The role of mononuclear phagocytes in Ebola virus infection

被引:31
作者
Rogers, Kai J. [1 ]
Maury, Wendy [1 ]
机构
[1] Univ Iowa, Dept Microbiol & Immunol, Iowa City, IA USA
关键词
ebola virus; filovirus; immune evasion; immune response; innate cell mediated immunity; viral pathogenesis; ALTERNATIVELY ACTIVATED MACROPHAGES; T-CELL IMMUNOGLOBULIN; DENDRITIC CELLS; HEMORRHAGIC-FEVER; DC-SIGN; ZAIRE-EBOLAVIRUS; VP35; PROTEIN; IMMUNE EVASION; PRIMATE MODELS; PATHOGENESIS;
D O I
10.1002/JLB.4RI0518-183R
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The filovirus, Zaire Ebolavirus (EBOV), infects tissue macrophages (M phi s) and dendritic cells (DCs) early during infection. Viral infection of both cells types is highly productive, leading to increased viral load. However, virus infection of these two cell types results in different consequences for cellular function. Infection of M phi s stimulates the production of proinflammatory and immunomodulatory cytokines and chemokines, leading to the production of a cytokine storm, while simultaneously increasing tissue factor production and thus facilitating disseminated intravascular coagulation. In contrast, EBOV infection of DCs blocks DC maturation and antigen presentation rendering these cells unable to communicate with adaptive immune response elements. Details of the known interactions of these cells with EBOV are reviewed here. We also identify a number of unanswered questions that remain about interactions of filoviruses with these cells.
引用
收藏
页码:717 / 727
页数:11
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