Across rheumatic diseases

Antibody response to the COVID-19 ChAdOx1nCov-19 and BNT162b vaccines after temporary suspension of DMARD therapy in immune-mediated inflammatory disease: an extension study (RESCUE 2)

RMD OpenPublished Extension study

Authors' conclusion

Antibody persistence was longer in the Pfizer group due to a higher peak antibody level following second vaccination with levels of protection in IMID on DMARD therapy similar to controls except in those on tsDMARDs where it was lower.

Study context

Population
Patients with immune-mediated inflammatory diseases (IMID) on DMARD therapy and controls vaccinated with two doses of ChAdO1nCov-19 (AZ) or BNT162b (Pfizer)
Participants
175 patients
Comparison
DMARD withhold vs continue vs controls, after AZ or Pfizer vaccination and mRNA booster
Outcome
SARS-CoV2 antibody decay kinetics after two doses of AZ or Pfizer and response after mRNA booster
Follow-up
6 months

Main finding

As reported in the abstract

Seropositive 6 months after initial AZ vaccination
P across groups
P = 0.756

Further findings

OutcomeValuesP value
Seropositive 6 months after initial Pfizer vaccinationWithhold 91.4% · Continue 100% · Control 100%
Mean SARS-CoV-2 antibody level, tsDMARD continuing therapy vs controltsDMARD (continued) mean 2.2 U/mL · Control mean 4.8 U/mLP = 0.010
Mean time until loss of protective antibodies, IMIDAZ mean 61 days · Pfizer mean 137.5 days
Time until loss of protective antibody titres by DMARD class, AZcsDMARD 68.3 days · bDMARD 71.8 days · tsDMARD 64.0 days
Time until loss of protective antibody titres by DMARD class, PfizercsDMARD 185.5 days · bDMARD 137.5 days · tsDMARD 116.0 days
Seropositive 6 months after initial Pfizer vaccination — P across groups
p=0.226

Seroconversion after booster

Seroconversion rates in all three intervention categories
100%

Original publication

Antibody response to the COVID-19 ChAdOx1nCov-19 and BNT162b vaccines after temporary suspension of DMARD therapy in immune-mediated inflammatory disease: an extension study (RESCUE 2). RMD Open. Published 2 March 2023. doi:10.1136/rmdopen-2022-002871

Composed by AI from the published abstract and checked against it. How Briefs are made →

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