Regulating the Adaptive Immune Response to Blood-Stage Malaria: Role of Dendritic Cells and CD4+Foxp3+ Regulatory T Cells

被引:24
作者
Stevenson, Mary M. [1 ]
Ing, Rebecca
Berretta, Floriana
Miu, Jenny
机构
[1] McGill Univ, Ctr Hlth, Res Inst, Ctr Study Host Resistance, Montreal, PQ H3G 1A4, Canada
基金
加拿大健康研究院;
关键词
malaria; Plasmodium; immune responses; dendritic cells; regulatory T cells; INFECTED ERYTHROCYTES; PLASMODIUM INFECTION; CUTTING EDGE; MOUSE MODELS; PARASITE; SUPPRESSION; MATURATION; INDUCTION; EXPANSION; CYTOKINES;
D O I
10.7150/ijbs.7.1311
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although a clearer understanding of the underlying mechanisms involved in protection and immunopathology during blood-stage malaria has emerged, the mechanisms involved in regulating the adaptive immune response especially those required to maintain a balance between beneficial and deleterious responses remain unclear. Recent evidence suggests the importance of CD11c(+) dendritic cells (DC) and CD4(+)Foxp3(+) regulatory T cells in regulating immune responses during infection and autoimmune disease, but information concerning the contribution of these cells to regulating immunity to malaria is limited. Here, we review recent findings from our laboratory and others in experimental models of malaria in mice and in Plasmodium-infected humans on the roles of DC and natural regulatory T cells in regulating adaptive immunity to blood-stage malaria.
引用
收藏
页码:1311 / 1322
页数:12
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