Anti-S1/RBD-Specific Antibody Formation After SARS-CoV-2 Vaccination in Elderly Rheumatoid Arthritis Patients:

Eun Song Kang1,2, Ji Seon Oh3, Eun-Ju Lee4

  • 1Division of Rheumatology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

Insights

The third mRNA vaccine dose significantly boosted antibody titers in rheumatoid arthritis (RA) patients previously vaccinated with ChAdOx1-S. This booster is particularly beneficial for RA patients with risk factors like older age, male sex, and corticosteroid use.

Area of Science:

  • Immunology
  • Vaccinology
  • Rheumatology

Background:

  • Rheumatoid arthritis (RA) patients face evolving COVID-19 vaccination guidelines.
  • Effectiveness of COVID-19 booster vaccines and antibody generation in RA patients is under continuous discussion.
  • Investigating the impact of a third mRNA vaccine dose on antibody titers in RA patients post-ChAdOx1-S vaccination.

Purpose of the Study:

  • To evaluate the effect of a third mRNA vaccine dose on antibody titers in rheumatoid arthritis (RA) patients.
  • To identify factors associated with antibody production in RA patients after initial ChAdOx1-S vaccination.
  • To compare antibody titers between RA patients receiving two ChAdOx1-S doses versus those with an additional mRNA booster.

Main Methods:

  • Prospective recruitment of two RA patient groups: one with two ChAdOx1-S doses, the other with an additional mRNA vaccine.
  • Quantification of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibody titers using electrochemiluminescence immunoassay.
  • Multivariate logistic regression to identify factors influencing antibody production, with follow-up of antibody titers post-third dose.

Main Results:

  • A third mRNA vaccine dose significantly increased high antibody titers (>250 U/mL) from 31% to 94% in RA patients.
  • Corticosteroid use, older age, and male sex were associated with lower high antibody titers after two ChAdOx1-S doses.
  • Minimal antibody titer waning was observed in patients followed up after the third mRNA vaccine dose.

Conclusions:

  • The third mRNA vaccine dose demonstrates significant benefit for RA patients, particularly those with risk factors.
  • Older age, male sex, and corticosteroid use are identified as risk factors for suboptimal antibody response post-initial vaccination.
  • The findings support the recommendation of a third mRNA vaccine dose for enhanced protection in vulnerable RA patient populations.
Abstract