Evidence map›Paper›PMID 33251011›Full record

ArticleClinical & translational immunology2020

A T-cell reporter platform for high-throughput and reliable investigation of TCR function and biology.

Thomas R Müller, Corinna Schuler, Monika Hammel, Amelie Köhler, Sabrina Jutz, Judith Leitner, Kilian Schober, Dirk H Busch, Peter Steinberger

Abstract read
In one paragraph

Article in Clinical & translational immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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  8. 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
    Article
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  14. Frontiers in endocrinology · 2022
    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

9 authors.

Thomas R MüllerInstitute for Medical Microbiology, Immunology and Hygiene Technical University of Munich (TUM) Munich Germany.ORCID https://orcid.org/0000-0001-5331-5522
Corinna SchulerInstitute for Medical Microbiology, Immunology and Hygiene Technical University of Munich (TUM) Munich Germany.
Monika HammelInstitute for Medical Microbiology, Immunology and Hygiene Technical University of Munich (TUM) Munich Germany.
Amelie KöhlerInstitute for Medical Microbiology, Immunology and Hygiene Technical University of Munich (TUM) Munich Germany.
Sabrina JutzDivision of Immune Receptors and T Cell Activation Center for Pathophysiology, Infectiology, and Immunology Institute of Immunology Medical University of Vienna Vienna Austria.
Judith LeitnerDivision of Immune Receptors and T Cell Activation Center for Pathophysiology, Infectiology, and Immunology Institute of Immunology Medical University of Vienna Vienna Austria.ORCID https://orcid.org/0000-0002-7156-1759
Kilian SchoberInstitute for Medical Microbiology, Immunology and Hygiene Technical University of Munich (TUM) Munich Germany.ORCID https://orcid.org/0000-0001-9323-9472
Dirk H BuschInstitute for Medical Microbiology, Immunology and Hygiene Technical University of Munich (TUM) Munich Germany.ORCID https://orcid.org/0000-0001-8713-093X
Peter SteinbergerDivision of Immune Receptors and T Cell Activation Center for Pathophysiology, Infectiology, and Immunology Institute of Immunology Medical University of Vienna Vienna Austria.ORCID https://orcid.org/0000-0001-6848-4097

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTransgenic re-expression enables unbiased investigation of T-cell receptor (TCR)-intrinsic characteristics detached from its original cellular context. Recent advancements in TCR repertoire sequencing and development of protocols for direct cloning of full TCRαβ constructs now facilitate large-scale transgenic TCR re-expression. Together, this offers unprecedented opportunities for the screening of TCRs for basic research as well as clinical use. However, the functional characterisation of re-expressed TCRs is still a complicated and laborious matter. Here, we propose a Jurkat-based triple parameter TCR signalling reporter endogenous TCR knockout cellular platform (TPR

methodsAs a proof-of-concept, we transgenically re-expressed 59 human cytomegalovirus-specific TCRs and systematically investigated and compared TCR function in TPR

resultsWe demonstrate that the TPR

conclusionOverall, our data show that the TPR

Indexed as

adoptive T‐cell therapyCas9CRISPRreporter T‐cell lineTCR biologyTCR functional avidityTCR gene editing

Identifiers

PMID33251011
PMCPMC7681835

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.