Key result
BNT162b2 is safe in prior PIMS-TS, though injection-site hardening is 5-fold higher vs controls.
Why the study?
The safety and immunologic reactogenicity of the Pfizer-BioNTech COVID-19 mRNA BNT162b2 vaccine in children with a history of paediatric multisystem inflammatory syndrome temporally associated with COVID-19 (PIMS-TS) were not established.
Is the COVID-19 mRNA BNT162b2 vaccine safe in children with a history of PIMS-TS compared to healthy controls?
Cohort (n=92)
Is the COVID-19 mRNA BNT162b2 vaccine safe in children with a history of PIMS-TS compared to healthy controls?
Absolute Event Rate: 20% vs 4%
p-value: p=0.02
The COVID-19 mRNA BNT162b2 vaccine appears safe and well-tolerated in children with a history of PIMS-TS, with no recurrence of PIMS-like symptoms.
May support vaccination in children with prior PIMS-TS; leaves open confirmation in larger prospective studies.
To assess the safety of Pfizer-BioNTech COVID-19 mRNA BNT162b2 vaccine (Comirnaty®) among patients with the anamnesis of paediatric inflammatory syndrome temporally associated with COVID-19 (PIMS-TS), we conducted a prospective cohort study of 21 patients with history of PIMS (PIMS group, median age 7.4 years, 71% male) and 71 healthy controls without such an anamnesis (CONTROL group, median age 9.0 years, 39% male) aged 5-18 years. Among them, 85 patients (all PIMS patients and 64 CONTROL patients) completed the two dose schedule of vaccination administered 21 days apart and 7 children in the CONTROL group received a single, age appropriate dose of a COVID-19 mRNA BNT162b2 vaccine during the study period. The frequency and character of reported adverse events (AEs) after each dose and results of flow cytometry (FC) 3 weeks after a second dose were compared between those groups. COVID-19 mRNA BNT162b2 vaccine safety profile was very good and comparable in both groups. No severe AEs were observed. 30% of all patients reported some general AE after any vaccine dose and 46% - some local AE. Frequency of reported AEs did not differ between groups except for local hardening at injection site, more common in PIMS group (20% vs 4% after any vaccine dose, p = 0,02). All AEs were benign, general AEs lasted up to 5 days and localised - up to 6 days after a vaccine dose. COVID-19 mRNA BNT162b2 vaccine did not induce any PIMS-like symptoms in any patient. We did not observe any significant T cells or B cells subset abnormalities in the PIMS group compared to the CONTROL group three weeks after a second dose except for terminally differentiated effector memory T cells that were higher in PIMS group (p < 0.0041). To sum up COVID-19 mRNA BNT162b2 vaccine in children with PIMS-TS was safe. Further studies are required to support our findings.
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Ludwikowska et al. (2023) conducted a cohort in Paediatric multisystem inflammatory syndrome temporally associated with COVID-19 (PIMS-TS) (n=92). Pfizer-BioNTech COVID-19 mRNA BNT162b2 vaccine vs. Healthy controls without a history of PIMS-TS was evaluated on Local hardening at injection site (p=0.02).
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