Evidence map›Paper›PMID 39311376›Full record

ArticleAntibodies (Basel, Switzerland)2024

Functional Activity of Cytokine-Induced Killer Cells Enhanced by CAR-CD19 Modification or by Soluble Bispecific Antibody Blinatumomab.

Silvia Zaninelli, Silvia Panna, Sarah Tettamanti, Giusi Melita, Andrea Doni, Francesca D'Autilia, Rut Valgardsdottir, Elisa Gotti, Alessandro Rambaldi, Josée Golay and 1 more

Abstract read
In one paragraph

Article in Antibodies (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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.

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

3 citing papers in PubMed.

  1. The evolution of cellular-based immunotherapy in the treatment of gastric cancer: an overview of clinical trials.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  2. Review
  3. Article
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

11 authors.

Silvia ZaninelliCenter of Cellular Therapy "G. Lanzani", Division of Hematology, ASST Papa Giovanni XXIII, 24122 Bergamo, Italy.
Silvia PannaCenter of Cellular Therapy "G. Lanzani", Division of Hematology, ASST Papa Giovanni XXIII, 24122 Bergamo, Italy.
Sarah TettamantiM. Tettamanti Center, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.
Giusi MelitaM. Tettamanti Center, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy.ORCID 0000-0001-9707-357X
Andrea DoniUnit of Multiscale and Nanostructural Imaging, IRCCS Humanitas Research Hospital, 20089 Milano, Italy.
Francesca D'AutiliaUnit of Multiscale and Nanostructural Imaging, IRCCS Humanitas Research Hospital, 20089 Milano, Italy.
Rut ValgardsdottirCenter of Cellular Therapy "G. Lanzani", Division of Hematology, ASST Papa Giovanni XXIII, 24122 Bergamo, Italy.
Elisa GottiCenter of Cellular Therapy "G. Lanzani", Division of Hematology, ASST Papa Giovanni XXIII, 24122 Bergamo, Italy.
Alessandro RambaldiHematology and Bone Marrow Transplant Unit, ASST Papa Giovanni XXIII Hospital, 24127 Bergamo, Italy.ORCID 0000-0002-3739-7502
Josée GolayCenter of Cellular Therapy "G. Lanzani", Division of Hematology, ASST Papa Giovanni XXIII, 24122 Bergamo, Italy.ORCID 0000-0002-7932-909X
Martino IntronaCenter of Cellular Therapy "G. Lanzani", Division of Hematology, ASST Papa Giovanni XXIII, 24122 Bergamo, Italy.

Funding

Fondazione Regionale per la Ricerca Biomedica Project N°CP2_10/ 2018Italian Association for Cancer Research 21147Italian Association for Cancer Research 22791
6 · The paper itself

Abstract

Strategies to increase the anti-tumor efficacy of cytokine-induced killer cells (CIKs) include genetic modification with chimeric antigen receptors (CARs) or the addition of soluble T-cell engaging bispecific antibodies (BsAbs). Here, CIKs were modified using a transposon system integrating two distinct anti-CD19 CARs (CAR-MNZ and CAR-BG2) or combined with soluble CD3xCD19 BsAb blinatumomab (CIK + Blina). CAR-MNZ bearing the CD28-OX40-CD3ζ signaling modules, and CAR-BG2, designed on the Tisagenlecleucel CAR sequence (Kymriah

Indexed as

B-cell neoplasiabispecific antibodyCAR signalingchimeric antigen receptorcytokine-induced killer

Identifiers

PMID39311376
PMCPMC11417890

What OpenQuestion holds

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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.