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Maintenance of antibody response to diphtheria/tetanus vaccine in patients aged 2–5 years with polyarticular-course juvenile idiopathic arthritis receiving subcutaneous abatacept.

Authors :
Brunner, Hermine I.
Tzaribachev, Nikolay
Cornejo, Gabriel Vega
Joos, Rik
Gervais, Elisabeth
Cimaz, Rolando
Calvo Penadés, Inmaculada
Cuttica, Rubén
Lutz, Thomas
Quartier, Pierre
Gandhi, Yash
Nys, Marleen
Wong, Robert
Martini, Alberto
Lovell, Daniel J.
Ruperto, Nicolino
for the Pediatric Rheumatology Collaborative Study Group and the Paediatric Rheumatology International Trials Organisation
Anton, Jordi
Espada, Graciela
Lauwerys, Bernard
Source :
Pediatric Rheumatology. 2/22/2020, Vol. 18 Issue 1, p1-7. 7p.
Publication Year :
2020

Abstract

Background: Patients with polyarticular-course juvenile idiopathic arthritis (pJIA), receiving disease-modifying anti-rheumatic drugs with immunosuppressive effects, may be at increased risk of vaccine-preventable infections. This substudy assessed protective antibody responses to diphtheria and tetanus vaccination given prior to study enrolment in patients with pJIA. Findings: This was a substudy of a 24-month, single-arm, open-label, multicenter, Phase III trial (NCT01844518) of subcutaneous abatacept in children with active pJIA (N = 219). Patients aged 2–5 years, with ≥2 continuous months of weekly weight-tiered (10–< 25 kg [50 mg], 25–< 50 kg [87.5 mg]) subcutaneous abatacept treatment (with/without methotrexate and/or low-dose corticosteroids), who received diphtheria/tetanus vaccine prior to enrolment, were eligible. Protective antibody levels to diphtheria/tetanus (> 0.1 IU/mL), and safety, were assessed. Overall, 29 patients were analyzed: 19 (65.5%), 1 (3.4%) and 9 (31.0%) patients had > 12, 6–12 and 2–< 6 months of abatacept exposure, respectively. All patients had protective antibody levels to tetanus and 26 (89.7%) patients had protective antibody levels to diphtheria. Of the 3 patients without protective antibody levels to diphtheria, each had an antibody level of 0.1 IU/mL, bordering the lower threshold of protection. Concomitant use of methotrexate and/or low-dose corticosteroids had no evident effect on antibody levels. No unexpected adverse events, including cases of diphtheria or tetanus, were reported during the 24-month period. Conclusions: Patients aged 2–5 years with pJIA who received 2–24 months of weekly subcutaneous abatacept, with or without concomitant methotrexate and/or low-dose corticosteroids, maintained effective diphtheria and tetanus vaccination protection without new safety signals. Trial registration: ClinicalTrials.gov (NCT01844518); registered May 1, 2013; https://clinicaltrials.gov/ct2/show/NCT01844518?term=NCT01844518&rank=1 [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15460096
Volume :
18
Issue :
1
Database :
Academic Search Index
Journal :
Pediatric Rheumatology
Publication Type :
Academic Journal
Accession number :
141879660
Full Text :
https://doi.org/10.1186/s12969-020-0410-x