TY - JOUR
T1 - CB2 and GPR55 receptors as therapeutic targets for systemic immune dysregulation
AU - Zhou, Juan
AU - Burkovskiy, Ian
AU - Yang, Hyewon
AU - Sardinha, Joel
AU - Lehmann, Christian
N1 - Publisher Copyright:
© 2016 Zhou, Burkovskiy, Yang, Sardinha and Lehmann.
PY - 2016/8/22
Y1 - 2016/8/22
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84988808466&partnerID=8YFLogxK
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U2 - 10.3389/fphar.2016.00264
DO - 10.3389/fphar.2016.00264
M3 - Short survey
AN - SCOPUS:84988808466
SN - 1663-9812
VL - 7
JO - Frontiers in Pharmacology
JF - Frontiers in Pharmacology
IS - AUG
M1 - 264
ER -