Long-Term Arthralgia after Mayaro Virus Infection Correlates with Sustained Pro-inflammatory Cytokine Response

Mayaro virus (MAYV), an alphavirus similar to chikungunya virus (CHIKV), causes an acute debilitating disease which results in the development of long-term arthralgia in more than 50% of infected individuals. Currently, the immune response and its role in the development of MAYV-induced persistent a...

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Published inPLoS neglected tropical diseases Vol. 9; no. 10; p. e0004104
Main Authors Santiago, Felix W, Halsey, Eric S, Siles, Crystyan, Vilcarromero, Stalin, Guevara, Carolina, Silvas, Jesus A, Ramal, Cesar, Ampuero, Julia S, Aguilar, Patricia V
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 23.10.2015
Public Library of Science (PLoS)
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Summary:Mayaro virus (MAYV), an alphavirus similar to chikungunya virus (CHIKV), causes an acute debilitating disease which results in the development of long-term arthralgia in more than 50% of infected individuals. Currently, the immune response and its role in the development of MAYV-induced persistent arthralgia remain unknown. In this study, we evaluated the immune response of individuals with confirmed MAYV infection in a one-year longitudinal study carried out in Loreto, Peru. We report that MAYV infection elicits robust immune responses that result in the development of a strong neutralizing antibody response and the secretion of pro-inflammatory immune mediators. The composition of these inflammatory mediators, in some cases, differed to those previously observed for CHIKV. Key mediators such as IL-13, IL-7 and VEGF were strongly induced following MAYV infection and were significantly increased in subjects that eventually developed persistent arthralgia. Although a strong neutralizing antibody response was observed in all subjects, it was not sufficient to prevent the long-term outcomes of MAYV infection. This study provides initial immunologic insight that may eventually contribute to prognostic tools and therapeutic treatments against this emerging pathogen.
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Conceived and designed the experiments: ESH JSA PVA. Performed the experiments: FWS CS SV CG JAS. Analyzed the data: FWS ESH JSA PVA. Wrote the paper: FWS ESH CS JSA PVA. Evaluation of patients: ESH CS SV CR JSA.
The authors have declared that no competing interests exist.
ISSN:1935-2735
1935-2727
1935-2735
DOI:10.1371/journal.pntd.0004104