Regulation of immunopathogenesis during Plasmodium and Toxoplasma infections: more parallels than distinctions?

被引:19
作者
Butler, Noah S. [1 ]
Harris, Tajie H. [2 ]
Blader, Ira J. [3 ]
机构
[1] Univ Oklahoma, Hlth Sci Ctr, Dept Microbiol & Immunol, Oklahoma City, OK 73104 USA
[2] Univ Virginia, Sch Med, Dept Neurosci, Charlottesville, VA 22908 USA
[3] SUNY Buffalo, Dept Microbiol & Immunol, Buffalo, NY 14214 USA
基金
美国国家卫生研究院;
关键词
Plasmodium; Toxoplasma; immunopathology; IL-10; IL-27; TGF-beta; GROWTH-FACTOR-BETA; CD4(+) T-CELLS; SEVERE MALARIAL ANEMIA; DENDRITIC CELLS; CEREBRAL MALARIA; INTERFERON-GAMMA; TGF-BETA; CUTTING EDGE; IFN-GAMMA; INTERLEUKIN-10-DEFICIENT MICE;
D O I
10.1016/j.pt.2013.10.002
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Toxoplasma and Plasmodium parasites exact a significant toll on public health. Host immunity required for efficient control of infection by these Apicomplexans involves the induction of potent T cell responses, which sometimes results in immunopathological damage. Thus, protective immune responses must be balanced by regulatory networks that limit immunopathology. We review several key cellular and molecular immunoregulatory networks operational during Toxoplasma and Plasmodium infections. Accumulating data show that despite differences in how the immune response controls these parasites, many host immunoregulatory pathways and cellular networks are common to both. Thus, understanding the cellular and molecular circuits that prevent or regulate immunopathological responses against one parasite is likely to inform our understanding of the host response to the other parasite.
引用
收藏
页码:593 / 602
页数:10
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