Evidence map›Paper›PMID 28950731›Full record

ArticleHuman gene therapy2017

Unbiased Identification of T-Cell Receptors Targeting Immunodominant Peptide-MHC Complexes for T-Cell Receptor Immunotherapy.

Felix K M Lorenz, Christian Ellinger, Elisa Kieback, Susanne Wilde, Maria Lietz, Dolores J Schendel, Wolfgang Uckert

Open access · bronzeAbstract read
In one paragraph

Article in Human gene therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
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  5. Article
  6. TCR and CAR Engineering of Primary Human T Cells.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  7. Review
  8. Review
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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 2 institutions in 1 country.

Felix K M Lorenz1 Max Delbrück Center for Molecular Medicine in the Helmholtz Association , Berlin, Germany .
Christian Ellinger2 Institute for Molecular Immunology, Helmholtz-Zentrum Munich , Munich, Germany .
Elisa Kieback1 Max Delbrück Center for Molecular Medicine in the Helmholtz Association , Berlin, Germany .
Susanne Wilde2 Institute for Molecular Immunology, Helmholtz-Zentrum Munich , Munich, Germany .
Maria Lietz1 Max Delbrück Center for Molecular Medicine in the Helmholtz Association , Berlin, Germany .
Dolores J Schendel2 Institute for Molecular Immunology, Helmholtz-Zentrum Munich , Munich, Germany .
Wolfgang Uckert1 Max Delbrück Center for Molecular Medicine in the Helmholtz Association , Berlin, Germany .
Max Delbrück Center · DEBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-cell receptor (TCR) immunotherapy uses T cells engineered with new TCRs to enable detection and killing of cancer cells. Efficacy of TCR immunotherapy depends on targeting antigenic peptides that are efficiently presented by the best-suited major histocompatibility complex (MHC) molecules of cancer cells. However, efficient strategies are lacking to easily identify TCRs recognizing immunodominant peptide-MHC (pMHC) combinations utilizing any of the six possible MHC class I alleles of a cancer cell. We generated an MHC cell library and developed a platform approach to detect, isolate, and re-express TCRs specific for immunodominant pMHCs. The platform approach was applied to identify a human papillomavirus (HPV16) oncogene E5-specific TCR, recognizing a novel, naturally processed pMHC (HLA-B*15:01) and a cytomegalovirus-specific TCR targeting an immunodominant pMHC (HLA-B*07:02). The platform provides a useful tool to isolate in an unbiased manner TCRs specific for novel and immunodominant pMHC targets for use in TCR immunotherapy.

Indexed as

HLA-B15 AntigenHLA-B7 AntigenNeoplasmsReceptors, Antigen, T-CellAdoptive TransferHumansK562 CellsPeptidesT-LymphocytesHLA-B15 AntigenHLA-B7 AntigenPeptidesReceptors, Antigen, T-Cellhuman papillomavirus ESimmunodominanceimmunotherapyMHC cell libraryT cell receptor (TCR) discoveryTCR gene therapy

Identifiers

PMID28950731
PMCPMC5737719
OpenAlexW2756985129

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.