免疫学
发病机制
免疫系统
CXCL10型
趋化因子
先天免疫系统
转录组
病毒学
黄热病疫苗
基因
炎症
生物
基因表达
黄热病
医学
病毒
遗传学
作者
André N. A. Gonçalves,Priscilla R. Costa,Mateus Vailant Thomazella,Carolina Argondizo Correia,Mariana Prado Marmorato,Juliana Zanatta de Carvalho Dias,Cássia Gisele Terrassani Silveira,Alvino Maestri,Natália B. Cerqueira,Carlos Henrique Valente Moreira,Renata Buccheri,Alvina Clara Félix,Felipe M. Martins,Vanessa Escolano Maso,Frederico Moraes Ferreira,José Deney Alves Araújo,Amanda Pereira Vasconcelos,Patrícia Gonzalez‐Dias,Adam‐Nicolas Pelletier,Rafick‐Pierre Sékaly
摘要
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.
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