一种明确的饮食结合超声接种提供了一种高发、中度的实验性自身免疫性脑脊髓炎(EAE)

Mariella Martorelli, Matthias Dengler, Julian Laux, Tina Fischer, Agne Vaiceliunaite, Ulrike Hahn, Thilo Weinstein, Santiago Cruces, Christina Pokoj, Luciano de Oliveira da Cunha, Lara Wohlbold, Pierre Koch, Stefan Laufer*, Michael Burnet* and Florian Maier, 
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引用次数: 0

摘要

背景:髓鞘少突胶质细胞糖蛋白35-55 (MOG35-55)肽诱导的实验性自身免疫性脑脊髓炎(EAE)是脑和脊髓炎症的一种模型。然而,其严重程度和发病率在实验室内部和不同实验室之间有所不同。严重的评分可能导致过早终止,而且对读数来说是不必要的,对动物福利也是有害的。理想情况下,该模型将具有高发生率、中等严重性和低个体间可变性,以实现3R概念的“细化”方面。然而,大多数增加发病率的努力也增加了严重程度。当测试潜在疗法的效果时,只要变化不大,中度的严重程度就足以检测出有用的药物效果。低变异还可以减少群体规模,这支持疾病建模中3R方法的“减少”方面。在MOG- eae模型中,我们通过评估小鼠年龄、膳食纤维、抗原乳剂、MOG和百日咳毒素剂量对发病率、变异性和严重程度的影响,着手减少变异和控制严重程度。方法:对14周龄和33周龄雌性C57BL/6小鼠进行对比研究,并改变两组小鼠的饮食和接种量。我们用免疫荧光法测定了体内的疾病体征以及脑、脊髓和组织学中的基因表达。多重比较采用普通单因素方差分析。结果:低发酵/纤维饲粮(AIN 93M)与mog35 - 55肽超声乳剂相结合是最可靠的诱导条件。高剂量百日咳毒素增加了14周龄小鼠EAE的严重程度和发病率(存活率为25%),而在成熟小鼠中则更为温和(存活率为100%)。改变所有参数表明,预先饲喂的规定日粮的持续时间、乳化液质量和小鼠成熟度是增加反应均匀性的因素,使发病率达到100%,而不会出现过度严重的情况。小胶质细胞和星形胶质细胞相关标志物成比例上调,评分与已知的EAE病理一致。结论:明确的纤维/高糖饮食和超声接种提供了中度、高发生率和较少变化的EAE。由此产生的动物反应和相关细胞因子模式的一致性,以及与特定饮食的紧密联系,表明这可能是诱导EAE的更具临床可翻译性的方案。这与报道的低发酵饮食对自身免疫性疾病患者免疫调节的影响是一致的。
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A Defined Diet Combined with Sonicated Inoculum Provides a High Incidence, Moderate Severity Form of Experimental Autoimmune Encephalomyelitis (EAE)

Background: Myelin oligodendrocyte glycoprotein 35–55 (MOG35–55)-peptide induced experimental autoimmune encephalomyelitis (EAE) is a model for inflammation of the brain and spinal cord. However, its severity and incidence vary within and between laboratories. Severe scores can lead to premature termination and are both unnecessary for readouts and detrimental to animal welfare. Ideally, the model would have high incidence, moderate severity, and low interindividual variability to fulfill the “Refine” aspect of the 3R concept. Nevertheless, most efforts to increase incidence also increase the severity. When the effects of potential therapies are tested, moderate severity is sufficient to detect useful drug effects as long as variation is low. Low variation can also reduce group sizes, which supports the “Reduce” aspect of 3R approaches in disease modeling. We set out to reduce variation and control severity by assessing the effects of mouse age, dietary fiber, antigen emulsion, and the dose of MOG and pertussis toxin on incidence, variability, and severity in the MOG-EAE model. Methods: We compared 14- and 33-week-old female C57BL/6 mice and varied the diet and inoculum in two studies. We measured disease signs in vivo as well as gene expression in the brain and spinal cord and histology by immunofluorescence. Ordinary one-way ANOVA was used for multiple comparisons. Results: The most reliable induction conditions were with a low-fermentative/fiber diet (AIN 93M) combined with a sonicated emulsion of the MOG35–55-peptide. High-dose pertussis toxin increased EAE severity and incidence in 14-week-old mice (25% survival) while being more moderate in mature mice (100% survival). Varying all parameters suggests that duration of prefeeding defined diet, emulsion quality, and mouse maturity were factors that increase uniformity of response allowing incidence to reach 100% without excess severity. Microglia and astrocyte-associated markers were upregulated proportionally to score consistent with known EAE pathology. Conclusions: A defined fiber/high-sugar diet with sonicated inoculum provides for a moderate severity, high incidence, and less variable EAE. The resulting uniformity in animal response and associated cytokine patterns, and the strong link to a defined diet, suggest that this may be a more clinically translatable protocol for the induction of EAE. This is consistent with reported effects of low-fermentable diets on immune modulation in human patients with autoimmune diseases.

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ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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