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耐受原性树突状细胞可减少慢性恰加斯病的心脏炎症和纤维化。

Tolerogenic Dendritic Cells Reduce Cardiac Inflammation and Fibrosis in Chronic Chagas Disease.

机构信息

Gonçalo Moniz Institute, FIOCRUZ, Salvador, Brazil.

Center for Biotechnology and Cell Therapy, Hospital São Rafael, Salvador, Brazil.

出版信息

Front Immunol. 2020 Apr 7;11:488. doi: 10.3389/fimmu.2020.00488. eCollection 2020.

Abstract

Chronic Chagas disease cardiomyopathy (CCC) is the most frequent and severe form of this parasitic disease. CCC is caused by a progressive inflammation in the heart, resulting in alterations that can culminate in heart failure and death. The use of dendritic cells (DCs) appears as an option for the development of treatments due to their important role in regulating immune responses. Here, we investigated whether tolerogenic cells (tDCs) could interfere with the progression of CCC in an experimental model of Chagas disease. The tDCs were generated and characterized as CD11b CD11c cells, low expression of MHC-II, CD86, CD80, and CD40, and increased expression of PD-L. These cells produced low levels of IL-6 and IL-12p70 and higher levels of IL-10, compared to mature DCs (mDCs). Interestingly, tDCs inhibited lymphoproliferation and markedly increased the population of FoxP3 Treg cells , compared to mature DCs. In a mouse model of CCC, treatment with tDCs reduced heart inflammation and fibrosis. Furthermore, tDCs treatment reduced the gene expression of pro-inflammatory cytokines ( and ) and of genes related to cardiac remodeling ( and ), while increasing the gene expression of IL-10. Finally, administration of tDCs, increased the percentage of Treg cells in the hearts and spleens of chagasic mice. Ours results show that tolerogenic dendritic cells have therapeutic potential on CCC, inhibiting disease progression.

摘要

慢性恰加斯病心肌病(CCC)是这种寄生虫病最常见和最严重的形式。CCC 是由心脏的进行性炎症引起的,导致的改变最终可导致心力衰竭和死亡。树突状细胞(DCs)的使用似乎是开发治疗方法的一种选择,因为它们在调节免疫反应方面起着重要作用。在这里,我们研究了耐受型细胞(tDCs)是否可以在恰加斯病的实验模型中干扰 CCC 的进展。tDCs 被生成并被鉴定为 CD11b CD11c 细胞,其 MHC-II、CD86、CD80 和 CD40 的表达较低,而 PD-L 的表达增加。与成熟的 DCs(mDCs)相比,这些细胞产生的 IL-6 和 IL-12p70 水平较低,而 IL-10 水平较高。有趣的是,与成熟的 DCs 相比,tDCs 抑制了淋巴细胞增殖,并显著增加了 FoxP3+Treg 细胞的数量。在 CCC 的小鼠模型中,tDCs 治疗可减少心脏炎症和纤维化。此外,tDCs 治疗降低了促炎细胞因子(和)和与心脏重塑相关的基因(和)的基因表达,同时增加了 IL-10 的基因表达。最后,tDCs 的给药增加了恰加斯病小鼠心脏和脾脏中 Treg 细胞的百分比。我们的结果表明,耐受型树突状细胞具有抑制疾病进展的 CCC 治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1905/7154094/c677a5c34d08/fimmu-11-00488-g0001.jpg

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