Evidence map›Paper›PMID 37973846›Full record

ArticleNature communications2023

High-sensitive spatially resolved T cell receptor sequencing with SPTCR-seq.

Jasim Kada Benotmane, Jan Kueckelhaus, Paulina Will, Junyi Zhang, Vidhya M Ravi, Kevin Joseph, Roman Sankowski, Jürgen Beck, Catalina Lee-Chang, Oliver Schnell and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
6.0field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

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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

11 authors at 2 institutions in 2 countries.

Jasim Kada BenotmaneDepartment of Neurosurgery, Medical Center - University of Freiburg, Freiburg, Germany.
Jan KueckelhausDepartment of Neurosurgery, Medical Center - University of Freiburg, Freiburg, Germany.
Paulina WillDepartment of Neurosurgery, Medical Center - University of Freiburg, Freiburg, Germany.
Junyi ZhangDepartment of Neurosurgery, Medical Center - University of Freiburg, Freiburg, Germany.ORCID 0000-0002-0001-2971
Vidhya M RaviDepartment of Neurosurgery, Medical Center - University of Freiburg, Freiburg, Germany.ORCID 0000-0003-0062-2099
Kevin JosephDepartment of Neurosurgery, Medical Center - University of Freiburg, Freiburg, Germany.ORCID 0000-0001-6317-8736
Roman SankowskiInstitute of Neuropathology, Medical Center-University of Freiburg, Freiburg, Germany.ORCID 0000-0001-9215-8021
Jürgen BeckDepartment of Neurosurgery, Medical Center - University of Freiburg, Freiburg, Germany.
Catalina Lee-ChangDepartment of Neurological Surgery, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.ORCID 0000-0002-7675-2124
Oliver SchnellDepartment of Neurosurgery, Medical Center - University of Freiburg, Freiburg, Germany.
Dieter Henrik HeilandDepartment of Neurosurgery, Medical Center - University of Freiburg, Freiburg, Germany. dieter.henrik.heiland@uniklinik-freiburg.de.ORCID 0000-0002-9258-3033
University of Freiburg · DENorthwestern University · US

Funding

Development of B-cell-based vaccine for GlioblastomaR37CA258426 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Catalina Lee Chang · 2021 to 2026
$2.2M
NCI NIH HHS R37 CA258426
6 · The paper itself

Abstract

Spatial resolution of the T cell repertoire is essential for deciphering cancer-associated immune dysfunction. Current spatially resolved transcriptomic technologies are unable to directly annotate T cell receptors (TCR). We present spatially resolved T cell receptor sequencing (SPTCR-seq), which integrates optimized target enrichment and long-read sequencing for highly sensitive TCR sequencing. The SPTCR computational pipeline achieves yield and coverage per TCR comparable to alternative single-cell TCR technologies. Our comparison of PCR-based and SPTCR-seq methods underscores SPTCR-seq's superior ability to reconstruct the entire TCR architecture, including V, D, J regions and the complementarity-determining region 3 (CDR3). Employing SPTCR-seq, we assess local T cell diversity and clonal expansion across spatially discrete niches. Exploration of the reciprocal interaction of the tumor microenvironmental and T cells discloses the critical involvement of NK and B cells in T cell exhaustion. Integrating spatially resolved omics and TCR sequencing provides as a robust tool for exploring T cell dysfunction in cancers and beyond.

Indexed as

Receptors, Antigen, T-CellT-LymphocytesComplementarity Determining RegionsGene Expression ProfilingHigh-Throughput Nucleotide SequencingReceptors, Antigen, T-Cell, alpha-betaComplementarity Determining RegionsReceptors, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID37973846
PMCPMC10654577
OpenAlexW4388718456

What OpenQuestion holds

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LicenceCC BY
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.