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Published on: November 5, 2019
Comparative long-term adverse effects elicited by invasive group B and C meningococcal infections
Magnus Gottfredsson1, Ingi K Reynisson, Ragnar F Ingvarsson
1Department of Medicine, The National University Hospital of Iceland, Reykjavik, Iceland. magnusgo@landspitali.is
Background:
Given the identity between Neisseria meningitidis serogroup B (MenB) capsular polysaccharide (polysialic acid; PSA) and PSA found on neural cell adhesion molecules, it has been proposed that infection with MenB or vaccination with PSA may be associated with subsequent autoimmune or neurological disease.
Methods:
We conducted 2 studies. The first was a retrospective nationwide study of invasive meningococcal disease (IMD) in Iceland (with 541 subjects) during the period 1975-2004, and we cross referenced this cohort with databases with respect to subsequent diagnosis of autoimmune disorders. A follow-up study involving 120 survivors of IMD was performed. The study included 70 patients with a history of MenB and 50 patients with N. meningitidis serogroup C (MenC) infection, who served as control subjects. Participants answered standardized questionnaires (Beck's Depression Inventory [BDI] II, Depression Anxiety Stress Scales [DASS], and Patient Health Questionnaire [PHQ]), and serum levels of immunoglobulin (Ig) G against MenB and MenC capsular polysaccharides were measured.
Results:
The nationwide cohort had 9166 patient-years of follow up. No evidence of increased autoimmunity was found to be associated with MenB, compared with MenC. In the follow-up study, patients were evaluated 16.6 years after the infection, representing 2022 patient-years of observation. Comparable rates of most complications were recorded, but MenC infections were associated with arthritis (P = .008) and migraine headaches (P = .01) more frequently than were MenB infections. No difference was observed with respect to scores on BDI-II, DASS, or PHQ. IgG anti-MenB and anti-MenC capsular polysaccharide levels were not related to patient complaints.
Conclusions:
This study does not support the hypothesis that MenB infection may predispose to autoimmunity. MenC infections are associated with a higher prevalence of arthritis and migraine headaches. No evidence of antibody-associated pathology was detected at long-term follow-up.
Insights
This study found no evidence that Neisseria meningitidis serogroup B (MenB) infection increases autoimmunity risk. MenC infections, however, were linked to higher rates of arthritis and migraine headaches.
Area of Science:
- Neuroscience
- Immunology
- Infectious Disease Epidemiology
Background:
- Neisseria meningitidis serogroup B (MenB) shares capsular polysaccharide (PSA) with neural cell adhesion molecules.
- This molecular mimicry raises concerns about MenB infection or PSA vaccination potentially triggering autoimmune or neurological diseases.
Purpose of the Study:
- To investigate the long-term association between MenB infection and autoimmune disorders.
- To compare the prevalence of neurological and autoimmune complications following MenB versus MenC infections.
Main Methods:
- A retrospective nationwide study in Iceland (1975-2004) linked invasive meningococcal disease (IMD) cases with autoimmune diagnoses.
- A follow-up study assessed 120 IMD survivors (70 MenB, 50 MenC) using standardized questionnaires and measured serum IgG levels against MenB and MenC capsular polysaccharides.
Main Results:
- No increased autoimmunity was observed in MenB cases compared to MenC.
- MenC infections were associated with higher rates of arthritis and migraine headaches (P = .008, P = .01, respectively).
- No significant differences in depression or anxiety scores were found; antibody levels did not correlate with reported symptoms.
Conclusions:
- The study does not support the hypothesis that MenB infection predisposes individuals to autoimmunity.
- MenC infections show a higher association with arthritis and migraine headaches.
- Long-term follow-up revealed no evidence of antibody-associated pathology in relation to MenB or MenC infections.
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