Department of Neuroimaging, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Department of Neuroimaging, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Brain Behav Immun. 2021 Jan;91:487-497. doi: 10.1016/j.bbi.2020.10.025. Epub 2020 Nov 5.
The relationship between peripheral and central immunity and how these ultimately may cause depressed behaviour has been the focus of a number of imaging studies conducted with Positron Emission Tomography (PET). These studies aimed at testing the immune-mediated model of depression that proposes a direct effect of peripheral cytokines and immune cells on the brain to elicit a neuroinflammatory response via a leaky blood-brain barrier and ultimately depressive behaviour. However, studies conducted so far using PET radioligands targeting the neuroinflammatory marker 18 kDa translocator protein (TSPO) in patient cohorts with depression have demonstrated mild inflammatory brain status but no correlation between central and peripheral immunity. To gain a better insight into the relationship between heightened peripheral immunity and neuroinflammation, we estimated blood-to-brain and blood-to-CSF perfusion rates for two TSPO radiotracers collected in two separate studies, one large cross-sectional study of neuroinflammation in normal and depressed cohorts (N = 51 patients and N = 25 controls) and a second study where peripheral inflammation in N = 7 healthy controls was induced via subcutaneous injection of interferon (IFN)-α. In both studies we observed a consistent negative association between peripheral inflammation, measured with c-reactive protein P (CRP), and radiotracer perfusion into and from the brain parenchyma and CSF. Importantly, there was no association of this effect with the marker of BBB leakage S100β, that was unchanged. These results suggest a different model of peripheral-to-central immunity interaction whereas peripheral inflammation may cause a reduction in BBB permeability. This effect, on the long term, is likely to disrupt brain homeostasis and induce depressive behavioural symptoms.
外周免疫和中枢免疫之间的关系,以及这些最终如何导致抑郁行为,一直是使用正电子发射断层扫描(PET)进行的许多成像研究的焦点。这些研究旨在测试抑郁症的免疫介导模型,该模型提出外周细胞因子和免疫细胞对大脑的直接影响,通过血脑屏障渗漏引发神经炎症反应,最终导致抑郁行为。然而,迄今为止,使用针对抑郁症患者队列中神经炎症标志物 18 kDa 转位蛋白(TSPO)的 PET 放射性配体进行的研究表明,大脑存在轻度炎症状态,但中枢免疫和外周免疫之间没有相关性。为了更深入地了解外周免疫增强与神经炎症之间的关系,我们评估了两种 TSPO 放射性示踪剂的血脑和血脑脊液灌注率,这些示踪剂分别来自两项单独的研究,一项是正常和抑郁队列的神经炎症的大型横断面研究(N=51 例患者和 N=25 例对照),另一项是在 7 例健康对照者中通过皮下注射干扰素(IFN)-α诱导外周炎症的研究。在这两项研究中,我们都观察到外周炎症(用 C 反应蛋白 P(CRP)测量)与放射性示踪剂向脑实质和脑脊液灌注以及从脑实质和脑脊液中流出之间存在一致的负相关。重要的是,这种效应与 BBB 渗漏标志物 S100β没有关联,S100β没有变化。这些结果表明了外周免疫与中枢免疫相互作用的不同模型,而外周炎症可能导致 BBB 通透性降低。这种效应从长远来看,可能会破坏大脑的内稳态并引发抑郁行为症状。