Evidence map›Paper›PMID 36844219›Full record

ArticleFrontiers in medicine2023

Familial CD45RA

Karima Al-Akioui Sanz, Carlos Echecopar Parente, Cristina Ferreras, Marta Menéndez Ribes, Alfonso Navarro, Carmen Mestre, Laura Clares, José Luis Vicario, Antonio Balas, Raquel De Paz and 7 more

Registry-linked trialAbstract read
In one paragraph

Article in Frontiers in medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06839456 (Phase 1/2 Study), which is not on this map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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.

NCT06839456 phase1 / phase2recruitingnot on this mapstarted 2025, after this paper: background citation

Phase 1/2 Study: CD45RA Depleted Peripheral Stem Cell Addback to Prevent Viral and Fungal Infections Following Alternative Donor TCRab/CD19 Depleted Hematopoietic Stem Cell Transplant

TypeinterventionalSponsorChildren's Hospital of PhiladelphiaRan2025 to 2032Enrolled100ConditionsLeukemia, High Risk Acute Lymphoblastic Leukemia, High Risk Acute Myeloid Leukemia, Relapse LeukemiaArmsPhase 1 Dose Level 1, Phase 1 Dose Level 2, Phase 1 Dose Level 3, Phase 2 Maximum Tolerated Dose determined in Phase 1, Phase 2 Established Dose from prior study, NCT03810196
3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. 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

17 authors.

Karima Al-Akioui SanzHospital La Paz Institute for Health Research, Madrid, Spain.
Carlos Echecopar ParenteDepartment of Pediatric Hemato-Oncology, La Paz University Hospital, Madrid, Spain.
Cristina FerrerasHospital La Paz Institute for Health Research, Madrid, Spain.
Marta Menéndez RibesHospital La Paz Institute for Health Research, Madrid, Spain.
Alfonso NavarroHospital La Paz Institute for Health Research, Madrid, Spain.
Carmen MestreHospital La Paz Institute for Health Research, Madrid, Spain.
Laura ClaresHospital La Paz Institute for Health Research, Madrid, Spain.
José Luis VicarioHistocompatibility Unit, Transfusion Center of Madrid, Madrid, Spain.
Antonio BalasHistocompatibility Unit, Transfusion Center of Madrid, Madrid, Spain.
Raquel De PazCell Therapy Unit, Department of Hematology, La Paz University Hospital, Madrid, Spain.
Eduardo López GranadosImmunology Unit, La Paz University Hospital, Madrid, Spain.
Elena Sánchez ZapardielImmunology Unit, La Paz University Hospital, Madrid, Spain.
Carlos JiménezDepartment of Nephrology, La Paz University Hospital, Madrid, Spain.
María López-OlivaDepartment of Nephrology, La Paz University Hospital, Madrid, Spain.
Esther RamosIntestinal Rehabilitation Unit, Pediatric Gastroenterology and Nutrition Unit, La Paz University Hospital, Madrid, Spain.
Francisco Hernández-OliverosDepartment of Pediatric Surgery, La Paz University Hospital, Madrid, Spain.
Antonio Pérez-MartínezHospital La Paz Institute for Health Research, Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Immunocompromised patients are susceptible to high-risk opportunistic infections and malignant diseases. Most antiviral and antifungal drugs are quite toxic, relatively ineffective, and induce resistance in the long term. The transfer of pathogen-specific Cytotoxic T-Lymphocytes has shown a minimal toxicity profile and effectiveness in treating Cytomegalovirus, Adenovirus, Epstein - Barr virus, BK Virus and Methods: We present preliminary data from six immunocompromised patients: four who had severe infectious diseases and two who had EBV lymphoproliferative disease. All of them underwent multiple safe familial CD45RA Results: The infusions were safe, there was no case of graft-versus host disease, and they showed a clear clinical benefit. The patients treated for BK virus nephritis, Cytomegalovirus encephalitis, Cytomegalovirus reactivation, and disseminated invasive aspergillosis experienced pathogen clearance, complete resolution of symptoms in 4-6 weeks and a lymphocyte increase in 3 of 4 cases after 3-4 months. Donor T cell transient microchimerism was detected in one patient. The two patients treated for EBV lymphoproliferative disease underwent chemotherapy and several infusions of CD45RA Conclusion: The use of familial CD45RA

Indexed as

adoptive cell therapy (ACT)AspergillusBK virus (BKV)CD45RA– T cellsCytomegalovirus (HCMV)Epstein-Barr virus (EBV)mDLI

Identifiers

PMID36844219
PMCPMC9944023

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.