Evidence map›Paper›PMID 16565865›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2006

Fas-ligand-expressing adenovirus-transfected dendritic cells decrease allergen-specific T cells and airway inflammation in a murine model of asthma.

Ya-Hui Chuang, Jau-Ling Suen, Bor-Luen Chiang

Abstract read
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Article in Journal of molecular medicine (Berlin, Germany), 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Blocking Fas ligand on leukocytes attenuates kidney ischemia-reperfusion injury.Journal of the American Society of Nephrology : JASN · 2011
    Article
  8. Article
  9. Article
  10. Review
  11. The role of costimulatory molecules in allergic disease and asthma.International archives of allergy and immunology · 2010
    Review
  12. Differential effects of dendritic cell transfer on airway hyperresponsiveness and inflammation.American journal of respiratory cell and molecular biology · 2009
    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

3 authors.

Ya-Hui ChuangGraduate Institute of Immunology, National Taiwan University, Taiwan, Republic of China.
Jau-Ling Suen
Bor-Luen Chiang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T cells expressing a type-2 T helper profile of cytokines (Th2 cells) have been demonstrated to play an important role in the initiation and progression of allergic asthma, and it is well known that Fas ligand (FasL) induces apoptosis when bound to its receptor, Fas. In the present study, we examined the possibility of modulating asthma manifestations by dendritic cells (DCs) genetically engineered to express FasL (DC-FasL), which could deliver a death signal to T cells in an antigen-specific manner. The delivery of DC-FasL into ovalbumin (OVA)-immunized allergic mice decreased the airway hyper-responsiveness (AHR). Moreover, we established a mouse model of airway inflammation by using an adoptive transfer of Th2 cells derived from ovalbumin T cell receptor transgenic mice to study the effect of DC-FasL on airway reactivity. The administration of DC-FasL in Th2-cell-induced allergic mice had significantly decreased AHR, airway inflammation, and IL-4, IL-5 and IL-13 production. Furthermore, the numbers of OVA-specific T cells were decreased in the lung of mice receiving DC-FasL. These results demonstrate that FasL-expressing dendritic cells might be applied for the modulation of allergic responses.

Indexed as

AdenoviridaeAllergensAnimalsAsthmaBronchial HyperreactivityCells, CulturedCytokinesDendritic CellsDisease Models, AnimalFas Ligand ProteinFemaleImmunizationInflammationMiceMice, Inbred BALB COvalbuminAllergensCytokinesFas Ligand ProteinOvalbumin

Identifiers

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Registered trials

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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.