Evidence map›Paper›PMID 36706534›Full record

ArticleJournal of autoimmunity2023

Accelerated waning of immune responses to a third COVID-19 vaccination in patients with immune-mediated inflammatory diseases.

Daniel Mrak, Felix Kartnig, Daniela Sieghart, Elisabeth Simader, Helga Radner, Peter Mandl, Lisa Göschl, Philipp Hofer, Thomas Deimel, Irina Gessl and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of autoimmunity, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.5field-weighted citation impact, top 9% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Observational
  4. Article
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

18 authors at 1 institution in 1 country.

Daniel MrakDivision of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Austria.
Felix KartnigDivision of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Austria.
Daniela SieghartDivision of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Austria.
Elisabeth SimaderDivision of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Austria.
Helga RadnerDivision of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Austria.
Peter MandlDivision of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Austria.
Lisa GöschlDivision of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Austria.
Philipp HoferDepartment of Pathology, Medical University of Vienna, Vienna, Austria.
Thomas DeimelDivision of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Austria.
Irina GesslDivision of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Austria.
Renate KainDepartment of Pathology, Medical University of Vienna, Vienna, Austria.
Stefan WinklerDivision of Infectious Diseases and Tropical Medicine, Department of Internal Medicine I, Medical University of Vienna, Austria.
Josef S SmolenDivision of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Austria.
Thomas PerkmannDepartment of Laboratory Medicine, Medical University of Vienna, Austria.
Helmuth HaslacherDepartment of Laboratory Medicine, Medical University of Vienna, Austria.
Daniel AletahaDivision of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Austria.
Leonhard X HeinzDivision of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Austria. Electronic address: leonhard.heinz@meduniwien.ac.at.
Michael BonelliDivision of Rheumatology, Department of Internal Medicine III, Medical University of Vienna, Austria. Electronic address: michael.bonelli@meduniwien.ac.at.
Medical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA 3

methods50 patients under immunosuppression and 42 healthy controls (HCs) received a 3

resultsAt week 12, reduced anti-RBD antibody levels were observed in IMID patients as compared to HCs (median antibody level 5345 BAU/ml [1781-10,208] versus 9650 BAU/ml [6633-16,050], p < 0.001). Reduction in relative antibody levels was significantly higher in IMID patients as compared to HCs at week 12 (p < 0.001). Lowest anti-RBD antibody levels were detected in IMID patients who received biological disease-modifying anti-rheumatic drugs (DMARDs) or a combination therapy with conventional synthetic and biological DMARDs. Number of SARS-CoV-2-specific T cells against wildtype and Omicron variants remained stable over 12 weeks in IMID patients. No serious adverse events were reported.

conclusionDue to a fast decline in anti-RBD antibodies in IMID patients an early 4

Indexed as

Antirheumatic AgentsCOVID-19AntibodiesAntibodies, ViralCOVID-19 VaccinesHumansImmunity, HumoralSARS-CoV-2Spike Glycoprotein, CoronavirusVaccinationAntibodiesAntibodies, ViralAntirheumatic AgentsCOVID-19 VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19ImmunosuppressionSARS-CoV-2Vaccination

Identifiers

PMID36706534
PMCPMC9771756
OpenAlexW4312193336

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.