# Vitamin D in Infectious Diseases: A Narrative Review Focusing on COVID-19, Long COVID, and Influenza

**Authors:** Olga Adriana Caliman-Sturdza, Roxana Elena Gheorghita, Iuliana Soldanescu, Mihai Dimian, Serghei Mangul

PMC · DOI: 10.3390/nu18040634 · Nutrients · 2026-02-14

## TL;DR

This paper reviews how vitamin D affects immune responses and outcomes in diseases like COVID-19, long COVID, and influenza.

## Contribution

It synthesizes current evidence on vitamin D's role in modulating immunity and disease outcomes for respiratory infections.

## Key findings

- Vitamin D enhances innate immunity through antimicrobial peptides and modulates adaptive immune responses.
- Low vitamin D levels are linked to severe COVID-19 outcomes, though causality is unclear.
- Supplementation may reduce ICU admissions and influenza risk in vitamin D-deficient populations.

## Abstract

Vitamin D is a secosteroid hormone traditionally recognized for its role in bone and mineral metabolism, but it is increasingly understood to also function as an important immunomodulator influencing susceptibility to and outcomes of infectious diseases. This narrative review summarizes current evidence on the immunological, clinical, and preventive effects of vitamin D in the context of novel coronavirus disease (COVID-19), post-acute sequelae of SARS-CoV-2 infection (long COVID), and influenza. Mechanistically, vitamin D enhances innate immune defenses through the induction of antimicrobial peptides, including cathelicidin and defensins, and modulates adaptive immunity by suppressing maladaptive Th1/Th17 responses while promoting regulatory T-cell activity. Observational studies have frequently associated vitamin D deficiency with more severe COVID-19 outcomes; however, these associations may be influenced by confounding factors and reverse causality. Some meta-analyses suggest that vitamin D supplementation reduced rates of intensive care unit admission and ventilatory support, particularly among older adults and individuals with low baseline serum 25-hydroxyvitamin D concentrations. Emerging evidence also indicates that inadequate vitamin D status may be associated with an increased risk and symptom burden of long COVID, although causality has not been established. In the case of influenza, a limited number of randomized controlled trials (RCTs) and meta-analyses report a modest but statistically significant reduction in infection risk, especially with daily or weekly vitamin D supplementation in populations with low baseline vitamin D levels. Clinical guidelines consistently recommend maintaining adequate vitamin D status for general health but do not endorse high-dose vitamin D as a treatment for COVID-19 due to inconsistent trial findings. Overall, vitamin D should not be considered a standalone therapeutic agent; rather, maintaining sufficient vitamin D levels represents a low-risk, potentially beneficial strategy to support immune resilience against respiratory viral infections.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096), influenza (MONDO:0005812)

## Full-text entities

- **Genes:** IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, CAMP (cathelicidin antimicrobial peptide) [NCBI Gene 820] {aka CAP-18, CAP18, CRAMP, FALL-39, FALL39, HSD26}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, VDR (vitamin D receptor) [NCBI Gene 7421] {aka NR1I1, PPP1R163}, CCL22 (C-C motif chemokine ligand 22) [NCBI Gene 6367] {aka A-152E5.1, ABCD-1, DC/B-CK, MDC, SCYA22, STCP-1}, IL23A (interleukin 23 subunit alpha) [NCBI Gene 51561] {aka IL-23, IL-23A, IL23P19, P19, SGRF}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, 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}
- **Diseases:** acute (MESH:D000208), acute respiratory distress syndrome (MESH:D012128), fever (MESH:D005334), tissue damage (MESH:D017695), Long COVID Symptoms (MESH:D000094024), Infectious Diseases (MESH:D003141), inflammatory cytokines (MESH:D000080424), autoimmune response (MESH:D001327), obese (MESH:D009765), fatigue (MESH:D005221), influenza pneumonia (MESH:D011014), Vitamin D deficiency (MESH:D014808), Infections (MESH:D007239), breathlessness (MESH:D004417), cardiovascular disease (MESH:D002318), diabetes (MESH:D003920), lung damage (MESH:D008171), COVID (MESH:D000086382), cancer (MESH:D009369), cough (MESH:D003371), toxicity (MESH:D064420), dermatologic problems (MESH:D000168), injury to (MESH:D014947), acute respiratory infection (MESH:D012141), long-term (MESH:D000088562), deficiencies in innate immunity (MESH:D007249), hypertension (MESH:D006973), influenza A infection (MESH:D007251), deaths (MESH:D003643), non-influenza respiratory diseases (MESH:D012140), deficiency (MESH:D007153), viral infections (MESH:D014777), reduced mobility (MESH:D014086)
- **Chemicals:** 1,25(OH)2D3 (MESH:D002117), magnesium (MESH:D008274), reactive oxygen species (MESH:D017382), lumisterol (MESH:D004875), cholecalciferol (MESH:D002762), vitamin K2 (MESH:D024482), cod liver oil (MESH:D003060), 1,25(OH)2D33 (-), Calcifediol (MESH:D002112), Vitamin D (MESH:D014807), 25-hydroxyvitamin D (MESH:C104450), oxygen (MESH:D010100)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Orthomyxoviridae (family) [taxon 11308]

## Full text

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## References

124 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943368/full.md

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Source: https://tomesphere.com/paper/PMC12943368