Evidence map›Paper›PMID 37667538›Full record

ArticleJournal of cellular and molecular medicine2023

Design and preclinical testing of an anti-CD41 CAR T cell for the treatment of acute megakaryoblastic leukaemia.

Adrian Bogdan Tigu, Catalin Sorin Constantinescu, Patric Teodorescu, David Kegyes, Raluca Munteanu, Richard Feder, Mareike Peters, Ioana Pralea, Cristina Iuga, Diana Cenariu and 13 more

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
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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 6 institutions in 4 countries.

Adrian Bogdan TiguMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Catalin Sorin ConstantinescuMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Patric TeodorescuDepartment of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
David KegyesMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Raluca MunteanuMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Richard FederMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Mareike PetersMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Ioana PraleaMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Cristina IugaMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Diana CenariuMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Andra MarcuDepartment of Pediatrics, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Alina TanaseDepartment of Pediatrics, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Anca ColitaDepartment of Pediatrics, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Rares DrulaMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Jon Thor BergthorssonStem Cell Research Unit, Biomedical Center, School of Health Sciences, University of Iceland, Reykjavík, Iceland.
Victor GreiffDepartment of Immunology, University of Oslo and Oslo University Hospital, Oslo, Norway.
Delia DimaDepartment of Hematology, Ion Chiricuta Clinical Cancer Center, Cluj Napoca, Romania.
Cristina SeliceanDepartment of Hematology, Ion Chiricuta Clinical Cancer Center, Cluj Napoca, Romania.
Ioana RusDepartment of Hematology, Ion Chiricuta Clinical Cancer Center, Cluj Napoca, Romania.
Mihnea ZdrengheaDepartment of Hematology, Ion Chiricuta Clinical Cancer Center, Cluj Napoca, Romania.
Diana GuleiMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Gabriel GhiaurMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.ORCID 0000-0002-3955-7944
Ciprian TomuleasaMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.ORCID 0000-0001-5500-1519
Iuliu Hațieganu University of Medicine and Pharmacy · ROInstitute of Oncology Prof. Dr. Ion Chiricuta · ROCarol Davila University of Medicine and Pharmacy · ROJohns Hopkins University · USOslo University Hospital · NOReykjavík University · IS

Funding

European Economic Space between Romania and Iceland 2021-2023Projects for Exploratory Medicine PCE 225/2021Romanian National Ministry of Research, Innovation and Digitalization PN-III-P4-ID-PCE-2020-1118 within PNCDI IVRomanian Society for Bone Marrow Transplantationthe Iuliu Hatieganu University - School of Doctoral StudiesYoung Research Teams PN-III-PI-1.1-TE-2019-0271
6 · The paper itself

Abstract

Acute megakaryoblastic leukaemia (AMkL) is a rare subtype of acute myeloid leukaemia (AML) representing 5% of all reported cases, and frequently diagnosed in children with Down syndrome. Patients diagnosed with AMkL have low overall survival and have poor outcome to treatment, thus novel therapies such as CAR T cell therapy could represent an alternative in treating AMkL. We investigated the effect of a new CAR T cell which targets CD41, a specific surface antigen for M7-AMkL, against an in vitro model for AMkL, DAMI Luc2 cell line. The performed flow cytometry evaluation highlighted a percentage of 93.8% CAR T cells eGFP-positive and a limited acute effect on lowering the target cell population. However, the interaction between effector and target (E:T) cells, at a low ratio, lowered the cell membrane integrity, and reduced the M7-AMkL cell population after 24 h of co-culture, while the cytotoxic effect was not significant in groups with higher E:T ratio. Our findings suggest that the anti-CD41 CAR T cells are efficient for a limited time spawn and the cytotoxic effect is visible in all experimental groups with low E:T ratio.

Indexed as

Immunotherapy, AdoptiveLeukemia, Megakaryoblastic, AcutePlatelet Membrane Glycoprotein IIbReceptors, Chimeric AntigenT-LymphocytesCell Line, TumorCoculture TechniquesHumansPlatelet Membrane Glycoprotein IIbReceptors, Chimeric AntigenB cellCAR T cellsCRSmegakaryoblastic leukaemia

Identifiers

PMID37667538
PMCPMC10538266
OpenAlexW4386439165

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.