Evidence map›Paper›PMID 33408405›Full record

ArticleNature methods2021

Mapping the functional landscape of T cell receptor repertoires by single-T cell transcriptomics.

Ze Zhang, Danyi Xiong, Xinlei Wang, Hongyu Liu, Tao Wang

Open access · greenAbstract read
In one paragraph

Article in Nature methods, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

66 citing papers in PubMed, 106 citations in OpenAlex.

  1. Review
  2. Gliadin-specific CD4Science advances · 2026
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6 more citing papers are in PubMed but not listed here.

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

5 authors at 3 institutions in 1 country.

Ze ZhangQuantitative Biomedical Research Center, Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0003-2717-0256
Danyi XiongDepartment of Statistical Science, Southern Methodist University, Dallas, TX, USA.
Xinlei WangDepartment of Statistical Science, Southern Methodist University, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-8561-6511
Hongyu LiuQuantitative Biomedical Research Center, Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Tao WangQuantitative Biomedical Research Center, Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA. Tao.Wang@UTSouthwestern.edu.ORCID http://orcid.org/0000-0002-4355-149X
Southern Methodist University · USThe University of Texas Southwestern Medical Center · USSouthwestern Medical Center · US

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MELANIE H. COBB · 2010 to 2026
$53.7M
Normalizing Gene Expression Data from Formalin-Fixed Paraffin-Embedded SamplesR15GM131390 · NIGMS · SOUTHERN METHODIST UNIVERSITY · PI WANG, XINLEI · 2019 to 2019
$432k
NCI NIH HHS P30 CA142543NIGMS NIH HHS R15 GM131390
6 · The paper itself

Abstract

Many experimental and bioinformatics approaches have been developed to characterize the human T cell receptor (TCR) repertoire. However, the unknown functional relevance of TCR profiling hinders unbiased interpretation of the biology of T cells. To address this inadequacy, we developed tessa, a tool to integrate TCRs with gene expression of T cells to estimate the effect that TCRs confer on the phenotypes of T cells. Tessa leveraged techniques combining single-cell RNA-sequencing with TCR sequencing. We validated tessa and showed its superiority over existing approaches that investigate only the TCR sequences. With tessa, we demonstrated that TCR similarity constrains the phenotypes of T cells to be similar and dictates a gradient in antigen targeting efficiency of T cell clonotypes with convergent TCRs. We showed this constraint could predict a functional dichotomization of T cells postimmunotherapy treatment and is weakened in tumor contexts.

Indexed as

TranscriptomeComputational BiologyHigh-Throughput Nucleotide SequencingHumansLymphocytes, Tumor-InfiltratingNeoplasmsReceptors, Antigen, T-CellSingle-Cell AnalysisT-LymphocytesReceptors, Antigen, T-Cell

Identifiers

PMID33408405
PMCPMC7799492
OpenAlexW3120050808

What OpenQuestion holds

Textmetadata
LicenceTDM
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.