Evidence map›Paper›PMID 34858733›Full record

ArticleOncoimmunology2021

Keratinocyte differentiation antigen-specific T cells in immune checkpoint inhibitor-treated NSCLC patients are associated with improved survival.

Fiamma Berner, Rebekka Niederer, Jolien J Luimstra, Oltin Tiberiu Pop, Ann-Kristin Jochum, Mette-Triin Purde, Omar Hasan Ali, David Bomze, Jens Bauer, Lena Katharina Freudenmann and 21 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. The role of tumor types in immune-related adverse events.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  3. Review
  4. A replicating LCMV-based vaccine for the treatment of solid tumors.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  5. 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

31 authors at 11 institutions in 5 countries.

Fiamma BernerInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Rebekka NiedererInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Jolien J LuimstraDepartment of Cell and Chemical Biology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.
Oltin Tiberiu PopInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Ann-Kristin JochumInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Mette-Triin PurdeInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Omar Hasan AliInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
David BomzeSackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Jens BauerClinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Department of Internal Medicine, University Hospital Tübingen, Tübingen, Germany.
Lena Katharina FreudenmannInterfaculty Institute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen, Germany.
Ana MarcuInterfaculty Institute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen, Germany.
Eva-Maria WolfschmittInterfaculty Institute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen, Germany.
Sebastian HaenInterfaculty Institute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen, Germany.
Thorben GrossInterfaculty Institute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen, Germany.
Marissa Lisa DubbelaarClinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Department of Internal Medicine, University Hospital Tübingen, Tübingen, Germany.
Marie-Therese AbdouInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Petra BaumgaertnerDepartment of Oncology, Ludwig Cancer Research, University of Lausanne, Switzerland.ORCID 0000-0002-5979-7654
Christina AppenzellerDepartment of Oncology and Hematology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Caroline Cicin-SainDepartment of Oncology and Hematology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Tobias LenzResearch Unit Evolutionary Immunogenomics, Department of Biology, University of Hamburg, Hamburg, Germany.
Daniel E SpeiserDepartment of Oncology, Ludwig Cancer Research, University of Lausanne, Switzerland.ORCID 0000-0003-2031-3250
Burkhard LudewigInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.ORCID 0000-0002-7685-573X
Christoph DriessenInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Markus JörgerDepartment of Oncology and Hematology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Martin FrühDepartment of Oncology and Hematology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Wolfram JochumInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Antonio CozzioDepartment of Dermatology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Hans-Georg RammenseeInterfaculty Institute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen, Germany.
Juliane WalzInterfaculty Institute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen, Germany.
Jacques NeefjesDepartment of Cell and Chemical Biology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.
Lukas FlatzInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.ORCID 0000-0001-9683-8390
Kantonsspital St. Gallen · CHGerman Cancer Research Center · DEUniversity of Tübingen · DELeiden University Medical Center · NLLudwig Cancer Research · CHTel Aviv University · ILUniversität Hamburg · DEUniversity Children's Hospital Tübingen · DEUniversity of Bern · CHUniversity of British Columbia · CAUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs) have improved the survival of patients with non-small cell lung cancer (NSCLC) by reinvigorating tumor-specific T cell responses. However, the specificity of such T cells and the human leukocyte antigen (HLA)-associated epitopes recognized, remain elusive. In this study, we identified NSCLC T cell epitopes of recently described NSCLC-associated antigens, termed keratinocyte differentiation antigens. Epitopes of these antigens were presented by HLA-A 03:01 and HLA-C 04:01 and were associated with responses to ICI therapy. Patients with CD8

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAntigens, DifferentiationHumansImmune Checkpoint InhibitorsKeratinocytesAntigens, DifferentiationImmune Checkpoint Inhibitorsautoimmune toxicityImmune checkpoint inhibitor therapyNSCLCtumor-associated antigen

Identifiers

PMID34858733
PMCPMC8632109
OpenAlexW3215925274

What OpenQuestion holds

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Registered trials

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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.