Evidence map›Paper›PMID 36768267›Full record

ArticleInternational journal of molecular sciences2023

Definition and Characterization of SOX11-Derived T Cell Epitopes towards Immunotherapy of Glioma.

Yibin Liu, Anna Keib, Brigitte Neuber, Lei Wang, Angelika B Riemer, Maria Bonsack, Angela Hückelhoven-Krauss, Anita Schmitt, Carsten Müller-Tidow, Michael Schmitt

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. SOX on tumors, a comfort or a constraint?Cell death discovery · 2024
    Review
  5. Bioactive Peptides in Human Health and Disease.International journal of molecular sciences · 2023
    Article
  6. 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

10 authors.

Yibin LiuDepartment of Internal Medicine V, Heidelberg University Hospital, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany.
Anna KeibDepartment of Internal Medicine V, Heidelberg University Hospital, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany.
Brigitte NeuberDepartment of Internal Medicine V, Heidelberg University Hospital, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany.
Lei WangDepartment of Internal Medicine V, Heidelberg University Hospital, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany.
Angelika B RiemerImmunotherapy and Immunoprevention, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.ORCID 0000-0002-5865-0714
Maria BonsackImmunotherapy and Immunoprevention, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.ORCID 0000-0003-2087-7451
Angela Hückelhoven-KraussDepartment of Internal Medicine V, Heidelberg University Hospital, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany.
Anita SchmittDepartment of Internal Medicine V, Heidelberg University Hospital, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany.
Carsten Müller-TidowDepartment of Internal Medicine V, Heidelberg University Hospital, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany.
Michael SchmittDepartment of Internal Medicine V, Heidelberg University Hospital, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany.ORCID 0000-0002-1579-1509

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transcription factor SOX11 is a tumor-associated antigen with low expression in normal cells, but overexpression in glioblastoma (GBM). So far, conventional surgery, chemotherapy, and radiotherapy have not substantially improved the dismal prognosis of relapsed/refractory GBM patients. Immunotherapy is considered a promising strategy against GBM, but there is a fervent need for better immunotargets in GBM. To this end, we performed an in silico prediction study on SOX11, which primarily yielded ten promising HLA-A*0201-restricted peptides derived from SOX11. We defined a novel peptide FMACSPVAL, which had the highest score according to in silico prediction (6.02 nM by NetMHC-4.0) and showed an exquisite binding affinity to the HLA-A*0201 molecule in the peptide-binding assays. In the IFN-γ ELISPOT assays, FMACSPVAL demonstrated a high efficiency for generating SOX11-specific CD8

Indexed as

GlioblastomaGliomaCD8-Positive T-LymphocytesEpitopes, T-LymphocyteHumansImmunotherapyPeptidesSOXC Transcription FactorsT-Lymphocytes, CytotoxicEpitopes, T-LymphocytePeptidesSOX11 protein, humanSOXC Transcription FactorsgliomaHLA-A*0201immunotherapySOX11tumor-associated antigen

Identifiers

PMID36768267
PMCPMC9916519

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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.