# SARS-CoV-2 and Influenza Co-Circulation and Co-Vaccination: A Narrative Review

**Authors:** Mohammad Kamransarkandi, Elena A. Varyushina, Andrey N. Gorshkov, Marina A. Stukova

PMC · DOI: 10.3390/vaccines14030283 · Vaccines · 2026-03-23

## TL;DR

This review discusses the overlapping spread of SARS-CoV-2 and influenza viruses and the benefits of combining their vaccinations to improve public health outcomes.

## Contribution

The paper provides a comprehensive analysis of co-circulation and co-vaccination strategies for SARS-CoV-2 and influenza, emphasizing their combined public health impact.

## Key findings

- Co-infection with SARS-CoV-2 and influenza increases risks of severe respiratory outcomes like pneumonia.
- Combined vaccination is convenient, improves compliance, and reduces healthcare burden.
- Available vaccines for both viruses are effective, immunogenic, and safe.

## Abstract

Background/Objectives: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and influenza virus are dangerous respiratory pathogens with high pandemic potential. Since 2021, these two viruses have been co-circulating, which implies additional risks of co-infection with both pathogens. Prophylactic vaccination is widely recognized as the most effective way to prevent COVID-19 and influenza and to reduce the severity of these diseases. This review analyzes recent data on the simultaneous circulation of influenza and SARS-CoV-2 viruses worldwide, including epidemiological data and the pathogenetic mechanisms of co-infection. Next, we focus on current approaches to simultaneous and combined vaccination against influenza and COVID-19. We outline the types of vaccines and summarize the available findings on the effectiveness and safety of co-vaccination. Methods: A comprehensive search was conducted using PubMed, Scopus, Web of Science, and ClinicalTrials to identify data relevant to SARS-CoV-2 and influenza co-circulation and dual vaccination. Results: Influenza and SARS-CoV-2 cause similar symptoms, and co-infection can significantly enhance the risks of pneumonia and acute respiratory distress syndrome progressing with a poor outcome, especially among children and the elderly. A range of influenza and COVID-19 vaccines built on different technological platforms is currently available on the market, with proven effectiveness, immunogenicity, and safety. A co-vaccination approach is more convenient for patients and is associated with better response to treatment, while also improving vaccine coverage and compliance and offering significant resource savings for healthcare systems. Conclusions: The concurrent circulation of SARS-CoV-2 and influenza viruses presents a growing public health challenge. Simultaneous and combination vaccination strategies have emerged as effective tools to streamline immunization, enhance protection, and reduce healthcare burden. Future studies should elucidate the mechanisms of the exacerbation of respiratory disease caused by co-infection, as well as the optimal strategies for co-administering influenza and COVID-19 vaccines for long-term control of seasonal and potentially pandemic respiratory viruses.

## Linked entities

- **Diseases:** pneumonia (MONDO:0005249), acute respiratory distress syndrome (MONDO:0006502), SARS-CoV-2 (MONDO:0100096), influenza (MONDO:0005812)

## Full-text entities

- **Genes:** CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, SPINK5 (serine peptidase inhibitor Kazal type 5) [NCBI Gene 11005] {aka LEKTI, LETKI, NETS, NS, VAKTI}, ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, Krt18 (keratin 18) [NCBI Gene 16668] {aka CK18, K18, Krt1-18}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, NEU1 (neuraminidase 1) [NCBI Gene 4758] {aka NANH, NEU, SIAL1}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, KRT31 (keratin 31) [NCBI Gene 3881] {aka HA1, Ha-1, KRTHA1, hHa1}, ACSM3 (acyl-CoA synthetase medium chain family member 3) [NCBI Gene 6296] {aka SA, SAH}, N (nucleocapsid phosphoprotein) [NCBI Gene 43740575], KRT18 (keratin 18) [NCBI Gene 3875] {aka CK-18, CYK18, K18}, S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}, VTN (vitronectin) [NCBI Gene 7448] {aka V75, VN, VNT}
- **Diseases:** injury to (MESH:D014947), respiratory infection (MESH:D012141), chest and abdominal pain (MESH:D015746), infected (MESH:D007239), deaths (MESH:D003643), sinus infections (MESH:D012852), pneumonia (MESH:D011014), adverse reactions (MESH:D064420), cardiovascular complications (MESH:D002318), pain (MESH:D010146), critically ill (MESH:D016638), lung tissue injury (MESH:D055370), organ damage (MESH:D000092124), bronchitis (MESH:D001991), acute respiratory distress syndrome (MESH:D012128), lung damage (MESH:D008171), loss of taste (MESH:D000370), viral infections (MESH:D014777), HAI (MESH:C565433), chills (MESH:D023341), symptoms (MESH:D012816), weight loss (MESH:D015431), eosinophilia (MESH:D004802), fever (MESH:D005334), diarrhea (MESH:D003967), sore throat (MESH:D010612), infectious disease (MESH:D003141), needle phobia (MESH:C000719195), respiratory disease (MESH:D012140), IAV infection (MESH:D007251), acute respiratory viral infections (MESH:D012120), anxiety (MESH:D001007), respiratory ailments (MESH:D012131), COVID (MESH:D000086382), vomiting (MESH:D014839), inflammatory (MESH:D007249), Co (MESH:D060085)
- **Chemicals:** AdC68 (-), Matrix-M (MESH:C000625666), PLGA (MESH:D000077182), AddaVax (MESH:C000590912), Lipid (MESH:D008055), glycolic acids (MESH:C031149), Betulin (MESH:C002503)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], H7N9 subtype (serotype) [taxon 333278], Qubevirus faecium (species) [taxon 39804], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606], Cricetus cricetus (black-bellied hamster, species) [taxon 10034], Enterovirus (genus) [taxon 12059], H3N2 subtype (serotype) [taxon 119210], H5N1 subtype (serotype) [taxon 102793], H1N1 subtype (serotype) [taxon 114727], Orthomyxoviridae (family) [taxon 11308], Influenza A virus (no rank) [taxon 11320], Bacteriophage sp. (species) [taxon 38018], Cricetinae (hamsters, subfamily) [taxon 10026], Respiratory syncytial virus (no rank) [taxon 12814]
- **Mutations:** D614G
- **Cell lines:** CHO — Cricetulus griseus (Chinese hamster), Spontaneously immortalized cell line (CVCL_0213), C57BL/6 — Mus musculus (Mouse), Transformed cell line (CVCL_C0MU)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13029830/full.md

## References

139 references — full list in the complete paper: https://tomesphere.com/paper/PMC13029830/full.md

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Source: https://tomesphere.com/paper/PMC13029830