Evidence map›Paper›PMID 34405140›Full record

ArticleEClinicalMedicine2021

Phase I dose-escalation single centre clinical trial to evaluate the safety of infusion of memory T cells as adoptive therapy in COVID-19 (RELEASE).

A Pérez-Martínez, M Mora-Rillo, C Ferreras, P Guerra-García, B Pascual-Miguel, C Mestre-Durán, A M Borobia, A J Carcas, J Queiruga-Parada, I García and 13 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in EClinicalMedicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07690943 (A Clinical Study to Evaluate the Safety and Efficacy of Autologous COVID-19 Antigen Specific T Cell Treatment in Prolonged SARS-CoV-2 Infected Patients), which is not on this map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 11% 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.

NCT07690943 nacompletednot on this mapstarted 2023, after this paper: background citation

A Clinical Study to Evaluate the Safety and Efficacy of Autologous COVID-19 Antigen Specific T Cell Treatment in Prolonged SARS-CoV-2 Infected Patients

TypeinterventionalSponsorLucasBioRan2023 to 2025Enrolled13ConditionsCOVID-19, COVID-19 (SARS-CoV-2 Infection)ArmsLB-DTK-COV19
3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Long COVID: Is mitochondria the target?Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Familial CD45RAFrontiers in medicine · 2023
    Article
  13. Review
  14. Review
  15. Spotlights on the latest opinions on identification, prevention, and management of newer CoV-2 variants: A roundup appraisal on innovative ideas and designer vaccines for Omicron.Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis · 2022
    Review
  16. ALVR109, an off-the-shelf partially HLA matched SARS-CoV-2-specific T cell therapy, to treat refractory severe COVID-19 pneumonia in a heart transplant patient: Case report.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2022
    Article
  17. Immunotherapy and CRISPR Cas Systems: Potential Cure of COVID-19?Drug design, development and therapy · 2022
    Review
  18. Article
  19. Article
  20. 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

23 authors at 5 institutions in 1 country.

A Pérez-MartínezPediatric Hemato-oncology Department, University Hospital La Paz, Madrid, Spain.
M Mora-RilloIdiPAZ, Hospital La Paz Institute for Health Research, University Hospital La Paz, Madrid, Spain.
C FerrerasIdiPAZ, Hospital La Paz Institute for Health Research, University Hospital La Paz, Madrid, Spain.
P Guerra-GarcíaPediatric Hemato-oncology Department, University Hospital La Paz, Madrid, Spain.
B Pascual-MiguelIdiPAZ, Hospital La Paz Institute for Health Research, University Hospital La Paz, Madrid, Spain.
C Mestre-DuránIdiPAZ, Hospital La Paz Institute for Health Research, University Hospital La Paz, Madrid, Spain.
A M BorobiaIdiPAZ, Hospital La Paz Institute for Health Research, University Hospital La Paz, Madrid, Spain.
A J CarcasIdiPAZ, Hospital La Paz Institute for Health Research, University Hospital La Paz, Madrid, Spain.
J Queiruga-ParadaIdiPAZ, Hospital La Paz Institute for Health Research, University Hospital La Paz, Madrid, Spain.
I GarcíaClinical Pharmacology Department University Hospital La Paz, Madrid, Spain.
E Sánchez-ZapardielImmunology Department, University Hospital La Paz, Madrid, Spain.
M GasiorCell Therapy Unit, Hematology Department, University Hospital La Paz, Madrid, Spain.
R De PazCell Therapy Unit, Hematology Department, University Hospital La Paz, Madrid, Spain.
A MarcosCell Therapy Unit, Hematology Department, University Hospital La Paz, Madrid, Spain.
J L VicarioHistocompatibility. Centro de Transfusión de Madrid. Madrid, Spain.
A BalasHistocompatibility. Centro de Transfusión de Madrid. Madrid, Spain.
M A MorenoHistocompatibility. Centro de Transfusión de Madrid. Madrid, Spain.
C EguizabalResearch Unit, Basque Centre for Blood Transfusion and Human Tissues, Osakidetza, Galdakao, Bizkaia, Spain.
C SolanoINCLIVA, Hospital Clínico Universitario de Valencia. Health Research Institute, University of Valencia, Spain.
J R ArribasIdiPAZ, Hospital La Paz Institute for Health Research, University Hospital La Paz, Madrid, Spain.
R de Miguel BuckleyIdiPAZ, Hospital La Paz Institute for Health Research, University Hospital La Paz, Madrid, Spain.
R MontejanoIdiPAZ, Hospital La Paz Institute for Health Research, University Hospital La Paz, Madrid, Spain.
B SoriaInstitute of Bioengineering, Miguel Hernández University, Elche, Alicante, Spain.
Hospital Universitario La Paz · ESHospital La Paz Institute for Health Research · ESBasque Center for Materials, Applications and Nanostructures · ESUniversitat de Miguel Hernández d'Elx · ESUniversitat de València · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEffective treatments are still needed to reduce the severity of symptoms, time of hospitalization, and mortality of COVID-19. SARS-CoV-2 specific memory T-lymphocytes obtained from convalescent donors recovered can be used as passive cell immunotherapy.

methodsBetween September and November 2020 a phase 1, dose-escalation, single centre clinical trial was conducted to evaluate the safety and feasibility of the infusion of CD45RA

findingsAll participants' clinical status measured by National Early Warning Score (NEWS) and 7-category point ordinal scales showed improvement six days after infusion. No serious adverse events were reported. Inflammatory parameters were stabilised post-infusion and the participants showed lymphocyte recovery two weeks after the procedure. Donor microchimerism was observed at least for three weeks after infusion in all patients.

interpretationThis study provides preliminary evidence supporting the idea that treatment of COVID-19 patients with moderate/severe symptoms using convalescent CD45RA

fundingClinical Trial supported by Spanish Clinical Research Network PT17/0017/0013. Co-funded by European Regional Development Fund/European Social Fund. CRIS CANCER Foundation Grant to AP-M and Agencia Valenciana de Innovación Grant AVI-GVA COVID-19-68 to BS.

Identifiers

PMID34405140
PMCPMC8361305
OpenAlexW3195832814

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.