Chronic distress and the vulnerable host: a new target for HIV treatment and prevention?

Neurobehavioral HIV medicine Pub Date : 2016-01-01 Epub Date: 2016-12-28 DOI:10.2147/nbhiv.s86309
Carlo Contoreggi, George P Chrousos, Michele Di Mascio
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Abstract

Pathologic stress (distress) disturbs immune, cardiovascular, metabolic, and behavioral homeostasis. Individuals living with HIV and those at risk are vulnerable to stress disorders. Corticotropin-releasing hormone (CRH) is critical in neuroendocrine immune regulation. CRH, a neuropeptide, is distributed in the central and peripheral nervous systems and acts principally on CRH receptor type 1 (CRHR1). CRH in the brain modulates neuropsychiatric disorders. CRH and stress modulation of immunity is two-pronged; there is a direct action on hypothalamic-pituitary-adrenal secretion of glucocorticoids and through immune organ sympathetic innervation. CRH is a central and systemic proinflammatory cytokine. Glucocorticoids and their receptors have gene regulatory actions on viral replication and cause central and systemic immune suppression. CRH and stress activation contributes to central nervous system (CNS) viral entry important in HIV-associated neurocognitive disorders and HIV-associated dementia. CNS CRH overproduction short-circuits reward, executive, and emotional control, leading to addiction, cognitive impairment, and psychiatric comorbidity. CRHR1 is an important therapeutic target for medication development. CRHR1 antagonist clinical trials have focused on psychiatric disorders with little attention paid to neuroendocrine immune disorders. Studies of those with HIV and those at risk show that concurrent stress-related disorders contribute to higher morbidity and mortality; stress-related conditions, addiction, immune dysfunction, and comorbid psychiatric illness all increase HIV transmission. Neuropsychiatric disease, chronic inflammation, and substance abuse are endemic, and chronic distress is a pathologic factor. It is being understood that stress and CRH are fundamental to neuroendocrine immunity; therapeutic interventions with existing and novel agents hold promise for restoring homeostasis, reducing morbidity and mortality for those with HIV and possibly reducing future disease transmission.

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长期痛苦和脆弱的宿主:艾滋病毒治疗和预防的新目标?
病理性压力(痛苦)会扰乱免疫、心血管、新陈代谢和行为的平衡。艾滋病病毒感染者和高危人群很容易出现应激障碍。促肾上腺皮质激素释放激素(CRH)对神经内分泌免疫调节至关重要。CRH是一种神经肽,分布于中枢和周围神经系统,主要作用于CRH受体1型(CRHR1)。大脑中的 CRH 可调节神经精神疾病。CRH 和应激对免疫的调节是双管齐下的:直接作用于下丘脑-垂体-肾上腺分泌糖皮质激素,并通过免疫器官交感神经支配。CRH 是一种中枢性和全身性促炎细胞因子。糖皮质激素及其受体对病毒复制具有基因调节作用,并导致中枢和全身免疫抑制。CRH和应激激活有助于中枢神经系统(CNS)病毒进入,这在艾滋病毒相关神经认知障碍和艾滋病毒相关痴呆症中非常重要。中枢神经系统 CRH 过度分泌会导致奖赏、执行和情绪控制短路,从而导致成瘾、认知障碍和精神病合并症。CRHR1 是药物开发的重要治疗靶点。CRHR1拮抗剂的临床试验主要集中在精神疾病上,很少关注神经内分泌免疫疾病。对艾滋病病毒感染者和高危人群的研究表明,并发压力相关疾病会导致更高的发病率和死亡率;压力相关疾病、成瘾、免疫功能紊乱和合并精神病都会增加艾滋病病毒的传播。神经精神疾病、慢性炎症和药物滥用已成为地方病,而长期焦虑则是一个病理因素。人们正在认识到,压力和 CRH 是神经内分泌免疫的基础;使用现有和新型药物进行治疗干预有望恢复平衡,降低艾滋病毒感染者的发病率和死亡率,并可能减少未来的疾病传播。
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