Evidence map›Paper›PMID 29541393›Full record

ArticleOncotarget2018

Effective screening of T cells recognizing neoantigens and construction of T-cell receptor-engineered T cells.

Taigo Kato, Tatsuo Matsuda, Yuji Ikeda, Jae-Hyun Park, Matthias Leisegang, Sachiko Yoshimura, Tetsuro Hikichi, Makiko Harada, Makda Zewde, Sho Sato and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.2field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 58 citations in OpenAlex.

  1. Review
  2. Review
  3. Personalizing DNA Cancer Vaccines.Journal of personalized medicine · 2025
    Review
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  6. Review
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  17. Review
  18. Immunogenomics in personalized cancer treatments.Journal of human genetics · 2021
    Review
  19. Article
  20. 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

13 authors at 4 institutions in 3 countries.

Taigo KatoDepartment of Medicine, The University of Chicago, Chicago, IL 60637, USA.
Tatsuo MatsudaDepartment of Medicine, The University of Chicago, Chicago, IL 60637, USA.
Yuji IkedaDepartment of Medicine, The University of Chicago, Chicago, IL 60637, USA.
Jae-Hyun ParkDepartment of Medicine, The University of Chicago, Chicago, IL 60637, USA.
Matthias LeisegangInstitute of Immunology - Campus Buch, Charité - Universitätsmedizin Berlin, Berlin 13125, Germany.
Sachiko YoshimuraOncoTherapy Science Inc., Kawasaki, Kanagawa 213-0012, Japan.
Tetsuro HikichiOncoTherapy Science Inc., Kawasaki, Kanagawa 213-0012, Japan.
Makiko HaradaOncoTherapy Science Inc., Kawasaki, Kanagawa 213-0012, Japan.
Makda ZewdeDepartment of Medicine, The University of Chicago, Chicago, IL 60637, USA.
Sho SatoDepartment of Gynecologic Oncology, Saitama Medical University International Medical Center, Hidaka, Saitama 350-1298, Japan.
Kosei HasegawaDepartment of Gynecologic Oncology, Saitama Medical University International Medical Center, Hidaka, Saitama 350-1298, Japan.
Kazuma KiyotaniDepartment of Medicine, The University of Chicago, Chicago, IL 60637, USA.
Yusuke NakamuraDepartment of Medicine, The University of Chicago, Chicago, IL 60637, USA.
University of Chicago · USOncoTherapy Science (Japan) · JPSaitama Medical University · JPBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neoantigens are the main targets of tumor-specific T cells reactivated by immune checkpoint-blocking antibodies or when using tumor-infiltrating T cells for adoptive therapy. While cancers often accumulate hundreds of mutations and harbor several immunogenic neoantigens, the repertoire of mutation-specific T cells in patients might be restricted. To bypass suboptimal conditions, which impede the reactivation of existing T cells or the priming of neoantigen-specific T cells in a patient, we employ T cells of healthy donors with an overlapping HLA repertoire to target cancer neoantigens. In this study, we focus on streamlining the process of

Indexed as

neoantigensneoantigen-specific T cellsT cell receptorTCR-engineered T cells

Identifiers

PMID29541393
PMCPMC5834292
OpenAlexW2784133529

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.