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CB2 and GPR55 Receptors as Therapeutic Targets for Systemic Immune Dysregulation
被引:24
|作者:
Zhou, Juan
[1
,2
]
Burkoyskiy, Ian
[1
,3
]
Yang, Hyewon
[1
,2
]
Sardinha, Joel
[1
]
Lehmann, Christian
[1
,2
,3
]
机构:
[1] Dalhousie Univ, Dept Anesthesia, Halifax, NS, Canada
[2] Dalhousie Univ, Dept Microbiol & Immunol, Halifax, NS, Canada
[3] Dalhousie Univ, Dept Pharmacol, Halifax, NS, Canada
来源:
关键词:
endocannabinoid system;
immune dysfunction;
sepsis;
central nervous system injury;
immunosuppression;
GPR55;
CNS injury-induced immunodeficiency syndrome;
CANNABINOID;
2;
RECEPTOR;
INDUCED IMMUNODEFICIENCY SYNDROME;
BLOOD-BRAIN-BARRIER;
CLOSED-HEAD INJURY;
INTERNATIONAL UNION;
SIGNALING PATHWAYS;
MICROGLIAL CELLS;
POTENTIAL ROLE;
SEPTIC SHOCK;
T-CELLS;
D O I:
10.3389/fphar.2016.00264
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
The endocannabinoid system (ECS) is involved in many physiological processes and has been suggested to play a critical role in the immune response and the central nervous system (CNS). Therefore, ECS modulation has potential therapeutic effects on immune dysfunctional disorders, such as sepsis and CNS injury-induced immunodeficiency syndrome (CIDS). In sepsis, excessive release of pro- and anti-inflammatory mediators results in multi-organ dysfunction, failure, and death. In CIDS, an acute CNS injury dysregulates a normally well-balanced interplay between CNS and the immune system, leading to increased patients' susceptibility to infections. In this review, we will discuss potential therapeutic modulation of the immune response in sepsis and CNS injury by manipulation of the ECS representing a novel target for immunotherapy.
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