Evidence map›Paper›PMID 18684917›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

CD28 controls differentiation of regulatory T cells from naive CD4 T cells.

Fei Guo, Cristina Iclozan, Woong-Kyung Suh, Claudio Anasetti, Xue-Zhong Yu

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 125 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
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  5. Article
  6. Review
  7. Article
  8. Article
  9. The Function of Ubiquitination in T-Cell Development.Advances in experimental medicine and biology · 2024
    Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. ICOS ligand and IL-10 synergize to promote host-microbiota mutualism.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  19. CTLA4-Ig prolongs graft survival specifically in young but not old mice.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2021
    Article
  20. Article

4 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 2 countries.

Fei GuoImmunology and Blood and Marrow Transplantation Programs, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA.
Cristina Iclozan
Woong-Kyung Suh
Claudio Anasetti
Xue-Zhong Yu
Moffitt Cancer Center · USUniversity of South Florida · USMontreal Clinical Research Institute · CA

Funding

Effects of Foxp3-Induced Regulatory T Cells on GVHD and GVT ActivityR01CA118116 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YU, XUE-ZHONG · 2006 to 2015
$2.2M
Antigen Specific T Cell Tolerance by Anti CD3 AntibodiesR01AI051693 · NIAID · H. LEE MOFFITT CANCER CTR &RES INST · PI ANASETTI, CLAUDIO · 2002 to 2006
$1.8M
Control of GVHD by Inducible T-Regulatory CellsR21AI063553 · NIAID · H. LEE MOFFITT CANCER CTR &RES INST · PI YU, XUE-ZHONG · 2005 to 2005
$243k
NCI NIH HHS CA 118116NCI NIH HHS R01 CA118116NIAID NIH HHS AI 51693NIAID NIH HHS AI 63553NIAID NIH HHS R01 AI051693NIAID NIH HHS R21 AI063553
6 · The paper itself

Abstract

CD28 is required for the development of regulatory T cells (Tregs; CD4(+)CD25(+)Foxp3(+)) in the thymus and also contributes to their survival and homeostasis in the periphery. We studied whether and how CD28 and ICOS control the differentiation of Tregs from naive T cells. By using wild-type, CD28-, ICOS-, or CD28/ICOS-double knockout mice on C57BL/6 background as T cell sources, we found that CD28 is essential, whereas ICOS is dispensable, for the development and homeostasis of Tregs. Furthermore, the differentiation of Tregs from naive CD4(+)CD25(-) T cells in vivo also depends on CD28. The requirement of CD28 for Treg differentiation was mediated by IL-2, because neutralization of IL-2 with its specific mAb-blocked Treg differentiation from wild-type CD4(+)CD25(-) T cells and addition of IL-2 restored Treg differentiation from CD28(-/-) T cells. Other common gamma-chain cytokines, IL-4, IL-7, or IL-15, do not share such a role with IL-2. Although CD28 is required for the differentiation of Tregs from naive T cells, already generated Tregs do not depend on CD28 to exert their suppressive function. Our study reveals a new aspect of CD28 function in regulating T cell response.

Indexed as

AnimalsAntigens, Differentiation, T-LymphocyteBALB 3T3 CellsCD28 AntigensCD4 AntigensCD4-Positive T-LymphocytesCell DifferentiationCells, CulturedForkhead Transcription FactorsHomeostasisInducible T-Cell Co-Stimulator ProteinInterleukin-2 Receptor alpha SubunitMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicAntigens, Differentiation, T-LymphocyteCD28 AntigensCD4 AntigensForkhead Transcription FactorsFoxp3 protein, mouseIcos protein, mouseInducible T-Cell Co-Stimulator ProteinInterleukin-2 Receptor alpha Subunit

Identifiers

PMID18684917
PMCPMC2688779
OpenAlexW1516873381

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.