Increased circulating levels of High Mobility Group Box 1 (HMGB1) in acute-phase Chikungunya virus infection: Potential disease biomarker

•HMGB1 serum levels are increased during CHIKV infections.•HMGB1 serum levels keeps increased all over the acute-phase of the disease.•HMGB1 serum levels positively correlates with CHIKV viremia.•Previous DENV infection or YFV vaccination does not affect HMGB1 serum levels. Chikungunya virus (CHIKV)...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of clinical virology 2022-01, Vol.146, p.105054-105054, Article 105054
Hauptverfasser: Rocha, Daniele C.P., Souza, Thiara Manuelle Alves, Nunes, Priscila Conrado Guerra, Mohana-Borges, Ronaldo, Paes, Marciano V., Guimarães, Gabriel M.C., Arcila, Juan C.S., Paiva, Iury Amâncio, Azeredo, Elzinandes Leal de, Damasco, Paulo Vieira, de Souza, Luiz José, dos Santos, Flavia B., Allonso, Diego
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:•HMGB1 serum levels are increased during CHIKV infections.•HMGB1 serum levels keeps increased all over the acute-phase of the disease.•HMGB1 serum levels positively correlates with CHIKV viremia.•Previous DENV infection or YFV vaccination does not affect HMGB1 serum levels. Chikungunya virus (CHIKV) causes a febrile syndrome with intense and debilitating arthralgia that can persist for several months or years after complete virus clearance. As there is no specific antiviral treatment or vaccine against CHIKV, identification of serological markers that help clinical management of CHIKV patients is urgent. The High Mobility Group Box 1 (HMGB1) protein is secreted to extracellular milieu and triggers an intense inflammatory process by inducing the overexpression of pro-inflammatory cytokines. HMGB1 plays an important role in several virus diseases as well as in rheumatoid arthritis. This study focus on the investigation of HMGB1 serum levels in a sera panel from CHIKV-infected patients in an attempt to assess its potential as a biomarker for chikungunya clinical management. Eighty CHIKV-positive samples and 32 samples from healthy donors were subjected to a quantitative HMGB1 ELISA assay to assess the HMGB1 circulating levels. HMGB1 levels were significantly higher in CHIKV-positive samples (516.12 ng/mL, SEM ± 48.83 ng/mL) compared to negative control (31.20 ng/mL, SEM ± 3.24 ng/mL, p 
ISSN:1386-6532
1873-5967
DOI:10.1016/j.jcv.2021.105054