# Dose-dependent immune modulation in arboviral coinfections among febrile patients

**Authors:** Peter Mac Asaga, Sunday Omilabu, Danaan Anthony Dakul

PMC · DOI: 10.3389/fcimb.2026.1776905 · Frontiers in Cellular and Infection Microbiology · 2026-02-23

## TL;DR

This study found high rates of arboviral infections and coinfections in Nigeria, with immune responses increasing with the number of viruses, highlighting the need for better diagnostics and control strategies.

## Contribution

The study provides new insights into dose-dependent immune modulation in arboviral coinfections and identifies circulating genotypes in Nigeria.

## Key findings

- Coinfection with two or more arboviruses was detected in 61.2% of participants.
- Cytokine levels like IL-6, TNF-α, IFN-γ, and IL-10 were significantly higher in dual and triple infections.
- DENV-2 and CHIKV East/Central/South African genotype were the most prevalent strains identified.

## Abstract

Arboviruses pose substantial diagnostic and public health challenges in tropical regions where multiple pathogens co-circulate. Nigeria, with diverse ecological zones and limited surveillance infrastructure, represents a critical nexus for arboviral transmission, yet comprehensive data on seroprevalence, coinfection dynamics, immune modulation, and viral genetic diversity remain scarce.

We conducted cross-sectional surveillance across three Nigerian ecological zones from January 2019 to December 2023. Sera from 871 participants were tested for IgG and IgM antibodies to dengue virus (DENV), chikungunya virus (CHIKV), Zika virus (ZIKV), yellow fever virus (YFV), West Nile virus (WNV), and Rift Valley fever virus (RVFV) using immunoblot assays. A stratified subset (n=300) underwent cytokine profiling for interleukin-6 (IL-6), tumour necrosis factor-alpha (TNF-α), interferon-gamma (IFN-γ), and interleukin-10 (IL-10). IgM-positive samples underwent RT-PCR confirmation with genotype assignment through sequence comparison against GenBank reference strains.

Overall IgM seropositivity indicating recent infection was 86.8% (756/871), with DENV most prevalent (59.6%; 95% CI: 56.3–62.8%), followed by CHIKV (49.4%), YFV (48.3%), ZIKV (19.7%), WNV (3.4%), and RVFV (2.3%). Coinfection with two or more arboviruses was detected in 61.2% (533/871) of participants. Seropositivity was highest in the tropical rainforest zone (94.2%) compared with Guinea savanna (84.5%) and Sudan savanna (80.4%; χ²=31.8, p<0.001). Cytokine profiling revealed significantly elevated concentrations of IL-6, TNF-α, IFN-γ, and IL-10 in dual and triple infections compared with mono-infections (all p<0.001), demonstrating dose-dependent immune modulation. All four DENV serotypes were identified, with DENV-2 predominating (59.9%). Molecular characterisation confirmed circulation of CHIKV East/Central/South African genotype (82.1%), DENV-2 Cosmopolitan genotype, and both African (71.2%) and Asian (28.8%) ZIKV lineages, with study sequences showing >99% nucleotide identity to established reference strains.

These findings reveal extraordinarily high levels of arboviral infection and coinfection across Nigerian ecological zones. The dose-dependent cytokine elevation in coinfections suggests distinct immunopathological mechanisms. These data underscore the urgent need for multiplex diagnostics, genotype-specific monitoring, and climate-informed vector control strategies.

## Linked entities

- **Proteins:** IL6 (interleukin 6), IL10 (interleukin 10)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IVNS1ABP (influenza virus NS1A binding protein) [NCBI Gene 10625] {aka ARA3, FLARA3, HSPC068, IMD70, KLHL39, ND1}
- **Diseases:** rash (MESH:D005076), febrile (MESH:D000071072), DENV (MESH:D003715), Fever (MESH:D005334), DD (MESH:C536170), headache (MESH:D006261), inflammation (MESH:D007249), myalgia (MESH:D063806), bacterial infection (MESH:D001424), congenital Zika syndrome (MESH:D000071243), immune dysregulation (OMIM:614878), malaria (MESH:D008288), arboviral (MESH:D004671), arboviral coinfections (MESH:D060085), arthralgia (MESH:D018771), infection (MESH:D007239)
- **Chemicals:** nuclease (-)
- **Species:** Zika virus (no rank) [taxon 64320], Yellow fever virus (no rank) [taxon 11089], Aedes albopictus (Asian tiger mosquito, species) [taxon 7160], Aedes aegypti (yellow fever mosquito, species) [taxon 7159], Dengue virus (no rank) [taxon 12637], Chikungunya virus (no rank) [taxon 37124], West Nile virus (no rank) [taxon 11082], flavivirus [taxon 11051], Aedes (subgenus) [taxon 149531], Homo sapiens (human, species) [taxon 9606], Rift Valley fever virus (no rank) [taxon 11588], Dothidea sp. ENV1 (species) [taxon 154308]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12968230/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12968230/full.md

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Source: https://tomesphere.com/paper/PMC12968230