# Dengue–SARS-CoV-2 interactions: immune crosstalk, variant emergence, and clinical outcomes

**Authors:** Mariana Parra-González, Lucio Nájera-Maldonado, Esperanza Peralta-Cuevas, Ashley Gutierrez-Onofre, Luis A. Jaimes-López, Juan A. Juarez-Antonio, Nahomi Y. Degollado-Hernández, Igor Garcia-Atutxa, Francisca Villanueva-Flores

PMC · DOI: 10.3389/fimmu.2026.1650425 · Frontiers in Immunology · 2026-02-05

## TL;DR

This paper reviews how dengue and SARS-CoV-2 co-infection may worsen disease severity and influence viral evolution through immune interactions.

## Contribution

The paper integrates molecular, immunological, and epidemiological evidence to propose mechanisms underlying dengue–SARS-CoV-2 co-infection outcomes.

## Key findings

- Co-infection can lead to severe complications like hemorrhagic stroke and acute kidney injury.
- Antibody-dependent enhancement and cross-reactive immune responses may worsen disease severity.
- Co-circulation of dengue and SARS-CoV-2 may influence viral evolution through selective pressures.

## Abstract

This review aims to provide an overview of dengue–COVID–19 co-infection, emphasizing recently described immunological, genomic, and eco-epidemiological interactions that may influence clinical outcomes and viral evolution. It brings together molecular evidence, immunological perspectives, and epidemiological insights to summarize current hypotheses and working models of these complex disease interactions. We summarize and critically discuss evidence on antibody-dependent enhancement (ADE), cross-reactive immune responses, and cytokine amplification pathways, and propose mechanisms that could underlie exacerbated disease severity. Published clinical data indicate heterogeneity in co-infection outcomes globally, from mild presentations to severe complications, such as hemorrhagic stroke, acute kidney injury, and increased mortality, particularly among populations with prior dengue exposure. Diagnostic complexities arising from serological cross-reactivity underscore the need for simultaneous molecular testing to ensure accurate pathogen identification. Additionally, we review current evidence on reciprocal selective pressures between SARS-CoV-2 variants and dengue serotypes, highlighting potential evolutionary impacts arising from their co-circulation. The available evidence suggests that co-infection may exacerbate inflammatory pathways, lead to increased vascular and organ damage, and complicate patient management. However, definitive clinical evidence for ADE remains inconclusive, underscoring an ongoing need for targeted mechanistic studies. By outlining significant knowledge gaps and summarizing proposed research directions, this review aims to provide a valuable reference for clinicians, immunologists, epidemiologists, and policymakers managing concurrent dengue and COVID-19 outbreaks.

Diagram illustrating immune crosstalk between Dengue and SARS-CoV-2. A mosquito and Dengue virus icon sit opposite the SARS-CoV-2 icon. An arrow labeled “Immune crosstalk” connects them. Below, the implications include “Antibody-dependent enhancement,” “Vascular and organ damage,” and “Variant emergence.” A sick person icon represents “Co-infection and severe illness."

## Linked entities

- **Diseases:** dengue (MONDO:0005502), SARS-CoV-2 (MONDO:0100096), COVID-19 (MONDO:0100096), hemorrhagic stroke (MONDO:1060199), acute kidney injury (MONDO:0002492)

## Full-text entities

- **Genes:** IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, FCGR1A (Fc gamma receptor Ia) [NCBI Gene 2209] {aka CD64, CD64A, FCG1, FCGR1, FCRI, FcgammaRI}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, FCGR2B (Fc gamma receptor IIb) [NCBI Gene 2213] {aka CD32, CD32B, FCG2, FCGR2, IGFR2}
- **Diseases:** inflammation (MESH:D007249), dengue hemorrhagic fever/shock syndrome (MESH:D019595), headache (MESH:D006261), arbovirus (MESH:D001102), shock (MESH:D012769), capillary leakage (MESH:D003763), respiratory complications (MESH:D012140), hemorrhagic fever (MESH:D006480), ADE (MESH:C564835), lymphopenia (MESH:D008231), dyspnea (MESH:D004417), hyperinflammatory lung injury (MESH:D055370), hemorrhagic stroke (MESH:D000083302), febrile (MESH:D000071072), bleeding (MESH:D006470), multi-organ dysfunction (MESH:D009102), dengue (MESH:D003715), Leukopenia (MESH:D007970), respiratory failure (MESH:D012131), rash (MESH:D005076), COVID pneumonia (MESH:D011014), confusion (MESH:D003221), Stroke (MESH:D020521), acute kidney injury (MESH:D058186), hypercoagulability (MESH:D019851), viremia (MESH:D014766), ARDS (MESH:D012128), fever (MESH:D005334), hypotension (MESH:D007022), vomiting (MESH:D014839), thrombosis (MESH:D013927), respiratory symptoms (MESH:D012818), Symptom (MESH:D012816), Co (MESH:D060085), ground-glass opacities (MESH:C000721427), death (MESH:D003643), DENV-SARS-CoV-2 infection (MESH:D000086382), thrombocytopenia (MESH:D013921), coagulopathy (MESH:D001778), -infection (MESH:D007239), vascular leak (MESH:D019559), cough (MESH:D003371), vascular and organ damage (MESH:D057772), kidney injury (MESH:D007674), cardiac damage (MESH:D006331), myalgia (MESH:D063806), MIS (MESH:C000718087), asthenia (MESH:D001247), septic shock (MESH:D012772), infectious disease (MESH:D003141), tissue damage (MESH:D017695), cognitive impairment (MESH:D003072)
- **Chemicals:** CYD-TDV (-), dexamethasone (MESH:D003907), steroid (MESH:D013256)
- **Species:** Middle East respiratory syndrome-related coronavirus (no rank) [taxon 1335626], Mus musculus (house mouse, species) [taxon 10090], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Gammacoronavirus (genus) [taxon 694013], Pseudovirus (genus) [taxon 186672], Aedes (subgenus) [taxon 149531], Dothidea sp. ENV1 (species) [taxon 154308], Homo sapiens (human, species) [taxon 9606], Dengue virus (no rank) [taxon 12637], flavivirus [taxon 11051]
- **Mutations:** A35R, A29L, 35F

## Full text

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## Figures

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## References

76 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916716/full.md

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Source: https://tomesphere.com/paper/PMC12916716