The Efficacy and Safety of Hepatitis A Vaccine in Children and Young Adults With an Autoinflammatory Diseases on Canakinumab and Tocilizumab Treatments: A Prospective Observational Controlled Study

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Özet

Intro: In this prospective interventional study, we aimed to assess the efficacy and safety of the hepatitis A vaccine in patients with autoinflammatory diseases undergoing canakinumab and tocilizumab treatments. Methods: A total of 24 patients with autoinflammatory diseases on canakinumab and tocilizumab treatments and 39 healthy children who were seronegative for hepatitis A were included in the study. All participants were vaccinated with 2 doses of inactivated hepatitis A vaccine at 6-month intervals. One month after the last vaccination, venous blood samples were collected from each participant, and the anti-HAV IgM and IgG titers were measured. Results: The patient group consisted of 19 patients with systemic juvenile idiopathic arthritis (sJIA) and 5 patients with cryopyrin-associated periodic fever. The mean age of the patient group and the healthy controls were 14.1 ± 3.7 and 12.4 ± 3.2 years, respectively. All patients with cryopyrin-associated periodic fever and 52.6% (10/19) of the patients with sJIA were on canakinumab. The remaining 9 patients (47.3%) with sJIA were using tocilizumab. Among sJIA patients, 15 were also on methotrexate, and 14 were on prednisolone. All of the participants were negative for hepatitis A serology. After two doses of hepatitis A vaccine, all the patients with autoinflammatory diseases (24/24) and 84.6% (33/39) of the healthy controls were detected as positive for anti-HAV IgG (p = 0.04). The mean anti-HAV Ig G titers of the patient group and the control group one month after the last dose of vaccination were 5.25 ± 1.49 IU/L and 10.5 ± 7.02 IU/L, respectively (p < 0.001). Neither disease flares nor adverse effects related to vaccination were observed within the study period. Conclusion: Hepatitis A vaccine is effective and safe in children with autoinflammatory diseases on biologic therapy. Long-term follow-up data, including larger patient cohorts, are needed to draw a solid conclusion about the safety of hepatitis A vaccine in patients receiving canakinumab and tocilizumab therapy.

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AlanDeğerDil
dc.contributor.authorBarut, Kenan
dc.contributor.authorYildiz, Mehmet
dc.contributor.authorBeşer, Ömer Faruk
dc.contributor.authorHaslak, Fatih
dc.contributor.authorGunalp, Aybuke
dc.contributor.authorKonte, Elif Kılıç
dc.contributor.authorAslan, Esma
dc.contributor.authorGül, Ümit
dc.contributor.authorAkay, Nergis
dc.contributor.authorAdrovic, Amra
dc.contributor.authorSahin, Sezgin
dc.contributor.authorMayda, Pelin Yüksel
dc.contributor.authorKocazeybek, Bekir
dc.contributor.authorKasapçopur, Özgür
dc.date.accessioned2026-10-27T23:47:38.022955180Z
dc.date.available2026-10-27T23:47:38.022955180Z
dc.date.issued2025
dc.description.abstractIntro: In this prospective interventional study, we aimed to assess the efficacy and safety of the hepatitis A vaccine in patients with autoinflammatory diseases undergoing canakinumab and tocilizumab treatments. Methods: A total of 24 patients with autoinflammatory diseases on canakinumab and tocilizumab treatments and 39 healthy children who were seronegative for hepatitis A were included in the study. All participants were vaccinated with 2 doses of inactivated hepatitis A vaccine at 6-month intervals. One month after the last vaccination, venous blood samples were collected from each participant, and the anti-HAV IgM and IgG titers were measured. Results: The patient group consisted of 19 patients with systemic juvenile idiopathic arthritis (sJIA) and 5 patients with cryopyrin-associated periodic fever. The mean age of the patient group and the healthy controls were 14.1 ± 3.7 and 12.4 ± 3.2 years, respectively. All patients with cryopyrin-associated periodic fever and 52.6% (10/19) of the patients with sJIA were on canakinumab. The remaining 9 patients (47.3%) with sJIA were using tocilizumab. Among sJIA patients, 15 were also on methotrexate, and 14 were on prednisolone. All of the participants were negative for hepatitis A serology. After two doses of hepatitis A vaccine, all the patients with autoinflammatory diseases (24/24) and 84.6% (33/39) of the healthy controls were detected as positive for anti-HAV IgG (p = 0.04). The mean anti-HAV Ig G titers of the patient group and the control group one month after the last dose of vaccination were 5.25 ± 1.49 IU/L and 10.5 ± 7.02 IU/L, respectively (p < 0.001). Neither disease flares nor adverse effects related to vaccination were observed within the study period. Conclusion: Hepatitis A vaccine is effective and safe in children with autoinflammatory diseases on biologic therapy. Long-term follow-up data, including larger patient cohorts, are needed to draw a solid conclusion about the safety of hepatitis A vaccine in patients receiving canakinumab and tocilizumab therapy.
dc.identifier.articlenumbere70196
dc.identifier.doi10.1111/1756-185x.70196
dc.identifier.eissn1756-185X
dc.identifier.issn1756-1841
dc.identifier.issue4
dc.identifier.pmid40172610
dc.identifier.scopus2-s2.0-105002075331
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/kostu/10555
dc.identifier.volume28
dc.identifier.wosWOS:001457892300001
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofInternational Journal of Rheumatic Diseases
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectanti-IL1
dc.subjectanti-IL6
dc.subjectautoinflammatory diseases
dc.subjectcanakinumab
dc.subjectCryopyrin-associated periodic syndrome
dc.subjectfamilial Mediterranean fever
dc.subjecthepatitis a vaccine
dc.subjectsystemic juvenile idiopathic arthritis
dc.subjecttocilizumab
dc.subject.classificationRheumatology
dc.subject.otherAdolescent
dc.subject.otherAge Factors
dc.subject.otherAntibodies, Monoclonal, Humanized
dc.subject.otherArthritis, Juvenile
dc.subject.otherCase-Control Studies
dc.subject.otherChild
dc.subject.otherCryopyrin-Associated Periodic Syndromes
dc.subject.otherFemale
dc.subject.otherHepatitis A
dc.subject.otherHepatitis A Vaccines
dc.subject.otherHumans
dc.subject.otherMale
dc.subject.otherProspective Studies
dc.subject.otherTime Factors
dc.subject.otherTreatment Outcome
dc.subject.otherVaccine Efficacy
dc.subject.otherYoung Adult
dc.subject.othercanakinumab
dc.subject.otherhepatitis A vaccine
dc.subject.othermethotrexate
dc.subject.otherprednisolone
dc.subject.othertocilizumab
dc.subject.othermonoclonal antibody
dc.subject.othervaccine
dc.subject.otheradult
dc.subject.otherantibody response
dc.subject.otherarthralgia
dc.subject.otherArticle
dc.subject.otherautoinflammatory disease
dc.subject.otherbiological therapy
dc.subject.otherblood sampling
dc.subject.otherclinical article
dc.subject.othercontrolled study
dc.subject.otherdrug efficacy
dc.subject.otherdrug safety
dc.subject.otherenzyme linked immunosorbent assay
dc.subject.otherfatigue
dc.subject.otherfever
dc.subject.otherhuman
dc.subject.otherjuvenile rheumatoid arthritis
dc.subject.othermyalgia
dc.subject.otherobservational study
dc.subject.otheroutcome variable
dc.subject.otherpediatrics
dc.subject.otherprospective study
dc.subject.otherschool child
dc.subject.othervaccination
dc.subject.othervisual analog scale
dc.subject.otherage
dc.subject.othercase control study
dc.subject.othercryopyrin-associated periodic syndrome
dc.subject.otherdiagnosis
dc.subject.otherdrug therapy
dc.subject.otherimmunology
dc.subject.otherprevention and control
dc.subject.othertime factor
dc.titleThe Efficacy and Safety of Hepatitis A Vaccine in Children and Young Adults With an Autoinflammatory Diseases on Canakinumab and Tocilizumab Treatments: A Prospective Observational Controlled Study
dc.typeArticle
rdl.citation.openalex1
rdl.citation.scopus1
rdl.citation.wos1
rdl.departmentDepartment of Pediatric Rheumatology, İstanbul University-Cerrahpaşa Cerrahpaşa, İstanbul, Turkey
rdl.departmentDepartment of Pediatric Gastroenterology, Hepatology, and Nutrition, İstanbul University-Cerrahpaşa Cerrahpaşa, İstanbul, Turkey
rdl.departmentKocaeli Health and Technology University, Faculty of Pharmacy, Kocaeli, Turkey
rdl.departmentİstanbul University-Cerrahpaşa Cerrahpaşa, Department of Medical Microbiology, İstanbul, Turkey
rdl.oa.statusbronze
rdl.oa.urlhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/1756-185X.70196
rdl.scopus.quartileQ3
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)