Evidence map›Paper›PMID 37686102›Full record

ArticleInternational journal of molecular sciences2023

Clinical Application of In Vitro Tests for COVID-19 Vaccine Delayed Hypersensitivity Diagnostics.

Jan Romantowski, Aleksandra Górska, Maciej Zieliński, Piotr Trzonkowski, Karolina Rucka, Marek Niedoszytko

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. 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

6 authors at 1 institution in 1 country.

Jan RomantowskiDepartment of Allergology, Medical University of Gdansk, 80-414 Gdańsk, Poland.ORCID 0000-0002-0487-0957
Aleksandra GórskaDepartment of Allergology, Medical University of Gdansk, 80-414 Gdańsk, Poland.
Maciej ZielińskiDepartment of Medical Immunology, Medical University of Gdansk, 80-414 Gdańsk, Poland.
Piotr TrzonkowskiDepartment of Medical Immunology, Medical University of Gdansk, 80-414 Gdańsk, Poland.ORCID 0000-0001-5287-5210
Karolina RuckaDepartment of Medical Immunology, Medical University of Gdansk, 80-414 Gdańsk, Poland.
Marek NiedoszytkoDepartment of Allergology, Medical University of Gdansk, 80-414 Gdańsk, Poland.
Gdańsk Medical University · PL

Funding

Gdańsk Medical University 01-10023/0004956/231
6 · The paper itself

Abstract

Drug hypersensitivity reactions can be classified as immediate or delayed. While diagnostic options for immediate reactions are well developed and standardized, delayed reactions (in many cases type IV according to Gell and Coombs) are a challenge for allergy work-up. In recent years, some in vitro markers have been proposed and used for delayed reactions, such as contact dermatitis. Primary strategy: Avoidance is difficult to achieve, especially for COVID-19 vaccinations, when immunity against infection is extremely important. The aim of our study was to evaluate the application of in vitro delayed hypersensitivity tests in COVID-19 vaccines. Seven patients with a positive history of severe delayed drug allergy were enrolled. Vein blood was collected to stimulate cells with the tested vaccines (Comirnaty, Janssen, Spikevax) and excipients with the assessment of CD40L, CD69, IL-2, IL-4, IL-6, IL-10, IFNgamma, TNFalfa, and intracellular markers: granulysin and INFgamma. In addition, basophile activation tests, patch tests, skin prick tests, and intradermal tests were performed with the tested vaccine. Finally, the decision was made to either administer a vaccine or resign. Two out of seven patients were considered positive for drug hypersensitivity in the in vitro test according to the high vaccine stimulation index measured with CD69 (6.91 and 12.18) and CD40L (5.38 and 15.91). All patch tests, BATs, and skin tests were negative. Serum interleukin measurements were inconclusive as the impact of the vaccine itself on the immunity system was high. Intracellular markers gave uncertain results due to the lack of stimulation on the positive control. CD69 and CD40L could be reliable in vitro markers for delayed hypersensitivity to COVID-19 vaccines. Patch tests, skin tests, BATs, and serum interleukins did not confirm their usefulness in our study.

Indexed as

COVID-19Drug HypersensitivityHypersensitivity, DelayedCD40 LigandCOVID-19 TestingCOVID-19 VaccinesHumansIn Vitro TechniquesCD40 LigandCOVID-19 VaccinesallergyCOVID-19cytometrydelayed hypersensitivityvaccine

Identifiers

PMID37686102
PMCPMC10487583
OpenAlexW4386221359

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.