Curciarello Renata, Canziani Karina E, Salto Ileana, Barbiera Romero Emanuel, Rocca Andrés, Doldan Ivan, Peton Emmanuel, Brayer Santiago, Sambuelli Alicia M, Goncalves Silvina, Tirado Pablo, Correa Gustavo J, Yantorno Martín, Garbi Laura, Docena Guillermo H, Serradell María de Los Ángeles, Muglia Cecilia I
Instituto de Estudios Inmunológicos y Fisiopatológicos (IIFP), CONICET-Departamento de Ciencias Biológicas, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, Asociado CIC PBA, La Plata, Argentina.
Unidad Endoscopía, Hospital de Gastroenterología Dr. Carlos Bonorino Udaondo, Ciudad Autónoma de Buenos Aires, Argentina.
Front Pharmacol. 2021 Apr 15;12:658026. doi: 10.3389/fphar.2021.658026. eCollection 2021.
Ulcerative colitis and Crohn's disease, the two main forms of inflammatory bowel disease (IBD), are immunologically mediated disorders. Several therapies are focused on activated T cells as key targets. Although has shown anti-inflammatory effects in animal models, few studies were done using human mucosal T cells. The aim of this work was to investigate the immunomodulatory effects of this bacterium on intestinal T cells from patients with active IBD. Mucosal biopsies and surgical samples from IBD adult patients ( = 19) or healthy donors (HC; = 5) were used. Lamina propria mononuclear cells were isolated by enzymatic tissue digestion, and entero-adhesive -specific lamina propria T cells (LPTC) were expanded. The immunomodulatory properties of CIDCA 8348 strain were evaluated on biopsies and on anti-CD3/CD28-activated LPTC. Secreted cytokines were quantified by ELISA, and cell proliferation and viability were assessed by flow cytometry. We found that reduced spontaneous release of IL-6 and IL-8 from inflamed biopsies Activated LPTC from IBD patients showed low proliferative rates and reduced secretion of TNF-α, IL-6, IFN-γ and IL-13 in the presence of . In addition, induced an increased frequency of CD4FOXP3 LPTC along with high levels of IL-10. This is the first report showing an immunomodulatory effect of CIDCA 8348 on human intestinal cells from IBD patients. Understanding the mechanisms of interaction between probiotics and immune mucosal cells may open new avenues for treatment and prevention of IBD.
溃疡性结肠炎和克罗恩病是炎症性肠病(IBD)的两种主要形式,是免疫介导的疾病。几种疗法聚焦于将活化的T细胞作为关键靶点。尽管[具体物质未提及]在动物模型中已显示出抗炎作用,但使用人类黏膜T细胞进行的研究很少。这项工作的目的是研究这种细菌对活动性IBD患者肠道T细胞的免疫调节作用。使用了IBD成年患者(n = 19)或健康供体(HC;n = 5)的黏膜活检组织和手术样本。通过酶促组织消化分离固有层单核细胞,并扩增肠黏附[具体细菌未提及]特异性固有层T细胞(LPTC)。在活检组织和抗CD3/CD28活化的LPTC上评估[具体细菌未提及] CIDCA 8348菌株的免疫调节特性。通过酶联免疫吸附测定法(ELISA)对分泌的细胞因子进行定量,并通过流式细胞术评估细胞增殖和活力。我们发现[具体细菌未提及]减少了炎症活检组织中IL-6和IL-8的自发释放。在[具体细菌未提及]存在的情况下,IBD患者活化的LPTC显示出低增殖率,并减少了TNF-α、IL-6、IFN-γ和IL-13的分泌。此外,[具体细菌未提及]诱导CD4FOXP3 LPTC的频率增加以及高水平的IL-10。这是首次报道[具体细菌未提及] CIDCA 8348对IBD患者人类肠道细胞具有免疫调节作用。了解益生菌与免疫黏膜细胞之间的相互作用机制可能为IBD的治疗和预防开辟新途径。