Evidence map›Paper›PMID 19646680›Full record

ArticleCellular immunology2009

CD28 and ICOS play complementary non-overlapping roles in the development of Th2 immunity in vivo.

Rebecca A Shilling, Bryan S Clay, Amanda G Tesciuba, Elizabeth L Berry, Tiffany Lu, Tamson V Moore, Hozefa S Bandukwala, Jiankun Tong, Joel V Weinstock, Richard A Flavell and 5 more

Open access · greenAbstract read
In one paragraph

Article in Cellular immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

8 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Endogenous matrix metalloproteinases 2 and 9 regulate activation of CD4+ and CD8+ T cells.American journal of respiratory cell and molecular biology · 2011
    Article
  8. 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

15 authors at 4 institutions in 1 country.

Rebecca A ShillingSection of Pulmonary and Critical Care Medicine, Department of Medicine, The University of Chicago, MC6076, Room M658, 5841 S. Maryland Avenue, Chicago, IL 60637, USA. rshillin@medicine.bsd.uchicago.edu
Bryan S Clay
Amanda G Tesciuba
Elizabeth L Berry
Tiffany Lu
Tamson V Moore
Hozefa S Bandukwala
Jiankun Tong
Joel V Weinstock
Richard A Flavell
Tom Horan
Steve K Yoshinaga
Andrew A Welcher
Judy L Cannon
Anne I Sperling
University of Chicago · USAmgen (United States) · USHoward Hughes Medical Institute · USTufts Medical Center · US

Funding

Vaccines and Therapies Against BotulismU54AI057153 · NIAID · UNIVERSITY OF CHICAGO · PI SCHNEEWIND, OLAF · 2003 to 2013
$87.6M
ZOLEDRONATE &OSTEOPOROTIC EFFECTS OF ANDROGEN DEPRIVATIM01RR000055 · NCRR · UNIVERSITY OF CHICAGO · PI GARFINKEL, MARC R · 1985 to 2007
$19.0M
Molecular Mechanisms of AsthmaP01AI056352 · NIAID · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2003 to 2007
$5.6M
The role of ICOS in allergic airway diseaseR01AI050180 · NIAID · UNIVERSITY OF CHICAGO · PI SPERLING, ANNE I. · 2001 to 2005
$1.7M
ICOS Expression Levels and Th DevelopmentK08AI059105 · NIAID · UNIVERSITY OF CHICAGO · PI SHILLING, REBECCA A. · 2006 to 2010
$576k
NCRR NIH HHS L30 RR021946NCRR NIH HHS M01 RR000055NIAID NIH HHS K08 AI 059105NIAID NIH HHS K08 AI059105NIAID NIH HHS P01 AI056352NIAID NIH HHS P01 AI56352NIAID NIH HHS R01 AI050180NIAID NIH HHS R01 AI50180NIAID NIH HHS U54 AI057153
6 · The paper itself

Abstract

Previous work has shown ICOS can function independently of CD28, but whether either molecule can compensate for the other in vivo is not known. Since ICOS is a potent inducer of Th2 cytokines and linked to allergy and elevated serum IgE in humans, we hypothesized that augmenting ICOS costimulation in murine allergic airway disease may overcome CD28 deficiency. While ICOS was expressed on T cells from CD28(-/-) mice, Th2-mediated airway inflammation was not induced in CD28(-/-) mice by increased ICOS costimulation. Further, we determined if augmenting CD28 costimulation could compensate for ICOS deficiency. ICOS(-/-) mice had a defect in airway eosinophilia that was not overcome by augmenting CD28 costimulation. CD28 costimulation also did not fully compensate for ICOS for antibody responses, germinal center formation or the development of follicular B helper T cells. CD28 and ICOS play complementary non-overlapping roles in the development of Th2 immunity in vivo.

Indexed as

AnimalsAntigens, Differentiation, T-LymphocyteBronchoalveolar Lavage FluidCD28 AntigensDisease Models, AnimalEnzyme-Linked Immunosorbent AssayFemaleFlow CytometryHistocytochemistryImmunity, CellularImmunoglobulin EInducible T-Cell Co-Stimulator ProteinLung DiseasesMiceMice, Inbred C57BLMice, KnockoutAntigens, Differentiation, T-LymphocyteCD28 AntigensICOS protein, humanIcos protein, mouseImmunoglobulin EInducible T-Cell Co-Stimulator Protein

Identifiers

PMID19646680
PMCPMC2748173
OpenAlexW1998259832

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.