducible nitric oxide synthase (iNOS), and produce reactive oxygen species (ROS), ARG-1, IL-10, induce Treg Gama et al. (26); Vollbrecht et al. (49); Qin et al. (24); Green et al. (93); Garg and Spector (23); Sui et al. (94); Wang et al. (54); O’Connor et al. (95); du Plessis et al. (28); Sui et al. (25); Garg et al. (96); Dross et al. (97)

Cytomegalovirus (CMV) M-MDSC-like Host detrimental; impair T-cell expansion, slowing viral clearance Daley-Bauer et al. (70)

Hepatitis C virus (HCV) M-MDSC and total MDSC Host detrimental; suppress CD4 T-cell and NK cell function, increase Treg Tacke et al. (21); Salem et al. (98); Zeng et al. (99); Nonnenman et al. (100); Ning et al. (101); Goh et al. (102); Ren et al. (22); Lei et al. (103); Pang et al. (19); Ren et al. (104)

Hepatitis B virus (HBV) M-MDSC and total MDSC Host detrimental; express IL-10, suppress T-cell function, promote disease chronicity Chen et al. (45); Huang et al. (105); Kondo et al. (106)

Viral coinfection (HIV/CMV, HCV/HIV) Host detrimental; impair T-cell function, accelerate disease progression Lei et al. (103); Garg et al. (96); Tumino et al. (107)

Bacteria
Staphylococcus aureus M-MDSC and PMN-MDSC Host detrimental; suppress T-cell function, express ARG-1, iNOS, IL-10, exacerbate disease, promote disease chronicity Skabytska et al. (32); Heim et al. (108); Heim et al. (47, 48); Tebartz et al. (33); Peng et al. (31)

Francisella tularensis Total MDSC Host detrimental; reduced phagocytosis, reduced survival Periasamy et al. (42)

Mycobacteria spp. M-MDSC and total MDSC Host beneficial/detrimental; suppress T-cell function; express ARG-1 and iNOS, impaired pathogen killing; TNF-dependent suppression of CD4 T cells Dietlin et al. (109); Martino et al. (65); Obregón-Henao et al. (41); Knaul et al. (30); Tsiganov et al. (50); Yang et al. (110); du Plessis et al. (28); Chavez-Galan et al. (80)

Klebsiella pneumoniae M-MDSC and PMN-MDSC Host beneficial/detrimental; pro-resolving, express ARG-1, IL-10/impair phagocytosis/killing Poe et al. (35); Ahn et al. (3); Chakraborty et al. (4)

Helicobacter pylori M-MDSC Host detrimental; suppress protective TH1 development. Zhuang et al. (111)

Polymicrobial sepsis M-MDSC and total MDSC Host beneficial/detrimental; suppress T-cell function, express nitric oxide and pro-inflammatory cytokines (early) and ARG-1, IL-10, and TGF-β (late) Delano et al. (55); Sander et al. (112); Brudecki et al. (75); McPeak et al. (76, 77)

Escherichia coli M-MDSC Host detrimental; suppress T-cell activation, innate immunity, impair bacterial uptake and increase disease severity, infection susceptibility Bernsmeier et al. (52)

Protozoa
Leishmania spp. M-MDSC and total MDSC Host beneficial/detrimental; species-specificity, suppress CD4 T-cell proliferation, improved killing of parasites Pereira et al. (73); Schmid et al. (74); Ribeiro-Gomes et al. (113); Bandyopadhyay et al. (114); Hammami et al. (115)

Trypanosoma cruzi M-MDSC and PMN-MDSC Host beneficial/detrimental; dependent on MDSC subset, express ROS, NO, suppress CD8 T-cell proliferation Goni et al. (116); Cuervo et al. (117); Arocena et al. (118)

Toxoplasma gondii Total MDSC Host protective; express NO, control parasite replication Voisin et al. (119); Dunay et al. (120)

Helminths
Schistosoma spp. Total MDSC Not evaluated; express ROS, suppress T-cell responses Yang et al. (121)

Echinnococcus granulosus Total MDSC Not evaluated; association with increased Treg and impaired T-cell L-selectin Pan et al. (122)

Nippostrongylus brasiliensis M-MDSC and PMN-MDSC Host beneficial/detrimental; dependent on MDSC subset, express TH2 cytokines, reduce parasite burden (PMN-MDSC) Saleem et al. (123)

Heligmosomoides polygyrus bakeri Total MDSC Host detrimental; suppress CD4 T-cell proliferation, increase parasite burden, and promote chronic infection Valanparambil et al. (124, 125)

M-MDSC are studied as a purified cell population or as part of the total MDSC population to measure their impact on the host control of infectious pathogens.