Evidence map›Paper›PMID 42498827›Full record

ArticlePediatric research2026

Immunogenicity and safety of BNT162b2 vaccine in patients with juvenile immune mediated inflammatory disease.

Carolina S E Gadelha, Maria Teresa Terreri, Ana Paula N Burian, Aline C M da Fraga, Ketty L L L Machado, Rita Elizabeth Checon, Daniel B Ferreira, Yhasmin O G Moraes, Sandra Lúcia E Ribeiro, Camila Maria P F Telles and 14 more

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Article in Pediatric research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

24 authors.

Carolina S E Gadelha *Federal University of Espírito Santo, Vitória, ES, Brazil.
Maria Teresa Terreri *Department of Pediatrics, Division of Pediatric Rheumatology, Federal University of São Paulo, São Paulo, SP, Brazil.
Ana Paula N BurianFederal University of Espírito Santo, Vitória, ES, Brazil.
Aline C M da FragaFederal University of Espírito Santo, Vitória, ES, Brazil.
Ketty L L L MachadoDepartment of Rheumatology, Federal University of Espírito Santo, Vitória, ES, Brazil.
Rita Elizabeth CheconFederal University of Espírito Santo, Vitória, ES, Brazil.
Daniel B FerreiraDepartment of Pediatrics, Division of Pediatric Rheumatology, Federal University of São Paulo, São Paulo, SP, Brazil.
Yhasmin O G MoraesDepartment of Pediatrics, Division of Pediatric Rheumatology, Federal University of São Paulo, São Paulo, SP, Brazil.
Sandra Lúcia E RibeiroDepartment of Rheumatology, Federal University of Amazonas, Manaus, AM, Brazil.
Camila Maria P F TellesDepartment of Rheumatology, Federal University of Amazonas, Manaus, AM, Brazil.
Rodrigo P V de RezendeDepartment of Rheumatology, Federal Fluminense University, Niterói, RJ, Brazil.
Katia LinoDepartment of Rheumatology, Federal Fluminense University, Niterói, RJ, Brazil.
Leonardo CamposDepartment of Rheumatology, Federal Fluminense University, Niterói, RJ, Brazil.
Lucélia P C SchimidtDepartment of Pediatrics, Federal University of Juiz de Fora, Juiz de Fora, MG, Brazil.
Gilda A FerreiraDepartment of Rheumatology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Ricardo M XavierDepartment of Rheumatology, Federal University of Rio Grande do Sul, Porto Alegre, RS, Brazil.
Odirlei André MonticieloDepartment of Rheumatology, Federal University of Rio Grande do Sul, Porto Alegre, RS, Brazil.
Edgard T Dos Reis-NetoDepartment of Rheumatology, Federal University of São Paulo, São Paulo, SP, Brazil.
Emília I SatoDepartment of Rheumatology, Federal University of São Paulo, São Paulo, SP, Brazil.
Viviane A de Souza *Department of Pediatrics, Federal University of Juiz de Fora, Juiz de Fora, MG, Brazil.
Gecilmara S Pileggi *Department of Rheumatology, Federal University of São Paulo, São Paulo, SP, Brazil.
Gleice Clemente *Department of Pediatrics, Division of Pediatric Rheumatology, Federal University of São Paulo, São Paulo, SP, Brazil. gleiceclemente@gmail.com.
SAFER STUDY GROUP
Valéria Valim *Department of Rheumatology, Federal University of Espírito Santo, Vitória, ES, Brazil. val.valim@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCOVID-19 vaccines have significantly reduced mortality and are safe for healthy children; however, research in pediatric populations with juvenile immune-mediated inflammatory diseases (IMIDs) is limited.

methodsThe Brazilian multicenter longitudinal SAFER-Study evaluates immunogenicity and safety of the BNT162b2/Pfizer vaccine in IMID patients. The juvenile cohort enrolled patients aged 12-17 years between August and December 2021 and compared them with adults under 40 years from the adult cohort. Safety was assessed by monitoring post-vaccination adverse events (AEs), immunogenicity was measured by IgG antibodies against the SARS-CoV-2 spike receptor-binding domain and seroconversion rates.

resultsA total of 123 participants were included: 86 adolescents and 37 adult controls. In adolescents, local AEs were most frequent; no serious or life-threatening AEs occurred. Significant increases in IgG-S levels were observed after the two doses in both cohorts (p < 0.001). Seroconversion after the second dose reached 97% overall and 100% after the third dose. In juvenile SLE and JIA patients, vaccination did not significantly affect disease activity.

conclusionThe BNT162b2 vaccine was safe and immunogenic in adolescents with IMIDs, including those with high immunosuppression and comorbidities, showing similar responses to adults. These findings support vaccination in this vulnerable population and contribute to evidence-based recommendations. IMPACT: BNT162b2 COVID-19 vaccine demonstrated a favorable safety profile and immunogenicity in adolescents with juvenile immune-mediated inflammatory diseases (IMID), with responses comparable to those observed in adults. Real life data on this population remain limited, and further evidence regarding vaccine safety and immunogenicity is needed. This study represents the first multicenter, longitudinal registry of Brazilian adolescents with IMID receiving BNT162b2. Comprehensive data on the safety and immunogenicity of BNT162b2 in highly immunosuppressed adolescents with IMID and comorbidities are crucial to guide clinical decision-making, mitigate vaccine hesitancy, and enhance vaccination coverage within this vulnerable population.

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.