Evidence map›Paper›PMID 19542428›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

Role of CD44 in the differentiation of Th1 and Th2 cells: CD44-deficiency enhances the development of Th2 effectors in response to sheep RBC and chicken ovalbumin.

Hongbing Guan, Prakash S Nagarkatti, Mitzi Nagarkatti

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
1.1field-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

46 citing papers in PubMed, 68 citations in OpenAlex.

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  10. A review of CD4Veterinary immunology and immunopathology · 2024
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  15. Article
  16. Review
  17. Article
  18. CD44 receptor targeted nanoparticles augment immunity against tuberculosis in mice.Journal of controlled release : official journal of the Controlled Release Society · 2022
    Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Hongbing GuanDepartment of Pathology, Microbiology and Immunology, University of South Carolina School of Medicine, Columbia, 29209, USA.
Prakash S Nagarkatti
Mitzi Nagarkatti
University of South Carolina · US

Funding

Use of Resveratrol to treat experimental multiple sclerosisP01AT003961 · NCCIH · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI NAGARKATTI, PRAKASH S · 2007 to 2018
$14.2M
TCDD-INDUCED APOPTOSIS EFFECT ON T CELLSR01ES009098 · NIEHS · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI NAGARKATTI, PRAKASH S · 1999 to 2008
$2.2M
Cytotoxic lymphocytes in acute lung injuryR01AI058300 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI NAGARKATTI, MITZI · 2004 to 2008
$1.5M
Role of CD44 in EC injury and melanoma therapyR01AI053703 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI NAGARKATTI, MITZI · 2003 to 2007
$1.4M
Cannabinoid-induced apoptosis in T cell regulationR01DA016545 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI NAGARKATTI, PRAKASH S. · 2003 to 2007
$1.2M
ENDOTHELIAL CELL INJURY BY CYTOLYTIC LYMPHOCYTESR01HL058641 · NHLBI · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI NAGARKATTI, MITZI · 1998 to 2006
$1.2M
NCCIH NIH HHS P01 AT003961NCCIH NIH HHS P01AT003961NHLBI NIH HHS HL058641NHLBI NIH HHS R01 HL058641NIAID NIH HHS AI053703NIAID NIH HHS AI058300NIAID NIH HHS R01 AI053703NIAID NIH HHS R01 AI058300NIDA NIH HHS DA016545NIDA NIH HHS R01 DA016545NIEHS NIH HHS ES09098NIEHS NIH HHS R01 ES009098
6 · The paper itself

Abstract

CD4 T cells can be primarily polarized to differentiate into Th1 or Th2 cells. CD44 is a marker of T cell activation and a property of long-lived memory cells and implicated in cell migration, activation, and differentiation. To date, whether CD44 has a role in regulating Th1-Th2 differentiation has not been determined. In this study, we compared Th1 and Th2 responses in wild-type and CD44-deficient mice in response to sheep RBC and chicken OVA, as well as examined Th1-Th2 differentiation in vivo and in vitro from CD44-sufficient and CD44-deficient naive CD4 T cells. We observed that deficiency of CD44 tended to inhibit Th1 while promoting Th2 differentiation. Furthermore, chimeric studies suggested that CD44 expression by CD4 T cells was essential for such Th2 bias. The regulation by CD44 occurred at the transcription level leading to up-regulated GATA3 and down-regulated T-bet expression in activated CD4 T cells. We also noted that CD44-deficiency could modify the state of dendritic cell subsets to induce a Th2-biased development. Results presented in this study demonstrate for the first time that CD44 participates in the regulation of Th1-Th2 differentiation.

Indexed as

AnimalsCell DifferentiationCells, CulturedChickensDown-RegulationErythrocytesErythrocyte TransfusionHyaluronan ReceptorsHypersensitivity, DelayedImmunoglobulin GMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicOvalbuminSheepCd44 protein, mouseHyaluronan ReceptorsImmunoglobulin GOvalbumin

Identifiers

PMID19542428
PMCPMC2723169
OpenAlexW1757683061

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.