Please use this identifier to cite or link to this item: http://hdl.handle.net/1843/61471
Type: Artigo de Periódico
Title: Serum Soluble Mediator Profiles and Networks During Acute Infection With Distinct DENV Serotypes
Authors: Mikelly Santos Coutinho-da-Silva
Lis Ribeiro do Valle Antonelli
Vitor Bortolo de Rezende
Fernanda Ludolf Ribeiro de Melo
Cristiana Couto Garcia
Jesuanne Carla Silva-Andrade
Ismael Artur da Costa-Rocha
Michele de Souza Bastos
Lucia Alves da Rocha
Valderjane Aprigio Silva
Ewerton da Silva Ferreira
Pedro Henrique Ferreira Sucupira
Eveny Perlize Melo Marinho
Allyson Guimarães Costa
Matheus de Souza Gomes
Laurence Rodrigues Amaral
Erilene Cristina da Silva Furtado
Eliana Vieira Pinto da Silva
Bruna Alves Ramos
Éder Barros Dos Santos
Maria Nazaré Oliveira Freitas
Pedro Fernando da Costa Vasconcelos
Kelly Alves Bicalho
Olindo Assis Martins-Filho
Márcio Sobreira Silva Araújo
Milene Silveira Ferreira
Livia Carício Martins
Ana Carolina Campi-Azevedo
Joaquim Pedro Brito-de-Sousa
Vanessa Peruhype-Magalhães
Maria Rios
Andrea Teixeira-Carvalho
Jordana Grazziela Alves Coelho Dos Reis
Abstract: A panoramic analysis of chemokines, pro-inflammatory/regulatory cytokines, and growth factors was performed in serum samples from patients with acute DENV infection (n=317) by a high-throughput microbeads array. Most soluble mediators analyzed were increased in DENV patients regardless of the DENV serotype. The substantial increase (≥10-fold) of CXCL10, IL-6, and IFN-γ, and decreased levels of PDGF (<0.4-fold) was universally identified in all DENV serotypes. Of note, increased levels of CXCL8, CCL4, and IL-12 (≥3-9-fold) were selectively observed in DENV2 as compared to DENV1 and DENV4. Heatmap and biomarker signatures further illustrated the massive release of soluble mediators observed in DENV patients, confirming the marked increase of several soluble mediators in DENV2. Integrative correlation matrices and networks showed that DENV infection exhibited higher connectivity among soluble mediators. Of note, DENV2 displayed a more complex network, with higher connectivity involving a higher number of soluble mediators. The timeline kinetics (Day 0-1, D2, D3, D4-6) analysis additionally demonstrated differences among DENV serotypes. While DENV1 triggers a progressive increase of soluble mediators towards D3 and with a decline at D4-6, DENV2 and DENV4 develop with a progressive increase towards D4-6 with an early plateau observed in DENV4. Overall, our results provided a comprehensive overview of the immune response elicited by DENV infection, revealing that infection with distinct DENV serotypes causes distinct profiles, rhythms, and dynamic network connectivity of soluble mediators. Altogether, these findings may provide novel insights to understand the pathogenesis of acute infection with distinct DENV serotypes.
Subject: Citocinas
Quimiocinas
Sorogrupo
Imunidade
Dengue
language: eng
metadata.dc.publisher.country: Brasil
Publisher: Universidade Federal de Minas Gerais
Publisher Initials: UFMG
metadata.dc.publisher.department: ICB - DEPARTAMENTO DE MICROBIOLOGIA
ICB - INSTITUTO DE CIÊNCIAS BIOLOGICAS
Rights: Acesso Aberto
metadata.dc.identifier.doi: https://doi.org/10.3389/fimmu.2022.892990
URI: http://hdl.handle.net/1843/61471
Issue Date: 31-May-2022
metadata.dc.url.externa: https://www.frontiersin.org/articles/10.3389/fimmu.2022.892990/full
metadata.dc.relation.ispartof: Frontiers in Immunology
Appears in Collections:Artigo de Periódico



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