Chikungunya-virus-specific CD4+ T cells are associated with chronic chikungunya viral arthritic disease in humans

• Published in: bioRxiv 2023-11
• Main Authors: Chang, James, Agarwal, Rimjhim, Cortes, Fernanda H, Ha, Calvin, Villalpando, John, Castillo, Izabella, Galvez, Rosa Isela, Grifoni, Alba, Sette, Alessandro, Romero-Vivas, Claudia M, Heise, Mark T, Lakshmanane, Prem, Falconar, Andrew Keith, Weiskopf, Daniela
• Format: Article
• Language: English
• Subjects: Arthralgia; CD4 antigen; CD8 antigen; Chikungunya virus; Chronic infection; Epidemics; Flow cytometry; Helper cells; Infections; Leukocytes (mononuclear); Lymphocytes; Lymphocytes T; Outbreaks; Peripheral blood mononuclear cells; Tumor necrosis factor-TNF; Viral infections
• DOI: 10.1101/2023.11.20.567688

Chikungunya virus (CHIKV) is a mosquito-borne re-emerging viral infection that can cause chronic chikungunya viral arthritic disease (CHIKVD), which is characterized by incapacitating arthralgia and inflammation that can last for months to years following infection. Despite CHIKV outbreaks occurring worldwide and several vaccines currently in development, immune responses to CHIKV in humans remains largely understudied, and targets of T cell response are currently unknown. In this study, we tested peripheral blood mononuclear cells (PBMCs) collected from patients diagnosed with CHIKV infection during the 2014-2015 outbreak in Colombia against pools of overlapping peptides sequentially spanning each CHIKV protein. Using high-resolution flow cytometry, we detected robust CHIKV-specific CD4+, but not CD8+ T cell responses, in these patients. Patients still experiencing disease symptoms six years after infection displayed significantly stronger CHIKV-specific CD4+ T cell responses against nsP1, nsP2 and E2 proteins, compared to patients that resolved the infection. CHIKV-specific CD4+ T cells in symptomatic patients displayed a significantly lower Th1 CD4+ helper T cell responses and were enriched within the Th17 CD4+ helper subset, identifying tumor necrosis factor-alpha (TNF α) as the predominantly produced cytokine. In conclusion, this study comprehensively characterizes the T cell response against CHIKV in humans during the chronic phase and provides insights into the role of T cells and possible treatment of CHIKVD.Competing Interest StatementD.W. is a consultant for Moderna. The remaining authors declare no competing interests.