Innate, adaptive, and cell-autonomous immunity against Toxoplasma gondii infection

被引:78
作者
Sasai, Miwa [1 ,2 ]
Yamamoto, Masahiro [1 ,2 ]
机构
[1] Osaka Univ, Microbial Dis Res Inst, Dept Immunoparasitol, Osaka, Japan
[2] Osaka Univ, WPI Immunol Frontier Res Ctr, Lab Immunoparasitol, Osaka, Japan
关键词
TUMOR-NECROSIS-FACTOR; PATHOGEN-CONTAINING VACUOLES; INDUCIBLY EXPRESSED GTPASE; IRG RESISTANCE GTPASES; IFN-GAMMA; INTERFERON-GAMMA; HOST-RESISTANCE; LYMPHOID-CELLS; MESSENGER-RNA; NITRIC-OXIDE;
D O I
10.1038/s12276-019-0353-9
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
Hosts have been fighting pathogens throughout the evolution of all infectious diseases. Toxoplasma gondii is one of the most common infectious agents in humans but causes only opportunistic infection in healthy individuals. Similar to antimicrobial immunity against other organisms, the immune response against T. gondii activates innate immunity and in turn induces acquired immune responses. After activation of acquired immunity, host immune cells robustly produce the proinflammatory cytokine interferon-gamma (IFN-gamma), which activates a set of IFN-gamma-inducible proteins, including GTPases. IFN-inducible GTPases are essential for cell-autonomous immunity and are specialized for effective clearance and growth inhibition of T. gondii by accumulating in parasitophorous vacuole membranes. Recent studies suggest that the cell-autonomous immune response plays a protective role in host defense against not only T. gondii but also various intracellular bacteria. Moreover, the negative regulatory mechanisms of such strong immune responses are also important for host survival after infection. In this review, we will discuss in detail recent advances in the understanding of host defenses against T. gondii and the roles played by cell-autonomous immune responses.
引用
收藏
页码:1 / 10
页数:10
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