Pyroptotic death storms and cytopenia

被引:44
作者
Croker, Ben A. [1 ]
O'Donnell, Joanne A. [2 ,3 ]
Gerlic, Motti [2 ,3 ]
机构
[1] Boston Childrens Hosp, Div Hematol Oncol, Boston, MA 02115 USA
[2] Walter & Eliza Hall Inst Med Res, Parkville, Vic 3052, Australia
[3] Univ Melbourne, Dept Med Biol, Parkville, Vic 3050, Australia
关键词
NLRP3 INFLAMMASOME ACTIVATION; PROTEIN PROMOTES VIRULENCE; LINKS OXIDATIVE STRESS; FACTOR-KAPPA-B; CASPASE-1; ACTIVATION; DIFFERENTIAL REQUIREMENT; NALP3; INFLAMMASOME; CELL-DEATH; DISTINCT PATHWAYS; INTERFERON-GAMMA;
D O I
10.1016/j.coi.2013.12.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
For over two decades, we have embraced the cytokine storm theory to explain sepsis, severe sepsis and septic shock. The failure of numerous large-scale clinical trials, which aimed to treat sepsis by neutralizing inflammatory cytokines and LPS, indicates that alternative pathophysiological mechanisms are likely to account for sepsis and the associated immune suppression in patients with severe infection. Recent insights that extricate pyroptotic death from inflammatory cytokine production in vivo have highlighted a need to investigate the consequences of apoptotic and non-apoptotic death in contributing to cytopenia and immune suppression. In this review, we will focus on the biochemical and cellular mechanisms controlling pyroptosis, a Caspase-1/11 dependent form of cell death during infection.
引用
收藏
页码:128 / 137
页数:10
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