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孤啡肽抑制体内适应性免疫反应,在体外以皮摩尔水平发挥作用。

Nociceptin/orphanin FQ suppresses adaptive immune responses in vivo and at picomolar levels in vitro.

机构信息

Molecular Neurobiology and Addictive Neurochemistry Laboratory, National Institute of Psychiatry, Mexico City, Mexico.

出版信息

J Neuroimmune Pharmacol. 2010 Mar;5(1):143-54. doi: 10.1007/s11481-010-9190-2. Epub 2010 Feb 2.

Abstract

Nociceptin/orphanin FQ (N/OFQ), added in vitro to murine spleen cells in the picomolar range, suppressed antibody formation to sheep red blood cells in a primary and a secondary plaque-forming cell assay. The activity of the peptide was maximal at 10(-12) M, with an asymmetric U-shaped dose-response curve that extended activity to 10(-14) M. Suppression was not blocked by pretreatment with naloxone. Specificity of the suppressive response was shown using affinity-purified rabbit antibodies against two N/OFQ peptides and with a pharmacological antagonist. Antisera against both peptides were active, in a dose-related manner, in neutralizing N/OFQ-mediated immunosuppression, when the peptide was used at concentrations from 10(-12.3) to 10(-11.6) M. In addition, nociceptin given in vivo by osmotic pump for 48 h suppressed the capacity of spleen cells placed ex vivo to make an anti-sheep red blood cell response. These studies show that nociceptin directly inhibits an adaptive immune response, i.e., antibody formation, both in vitro and in vivo.

摘要

孤啡肽(Nociceptin/Orphanin FQ,N/OFQ)在毫微微摩尔范围内添加到体外的小鼠脾细胞中,可抑制初次和二次噬斑形成细胞测定中对抗绵羊红细胞的抗体形成。该肽的活性在 10(-12) M 时达到最大值,呈非对称 U 形剂量反应曲线,其活性延伸至 10(-14) M。纳洛酮预处理不能阻断该肽的抑制作用。使用针对两种 N/OFQ 肽的亲和纯化兔抗体和药理学拮抗剂证明了抑制反应的特异性。针对两种肽的抗血清在中和 N/OFQ 介导的免疫抑制方面具有活性,呈剂量依赖性,当肽的浓度在 10(-12.3)至 10(-11.6) M 时。此外,通过渗透泵在体内给予孤啡肽 48 小时可抑制体外放置的脾细胞产生抗绵羊红细胞反应的能力。这些研究表明,孤啡肽直接抑制适应性免疫反应,即体外和体内的抗体形成。

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