# Interleukins in COVID-19 and SARS-CoV-2 Variants: Immunopathogenesis, Therapeutic Perspectives and Vaccine-Induced Immune Responses

**Authors:** Supriya Mahajan, Saurabh Mahajan, Akanksha Gusain

PMC · DOI: 10.3390/ijms27031391 · International Journal of Molecular Sciences · 2026-01-30

## TL;DR

This paper reviews how interleukins influence the severity of COVID-19 and immune responses to vaccines, focusing on differences between SARS-CoV-2 variants.

## Contribution

The paper provides a comprehensive analysis of interleukin roles across SARS-CoV-2 variants and their impact on disease severity and vaccine responses.

## Key findings

- Pro-inflammatory interleukins like IL-1β, IL-6, and IL-18 are linked to severe disease outcomes in COVID-19.
- Delta variant shows elevated levels of several interleukins compared to Omicron.
- Tocilizumab, an IL-6 inhibitor, shows some promise in treating severe COVID-19.

## Abstract

The Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is characterized by profound immune dysregulation where interleukins play a central role in determining disease severity and response to interventions. This review summarizes the role of interleukins in the immunopathogenesis of COVID-19, with particular emphasis on differences observed across major SARS-CoV-2 variants. Pro-inflammatory interleukins like IL-1β, IL-6, IL-2, IL-17 and IL-18 are critically involved in cytokine storm, hyperinflammation, and acute respiratory distress syndrome, whereas anti-inflammatory cytokines like IL-10 contribute to immune regulation and resolution of inflammation. Elevated levels of IL-1α, IL-1β, IL-4, IL-8, IL-9, IL-16, IL-18 have been documented in the Delta variant as compared with the Omicron variant, with IL-6 being the most frequent interleukin reported to be increased across all SARS-CoV-2 variants relative to the ancestral Wuhan strain. Elevated IL-2, IL-4, IL-6, and IL-10 levels have been associated with Omicron sub-variants. The review encompasses interleukin-based therapeutic strategies, where several IL-1 and IL-6 inhibitors were studied across clinical trials, but only tocilizumab has shown some promise against severe COVID-19. IL-2, IL-6, IL-15 and IL-21 levels were positively correlated with IgG and neutralizing antibody activity after vaccination with longevity of post-vaccination immunity being determined by IL-2 and IL-7.

## Linked entities

- **Proteins:** IL1B (interleukin 1 beta), IL6 (interleukin 6), IL2 (interleukin 2), IL17A (interleukin 17A), IL18 (interleukin 18), IL10 (interleukin 10), IL1A (interleukin 1 alpha), IL4 (interleukin 4), CXCL8 (C-X-C motif chemokine ligand 8), IL9 (interleukin 9), IL16 (interleukin 16), IL15 (interleukin 15), IL21 (interleukin 21), IL7 (interleukin 7)
- **Diseases:** Coronavirus disease 2019 (MONDO:0100096), severe acute respiratory syndrome coronavirus 2 (MONDO:0100096), cytokine storm (MONDO:0600008), acute respiratory distress syndrome (MONDO:0006502)

## Full-text entities

- **Genes:** IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, IL15 (interleukin 15) [NCBI Gene 3600] {aka IL-15}, IL9 (interleukin 9) [NCBI Gene 3578] {aka HP40, IL-9, P40}, IL7 (interleukin 7) [NCBI Gene 3574] {aka IL-7, IMD130}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, IL16 (interleukin 16) [NCBI Gene 3603] {aka LCF, NIL16, PRIL16, prIL-16}, IL21 (interleukin 21) [NCBI Gene 59067] {aka CVID11, IL-21, Za11}, IL18 (interleukin 18) [NCBI Gene 3606] {aka IGIF, IL-18, IL-1g, IL1F4}
- **Diseases:** COVID-19 (MESH:D000086382), acute respiratory distress syndrome (MESH:D012128), inflammation (MESH:D007249), immune dysregulation (OMIM:614878)
- **Chemicals:** tocilizumab (MESH:C502936)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12897649/full.md

## References

137 references — full list in the complete paper: https://tomesphere.com/paper/PMC12897649/full.md

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Source: https://tomesphere.com/paper/PMC12897649