Taking Advantage of the Systemic Immune System to Cure Brain Diseases

被引:139
作者
Yong, V. Wee [1 ,2 ,3 ]
Rivest, Serge [4 ,5 ]
机构
[1] Univ Calgary, Hotchkiss Brain Inst, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Dept Clin Neurosci, Calgary, AB T2N 4N1, Canada
[3] Univ Calgary, Dept Oncol, Calgary, AB T2N 4N1, Canada
[4] Univ Laval, Dept Mol Med, Quebec City, PQ G1V 4G2, Canada
[5] Univ Laval, CHUL Res Ctr, Lab Endocrinol & Genom, Quebec City, PQ G1V 4G2, Canada
基金
加拿大健康研究院;
关键词
AMYOTROPHIC-LATERAL-SCLEROSIS; MARROW-DERIVED MICROGLIA; ALZHEIMERS-DISEASE; MOUSE MODEL; INNATE; CELLS; MONOCYTES; CNS; REGENERATION; ACTIVATION;
D O I
10.1016/j.neuron.2009.09.035
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The systemic immune system has the ability to modulate multiple brain functions, including autonomic responses, glial reactivity following neural injuries, and neuronal excitability. Immune stimuli also influence microglia subpopulations originating from blood progenitors, and neuroprotective and reparative capacities of blood-derived microglia, were recently described in mouse models of spinal cord injury and brain disorders. Furthermore, reparative roles for various immune subsets have been recognized, such as in inducing myelin repair. Nonetheless, uncontrolled and excessive activation of immune responses can be detrimental. The development of strategies to stimulate the systemic immune system safely to protect or repair brain disorders remains a major challenge ahead, but important inroads have been made. We discuss here some of the mechanisms underlying the neuroprotective and reparative effects of the systemic immune system and the most promising immunotherapies tested in mouse models of injuries and diseases, such as Alzheimer's disease, amyotrophic lateral sclerosis, and multiple sclerosis.
引用
收藏
页码:55 / 60
页数:6
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