Evidence map›Paper›PMID 34203833›Full record

ArticleJournal of clinical medicine2021

Engineering of CD19 Antibodies: A CD19-TRAIL Fusion Construct Specifically Induces Apoptosis in B-Cell Precursor Acute Lymphoblastic Leukemia (BCP-ALL) Cells In Vivo.

Dorothee Winterberg, Lennart Lenk, Maren Oßwald, Fotini Vogiatzi, Carina Lynn Gehlert, Fabian-Simon Frielitz, Katja Klausz, Thies Rösner, Thomas Valerius, Anna Trauzold and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2021. 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
0.8field-weighted citation impact, top 25% 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, 10 citations in OpenAlex.

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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

13 authors at 3 institutions in 1 country.

Dorothee WinterbergALL-BFM Study Group, Department of Pediatrics I, Christian-Albrechts University Kiel and University Medical Center Schleswig-Holstein, Arnold-Heller Str. 3, Haus C, 24105 Kiel, Germany.
Lennart LenkALL-BFM Study Group, Department of Pediatrics I, Christian-Albrechts University Kiel and University Medical Center Schleswig-Holstein, Arnold-Heller Str. 3, Haus C, 24105 Kiel, Germany.
Maren OßwaldDepartment of Medicine II Christian-Albrechts, Division of Stem Cell Transplantation and Immunotherapy, Campus Kiel, University Kiel and University Hospital Schleswig-Holstein, 24105 Kiel, Germany.
Fotini VogiatziALL-BFM Study Group, Department of Pediatrics I, Christian-Albrechts University Kiel and University Medical Center Schleswig-Holstein, Arnold-Heller Str. 3, Haus C, 24105 Kiel, Germany.
Carina Lynn GehlertDepartment of Medicine II Christian-Albrechts, Division of Stem Cell Transplantation and Immunotherapy, Campus Kiel, University Kiel and University Hospital Schleswig-Holstein, 24105 Kiel, Germany.
Fabian-Simon FrielitzInstitute for Social Medicine and Epidemiology, University of Lübeck, 23538 Lübeck, Germany.
Katja KlauszDepartment of Medicine II Christian-Albrechts, Division of Stem Cell Transplantation and Immunotherapy, Campus Kiel, University Kiel and University Hospital Schleswig-Holstein, 24105 Kiel, Germany.
Thies RösnerDepartment of Medicine II Christian-Albrechts, Division of Stem Cell Transplantation and Immunotherapy, Campus Kiel, University Kiel and University Hospital Schleswig-Holstein, 24105 Kiel, Germany.
Thomas ValeriusDepartment of Medicine II Christian-Albrechts, Division of Stem Cell Transplantation and Immunotherapy, Campus Kiel, University Kiel and University Hospital Schleswig-Holstein, 24105 Kiel, Germany.ORCID 0000-0001-9181-8067
Anna TrauzoldInstitute for Experimental Cancer Research, Christian-Albrechts-University Kiel, 24104 Kiel, Germany.ORCID 0000-0003-4697-556X
Matthias PeippDepartment of Medicine II Christian-Albrechts, Division of Stem Cell Transplantation and Immunotherapy, Campus Kiel, University Kiel and University Hospital Schleswig-Holstein, 24105 Kiel, Germany.
Christian KellnerDepartment of Transfusion Medicine, Cell Therapeutics and Hemostaseology, LMU University Hospital Munich, 81377 Munich, Germany.
Denis Martin ScheweALL-BFM Study Group, Department of Pediatrics I, Christian-Albrechts University Kiel and University Medical Center Schleswig-Holstein, Arnold-Heller Str. 3, Haus C, 24105 Kiel, Germany.ORCID 0000-0002-1070-0217
Christian-Albrechts-Universität zu Kiel · DELMU Klinikum · DEUniversity of Lübeck · DE

Funding

Deutsche Krebshilfe 70113524Deutsche Krebshilfe Mildred-Scheel-Professorship-ProgramJosé Carreras Leukämie-Stiftung DJCLS17R/2017, DJCLS13R/2020Wilhelm Sander-Stiftung 2016.110.1, 2019.119.1
6 · The paper itself

Abstract

B-cell precursor acute lymphoblastic leukemia (BCP-ALL) is the most frequent malignancy in children and also occurs in adulthood. Despite high cure rates, BCP-ALL chemotherapy can be highly toxic. This type of toxicity can most likely be reduced by antibody-based immunotherapy targeting the CD19 antigen which is commonly expressed on BCP-ALL cells. In this study, we generated a novel Fc-engineered CD19-targeting IgG1 antibody fused to a single chain tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) domain (CD19-TRAIL). As TRAIL induces apoptosis in tumor cells but not in healthy cells, we hypothesized that CD19-TRAIL would show efficient killing of BCP-ALL cells. CD19-TRAIL showed selective binding capacity and pronounced apoptosis induction in CD19-positive (CD19

Indexed as

antibodyBCP-ALLCD19Fc-engineeringleukemiaTRAILxenograft

Identifiers

PMID34203833
PMCPMC8232684
OpenAlexW3168084241

What OpenQuestion holds

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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.