Rubella virus seropositivity after infection or vaccination as a risk factor for multiple sclerosisVisa övriga samt affilieringar
2024 (Engelska)Ingår i: European Journal of Neurology, ISSN 1351-5101, E-ISSN 1468-1331, Vol. 31, nr 10, artikel-id e16387Artikel i tidskrift (Refereegranskat) Published
Abstract [en]
Background: Multiple sclerosis (MS) is a demyelinating disease affecting millions of people worldwide. Hereditary susceptibility and environmental factors contribute to disease risk. Infection with Epstein–Barr virus (EBV) and human herpesvirus 6A (HHV-6A) have previously been associated with MS risk. Other neurotropic viruses, such as rubella virus (RV), are possible candidates in MS aetiopathogenesis, but previous results are limited and conflicting.
Methods: In this nested case–control study of biobank samples in a Swedish cohort, we analysed the serological response towards RV before the clinical onset of MS with a bead-based multiplex assay in subjects vaccinated and unvaccinated towards RV. The association between RV seropositivity and MS risk was analysed with conditional logistic regression.
Results: Seropositivity towards RV was associated with an increased risk of MS for unvaccinated subjects, even when adjusting for plausible confounders including EBV, HHV-6A, cytomegalovirus and vitamin D (adjusted odds ratio [AOR] = 4.0, 95% confidence interval [CI] 1.8–8.8). Cases also had stronger antibody reactivity towards rubella than controls, which was not seen for other neurotropic viruses such as herpes simplex or varicella zoster. Furthermore, we observed an association between RV seropositivity and MS in vaccinated subjects. However, this association was not significant when adjusting for the aforementioned confounders (AOR = 1.7, 95% CI 1.0–2.9).
Conclusions: To our knowledge, these are the first reported associations between early RV seropositivity and later MS development. This suggests a broadening of the virus hypothesis in MS aetiology, where molecular mimicry between rubella epitopes and human central nervous system molecules could be an attractive possible mechanism.
Ort, förlag, år, upplaga, sidor
John Wiley & Sons, 2024. Vol. 31, nr 10, artikel-id e16387
Nationell ämneskategori
Infektionsmedicin Mikrobiologi inom det medicinska området Neurologi
Identifikatorer
URN: urn:nbn:se:umu:diva-228037DOI: 10.1111/ene.16387ISI: 001270657500001PubMedID: 39023088Scopus ID: 2-s2.0-85198855623OAI: oai:DiVA.org:umu-228037DiVA, id: diva2:1885818
Forskningsfinansiär
Forte, Forskningsrådet för hälsa, arbetsliv och välfärd, 2015-00195Forte, Forskningsrådet för hälsa, arbetsliv och välfärd, 2017-00687Hjärnfonden, FO2020-0077EU, Horisont 2020, 733161Vetenskapsrådet, 2015-02419Vetenskapsrådet, 2016- 02349Vetenskapsrådet, 2020-01998Vetenskapsrådet, 521-2012-2917Region Jämtland Härjedalen2024-07-252024-07-252024-10-28Bibliografiskt granskad