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预先用α-生育酚处理的 C57BL/6 小鼠在感染后表现出更好的结果,组织炎症和纤维化程度较低。

C57BL/6 Mice Pretreated With Alpha-Tocopherol Show a Better Outcome of Infection With Less Tissue Inflammation and Fibrosis.

机构信息

Laboratory of Molecular and Structural Pathology, Gonçalo Moniz Institute, Fiocruz, Salvador, Brazil.

Department of Pathology, Faculty of Medicine, Federal University of Bahia, UFBA, Salvador, Brazil.

出版信息

Front Immunol. 2022 Jan 28;13:833560. doi: 10.3389/fimmu.2022.833560. eCollection 2022.

DOI:10.3389/fimmu.2022.833560
PMID:35154155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8832012/
Abstract

Chagas disease is accompanied by a multisystem inflammatory disorder that follows infection. Alpha-tocopherol has been described as an antioxidant and a potential adjuvant to enhance immune responses to vaccines. Therefore, we have evaluated the immune response to infection upon alpha-tocopherol pre-administration. The results show that administration of alpha-tocopherol before the infection results in lower parasitemia and lower mortality of C57BL/6 mice infected with the strain. Alpha-tocopherol administration in normal C57BL/6 mice resulted in higher levels of IFN-γ production by T and NK cells before and after the infection with . More importantly, previous administration of alpha-tocopherol increased the production of IL-10 by T and myeloid suppressor cells and the formation of effector memory T cells while decreasing the expression of PD-1 on T cells. These results suggest that alpha-tocopherol may limit the appearance of dysfunctional T cells during the acute and early chronic phases of infection, contributing to control infection. In addition, alpha-tocopherol could diminish tissue inflammation and fibrosis in late acute disease. These results strongly suggest that alpha-tocopherol may be a helpful agent to be considered in Chagas disease.

摘要

恰加斯病伴随着感染后的多系统炎症性疾病。α-生育酚已被描述为一种抗氧化剂,可作为增强疫苗免疫反应的辅助剂。因此,我们评估了α-生育酚预先给药对 感染的免疫反应。结果表明,在感染前给予α-生育酚可导致感染 株的 C57BL/6 小鼠的寄生虫血症降低和死亡率降低。在正常的 C57BL/6 小鼠中给予α-生育酚,可导致在感染 前后 T 和 NK 细胞产生更高水平的 IFN-γ。更重要的是,α-生育酚的预先给药增加了 T 和髓样抑制细胞产生 IL-10 的能力,并形成效应记忆 T 细胞,同时降低 T 细胞上 PD-1 的表达。这些结果表明,α-生育酚可能限制了 感染急性和早期慢性阶段中功能失调的 T 细胞的出现,有助于控制感染。此外,α-生育酚可减少晚期急性疾病中的组织炎症和纤维化。这些结果强烈表明,α-生育酚可能是一种有助于治疗恰加斯病的药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6701/8832012/bfbee83d1d27/fimmu-13-833560-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6701/8832012/9851845785b5/fimmu-13-833560-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6701/8832012/33ef64827c24/fimmu-13-833560-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6701/8832012/fde1a42c9f86/fimmu-13-833560-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6701/8832012/7bf509501ef0/fimmu-13-833560-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6701/8832012/ef99b0d51f56/fimmu-13-833560-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6701/8832012/bfbee83d1d27/fimmu-13-833560-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6701/8832012/9851845785b5/fimmu-13-833560-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6701/8832012/33ef64827c24/fimmu-13-833560-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6701/8832012/fde1a42c9f86/fimmu-13-833560-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6701/8832012/7bf509501ef0/fimmu-13-833560-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6701/8832012/ef99b0d51f56/fimmu-13-833560-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6701/8832012/bfbee83d1d27/fimmu-13-833560-g006.jpg

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Signal Transducer and Activator of Transcription-3 Modulation of Cardiac Pathology in Chronic Chagasic Cardiomyopathy.信号转导子和转录激活子 3 调节慢性恰加斯心肌病中心脏病理学。
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