Increased Indoleamine 2,3-Dioxygenase 1 (IDO-1) Activity and Inflammatory Responses during Chikungunya Virus Infection

Author:

Alves de Souza Thiara1,Fernandes-Santos Caroline1ORCID,Araújo da Paixão de Oliveira Jéssica2,Tomé Larissa1,Fiestas-Solórzano Victor1ORCID,Nunes Priscila1ORCID,Guimaraes Gabriel1,Sánchez-Arcila Juan1ORCID,Paiva Iury1ORCID,de Souza Luís3,Damasco Paulo4,da Silva Frutuoso Válber5,Heringer Manoela6,de Oliveira-Pinto Luzia1,Pinheiro Roberta2ORCID,dos Santos Flavia1ORCID,Leal de Azeredo Elzinandes1

Affiliation:

1. Viral Immunology Laboratory, Oswaldo Cruz Institute, Oswaldo Cruz Foundation (Fiocruz), Rio de Janeiro 21040-360, Brazil

2. Leprosy Laboratory, Oswaldo Cruz Institute, Oswaldo Cruz Foundation (Fiocruz), Rio de Janeiro 21040-360, Brazil

3. Reference Center for Immune and Infectious Diseases (CRDI), Faculty of Medicine, Campos dos Goytacazes, Brazil Campos dos Goytacazes, Rio de Janeiro 28025-496, Brazil

4. Department of General Medicine, Medicine and Surgery School, Gaffrée Guinle University Hospital, Federal University of State of Rio de Janeiro (UniRio), Rio de Janeiro 20270-004, Brazil

5. Laboratory of Immunopharmacology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation (Fiocruz), Rio de Janeiro 21040-360, Brazil

6. Brain Biomedicine Laboratory, Paulo Niemeyer State Brain Institute, Rio de Janeiro 20231-092, Brazil

Abstract

Chikungunya virus (CHIKV) infection causes intense cytokine/chemokine inflammatory responses and debilitating joint pain. Indoleamine2,3–dioxygenase 1 (IDO-1) is an enzyme that initiates the tryptophan degradation that is important in initial host innate immune defense against infectious pathogens. Besides that, IDO-1 activation acts as a regulatory mechanism to prevent overactive host immune responses. In this study, we evaluated IDO-1 activity and cytokine/chemokine patterns in CHIKV patients. Higher IDO-1 (Kyn/Trp ratio) activation was observed during the early acute phase of CHIKV infection and declined in the chronic phase. Importantly, increased concentrations of Tumor Necrosis Factor-α (TNF-α), Interleukin-6 (IL-6), Interferon γ (IFN-γ), C-C motif chemokine ligand 2/Monocyte Chemoattractant Protein-1 (CCL2/MCP-1) and C-X-C motif chemokine ligand 10/Interferon Protein-10 (CXCL10/IP-10) were found in the acute phase of infection, while C-C motif chemokine ligand 4/Macrophage Inflammatory Protein 1 β (CCL4/MIP-1β) was found at increased concentrations in the chronic phase. Likewise, CHIKV patients with arthritis had significantly higher concentrations of CCL4/MIP-1β compared to patients without arthritis. Taken together, these data demonstrated increased IDO-1 activity, possibly exerting both antiviral effects and regulating exacerbated inflammatory responses. CCL4/MIP-1β may have an important role in the persistent inflammation and arthritic symptoms following chikungunya infection.

Funder

Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro

Publisher

MDPI AG

Subject

Infectious Diseases,Microbiology (medical),General Immunology and Microbiology,Molecular Biology,Immunology and Allergy

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