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J Neuroimmune Pharmacol. 2014 Sep;9(4):447-53. doi: 10.1007/s11481-014-9554-0.
2
Histone modifications are associated with Δ9-tetrahydrocannabinol-mediated alterations in antigen-specific T cell responses.组蛋白修饰与Δ9-四氢大麻酚介导的抗原特异性T细胞反应改变有关。
J Biol Chem. 2014 Jul 4;289(27):18707-18. doi: 10.1074/jbc.M113.545210. Epub 2014 May 19.
3
Modulation of gut-specific mechanisms by chronic δ(9)-tetrahydrocannabinol administration in male rhesus macaques infected with simian immunodeficiency virus: a systems biology analysis.慢性给予δ(9)-四氢大麻酚对感染猴免疫缺陷病毒的雄性恒河猴肠道特异性机制的调节:一项系统生物学分析
AIDS Res Hum Retroviruses. 2014 Jun;30(6):567-78. doi: 10.1089/aid.2013.0182. Epub 2014 Feb 7.
4
Cannabinoids inhibit T-cells via cannabinoid receptor 2 in an in vitro assay for graft rejection, the mixed lymphocyte reaction.在一项用于移植排斥反应的体外实验即混合淋巴细胞反应中,大麻素通过大麻素受体2抑制T细胞。
J Neuroimmune Pharmacol. 2013 Dec;8(5):1239-50. doi: 10.1007/s11481-013-9485-1. Epub 2013 Jul 4.
5
Differential expression of intracellular and extracellular CB(2) cannabinoid receptor protein by human peripheral blood leukocytes.人外周血白细胞中细胞内和细胞外 CB(2)大麻素受体蛋白的差异表达。
J Neuroimmune Pharmacol. 2013 Mar;8(1):323-32. doi: 10.1007/s11481-012-9430-8. Epub 2013 Jan 10.
6
Differential modulation by delta9-tetrahydrocannabinol (∆9)-THC) of CD40 ligand (CD40L) expression in activated mouse splenic CD4+ T cells.δ9-四氢大麻酚(∆9-THC)对激活的小鼠脾 CD4+T 细胞中 CD40 配体(CD40L)表达的差异调节。
J Neuroimmune Pharmacol. 2012 Dec;7(4):969-80. doi: 10.1007/s11481-012-9390-z. Epub 2012 Aug 1.
7
Cannabinoid receptor 2-mediated attenuation of CXCR4-tropic HIV infection in primary CD4+ T cells.大麻素受体 2 介导的对原代 CD4+T 细胞中趋化因子受体 4 嗜性 HIV 感染的抑制作用。
PLoS One. 2012;7(3):e33961. doi: 10.1371/journal.pone.0033961. Epub 2012 Mar 20.
8
Activation of cannabinoid receptor 2 attenuates leukocyte-endothelial cell interactions and blood-brain barrier dysfunction under inflammatory conditions.大麻素受体 2 的激活可减轻炎症状态下白细胞-内皮细胞相互作用和血脑屏障功能障碍。
J Neurosci. 2012 Mar 21;32(12):4004-16. doi: 10.1523/JNEUROSCI.4628-11.2012.
9
Cannabinoid receptor-2 (CB2) agonist ameliorates colitis in IL-10(-/-) mice by attenuating the activation of T cells and promoting their apoptosis.大麻素受体 2 (CB2) 激动剂通过抑制 T 细胞的激活并促进其凋亡来改善 IL-10(-/-) 小鼠的结肠炎。
Toxicol Appl Pharmacol. 2012 Jan 15;258(2):256-67. doi: 10.1016/j.taap.2011.11.005. Epub 2011 Nov 18.
10
Deletion of cannabinoid receptors 1 and 2 exacerbates APC function to increase inflammation and cellular immunity during influenza infection.大麻素受体 1 和 2 的缺失会加剧 APC 功能,在流感感染期间增加炎症和细胞免疫。
J Leukoc Biol. 2011 Nov;90(5):983-95. doi: 10.1189/jlb.0511219. Epub 2011 Aug 26.

大麻素对T细胞功能及抗感染能力的影响

Effects of Cannabinoids on T-cell Function and Resistance to Infection.

作者信息

Eisenstein Toby K, Meissler Joseph J

机构信息

Center for Substance Abuse Research, Temple University School of Medicine, Room 859, 3500 N. Broad St., Philadelphia, PA, 19140, USA,

出版信息

J Neuroimmune Pharmacol. 2015 Jun;10(2):204-16. doi: 10.1007/s11481-015-9603-3. Epub 2015 Apr 16.

DOI:10.1007/s11481-015-9603-3
PMID:25876735
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4470840/
Abstract

This review examines the effects of cannabinoids on immune function, with a focus on effects on T-cells, as well as on resistance to infection. The paper considers the immune modulating capacity of marijuana, of ∆(9)-THC extracted from the marijuana plant, and synthetic cannabinoids. Of particular interest are synthetic compounds that are CB2 receptor (CB2R) selective agonists. As the CB2R is principally expressed on cells of the immune system, agonists that target this receptor, and not CB1 (which is mainly expressed on neurons), have the possibility of altering immune function without psychoactive effects. The overall conclusion of the studies discussed in this review is that cannabinoids that bind to the CB2 receptor, including ∆(9)-THC and CB2 selective agonists are immunosuppressive. The studies provide objective evidence for potentially beneficial effects of marijuana and ∆(9)-THC on the immune system in conditions where it is desirable to dampen immune responses. Evidence is also reviewed supporting the conclusion that these same compounds can sensitize to some infections through their immunosuppressive activities, but not to others. An emerging area of investigation that is reviewed is evidence to support the conclusion that CB2 selective agonists are a new class of immunosuppressive and anti-inflammatory compounds that may have exceptional beneficial effects in a variety of conditions, such as autoimmune diseases and graft rejection, where it is desirable to dampen the immune response without psychoactive effects.

摘要

本综述探讨了大麻素对免疫功能的影响,重点关注其对T细胞的作用以及对感染抵抗力的影响。本文考量了大麻、从大麻植物中提取的∆(9)-四氢大麻酚(∆(9)-THC)以及合成大麻素的免疫调节能力。特别值得关注的是那些对CB2受体(CB2R)具有选择性的合成激动剂。由于CB2R主要在免疫系统细胞上表达,靶向该受体而非CB1(主要在神经元上表达)的激动剂有可能在不产生精神活性作用的情况下改变免疫功能。本综述中所讨论研究的总体结论是,与CB2受体结合的大麻素,包括∆(9)-THC和CB2选择性激动剂,具有免疫抑制作用。这些研究为大麻和∆(9)-THC在需要抑制免疫反应的情况下对免疫系统产生潜在有益影响提供了客观证据。同时也对支持以下结论的证据进行了综述:这些相同的化合物可因其免疫抑制活性而使机体对某些感染更易感,但对其他感染则不然。本文所综述的一个新兴研究领域是支持以下结论的证据:CB2选择性激动剂是一类新型的免疫抑制和抗炎化合物,在各种需要在不产生精神活性作用的情况下抑制免疫反应的病症中,如自身免疫性疾病和移植排斥反应,可能具有特殊的有益效果。