Evidence map›Paper›PMID 35217611›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Heritable changes in division speed accompany the diversification of single T cell fate.

Marten Plambeck, Atefeh Kazeroonian, Dirk Loeffler, Lorenz Kretschmer, Ciro Salinno, Timm Schroeder, Dirk H Busch, Michael Flossdorf, Veit R Buchholz

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Cell Cycle Sensing Shapes Human T Cell Fate and Exhaustion Programs.bioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Article
  6. Design principles of the cytotoxic CD8Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Design principles of the cytotoxic CD8bioRxiv : the preprint server for biology · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Picking up speed: cell cycle regulation during effector CD8Medical microbiology and immunology · 2023
    Article
  18. Modeling T Cell Fate.Annual review of immunology · 2023
    Review
  19. T cell memories of past divisions.Nature immunology · 2022
    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

9 authors.

Marten PlambeckInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich 81675, Germany.ORCID 0000-0003-1323-7026
Atefeh KazeroonianInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich 81675, Germany.ORCID 0000-0002-5180-8937
Dirk LoefflerDepartment of Biosystems Science and Engineering, Eidgenössische Technische Hochschule Zürich (ETH Zurich), 4058 Basel, Switzerland.ORCID 0000-0001-9870-0088
Lorenz KretschmerInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich 81675, Germany.
Ciro SalinnoInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich 81675, Germany.ORCID 0000-0003-4364-3236
Timm SchroederDepartment of Biosystems Science and Engineering, Eidgenössische Technische Hochschule Zürich (ETH Zurich), 4058 Basel, Switzerland.ORCID 0000-0001-9320-0252
Dirk H BuschInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich 81675, Germany; dirk.busch@tum.de michael.flossdorf@tum.de veit.buchholz@tum.de.ORCID 0000-0001-8713-093X
Michael FlossdorfInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich 81675, Germany; dirk.busch@tum.de michael.flossdorf@tum.de veit.buchholz@tum.de.
Veit R BuchholzInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich (TUM), Munich 81675, Germany; dirk.busch@tum.de michael.flossdorf@tum.de veit.buchholz@tum.de.ORCID 0000-0003-0441-3913

Funding

European Research Council 949719
6 · The paper itself

Abstract

Rapid clonal expansion of antigen-specific T cells is a fundamental feature of adaptive immune responses. It enables the outgrowth of an individual T cell into thousands of clonal descendants that diversify into short-lived effectors and long-lived memory cells. Clonal expansion is thought to be programmed upon priming of a single naive T cell and then executed by homogenously fast divisions of all of its descendants. However, the actual speed of cell divisions in such an emerging "T cell family" has never been measured with single-cell resolution. Here, we utilize continuous live-cell imaging in vitro to track the division speed and genealogical connections of all descendants derived from a single naive CD8

Indexed as

Cell LineageAnimalsAntigens, CDBiomarkersCD8-Positive T-LymphocytesCell DifferentiationCell DivisionMiceMice, Inbred C57BLAntigens, CDBiomarkerscomputational modelingcontinuous imagingimmunological memorysingle-cell analysisT cell response

Identifiers

PMID35217611
PMCPMC8892279

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.