Evidence map›Paper›PMID 30348802›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Isolation and characterization of NY-ESO-1-specific T cell receptors restricted on various MHC molecules.

Michael T Bethune, Xiao-Hua Li, Jiaji Yu, Jami McLaughlin, Donghui Cheng, Colleen Mathis, Blanca Homet Moreno, Katherine Woods, Ashley J Knights, Angel Garcia-Diaz and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
3.0field-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

61 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
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  7. CD8 co-receptor modulates the specificity profile of the 1G4 TCR against NY-ESO-1.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
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  12. Review
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  18. Article
  19. Heliyon · 2024
    Article
  20. Defining T cell receptor repertoires using nanovial-based binding and functional screening.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article

1 more citing papers are in PubMed but not listed here.

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

18 authors at 6 institutions in 2 countries.

Michael T BethuneDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125.
Xiao-Hua LiDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095.
Jiaji YuDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095.
Jami McLaughlinDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095.
Donghui ChengDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095.
Colleen MathisDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095.
Blanca Homet MorenoDivision of Hematology and Oncology, Department of Medicine, University of California, Los Angeles, CA 90095.
Katherine WoodsCancer Immunobiology Laboratory, Olivia Newton-John Cancer Research Institute, Austin Hospital, Heidelberg, VIC 3084, Australia.
Ashley J KnightsCancer Immunobiology Laboratory, Ludwig Institute for Cancer Research, Heidelberg, VIC 3084, Australia.
Angel Garcia-DiazDivision of Hematology and Oncology, Department of Medicine, University of California, Los Angeles, CA 90095.
Stephanie WongDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125.
Siwen Hu-LieskovanDivision of Hematology and Oncology, Department of Medicine, University of California, Los Angeles, CA 90095.
Cristina Puig-SausDivision of Hematology and Oncology, Department of Medicine, University of California, Los Angeles, CA 90095.
Jonathan CebonCancer Immunobiology Laboratory, Olivia Newton-John Cancer Research Institute, Austin Hospital, Heidelberg, VIC 3084, Australia.
Antoni RibasDivision of Hematology and Oncology, Department of Medicine, University of California, Los Angeles, CA 90095.
Lili YangDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095; liliyang@ucla.edu owenwitte@mednet.ucla.edu baltimo@caltech.edu.
Owen N WitteDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095; liliyang@ucla.edu owenwitte@mednet.ucla.edu baltimo@caltech.edu.
David BaltimoreDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125; liliyang@ucla.edu owenwitte@mednet.ucla.edu baltimo@caltech.edu.
University of California, Los Angeles · USBroad Center · USCalifornia Institute of Technology · USAustin Hospital · AULudwig Cancer Research · AUOlivia Newton-John Cancer Wellness & Research Centre · AU

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Transduction of Hematopoietic Stem Cells for Enhanced Immunotherapy of MelanomaP01CA132681 · NCI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI BALTIMORE, DAVID · 2010 to 2014
$14.4M
Next Generation Cancer Immunotherapies to Defeat MelanomaR35CA197633 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ANTONI RIBAS · 2015 to 2026
$10.4M
NCI NIH HHS P01 CA132681NCI NIH HHS P30 CA016042NCI NIH HHS R35 CA197633
6 · The paper itself

Abstract

Tumor-specific T cell receptor (TCR) gene transfer enables specific and potent immune targeting of tumor antigens. Due to the prevalence of the HLA-A2 MHC class I supertype in most human populations, the majority of TCR gene therapy trials targeting public antigens have employed HLA-A2-restricted TCRs, limiting this approach to those patients expressing this allele. For these patients, TCR gene therapy trials have resulted in both tantalizing successes and lethal adverse events, underscoring the need for careful selection of antigenic targets. Broad and safe application of public antigen-targeted TCR gene therapies will require (

Indexed as

AnimalsCloning, MolecularHomeodomain ProteinsHumansMajor Histocompatibility ComplexReceptors, Antigen, T-CellEso-1 protein, mouseHomeodomain ProteinsReceptors, Antigen, T-CellimmunotherapyMHCNY-ESO-1T cell receptor gene therapyTCR

Identifiers

PMID30348802
PMCPMC6233129
OpenAlexW2897545222

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.