Evidence map›Paper›PMID 37438402›Full record

ReviewNature reviews. Rheumatology2023

Effect of DMARDs on the immunogenicity of vaccines.

Yannick van Sleen, Kornelis S M van der Geest, Anke L W Huckriede, Debbie van Baarle, Elisabeth Brouwer

Registry-linked trialOpen access · greenAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Rheumatology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07280741 (Efficacy, Immunogenicity, and Safety of the Recombinant Herpes Zoster Vaccine), which is not on this map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.4field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

NCT07280741 phase4recruitingnot on this mapstarted 2025, after this paper: background citation

Efficacy, Immunogenicity, and Safety of the Recombinant Herpes Zoster Vaccine (RZV) in Patients With Autoimmune Rheumatic Diseases Under Immunomodulators

TypeinterventionalSponsorUniversity of Sao Paulo General HospitalRan2025 to 2028Enrolled200ConditionsAutoimmune Rheumatic DiseasesArmsRecombinant Zoster Vaccine (RZV)
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 28 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Yannick van SleenDepartment of Rheumatology and Clinical Immunology, University Medical Center Groningen, Groningen, the Netherlands. y.van.sleen@umcg.nl.ORCID 0000-0002-7382-8322
Kornelis S M van der GeestDepartment of Rheumatology and Clinical Immunology, University Medical Center Groningen, Groningen, the Netherlands.ORCID 0000-0003-2798-6765
Anke L W HuckriedeDepartment of Medical Microbiology and Infection Prevention, University Medical Center Groningen, Groningen, the Netherlands.
Debbie van BaarleDepartment of Medical Microbiology and Infection Prevention, University Medical Center Groningen, Groningen, the Netherlands.
Elisabeth BrouwerDepartment of Rheumatology and Clinical Immunology, University Medical Center Groningen, Groningen, the Netherlands. e.brouwer@umcg.nl.ORCID 0000-0002-5652-4423
University Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vaccines are important for protecting individuals at increased risk of severe infections, including patients undergoing DMARD therapy. However, DMARD therapy can also compromise the immune system, leading to impaired responses to vaccination. This Review focuses on the impact of DMARDs on influenza and SARS-CoV-2 vaccinations, as such vaccines have been investigated most thoroughly. Various data suggest that B cell depletion therapy, mycophenolate mofetil, cyclophosphamide, azathioprine and abatacept substantially reduce the immunogenicity of these vaccines. However, the effects of glucocorticoids, methotrexate, TNF inhibitors and JAK inhibitors on vaccine responses remain unclear and could depend on the dosage and type of vaccination. Vaccination is aimed at initiating robust humoral and cellular vaccine responses, which requires efficient interactions between antigen-presenting cells, T cells and B cells. DMARDs impair these cells in different ways and to different degrees, such as the prevention of antigen-presenting cell maturation, alteration of T cell differentiation and selective inhibition of B cell subsets, thus inhibiting processes that are necessary for an effective vaccine response. Innovative modified vaccination strategies are needed to improve vaccination responses in patients undergoing DMARD therapy and to protect these patients from the severe outcomes of infectious diseases.

Indexed as

Antirheumatic AgentsCOVID-19VaccinesAzathioprineHumansSARS-CoV-2VaccinationAntirheumatic AgentsAzathioprineVaccines

Identifiers

PMID37438402
OpenAlexW4384071185

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.