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精神药理学:精神疾病中的神经免疫信号——使用 Toll 样受体激动剂开发针对滥用药物的疫苗。

Psychopharmacology: neuroimmune signaling in psychiatric disease-developing vaccines against abused drugs using toll-like receptor agonists.

机构信息

Department of Psychiatry, Baylor College of Medicine, 1977 Butler Blvd, Suite E4.207, Houston, TX, 77030, USA.

出版信息

Psychopharmacology (Berl). 2019 Oct;236(10):2899-2907. doi: 10.1007/s00213-019-5176-9. Epub 2019 Feb 6.

Abstract

RATIONALE

Since substance use disorders have few or no effective pharmacotherapies, researchers have developed vaccines as immune-therapies against nicotine, cocaine, methamphetamine, and opioids including fentanyl.

OBJECTIVES

We focus on enhancing antibody (AB) production through stimulation of toll-like receptor-5 (TLR5) during active vaccination. The stimulating adjuvant is Entolimod, a novel protein derivative of flagellin. We review the molecular and cellular mechanisms underlying Entolimod's actions on TLR5.

RESULTS

Entolimod shows excellent efficacy for increasing AB levels to levels well beyond those produced by anti-addiction vaccines alone in animal models and humans. These ABs also significantly block the behavioral effects of the targeted drug of abuse. The TLR5 stimulation involves a wide range of immune cell types such as dendritic, antigen presenting, T and B cells. Entolimod binding to TLR5 initiates an intracellular signaling cascade that stimulates cytokine production of tumor necrosis factor and two interleukins (IL-6 and IL-12). While cytokine release can be catastrophic in cytokine storm, Entolimod produces a modulated release with few side effects even at doses 30 times greater than doses needed in these vaccine studies. Entolimod has markedly increased AB responses to all of our anti-addiction vaccines in rodent models, and in normal humans.

CONCLUSIONS

Entolimod and TLR5 stimulation has broad application to vaccines and potentially to other psychiatric disorders like depression, which has critical inflammatory contributions that Entolimod could reduce.

摘要

理由

由于物质使用障碍几乎没有有效的药物治疗方法,研究人员已经开发出针对尼古丁、可卡因、冰毒和包括芬太尼在内的阿片类药物的疫苗作为免疫疗法。

目的

我们专注于通过在主动免疫接种过程中刺激 Toll 样受体 5(TLR5)来增强抗体(AB)的产生。刺激佐剂是 Entolimod,一种鞭毛蛋白的新型蛋白衍生物。我们回顾了 Entolimod 对 TLR5 作用的分子和细胞机制。

结果

在动物模型和人类中,Entolimod 表现出极好的功效,可将 AB 水平提高到远远超过单独使用抗成瘾疫苗产生的水平。这些 AB 还显著阻断了靶向滥用药物的行为效应。TLR5 刺激涉及多种免疫细胞类型,如树突状细胞、抗原呈递细胞、T 和 B 细胞。Entolimod 与 TLR5 结合启动细胞内信号级联反应,刺激肿瘤坏死因子和两种白细胞介素(IL-6 和 IL-12)的细胞因子产生。虽然细胞因子释放可能在细胞因子风暴中造成灾难性后果,但 Entolimod 产生的调制释放几乎没有副作用,即使在剂量是这些疫苗研究所需剂量的 30 倍时也是如此。Entolimod 显著增加了我们在啮齿动物模型和正常人类中的所有抗成瘾疫苗的 AB 反应。

结论

Entolimod 和 TLR5 刺激具有广泛的应用于疫苗的潜力,并且可能对其他精神疾病(如抑郁症)有潜在作用,抑郁症具有关键的炎症贡献,Entolimod 可以减轻这些炎症。

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