Evidence map›Paper›PMID 12669034›Full record

ArticleNature medicine2003

Essential role of NKT cells producing IL-4 and IL-13 in the development of allergen-induced airway hyperreactivity.

Omid Akbari, Philippe Stock, Everett Meyer, Mitchell Kronenberg, Stephane Sidobre, Toshinori Nakayama, Masaru Taniguchi, Michael J Grusby, Rosemarie H DeKruyff, Dale T Umetsu

Abstract read
PubMed Publisher
In one paragraph

Article in Nature medicine, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 294 papers.

0numbers the graph read from it
0cells of the map it votes in
294citing papers in PubMed
14.8field-weighted citation impact, top 1% 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

294 citing papers in PubMed, 704 citations in OpenAlex.

  1. Trial
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  7. Article
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  9. Article
  10. Review
  11. G protein subunit GeLife · 2024
    Article
  12. CAR-NKT Cells in Asthma: Use of NKT as a Promising Cell for CAR Therapy.Clinical reviews in allergy & immunology · 2024
    Review
  13. Review
  14. Review
  15. Article
  16. Invariant natural killer T cells in lung diseases.Experimental & molecular medicine · 2023
    Review
  17. Review
  18. Development of Adaptive Immunity and Its Role in Lung Remodeling.Advances in experimental medicine and biology · 2023
    Article
  19. Review
  20. Article

234 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 2 countries.

Omid AkbariDivision of Immunology and Allergy, Department of Pediatrics, Stanford University, Stanford, California, USA.
Philippe Stock
Everett Meyer
Mitchell Kronenberg
Stephane Sidobre
Toshinori Nakayama
Masaru Taniguchi
Michael J Grusby
Rosemarie H DeKruyff
Dale T Umetsu
Stanford University · USChiba University · JPLa Jolla Institute for Immunology · USHarvard University · US

Funding

MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
HETEROGENEITY AMONG HUMAN CD4+ T LYMPHOCYTESR01AI026322 · NIAID · STANFORD UNIVERSITY · PI UMETSU, DALE T · 1989 to 2010
$2.7M
THE ROLE OF TH CELL SUBSETS AND ALLERGIC LUNG INFLAMMATIR01HL062348 · NHLBI · STANFORD UNIVERSITY · PI UMETSU, DALE T · 1999 to 2007
$2.6M
REGULATION OF THE DIFFERENTIATION AND FUNCTION OF TH2 CER01AI040171 · NIAID · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI GRUSBY, MICHAEL J · 1997 to 2006
$1.9M
EXPRESSION AND FUNCTION OF THE MHC-ENCODED TL MOLECULER01CA052511 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KRONENBERG, MITCHELL · 1991 to 2004
$1.8M
REGULATION OF STAT FUNCTIONR01GM062135 · NIGMS · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI GRUSBY, MICHAEL J · 2001 to 2004
$1.4M
ALTERING INTERLEUKIN 4 FUNCTION IN VIVOR21AI040171 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GRUSBY, MICHAEL J · 1996 to 1996
–
NCI NIH HHS R01 CA52511NHLBI NIH HHS R01 HL62348NIAID NIH HHS AI40171NIAID NIH HHS R01 AI26322NIAID NIH HHS T32AI07290NIGMS NIH HHS GM62135
6 · The paper itself

Abstract

Using natural killer T (NKT) cell-deficient mice, we show here that allergen-induced airway hyperreactivity (AHR), a cardinal feature of asthma, does not develop in the absence of V(alpha)14i NKT cells. The failure of NKT cell-deficient mice to develop AHR is not due to an inability of these mice to produce type 2 T-helper (Th2) responses because NKT cell-deficient mice that are immunized subcutaneously at non-mucosal sites produce normal Th2-biased responses. The failure to develop AHR can be reversed by the adoptive transfer of tetramer-purified NKT cells producing interleukin (IL)-4 and IL-13 to Ja281(-/-) mice, which lack the invariant T-cell receptor (TCR) of NKT cells, or by the administration to Cd1d(-/-) mice of recombinant IL-13, which directly affects airway smooth muscle cells. Thus, pulmonary V(alpha)14i NKT cells crucially regulate the development of asthma and Th2-biased respiratory immunity against nominal exogenous antigens. Therapies that target V(alpha)14i NKT cells may be clinically effective in limiting the development of AHR and asthma.

Indexed as

Adoptive TransferAllergensAnimalsAntigens, CD1Antigens, CD1dBronchial HyperreactivityInterleukin-13Interleukin-4Killer Cells, NaturalMiceMice, Inbred BALB CAllergensAntigens, CD1Antigens, CD1dInterleukin-13Interleukin-4

Identifiers

PMID12669034
OpenAlexW2092599690

What OpenQuestion holds

Textmetadata
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.