Evidence map›Paper›PMID 31527633›Full record

ArticleScientific reports2019

Direct comparison of target-reactivity and cross-reactivity induced by CAR- and BiTE-redirected T cells for the development of antibody-based T-cell therapy.

Masaki Maruta, Toshiki Ochi, Kazushi Tanimoto, Hiroaki Asai, Takashi Saitou, Hiroshi Fujiwara, Takeshi Imamura, Katsuto Takenaka, Masaki Yasukawa

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

23 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Bystander CARJournal for immunotherapy of cancer · 2025
    Article
  4. Review
  5. Development of a highly sensitive platform for protein-protein interaction detection and regulation of T cell function.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. Article
  7. Review
  8. Exploring TCR-like CAR-Engineered Lymphocyte Cytotoxicity against MAGE-A4.International journal of molecular sciences · 2023
    Article
  9. Review
  10. Article
  11. Article
  12. Single-cell imaging of T cell immunotherapy responses in vivo.The Journal of experimental medicine · 2021
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  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

9 authors at 1 institution in 1 country.

Masaki MarutaDepartment of Hematology, Clinical Immunology, and Infectious Diseases, Ehime University Graduate School of Medicine, 791-0295, Toon, Ehime, Japan.
Toshiki OchiDepartment of Hematology, Clinical Immunology, and Infectious Diseases, Ehime University Graduate School of Medicine, 791-0295, Toon, Ehime, Japan. ochi.toshiki.eg@ehime-u.ac.jp.ORCID http://orcid.org/0000-0001-8440-6144
Kazushi TanimotoDepartment of Hematology, Clinical Immunology, and Infectious Diseases, Ehime University Graduate School of Medicine, 791-0295, Toon, Ehime, Japan.
Hiroaki AsaiDepartment of Hematology, Clinical Immunology, and Infectious Diseases, Ehime University Graduate School of Medicine, 791-0295, Toon, Ehime, Japan.
Takashi SaitouDepartment of Molecular Medicine for Pathogenesis, Ehime University Graduate School of Medicine, 791-0295, Toon, Ehime, Japan.
Hiroshi FujiwaraDepartment of Hematology, Clinical Immunology, and Infectious Diseases, Ehime University Graduate School of Medicine, 791-0295, Toon, Ehime, Japan.
Takeshi ImamuraDepartment of Molecular Medicine for Pathogenesis, Ehime University Graduate School of Medicine, 791-0295, Toon, Ehime, Japan.
Katsuto TakenakaDepartment of Hematology, Clinical Immunology, and Infectious Diseases, Ehime University Graduate School of Medicine, 791-0295, Toon, Ehime, Japan.
Masaki YasukawaDivision of Immune Regulation, Proteo-Science Center, Ehime University, 791-0295, Toon, Ehime, Japan.ORCID http://orcid.org/0000-0002-1538-433X
Ehime University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of chimeric antigen receptor (CAR) and bispecific T-cell engager (BiTE) has led to the successful application of cancer immunotherapy. The potential reactivity mediated by CAR- and BiTE-redirected T cells needs to be assessed to facilitate the application of these treatment options to a broader range of patients. Here, we have generated CAR and BiTE possessing the same single chain fragment variable (scFv) specific for the HLA-A2/NY-ESO-1

Indexed as

Antigens, NeoplasmCell Line, TumorHLA-A2 AntigenHumansImmunoglobulin Variable RegionImmunotherapy, AdoptiveLymphocyte ActivationMembrane ProteinsMultiple MyelomaReceptors, Chimeric AntigenT-Lymphocytes, CytotoxicAntigens, NeoplasmCTAG1B protein, humanHLA-A2 AntigenImmunoglobulin Variable RegionMembrane ProteinsReceptors, Chimeric Antigen

Identifiers

PMID31527633
PMCPMC6746725
OpenAlexW2972825300

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.