Pediatric rheumatology

Immunogenicity and safety of BNT162b2 vaccination in adolescents with systemic lupus erythematosus

LupusPublished Prospective cohort study

Authors' conclusion

AdoSLE on High-IS induced lower SARS-CoV-2 vaccine immune responses than Low-IS.

Study context

Population
Patients aged 12–18 years diagnosed with SLE receiving two doses of BNT162b2 4 weeks apart and a booster at 4–6 months
Participants
73 patients
Exposure
High-dose vs low-dose immunosuppressant in adolescents with SLE receiving BNT162b2
  • High-ISn = 40
  • Low-ISn = 33reference
Outcome
Anti-RBD IgG seropositivity (overall)
Follow-up
4 weeks after 2nd dose

Main finding

As reported in the abstract

Overall anti-RBD IgG seropositivity

97.3%

Observational data: associations, not effects.

Further findings

OutcomeP value
Anti-RBD IgG, Wuhan NT and IFN-γ-ELISpot · 4 weeks after 2nd doseHigh-IS vs Low-ISP < 0.001
Anti-RBD IgG, Wuhan NT and IFN-γ-ELISpot · 4 weeks after 2nd doseHigh-IS vs Low-ISP < 0.001
Anti-RBD IgG, Wuhan NT and IFN-γ-ELISpot · 4 weeks after 2nd doseHigh-IS vs Low-ISP = 0.022

Antibody response after 3rd dose vs after 2nd dose

Significantly higher antibody responses after 3rd dose in both groups, with seroconversion against Omicron; persistently lower antibody levels in High-IS
P < 0.001

Safety

SELENA-SLEDAI score within 12 weeks after 2-dose vaccination vs before

After vs before vaccination
3.1 vs 2.5; p < .036
Disease flare by SELENA-SLEDAI flare index not different after vs before vaccination, consistent across groups

Non-severe adverse events (AEs)

Occurred similarly in both groups

Original publication

Immunogenicity and safety of BNT162b2 vaccination in adolescents with systemic lupus erythematosus. Lupus. Published 9 February 2024. doi:10.1177/09612033241232576

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