Inflammation and Immune System Activation After Traumatic Brain Injury

被引:47
作者
Balu, Ramani [1 ]
机构
[1] Univ Penn, Div Neurocrit Care, Dept Neurol, Perelman Sch Med, Philadelphia, PA 19104 USA
关键词
Inflammation; Traumatic brain injury; Microglia; Damage-associated molecular patterns; Cytokine; Pattern recognition receptor; CENTRAL-NERVOUS-SYSTEM; PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY; PLACEBO-CONTROLLED TRIAL; CEREBRAL EDEMA; NATALIZUMAB; INFLAMMASOMES; NEUTRALIZATION; SURVEILLANCE; MECHANISMS; AUTOIMMUNE;
D O I
10.1007/s11910-014-0484-2
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Treatment options for managing traumatic brain injury remain limited. Therapies that limit the development of secondary brain injury-the delayed injury that can occur days to weeks after initial presentation-would have a major impact on outcomes and reduce the medical, social, and economic burden of this devastating disease. A growing body of evidence suggests that inflammation and activation of the immune system is a central driver of secondary brain injury. This article reviews the evidence for inflammation mediating secondary injury after head trauma and outlines potential approaches for immunomodulatory therapies after traumatic brain injury.
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页数:8
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