Evidence map›Paper›PMID 25548167›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

HLA ligandome analysis identifies the underlying specificities of spontaneous antileukemia immune responses in chronic lymphocytic leukemia (CLL).

Daniel J Kowalewski, Heiko Schuster, Linus Backert, Claudia Berlin, Stefan Kahn, Lothar Kanz, Helmut R Salih, Hans-Georg Rammensee, Stefan Stevanovic, Juliane Sarah Stickel

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 115 papers.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

115 citing papers in PubMed, 161 citations in OpenAlex.

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  9. Dual role of the peptide-loading complex as proofreader and limiter of MHC-I presentation.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  11. TOFNature communications · 2023
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55 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Daniel J KowalewskiInstitute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen 72076, Germany;
Heiko SchusterInstitute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen 72076, Germany;
Linus BackertInstitute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen 72076, Germany; Applied Bioinformatics, Center for Bioinformatics and Department of Computer Science, University of Tübingen, Tübingen 72076, Germany;
Claudia BerlinInstitute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen 72076, Germany; Department of Hematology and Oncology, University of Tübingen, Tübingen 72076, Germany;
Stefan KahnInstitute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen 72076, Germany;
Lothar KanzDepartment of Hematology and Oncology, University of Tübingen, Tübingen 72076, Germany;
Helmut R SalihDepartment of Hematology and Oncology, University of Tübingen, Tübingen 72076, Germany; Clinical Cooperation Unit Translational Immunology, DKFZ Partner Site Tübingen, German Cancer Consortium (DKTK), Tübingen 72076, Germany; and.
Hans-Georg RammenseeInstitute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen 72076, Germany; DKFZ Partner Site Tübingen, German Cancer Consortium (DKTK), Tübingen 72076, Germany.
Stefan StevanovicInstitute for Cell Biology, Department of Immunology, University of Tübingen, Tübingen 72076, Germany; DKFZ Partner Site Tübingen, German Cancer Consortium (DKTK), Tübingen 72076, Germany.
Juliane Sarah StickelDepartment of Hematology and Oncology, University of Tübingen, Tübingen 72076, Germany; juliane.stickel@med.uni-tuebingen.de.
University of Tübingen · DEGerman Cancer Research Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The breakthrough development of clinically effective immune checkpoint inhibitors illustrates the potential of T-cell-based immunotherapy to effectively treat malignancies. A remaining challenge is to increase and guide the specificities of anticancer immune responses, e.g., by therapeutic vaccination or by adoptive T-cell transfer. By analyzing the landscape of naturally presented HLA class I and II ligands of primary chronic lymphocytic leukemia (CLL), we delineated a novel category of tumor-associated T-cell antigens based on their exclusive and frequent representation in the HLA ligandome of leukemic cells. These antigens were validated across different stages and mutational subtypes of CLL and found to be robustly represented in HLA ligandomes of patients undergoing standard chemo-/immunotherapy. We demonstrate specific immune recognition of these antigens exclusively in CLL patients, with the frequencies of representation in CLL ligandomes correlating with the frequencies of immune recognition by patient T cells. Moreover, retrospective survival analysis revealed survival benefits for patients displaying immune responses to these antigens. These results directly imply these nonmutant self-peptides as pathophysiologically relevant tumor antigens and encourages their implementation for cancer immunotherapy.

Indexed as

AgedAged, 80 and overAmino Acid SequenceAntigen PresentationAntigens, Differentiation, T-LymphocyteAntigens, NeoplasmCancer VaccinesCD4-Positive T-LymphocytesFemaleHLA AntigensHumansImmunity, InnateImmunotherapyLeukemia, Lymphocytic, Chronic, B-CellLigandsMaleAntigens, Differentiation, T-LymphocyteAntigens, NeoplasmCancer VaccinesHLA AntigensLigandsVaccines, Subunitcancer immunotherapychronic lymphocytic leukemiaHLAtherapeutic vaccinationtumor-associated antigens

Identifiers

PMID25548167
PMCPMC4299203
OpenAlexW2154707187

What OpenQuestion holds

Textmetadata
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.