In March 2021, the CDC stated: “People with autoimmune conditions (including preceding Guillain-Barré syndrome) may receive a COVID-19 vaccine. However, it should be noted that no data are currently available on the safety of COVID-19 vaccines for people with autoimmune conditions.” This was the rationale for a group of Italian researchers to assess the risk of relapse after SARS-CoV-2 vaccination in patients with CIDP or MMN [1]. In this multicentre, cohort, case-crossover study, the frequency of relapse in CIDP and MMN patients who received and did not receive a vaccination were compared.
Researchers included 336 patients: 278 with CIDP and 58 with MMN. Most patients were treated with intravenous or subcutaneous immunoglobulin therapy (IVIg 44%, SCIg 23%) and 16% received no treatment. In total, 307 (91%) underwent SARS-CoV-2 vaccination: 269 (88%) with BNT-162b2 (Pfizer/BioNTech), 28 (9%) with mRNA-1273 (Moderna), and 10 (3%) with ChAdOx1 (AstraZeneca).
In the group of 29 unvaccinated patients, no clinical relapse was observed during the 3 months of follow-up. In the vaccinated group, 16 patients (5%; 13 CIDP, 3 MMN) had a relapse (RR 3.21; 95% CI 0.19–52.25). This difference was not statistically significant. However, during the 3-month control period before vaccination, only 3 patients (1%) relapsed. Therefore, the risk of relapse was increased after vaccination (RR 4.00; 95% CI 1.35–11.82). This increase was mainly driven by CIDP patients (RR 3.25; 95% CI 1.07–9.84). Of the 16 patients who relapsed, 4 did so after the first vaccination and 12 after the second. About 30% of these patients relapsed within a week after vaccination, which might indicate a causal relationship. In 12 patients, relapse required adjustment of therapy. The short-term safety profile of SARS-CoV-2 vaccination in this study was acceptable, with local and systemic adverse events almost exclusively being mild to moderate.
- Doneddu PE, et al. Risk of disease relapse and safety of SARS-CoV-2 vaccination in patients with chronic inflammatory neuropathies. EAN 2023 Annual Meeting, 1–4 July, Budapest, Hungary.
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Table of Contents: EAN 2023
Featured articles
Letter from the Editor
Alzheimer’s disease and dementia: the road towards proactive and preventive care
Overarching Theme: Big Data
Contribution of genomics and genetics to personalised medicine
How big data can boost care for neurodegenerative disorders
COVID-19
Amantadine in early COVID-19 enhances recovery
SARS-CoV-2 vaccination in CIDP and MMN: more benefit than harm
Cerebrovascular Disease and Stroke
Intensive BP reduction associated with smaller haematoma
Cognition and Dementia
Towards cell biology of Alzheimer’s disease
Epilepsy
Minimising co-medication optimises cenobamate efficacy in drug-resistant epilepsy
Headache and Pain
GLP-1 agonists induce weight loss and alleviate headache in idiopathic intracranial hypertension
Cannabis-based medicine does not beat placebo in central neuropathic pain
80% of patients reverse from chronic to episodic migraine on anti-CGRP antibodies
Multiple Sclerosis
Which patients can initially be treated with platform DMT?
Retinal layer thickness predicts disability accumulation in early RMS
Withdrawing DMF in early pregnancy does not increase relapse risk in pregnant patients with MS
Immunosenescence and MS: relevance to immunopathogenesis and treatment
Sleep Disorders
Nightmares during childhood linked to cognitive decline later in life
Sleep changes contribute to the pathogenesis of neurodegenerative diseases
Miscellaneous
EAN guidelines on the management of ALS
What neurologists should know about bladder and sexual problems
Laughing gas abuse often leads to polyneuropathy, myelopathy, and encephalopathy
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