Splenic macrophage subsets and their function during blood-borne infections

被引:140
作者
da Silva, Henrique Borges [1 ]
Fonseca, Raissa [1 ]
Pereira, Rosana Moreira [1 ]
Cassado, Alexandra dos Anjos [1 ]
Alvarez, Jose Maria [1 ]
D'Imperio Lima, Maria Regina [1 ]
机构
[1] Univ Sao Paulo, Dept Immunol, Inst Ciencias Biomed, BR-05508000 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会; 瑞典研究理事会;
关键词
spleen; macrophages; phagocytosis; pattern-recognition receptors; tissue remodeling; MARGINAL ZONE MACROPHAGES; RED PULP MACROPHAGES; PLASMODIUM-FALCIPARUM; SCAVENGER RECEPTORS; DC-SIGN; T-CELL; SPI-C; BINDING; ANTIGEN; SPLEEN;
D O I
10.3389/fimmu.2015.00480
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The spleen is one of the major immunological sites for maintaining blood homeostasis. Previous studies showed that heterogeneous splenic macrophage populations contribute in complimentary ways to control blood-borne infections and induce effective immune responses. Marginal metallophilic macrophages (MMM Phi s) and marginal zone macrophages (MZM Phi s) are cells with great ability to internalize blood-borne pathogens such as virus or bacteria. Their localization adjacent to T- and B-cell-rich splenic areas favors the rapid contact between these macrophages and cells from adaptive immunity. Indeed, MMM Phi s and MZM Phi s are considered important bridges between innate and adaptive immunity. Although red pulp macrophages (RpM Phi s) are mainly considered scavengers for senescent erythrocytes, several data indicate a role for RpM Phi s in control of infections such as blood-stage malaria as well as in the induction of innate and adaptive immunity. Here, we review current data on how different macrophage subsets recognize and help eliminate blood-borne pathogens, and, in turn, how the inflammatory microenvironment in different phases of infection (acute, chronic, and after pathogen clearance) influences macrophage function and survival.
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页数:9
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