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在进行中的球孢子菌病中耗竭调节性 T 细胞可挽救保护性 Th1/Th17 免疫并防止致命疾病结局。

Depletion of regulatory T cells in ongoing paracoccidioidomycosis rescues protective Th1/Th17 immunity and prevents fatal disease outcome.

机构信息

Departamento de Imunologia, Instituto de Ciências Biomédicas, Universidade de São Paulo, São Paulo, SP, Brazil.

Instituto de Ciência e Tecnologia, Universidade Federal de São Paulo, São José dos Campos, SP, Brazil.

出版信息

Sci Rep. 2018 Nov 8;8(1):16544. doi: 10.1038/s41598-018-35037-8.

Abstract

In human paracoccidioidomycosis (PCM), a primary fungal infection typically diagnosed when the disease is already established, regulatory T cells (Treg) cells are associated with disease severity. Experimental studies in pulmonary PCM confirmed the detrimental role of these cells, but in most studies, Tregs were depleted prior to or early during infection. These facts led us to study the effects of Treg cell depletion using a model of ongoing PCM. Therefore, Treg cell depletion was achieved by treatment of transgenic C57BL/6 (DEREG) mice with diphtheria toxin (DT) after 3 weeks of intratracheal infection with 1 × 10 Paracoccidioides brasiliensis yeasts. At weeks 6 and 10 post-infection, DT-treated DEREG mice showed a reduced number of Treg cells associated with decreased fungal burdens in the lungs, liver and spleen, reduced tissue pathology and mortality. Additionally, an increased influx of activated CD4 and CD8 T cells into the lungs and elevated production of Th1/Th17 cytokines was observed in DT-treated mice. Altogether, our data demonstrate for the first time that Treg cell depletion in ongoing PCM rescues infected hosts from progressive and potentially fatal PCM; furthermore, our data indicate that controlling Treg cells could be explored as a novel immunotherapeutic procedure.

摘要

在人类副球孢子菌病(PCM)中,原发性真菌感染通常在疾病已经确立时诊断,调节性 T 细胞(Treg)与疾病严重程度相关。肺部 PCM 的实验研究证实了这些细胞的有害作用,但在大多数研究中,Tregs 在感染前或早期被耗尽。这些事实促使我们使用正在进行的 PCM 模型研究 Treg 细胞耗竭的影响。因此,通过在气管内感染 1×10 个巴西副球孢子菌酵母 3 周后,用白喉毒素(DT)处理转基因 C57BL/6(DEREG)小鼠来实现 Treg 细胞耗竭。在感染后第 6 和第 10 周,DT 处理的 DEREG 小鼠显示与肺部、肝脏和脾脏中的真菌负荷减少相关的 Treg 细胞数量减少,组织病理学和死亡率降低。此外,在 DT 处理的小鼠中观察到激活的 CD4 和 CD8 T 细胞向肺部的流入增加和 Th1/Th17 细胞因子的产生增加。总之,我们的数据首次表明,在正在进行的 PCM 中耗尽 Treg 细胞可使感染宿主免于进行性和潜在致命的 PCM;此外,我们的数据表明,控制 Treg 细胞可能被探索为一种新的免疫治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f95/6224548/1688deafff3c/41598_2018_35037_Fig1_HTML.jpg

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