Evidence map›Paper›PMID 35565389›Full record

ArticleCancers2022

HLA-DR Presentation of the Tumor Antigen MSLN Associates with Clinical Outcome of Ovarian Cancer Patients.

Christian M Tegeler, Jonas Scheid, Hans-Georg Rammensee, Helmut R Salih, Juliane S Walz, Jonas S Heitmann, Annika Nelde

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
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  8. TOFNature communications · 2023
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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

7 authors at 3 institutions in 1 country.

Christian M TegelerClinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Department of Internal Medicine, University Hospital Tübingen, 72076 Tübingen, Germany.ORCID 0000-0001-6688-7351
Jonas ScheidDepartment of Peptide-Based Immunotherapy, University Hospital Tübingen, 72076 Tübingen, Germany.ORCID 0000-0002-5923-1343
Hans-Georg RammenseeInstitute for Cell Biology, Department of Immunology, University of Tübingen, 72076 Tübingen, Germany.
Helmut R SalihClinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Department of Internal Medicine, University Hospital Tübingen, 72076 Tübingen, Germany.ORCID 0000-0002-6719-1847
Juliane S WalzClinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Department of Internal Medicine, University Hospital Tübingen, 72076 Tübingen, Germany.ORCID 0000-0001-6404-7391
Jonas S HeitmannClinical Collaboration Unit Translational Immunology, German Cancer Consortium (DKTK), Department of Internal Medicine, University Hospital Tübingen, 72076 Tübingen, Germany.
Annika NeldeDepartment of Peptide-Based Immunotherapy, University Hospital Tübingen, 72076 Tübingen, Germany.ORCID 0000-0001-8504-8481
University Children's Hospital Tübingen · DEDeutschen Konsortium für Translationale Krebsforschung · DEGerman Cancer Research Center · DE

Funding

Deutsche Forschungsgemeinschaft WA 4608/1-2Deutsche Forschungsgemeinschaft under Germany`s Excellence Stategy EXC2180-390900677Deutsche José Carreras Leukämie-Stiftung DJCLS 05R/2017Federal Ministry of Education and Research FKZ:01KI20130Fortüne Program of the University of Tübingen Fortüne no. 2451-0-0German Cancer Consortium n.a.Wilhelm Sander Stiftung 2016.177.2
6 · The paper itself

Abstract

T-cell recognition of HLA-presented antigens is central for the immunological surveillance of malignant disease and key for the development of novel T-cell-based immunotherapy approaches. In recent years, large-scale immunopeptidome studies identified naturally presented tumor-associated antigens for several malignancies. Regarding ovarian carcinoma (OvCa), Mucin-16 (MUC16) and Mesothelin (MSLN) were recently described as the top HLA class I- and HLA class II-presented tumor antigens, respectively. Here, we investigate the role and impact of immunopeptidome-presented tumor antigens on the clinical outcomes of 39 OvCa patients with a follow-up time of up to 50 months after surgery. Patients with a HLA-restricted presentation of high numbers of different MSLN-derived peptides on their tumors exhibited significantly prolonged progression-free (PFS) and overall survival (OS), whereas the presentation of MUC16-derived HLA class I-restricted peptides had no impact. Furthermore, a high HLA-DRB gene expression was associated with increased PFS and OS. In line, in silico prediction revealed that MSLN-derived HLA class II-presented peptides are predominantly presented on HLA-DR allotypes. In conclusion, the correlation of MSLN tumor antigen presentation and HLA-DRB gene expression with prolonged survival indicates a central role of CD4

Indexed as

clinical dataimmunopeptidomemesothelinmucin-16ovarian cancersurvival

Identifiers

PMID35565389
PMCPMC9101593
OpenAlexW4225246745

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.