Trial reportRheumatology (Oxford, England)2026
Impaired cellular immune responses to herpes zoster subunit vaccine in patients with rheumatoid arthritis receiving Janus kinase inhibitors.
Trial report in Rheumatology (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03886038 (The Immunogenicity and Efficacy of Subunit Vaccine Against Herpes Zoster in RA Treated With JAK-inhibitors), which is not on this map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
The Immunogenicity and Efficacy of Subunit Vaccine Against Herpes Zoster in RA Treated With JAK-inhibitors (VACCIMIL-ZOSTER)
Who cites it
1 citing paper in PubMed.
- CD4 T cell phenotype after AS01-adjuvanted immunization is shaped by prior antigen or pathogen exposure.Frontiers in immunology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
objectiveTo investigate cellular immune responses to the herpes zoster (HZ) subunit (HZ/su) vaccine in patients with rheumatoid arthritis (RA) treated with Janus kinase inhibitors (JAKis).
methodsRA patients treated with JAKi (n = 46) at the Department of Rheumatology, Skåne University Hospital, Sweden, and healthy controls (n = 37) received two doses of the HZ/su vaccine. Blood samples were collected before and ∼6 weeks after vaccination. Varicella zoster virus (VZV) glycoprotein E (gE)-specific lymphocyte proliferation was analysed using flow cytometry. gE-specific production of tumour necrosis factor (TNF)α and IFNγ was analysed using an immunoassay. gE-specific responses were compared before and after vaccination within the groups (Wilcoxon signed-rank test), and between the patients and the controls (Mann-Whitney, ANCOVA). Proportions achieving a positive vaccine response were compared between the groups (Chi2 test).
resultsFollowing vaccination, gE-specific proliferation of CD19+ cells increased significantly in both the patients (P = 0.016) and the controls (P < 0.001). For patients, no statistically significant differences were seen after vaccination for gE-specific proliferation of CD4+ or CD8+ cells or production of TNFα or IFNγ. Lower proportions of patients than the controls achieved a positive vaccine response for gE-specific proliferation of CD4+, CD8+ and CD19+ cells and gE-specific TNFα.
conclusionThe lack of significant increases in both vaccine-specific proliferation of CD4+ and CD8+ cells and proinflammatory cytokines after vaccination indicate impaired T cell responses to the HZ/su vaccination in patients with RA treated with JAKi. These results suggest that to ensure satisfactory cellular immunity in patients with RA, vaccination against HZ should preferably be performed before the initiation of JAKi treatment. CLINICAL
trial registrationClinicalTrials.gov; NCT03886038.
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