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系统免疫学方法用于理解黄热病患者急性感染中的免疫反应

Systems Immunology Approaches to Understanding Immune Responses in Acute Infection of Yellow Fever Patients.

作者信息

Gonçalves André N A, Costa Priscilla R, Thomazella Mateus V, Correia Carolina A, Marmorato Mariana P, Dias Juliana Z C, Silveira Cassia G T, Maestri Alvino, Cerqueira Natalia B, Moreira Carlos H V, Buccheri Renata, Félix Alvina C, Martins Felipe M, Maso Vanessa E, Ferreira Frederico M, Araújo José D A, Vasconcelos Amanda P, Gonzalez-Dias Patrícia, Pelletier Adam-Nicolas, Sékaly Rafick-Pierre, Cabral-Marques Otavio, Coelho-Dos-Reis Jordana G A, Ferreira Daniela M, Kallas Esper G, Nakaya Helder I

机构信息

Oxford Vaccine Group, NIHR Oxford Biomedical Research Centre, Oxford, UK.

Department of Clinical and Toxicological Analyses, School of Pharmaceutical Sciences, University of São Paulo, São Paulo, Brazil.

出版信息

J Med Virol. 2024 Dec;96(12):e70099. doi: 10.1002/jmv.70099.

Abstract

In the 2018 yellow fever (YF) outbreak in Brazil, we generated new transcriptomic data and combined it with clinical and immunological data to decode the pathogenesis of YF. Analyzing 79 patients, we found distinct gene expression patterns between acute YF, other viral infections, and the milder YF-17D vaccine infection. We identified a critical role for low-density, immature neutrophils in severe outcomes, marked by the downregulation of genes essential for neutrophil migration and maturation, such as PADI4, CSF3R, and ICAM1, in deceased patients. Our study also revealed complex interactions among inflammation-related genes, including increased CXCL10 and IL1R2 expression and decreased IL-1b expression in the acute phase. The diminished expression of HLA class II genes indicates impaired antigen presentation. These findings highlight the delicate balance of immune responses in YF pathogenesis and lay the groundwork for future therapeutic and diagnostic advancements.

摘要

在2018年巴西黄热病(YF)疫情中,我们生成了新的转录组数据,并将其与临床和免疫学数据相结合,以解读黄热病的发病机制。通过分析79名患者,我们发现急性黄热病、其他病毒感染以及症状较轻的YF-17D疫苗感染之间存在不同的基因表达模式。我们确定了低密度、未成熟中性粒细胞在严重后果中起关键作用,这在死亡患者中表现为中性粒细胞迁移和成熟所必需的基因(如PADI4、CSF3R和ICAM1)下调。我们的研究还揭示了炎症相关基因之间的复杂相互作用,包括急性期CXCL10和IL1R2表达增加以及IL-1b表达降低。HLA II类基因表达的减少表明抗原呈递受损。这些发现突出了黄热病发病机制中免疫反应的微妙平衡,并为未来的治疗和诊断进展奠定了基础。

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