Evidence map›Paper›PMID 33201171›Full record

ArticleThe Journal of experimental medicine2021

Single-cell lineage mapping of a diverse virus-specific naive CD4 T cell repertoire.

Achia Khatun, Moujtaba Y Kasmani, Ryan Zander, David M Schauder, Jeremy P Snook, Jian Shen, Xiaopeng Wu, Robert Burns, Yi-Guang Chen, Chien-Wei Lin and 2 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

43 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Tissue determinants of the human T cell receptor repertoire.bioRxiv : the preprint server for biology · 2024
    Article
  19. Article
  20. 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

12 authors at 3 institutions in 1 country.

Achia KhatunDepartment of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI.
Moujtaba Y KasmaniDepartment of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI.
Ryan ZanderBlood Research Institute, Versiti Wisconsin, Milwaukee, WI.
David M SchauderDepartment of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI.
Jeremy P SnookDivision of Microbiology and Immunology, Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT.
Jian ShenDepartment of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI.
Xiaopeng WuBlood Research Institute, Versiti Wisconsin, Milwaukee, WI.
Robert BurnsBlood Research Institute, Versiti Wisconsin, Milwaukee, WI.
Yi-Guang ChenDepartment of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI.
Chien-Wei LinInstitute for Health and Equity, Division of Biostatistics, Medical College of Wisconsin, Milwaukee, WI.
Matthew A WilliamsDivision of Microbiology and Immunology, Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT.
Weiguo CuiDepartment of Microbiology and Immunology, Medical College of Wisconsin, Milwaukee, WI.
Medical College of Wisconsin · USVersiti Blood Center of Wisconsin · USUniversity of Utah · US

Funding

Medical Scientist Training ProgramT32GM080202 · NIGMS · MEDICAL COLLEGE OF WISCONSIN · PI BARBIERI, JOSEPH T, SALZMAN, NITA H · 2010 to 2024
$5.7M
Mechanistic and Therapeutic Role of the CD137-CD137L Axis in Type 1 DiabetesR01DK107541 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI CHEN, YI-GUANG, RIDGWAY, WILLIAM M · 2016 to 2025
$5.6M
TCR-dependent activation, functional differentiation and memory formation of CD4+ T cells following infectionR01AI137248 · NIAID · UNIVERSITY OF UTAH · PI WILLIAMS, MATTHEW A · 2018 to 2022
$2.5M
The Cellular and Transcriptional Control of CD8 T Cell Functional Adaptation to Chronic VirusesR01AI125741 · NIAID · VERSITI WISCONSIN, INC. · PI CUI, WEIGUO · 2016 to 2020
$2.1M
Shaping diabetogenic T cells by IL-27 in type 1 diabetesR01DK121747 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI CHEN, YI-GUANG · 2019 to 2022
$1.5M
Defining the transcriptional, phenotypic, and functional heterogeneity of virus-specific CD4 T cells during chronic viral infectionR00AI153537 · NIAID · UNIVERSITY OF IOWA · PI ZANDER, RYAN · 2022 to 2023
$498k
Genetic analysis of islet-infiltrating IL-21-expressing CD4 T cells in type 1 diabetesR21AI144360 · NIAID · MEDICAL COLLEGE OF WISCONSIN · PI CHEN, YI-GUANG · 2020 to 2021
$418k
Defining the transcriptional, phenotypic, and functional heterogeneity of virus-specific CD4 T cells during chronic viral infectionK99AI153537 · NIAID · VERSITI WISCONSIN, INC. · PI ZANDER, RYAN · 2020 to 2021
$224k
Mechanistic study of TCR signaling strength in CD8 T cell differentiation during pathogenesis of T1DMF30DK127526 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI KASMANI, MOUJTABA Y · 2020 to 2023
$198k
BATF-IRF4 complex controls transcriptional regulation and effector function of autoreactive CD8 T cells in type 1 diabetesF30DK108557 · NIDDK · VERSITI WISCONSIN, INC. · PI SCHAUDER, DAVID · 2016 to 2019
$191k
NIAID NIH HHS K99 AI153537NIAID NIH HHS R00 AI153537NIAID NIH HHS R01 AI125741NIAID NIH HHS R01 AI137248NIAID NIH HHS R21 AI144360NIDDK NIH HHS F30 DK108557NIDDK NIH HHS F30 DK127526NIDDK NIH HHS R01 DK107541NIDDK NIH HHS R01 DK121747NIGMS NIH HHS T32 GM080202
6 · The paper itself

Abstract

Tracking how individual naive T cells from a natural TCR repertoire clonally expand, differentiate, and make lineage choices in response to an infection has not previously been possible. Here, using single-cell sequencing technology to identify clones by their unique TCR sequences, we were able to trace the clonal expansion, differentiation trajectory, and lineage commitment of individual virus-specific CD4 T cells during an acute lymphocytic choriomeningitis virus (LCMV) infection. Notably, we found previously unappreciated clonal diversity and cellular heterogeneity among virus-specific helper T cells. Interestingly, although most naive CD4 T cells gave rise to multiple lineages at the clonal level, ∼28% of naive cells exhibited a preferred lineage choice toward either Th1 or TFH cells. Mechanistically, we found that TCR structure, in particular the CDR3 motif of the TCR α chain, skewed lineage decisions toward the TFH cell fate.

Indexed as

Cell LineageAmino Acid MotifsAnimalsCD4-Positive T-LymphocytesClone CellsLymphocyte SubsetsLymphocytic ChoriomeningitisLymphocytic choriomeningitis virusMiceMice, Inbred C57BLReceptors, Antigen, T-CellSpecies SpecificityReceptors, Antigen, T-Cell

Identifiers

PMID33201171
PMCPMC7676493
OpenAlexW3102577481

What Socratic holds

Textmetadata
LicenceCC BY-NC-SA
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 Socratic graph.