Safety and immunogenicity of BNT162b2 mRNA COVID-19 vaccine in adolescents with rheumatic diseases treated with immunomodulatory medications

Author:

Heshin-Bekenstein Merav12ORCID,Ziv Amit23,Toplak Natasa45,Hagin David26,Kadishevich Danielle7,Butbul Yonatan A8,Saiag Esther9,Kaufman Alla10,Shefer Gabi11,Sharon Orli11,Pel Sara12,Elkayam Ori212,Uziel Yosef23

Affiliation:

1. Pediatric Rheumatology Service, Dana-Dwek Children’s Hospital, Tel Aviv Sourasky Medical Center

2. Sackler Faculty of Medicine, Tel Aviv University , Tel Aviv

3. Pediatric Rheumatology Unit, Meir Medical Center , Kfar Saba, Israel

4. Department of Allergology, Rheumatology and Clinical Immunology, University Children’s Hospital, University Medical Center Ljubljana

5. Faculty of Medicine, University of Ljubljana , Ljubljana, Slovenia

6. Allergy and Clinical Immunology Unit, Department of Medicine, Tel Aviv Sourasky Medical Center , Tel Aviv

7. Pediatric Department, Meir Medical Center , Kfar Saba

8. Pediatric Rheumatology Unit, Rambam Medical Center , Haifa

9. Hospital Management, Information and Operation Branch

10. Pediatric Department, Dana-Dwek Children’s Hospital

11. Department of Endocrinology Metabolism and Hypertension

12. Rheumatology Department, Tel Aviv Sourasky Medical Center , Tel Aviv, Israel

Abstract

Abstract Objectives Adolescents with juvenile-onset autoimmune inflammatory rheumatic diseases (AIIRDs) could be at risk for disease flare secondary to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection or to withholding anti-inflammatory therapy. While vaccination can protect against coronavirus disease 2019 (COVID-19), safety and immunogenicity data regarding anti-SARS-CoV-2 vaccines among adolescents with AIIRDs are limited. This international, prospective, multicentre study evaluated the safety and immunogenicity of the BNT162b2 anti-SARS-CoV-2 vaccine among adolescents and young adults with juvenile-onset AIIRDs, 80% of whom are on chronic immunomodulatory therapy. Methods Vaccine side effects, disease activity and short-term efficacy were evaluated after 3 months in 91 patients. Anti-spike S1/S2 IgG antibody levels were evaluated in 37 patients and 22 controls 2–9 weeks after the second dose. Results A total of 91 patients and 40 healthy controls were included. The safety profile was good, with 96.7% (n = 88) of patients reporting mild or no side effects and no change in disease activity. However, three patients had transient acute symptoms: two following the first vaccination (renal failure and pulmonary haemorrhage) and one following the second dose (mild lupus flare vs viral infection). The seropositivity rate was 97.3% in the AIIRD group compared with 100% among controls. However, anti-S1/S2 antibody titres were significantly lower in the AIIRD group compared with controls [242 (s.d. 136.4) vs 387.8 (57.3) BAU/ml, respectively; P < 0.0001]. No cases of COVID-19 were documented during the 3 month follow-up. Conclusion Vaccination of juvenile-onset AIIRD patients demonstrated good short-term safety and efficacy and a high seropositivity rate but lower anti-S1/S2 antibody titres compared with healthy controls. These results should encourage vaccination of adolescents with juvenile-onset AIIRDs, even while on immunomodulation.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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