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开发一种临床上可行的海洛因疫苗。

Development of a Clinically Viable Heroin Vaccine.

机构信息

Departments of Chemistry and Immunology, The Skaggs Institute for Chemical Biology, Worm Institute of Research and Medicine (WIRM), The Scripps Research Institute , 10550 N Torrey Pines Road, La Jolla, California 92037, United States.

Department of Pharmacology and Toxicology, Virginia Commonwealth University , 410 N 12th Street, Richmond, Virginia 23298, United States.

出版信息

J Am Chem Soc. 2017 Jun 28;139(25):8601-8611. doi: 10.1021/jacs.7b03334. Epub 2017 Jun 20.

Abstract

Heroin is a highly abused opioid and incurs a significant detriment to society worldwide. In an effort to expand the limited pharmacotherapy options for opioid use disorders, a heroin conjugate vaccine was developed through comprehensive evaluation of hapten structure, carrier protein, adjuvant and dosing. Immunization of mice with an optimized heroin-tetanus toxoid (TT) conjugate formulated with adjuvants alum and CpG oligodeoxynucleotide (ODN) generated heroin "immunoantagonism", reducing heroin potency by >15-fold. Moreover, the vaccine effects proved to be durable, persisting for over eight months. The lead vaccine was effective in rhesus monkeys, generating significant and sustained antidrug IgG titers in each subject. Characterization of both mouse and monkey antiheroin antibodies by surface plasmon resonance (SPR) revealed low nanomolar antiserum affinity for the key heroin metabolite, 6-acetylmorphine (6AM), with minimal cross reactivity to clinically used opioids. Following a series of heroin challenges over six months in vaccinated monkeys, drug-sequestering antibodies caused marked attenuation of heroin potency (>4-fold) in a schedule-controlled responding (SCR) behavioral assay. Overall, these preclinical results provide an empirical foundation supporting the further evaluation and potential clinical utility of an effective heroin vaccine in treating opioid use disorders.

摘要

海洛因是一种高度滥用的阿片类药物,给全世界的社会带来了重大危害。为了扩大阿片类药物使用障碍的有限药物治疗选择,通过对手性结构、载体蛋白、佐剂和剂量的综合评估,开发了一种海洛因结合疫苗。用佐剂明矾和 CpG 寡脱氧核苷酸(ODN)优化的海洛因-破伤风类毒素(TT)缀合物免疫小鼠产生了海洛因“免疫拮抗作用”,使海洛因效力降低了 >15 倍。此外,疫苗效果持久,持续超过八个月。该领先疫苗在恒河猴中有效,在每个研究对象中都产生了显著且持续的抗毒品 IgG 滴度。通过表面等离子体共振(SPR)对小鼠和猴子的抗海洛因抗体进行表征,发现抗血清对关键海洛因代谢物 6-乙酰吗啡(6AM)的亲和力低至纳摩尔级,与临床使用的阿片类药物的交叉反应最小。在接种疫苗的猴子中进行了六个月的一系列海洛因挑战后,在行为分析中,药物隔离抗体导致海洛因效力明显减弱(>4 倍)。总的来说,这些临床前结果为评估有效海洛因疫苗治疗阿片类药物使用障碍的进一步评估和潜在临床应用提供了经验基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b24a/5612493/580998f4859e/nihms906760f1.jpg

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