Immunogenicity and Safety of MenB Vaccine in Pediatric Patients With Autoimmune Rheumatic Diseases

Invasive meningococcal disease (IMD) is a severe infection caused by Neisseria meningitidis and can be life-threatening. In Brazil, the incidence of IMD has been reported as 2 per 100,000 children and adolescents, with serogroups B and C being the most prevalent. Severe infections are a major concern in patients with autoimmune rheumatic diseases (ARDs), as they are recognized as a leading cause of morbidity and mortality, accounting for up to one-third of all deaths in this population. In this context, there are currently two licensed vaccines against serogroup B in Brazil: the MenB-4C vaccine (Bexsero©) by GlaxoSmithKline (GSK), which includes four components, and the MenB-FHbp vaccine (Trumenba©) by Pfizer, which includes two components. The MenB-4C (Bexsero©) vaccine has broader coverage and is recommended in Brazil from 2 months of age. MenB-FHbp (Trumenba©, Pfizer) is approved in Brazil only for adolescents and young adults aged 10 to 25 years. Neither of these vaccines is included in Brazil's National Immunization Program (PNI) due to their high cost. Currently, the MenB-4C vaccine is licensed in over 35 countries and consists of three recombinant antigenic proteins. The Brazilian Society of Pediatrics recommends MenB-4C vaccination for children and adolescents aged 2 to 18 years, administered in two doses at least one month apart. The immunogenicity and safety of MenB-4C has been demonstrated in the general population through a meta-analysis of 18 studies, including phase I, II, and III randomized controlled clinical trials, involving 6,637 children and adolescents aged 2 months to 17 years. The incidence of serious adverse events (SAEs) potentially related to the vaccine was very low (0.54%) but significantly higher than in controls (0.12%) who received routine childhood vaccines. Despite this, the safety profile of MenB-4C is considered acceptable. Physical activity is a low-cost, scalable behavioral intervention that may enhance immune function, particularly relevant in immunocompromised populations such as children and adolescents with ARDs. While higher physical activity levels have been linked to improved vaccine responses in adults, its role in pediatric ARD patients remains unexplored. This study aims to fill this knowledge gap by investigating the association between physical activity and the humoral immune response to the MenB-4C vaccine, using both subjective and objective assessment methods. However, to date, no studies have evaluated the immunogenicity, safety and physical activity levels after MenB vaccines in pediatric patients with ARDs. Our study is a prospective, controlled, phase IV study that aims to evaluate the humoral immunogenicity of the MenB-4C vaccine in pediatric patients with ARDs compared to age and sex matched non-immunosuppressed controls. As secondary objectives we will assess the influence of short- and long-term immunosuppressive treatment on the vaccine response in patients with ARDs; to evaluate the impact of vaccination on disease activity in patients with ARDs; to assess the safety of the vaccine in pediatric ARD patients and controls and to evaluate the association between physical activity levels and vaccine-induced humoral immune responses in patients with ARDs. Participants will be between 2 and 25 years of age. Patients with JIA will be diagnosed based on the classification criteria of the International League of Associations for Rheumatology (ILAR); patients with JSLE, according to the American College of Rheumatology (ACR); and those with JDM, according to Bohan \& Peter criteria. A total of 263 patients will be included, of these,197 with ARDs and 66 healthy-matched controls. All participants will receive the MenB-4C vaccine (Bexsero©), administered intramuscularly in the deltoid muscle, in two doses (0.5 mL each) one month apart. Blood samples will be collected immediately before vaccination at baseline (D0), and the first vaccine dose will be administered on the same day (D0). The second dose will be administered 4 weeks after the first dose (D28). Blood samples will be collected on D0, D28, and D56. A final sample will be collected one year after the last dose (D208) to assess the persistence of the immune response. At baseline and one month after each dose, patients will also be assessed for clinical and laboratory disease activity using disease-specific inflammatory activity indices: * JSLE: Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI-2K): complete blood count (hemoglobin in g/dL, white blood cells and platelets in 1000/mm3, anti-dsDNA antibodies (in UI/mL), complement (in mg/dL), urinalysis (heme-granular or red blood cells urinary casts, hematuria \>5RBC/higpower field, proteinuria \>0.5g/24 hours, pyuria (\>5 white blood cells/ high-power field) and urine protein/creatinine ratio (in mg/dL); * JIA: Juvenile Arthritis Disease Activity Score (JADAS): erythrocyte sedimentation rate (in mm), and C-reactive protein (in mg/L); * JDM: Manual Muscle Testing (MMT) and Childhood Myositis Assessment Scale (CMAS): creatine phosphokinase (in U/L), transaminases (in U/L), and lactate dehydrogenase (in U/L). Safety will be closely monitored, and all serious adverse events will be classified as related or unrelated to the vaccine. A standardized adverse event diary will be provided to all patients and healthy controls for recording local and systemic reactions during the 4 weeks following each vaccine dose (D28 and D56). Local reactions include: injection site pain, redness, swelling, bruising, itching, and induration. Systemic reactions include: fever, fatigue, chills, malaise, drowsiness, loss of appetite, nausea, vomiting, diarrhea, abdominal pain, dizziness, tremors, headache, fatigue, myalgia, muscle weakness, arthralgia, pruritus, and skin rash. The severity of adverse events will be determined according to World Health Organization (WHO) criteria. Immunosuppressive treatments at each time point-including nonsteroidal anti-inflammatory drugs, prednisone/prednisolone, intra-articular corticosteroids, hydroxychloroquine, methotrexate, azathioprine, leflunomide, cyclosporine, tacrolimus, mycophenolate mofetil, and biologics (anti-TNF, tocilizumab, abatacept, belimumab, and rituximab) -will be systematically evaluated and correlated with possible impact with seroconversion. Humoral immunogenicity will be assessed by serum bactericidal activity (SBA) assay using exogenous complement (Baby rabbit, Pel Freez) against four test strains: H44/76 (fHBP), 5/99 (NadA), NZ98/254 (PorA), and M10713 (NHBA), from blood samples collected at D0, D30, D60, and D208. SBA assays will be performed at the Immunology Center of the Adolfo Lutz Institute, São Paulo. Briefly, exogenous complement will be added to serially diluted serum samples, followed by the addition of a bacterial suspension. The humoral response rate induced by the vaccine, or seroconversion, will be defined by the bactericidal titer (the dilution that results in 50% bacterial killing within 60 minutes compared to the control), with titers ≥ 1:4 considered bactericidal. The geometric mean titers will be calculated using the exponential of the mean of the log-transformed concentrations. Physical activity will be evaluated using age-appropriate validated questionnaires (IPAQ, PAQ-A, PAQ-C), classifying participants as active or inactive based on WHO guidelines (≥150 minutes/week of moderate-to-vigorous activity). Additionally, participants will wear a triaxial accelerometer (ActiGraph GTex®) continuously between days 7 and 14 after the first vaccine dose to objectively record movement intensity and volume.