Julliard Walker, De Wolfe Travis J, Fechner John H, Safdar Nasia, Agni Rashmi, Mezrich Joshua D
*Division of Transplant Surgery, Department of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, WI †Department of Food Sciences, University of Wisconsin, Madison, WI ‡William S. Middleton Memorial Veterans Hospital and the Division of Infectious Diseases, University of Wisconsin School of Medicine and Public Health, Madison, WI §Department of Pathology and Laboratory Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI.
Ann Surg. 2017 Jun;265(6):1183-1191. doi: 10.1097/SLA.0000000000001830.
To determine the therapeutic effects of dietary supplementation on Clostridium difficile infection (CDI).
With limited treatment options, the rise of C. difficile-associated disease has spurred on the search for novel therapies. Recent data define a role for the aryl hydrocarbon receptor (AHR) and diet-derived AHR ligands in mucosal immunity. We investigated the efficacy of indole-3-carbinol (I3C), a dietary supplement, and AHR precursor ligand in a murine model of CDI.
C57BL/6 (B6), AHR, and AHR mice were placed on either grain-based or semipurified diets with or without I3C before and during CDI. Mice were followed clinically for a minimum of 6 days or euthanized between days 0 and 4 of inoculation for analysis of the inflammatory response and microbiota.
B6 mice fed an AHR ligand-deficient, semipurified diet have significantly increased disease severity (P<0.001) and mortality (P < 0.001) compared with mice fed on diet containing I3C. The addition of I3C to the diet of AHR null mice had less of an impact than in AHR heterozygous littermates, although some protection was seen. Mice on semipurified I3C-diet had increased cecal Tregs, ILC3s, and γδ T cells and an increased neutrophilic response without increased inflammation or bacterial translocation compared with controls.
I3C is a powerful treatment to reduce impact of CDI in mice. The findings indicate I3C may be acting through both AHR-dependent and -independent mechanisms in this model. Dietary supplementation with I3C is a potential new therapy for prevention and amelioration of C. difficile disease.
确定膳食补充剂对艰难梭菌感染(CDI)的治疗效果。
由于治疗选择有限,艰难梭菌相关疾病的增加促使人们寻找新的治疗方法。最近的数据表明芳烃受体(AHR)和饮食来源的AHR配体在粘膜免疫中发挥作用。我们在CDI小鼠模型中研究了膳食补充剂吲哚 - 3 - 甲醇(I3C)和AHR前体配体的疗效。
在CDI之前和期间,将C57BL / 6(B6)、AHR和AHR敲除小鼠置于含或不含I3C的谷物类或半纯化饮食中。对小鼠进行至少6天的临床随访,或在接种后第0至4天实施安乐死,以分析炎症反应和微生物群。
与喂食含I3C饮食的小鼠相比,喂食缺乏AHR配体的半纯化饮食的B6小鼠疾病严重程度(P<0.001)和死亡率(P < 0.001)显著增加。在AHR基因敲除小鼠的饮食中添加I3C的影响小于AHR杂合子同窝小鼠,尽管也观察到了一些保护作用。与对照组相比,食用半纯化I3C饮食的小鼠盲肠调节性T细胞、3型固有淋巴细胞和γδ T细胞增加,中性粒细胞反应增强,且炎症或细菌易位未增加。
I3C是减轻小鼠CDI影响的有效治疗方法。研究结果表明,在该模型中I3C可能通过AHR依赖性和非依赖性机制发挥作用。膳食补充I3C是预防和改善艰难梭菌疾病的一种潜在新疗法。