Nociceptin/Orphanin FQ Suppresses Adaptive Immune Responses In Vivo and at Picomolar Levels In Vitro

被引:0
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作者
Benito Anton
Phillipe Leff
Joseph J. Meissler
Juan C. Calva
Rodolfo Acevedo
Alberto Salazar
Maura Matus
Anabel Flores
Martin Martinez
Martin W. Adler
John P. Gaughan
Toby K. Eisenstein
机构
[1] Temple University School of Medicine,Center for Substance Abuse Research
[2] Temple University School of Medicine,Department of Microbiology & Immunology
[3] Temple University School of Medicine,Department of Pharmacology
[4] Temple University School of Medicine,Biostatistics Consulting Center, Department of Physiology
[5] National Institute of Psychiatry,Molecular Neurobiology and Addictive Neurochemistry Laboratory
[6] National Institute of Cardiology,Department of Physiology
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关键词
nociceptin; orphanin FQ; N/OFQ; ORL-1; immunosuppression; mouse; plaque-forming cell assay; anti-N/OFQ antibodies; neutralizing antibodies; RIA;
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摘要
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.
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页码:143 / 154
页数:11
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