# Association between vaccination and myasthenia gravis: a systematic review and meta-analysis

**Authors:** Chang Guan, Ruonan Zhang, Peixi Zhao, Ying Zhang, Lan Yu, Huijing Cui, Li Jiang, Tong Wu, Fang Liu, Yang Wu, Lin Huang, Hongmei Nan, Jian Wang, Peng Xu

PMC · DOI: 10.3389/fimmu.2026.1739730 · Frontiers in Immunology · 2026-02-11

## TL;DR

This study finds that vaccination reduces the risk of COVID-19 infection without significantly increasing myasthenia gravis flare-ups.

## Contribution

The study provides the first meta-analysis on the safety and effectiveness of vaccination in myasthenia gravis patients.

## Key findings

- Vaccination significantly reduces the risk of COVID-19 infection in MG patients.
- No significant increase in MG exacerbation was observed following vaccination.

## Abstract

Myasthenia gravis (MG) is a rare autoimmune disorder characterized by fluctuating muscle weakness due to impaired neuromuscular transmission. Vaccination remains a cornerstone of infectious disease prevention, yet concerns persist regarding potential autoimmune exacerbation in susceptible individuals. This systematic review and meta-analysis aimed to synthesize available evidence on the association between vaccination and MG, evaluating both vaccine effectiveness and safety in this population.

Observational studies in cohort or case-control formats were identified through systematic searches of PubMed, Web of Science, Embase, Cochrane Library, SinoMed, CNKI, Wanfang, and VIP databases from inception to June 24, 2025. Study quality was assessed using the Newcastle–Ottawa Scale (NOS). Pooled odds ratios (OR) with 95% confidence intervals (CI) were calculated using fixed- or random-effects models based on heterogeneity. Publication bias was assessed using funnel plots and Egger’s test.

Five studies encompassing 27,193 participants (22,618 vaccinated and 4,575 unvaccinated) met inclusion criteria. Meta-analysis demonstrated a significant protective effect of vaccination against COVID-19 infection (fixed-effects model: OR = 0.23, 95% CI [0.20–0.26], P < 0.001). Conversely, vaccination was not associated with a statistically significant increase in MG exacerbation (random-effects model: OR = 0.67, 95% CI [0.10–4.54], P = 0.68).

This study provides quantitative evidence that COVID-19 vaccination effectively reduces infection risk without significantly increasing MG exacerbation. These findings support the safety and clinical utility of vaccination in MG patients, emphasizing the need for individualized risk–benefit assessment and ongoing pharmacovigilance in this population.

https://www.crd.york.ac.uk/prospero/, identifier CRD420251078995.

## Linked entities

- **Diseases:** myasthenia gravis (MONDO:0009688), COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** MUSK (muscle associated receptor tyrosine kinase) [NCBI Gene 4593] {aka CMS9, FADS}
- **Diseases:** autoimmune inflammatory rheumatic diseases (MESH:D012213), muscle weakness (MESH:D018908), COVID-19 (MESH:D000086382), Infections (MESH:D007239), MMR (MESH:D009107), Influenza (MESH:D007251), inflammatory (MESH:D007249), myasthenic crisis (MESH:D020294), disease (MESH:D004194), infectious (MESH:D003141), MG (MESH:D009157), jSLE (MESH:D008180), smallpox (MESH:D012899), autoimmune neuromuscular disorders (MESH:D009468), autoimmune neuromuscular junction disorder (MESH:D020511), immune dysregulation (OMIM:614878), poliomyelitis (MESH:D011051), autoimmune (MESH:D001327), measles (MESH:D008457), respiratory compromise (MESH:D012131)
- **Chemicals:** methotrexate (MESH:D008727)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human papillomavirus (species) [taxon 10566], Legionella sp. H (species) [taxon 66966], Human alphaherpesvirus 3 (Varicella-zoster virus, no rank) [taxon 10335]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12932598/full.md

## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932598/full.md

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Source: https://tomesphere.com/paper/PMC12932598