Evidence map›Paper›PMID 21149551›Full record

ArticleThe Journal of experimental medicine2010

A peripheral CD4+ T cell precursor for naive, memory, and regulatory T cells.

Chunfang Zhao, Joanna D Davies

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2010. 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
1.0field-weighted citation impact, top 23% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

  1. Aging and Thymosin Alpha-1.International journal of molecular sciences · 2025
    Review
  2. Antigen-Specific CD4 T Cell and B Cell Responses to Borrelia burgdorferi.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Article
  3. Article
  4. Review
  5. T Cell Calcium Signaling Regulation by the Co-Receptor CD5.International journal of molecular sciences · 2018
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Analysis of naïve lung CD4 T cells provides evidence of functional lung to lymph node migration.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  13. Article
  14. Distinct CD4+ helper T cells involved in primary and secondary responses to infection.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  15. Article
  16. Review
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

2 authors at 1 institution in 1 country.

Chunfang ZhaoTorrey Pines Institute for Molecular Studies, 3550 General Atomics Court, San Diego, CA 92121, USA.
Joanna D Davies
Torrey Pines Institute For Molecular Studies · US

Funding

CD4+ T cells in the control of cachexiaR01CA109729 · NCI · TORREY PINES INST FOR MOLECULAR STUDIES · PI DAVIES, JOANNA D · 2006 to 2008
$760k
NCI NIH HHS CA109729NCI NIH HHS R01 CA109729
6 · The paper itself

Abstract

Mechanisms that control the size of the T cell pool, the ratio between naive cells and memory cells, the number and frequency of regulatory T cells, and T cell receptor (TCR) diversity are necessary to maintain immune integrity and avoid disease. We have previously shown that a subset of naive CD4(+) T cells, defined by the expression on their surface of a very low density of CD44 (CD44(v.low) cells), can inhibit wasting and wasting-associated lymphopenia in mice with cancer. In this study, we further investigate the properties of CD44(v.low) cells and show that they are significantly more efficient than the remaining naive (CD44(low) or CD44(int)) and memory CD4(+) cell subsets in reconstituting the overall size of the CD4(+) T cell pool, creating a T cell pool with a diverse TCR repertoire, generating regulatory T cells that express forkhead box P3 (FoxP3), and promoting homeostatic equilibrium between naive, memory, and Foxp3(+) regulatory T cell numbers. T cell population reconstitution by CD44(v.low) cells is thymus independent. Compared with CD44(int) cells, a higher percentage of CD44(v.low) cells express B cell leukemia/lymphoma 2, interleukin-7 receptor, and CD5. The data support a key role for CD4(+) CD44(v.low) cells as peripheral precursors that maintain the integrity of the CD4(+) T cell pool.

Indexed as

Adoptive TransferAnimalsCD4-Positive T-LymphocytesCD5 AntigensCell ProliferationFlow CytometryForkhead Transcription FactorsHyaluronan ReceptorsImmunologic MemoryInterleukin-2Interleukin-7 Receptor alpha SubunitLymphocyte CountMiceMice, Inbred BALB CMice, SCIDPrecursor Cells, T-LymphoidCD5 AntigensForkhead Transcription FactorsFoxp3 protein, mouseHyaluronan ReceptorsInterleukin-2Interleukin-7 Receptor alpha SubunitProto-Oncogene Proteins c-bcl-2Receptors, Antigen, T-Cell

Identifiers

PMID21149551
PMCPMC3005223
OpenAlexW2165578636

What OpenQuestion 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 OpenQuestion graph.