Evidence map›Paper›PMID 36585293›Full record

ArticleCytotherapy2023

Donor selection for adoptive cell therapy with CD45RA

Karima Al-Akioui-Sanz, Bárbara Pascual-Miguel, Mariana Díaz-Almirón, Carmen Mestre-Durán, Alfonso Navarro-Zapata, Laura Clares-Villa, Carla Martín-Cortázar, José Luis Vicario, Miguel Ángel Moreno, Antonio Balas and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Cytotherapy, 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
0.4field-weighted citation impact, top 38% 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, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
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

14 authors at 2 institutions in 1 country.

Karima Al-Akioui-SanzIdiPAZ, Hospital La Paz Institute for Health Research, La Paz University Hospital, Madrid, Spain.
Bárbara Pascual-MiguelIdiPAZ, Hospital La Paz Institute for Health Research, La Paz University Hospital, Madrid, Spain.
Mariana Díaz-AlmirónBiostatistics Department, La Paz University Hospital, Madrid, Spain.
Carmen Mestre-DuránIdiPAZ, Hospital La Paz Institute for Health Research, La Paz University Hospital, Madrid, Spain.
Alfonso Navarro-ZapataIdiPAZ, Hospital La Paz Institute for Health Research, La Paz University Hospital, Madrid, Spain.
Laura Clares-VillaIdiPAZ, Hospital La Paz Institute for Health Research, La Paz University Hospital, Madrid, Spain.
Carla Martín-CortázarIdiPAZ, Hospital La Paz Institute for Health Research, La Paz University Hospital, Madrid, Spain.
José Luis VicarioHistocompatibility Unit, Transfusion Center of Madrid, Madrid, Spain.
Miguel Ángel MorenoHistocompatibility Unit, Transfusion Center of Madrid, Madrid, Spain.
Antonio BalasHistocompatibility Unit, Transfusion Center of Madrid, Madrid, Spain.
Raquel De PazCell Therapy Unit, Hematology Department, La Paz University Hospital, Madrid, Spain.
Jordi MinguillónIdiPAZ, Hospital La Paz Institute for Health Research, La Paz University Hospital, Madrid, Spain.
Antonio Pérez-MartínezIdiPAZ, Hospital La Paz Institute for Health Research, La Paz University Hospital, Madrid, Spain; Pediatric Hemato-oncology Department, La Paz University Hospital, Madrid, Spain; Faculty of Medicine Autonomous, University of Madrid, Madrid, Spain.
Cristina FerrerasIdiPAZ, Hospital La Paz Institute for Health Research, La Paz University Hospital, Madrid, Spain. Electronic address: cristina.ferreras@salud.madrid.org.
Hospital La Paz Institute for Health Research · ESHospital Universitario La Paz · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND

aimsWe have previously demonstrated the safety and feasibility of adoptive cell therapy with CD45RA

methodsWe performed a longitudinal analysis from previously severe acute respiratory syndrome coronavirus 2-infected and infection-naïve individuals covering 21 months from infection and 10 months after full vaccination with the BNT162b2 Pfizer/BioNTech vaccine.

resultsWe observed that cellular responses are maintained over time. Humoral responses increased after vaccination but were gradually lost. In addition, dexamethasone did not alter cell functionality or proliferation of CD45RA

conclusionsOur results suggest that the best donors for adoptive cell therapy would be recovered individuals and 2 months after vaccination, although further studies with larger cohorts would be needed to confirm this finding. Dexamethasone did not affect the characteristics of the memory T cells at a concentration used in the clinical practice and IL-15 showed a positive effect on SARS-CoV-2-specific CD45RA

Indexed as

COVID-19Interferon-gammaAntibodies, ViralBNT162 VaccineCell ProliferationCOVID-19 Drug TreatmentDexamethasoneDonor SelectionHumansInterleukin-15Leukocyte Common AntigensMemory T CellsPhenotypeSARS-CoV-2VaccinationAntibodies, ViralBNT162 VaccineDexamethasoneInterferon-gammaInterleukin-15Leukocyte Common AntigensCD45RA(−) memory T cellscellular immunityCOVID-19 treatmenthumoral immunity

Identifiers

PMID36585293
PMCPMC9742221
OpenAlexW4311424369

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.