Myeloid-derived suppressor cells in parasitic infections

被引:117
作者
Van Ginderachter, Jo A. [1 ,2 ]
Beschin, Alain [1 ,2 ]
De Baetselier, Patrick [1 ,2 ]
Raes, Geert [1 ,2 ]
机构
[1] Vrije Univ Brussel VIB, Dept Mol & Cellular Interact, Cellular & Mol Immunol Lab, B-1050 Brussels, Belgium
[2] Vrije Univ Brussel, Cellular & Mol Immunol Lab, Brussels, Belgium
关键词
Myeloid-derived suppressor cells; Myelopoiesis; Parasitic infection; T-cell suppression; ALTERNATIVELY ACTIVATED MACROPHAGES; REGULATORY T-CELLS; TRYPANOSOMA-BRUCEI INFECTION; ANTIGEN-PRESENTING CELLS; L-ARGININE METABOLISM; TUMOR-BEARING MICE; NITRIC-OXIDE; BONE-MARROW; ACUTE TOXOPLASMOSIS; LEISHMANIA-MAJOR;
D O I
10.1002/eji.201040911
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Myeloid-derived suppressor cells (MDSC) are a heterogeneous population of immature myeloid cells that share a common property of suppressing immune responses. Several helminth and protozoan parasite species have developed efficient strategies to increase the rate of medullary or extramedullary myelopoiesis and to induce the expansion and accumulation of immature myeloid cells such as MDSC. In this review, we examine current knowledge on the factors mediating enhanced myelopoiesis and MDSC induction and recruitment during parasitic infections and how the MDSC phenotype and mechanism of immune modulation and suppression depends on the factors they encounter within the host. Finally, we place MDSC expansion in the context of the critical balance between parasite elimination and pathogenicity to the host and suggest attractive avenues for future research.
引用
收藏
页码:2976 / 2985
页数:10
相关论文
共 90 条
[1]  
ABRAHAMSOHN IA, 1995, J IMMUNOL, V155, P3955
[2]   ROLE OF MACROPHAGE-DERIVED NITRIC-OXIDE IN SUPPRESSION OF LYMPHOCYTE-PROLIFERATION DURING BLOOD-STAGE MALARIA [J].
AHVAZI, BC ;
JACOBS, P ;
STEVENSON, MM .
JOURNAL OF LEUKOCYTE BIOLOGY, 1995, 58 (01) :23-31
[3]   Profound suppression of cellular proliferation mediated by the secretions of nematodes [J].
Allen, JE ;
Macdonald, AS .
PARASITE IMMUNOLOGY, 1998, 20 (05) :241-247
[4]  
ALVAREZSILVA M, 1993, J CELL SCI, V104, P477
[5]   A COMPARATIVE-STUDY OF THE KINETIC CHANGES OF HEMATOPOIETIC STEM-CELLS IN MICE INFECTED WITH LETHAL AND NONLETHAL MALARIA [J].
ASAMI, M ;
OWHASHI, M ;
ABE, T ;
NAWA, Y .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 1992, 22 (01) :43-47
[6]   A schistosome-expressed immunomodulatory glycoconjugate expands peritoneal Gr1+ macrophages that suppress naive CD4+ T cell proliferation via an IFN-γ and nitric oxide-dependent mechanism [J].
Atochina, O ;
Daly-Engel, T ;
Piskorska, D ;
McGuire, E ;
Harn, DA .
JOURNAL OF IMMUNOLOGY, 2001, 167 (08) :4293-4302
[7]   CD4+CD25+ regulatory T cells control Leishmania major persistence and immunity [J].
Belkaid, Y ;
Piccirillo, CA ;
Mendez, S ;
Shevach, EM ;
Sacks, DL .
NATURE, 2002, 420 (6915) :502-507
[8]   Induction of an IL7-R+c-Kithi myelolymphoid progenitor critically dependent on IFN-γ signaling during acute malaria [J].
Belyaev, Nikolai N. ;
Brown, Douglas E. ;
Diaz, Ana-Isabel Garcia ;
Rae, Aaron ;
Jarra, William ;
Thompson, Joanne ;
Langhorne, Jean ;
Potocnik, Alexandre J. .
NATURE IMMUNOLOGY, 2010, 11 (06) :477-U41
[9]   Trypanosoma brucei infection elicits nitric oxide-dependent and nitric oxide-independent suppressive mechanisms [J].
Beschin, A ;
Brys, L ;
Magez, S ;
Radwanska, M ;
De Baetselier, P .
JOURNAL OF LEUKOCYTE BIOLOGY, 1998, 63 (04) :429-439
[10]   IL-4-induced arginase 1 suppresses alloreactive T cells in tumor-bearing mice [J].
Bronte, V ;
Serafini, P ;
De Santo, C ;
Marigo, I ;
Tosello, V ;
Mazzoni, A ;
Segal, DM ;
Staib, C ;
Lowel, M ;
Sutter, G ;
Colombo, MP ;
Zanovello, P .
JOURNAL OF IMMUNOLOGY, 2003, 170 (01) :270-278