RMD Open (Feb 2024)

Immunogenicity and influence on disease activity of recombinant zoster vaccine in patients with rheumatoid arthritis treated with DMARDs

  • Kei Ikeda,
  • Taro Iwamoto,
  • Shunsuke Furuta,
  • Hiroshi Nakajima,
  • Yoshihisa Kobayashi,
  • Shotaro Kojima,
  • Arifumi Iwata,
  • Tomoaki Ida,
  • Manami Kato,
  • Fumiyoshi Takizawa,
  • Junya Suzuki,
  • Yosuke Toda,
  • Kazusa Miyachi

DOI
https://doi.org/10.1136/rmdopen-2023-003902
Journal volume & issue
Vol. 10, no. 1

Abstract

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Objectives This study aimed to determine the immunogenicity and the influence on disease activity of an adjuvanted recombinant varicella-zoster virus (VZV) subunit vaccine (RZV) in patients with rheumatoid arthritis (RA) treated with disease-modifying antirheumatic drugs (DMARDs).Methods This prospective longitudinal study enrolled 53 patients with RA (aged ≥50 years) treated with DMARDs (conventional synthetic (cs)DMARDs 20, biological (b)DMARDs 23 and targeted synthetic (ts)DMARDs 10) and 10 control individuals. The participants received two intramuscular RZV 2 months apart. VZV-specific CD4+ T cell responses (cell-mediated immunity; CMI) and IgG antibody responses (humoral immunity; HI) were assessed at 0 and 3 months after the first RZV administration using flow cytometry and enzyme immunoassay, respectively. Disease activity (Disease Activity Score 28-C reactive protein and Clinical Disease Activity Index), flares and adverse events were monitored for 6 months after the first vaccination.Results VZV-specific CMI and HI significantly increased in the three DMARDs-treated patients with RA after RZV administration compared with the corresponding prevaccination values (p<0.001–0.014), and the magnitudes and fold-increases of those responses were not significantly different among the three DMARDs-treated patients with RA. Furthermore, the vaccine response rates of CMI and HI were not significantly different between csDMARDs-treated patients and b-DMARDs or ts-DMARDs-treated patients. Meanwhile, no significant increases in disease activity indices or adverse events were observed in these patients during the 6-month follow-up period after the first vaccination. RZV-induced RA flares occurred in two patients (3.8%) but were mild and controllable.Conclusion RZV is robustly immunogenic and has a clinically acceptable safety profile in elderly patients with RA receiving DMARDs.