Evidence map›Paper›PMID 22812678›Full record

ArticleJournal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research2012

Ethanol exposure suppresses bone marrow-derived dendritic cell inflammatory responses independent of TLR4 expression.

Juan L Rendon, Brian A Janda, Monica E Bianco, Mashkoor A Choudhry

Abstract read
In one paragraph

Article in Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Alcohol, aging, and innate immunity.Journal of leukocyte biology · 2017
    Review
  7. Article
  8. Review
  9. Article
  10. 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

4 authors at 1 institution in 1 country.

Juan L RendonHealth Sciences Division, Alcohol Research Program, Loyola University Chicago, Maywood, Illinois 60153, USA.
Brian A Janda
Monica E Bianco
Mashkoor A Choudhry
Loyola University Chicago · US

Funding

Training in Neuroimmunoendocrine Effects of AlcoholT32AA013527 · NIAAA · LOYOLA UNIVERSITY CHICAGO · PI CHOUDHRY, MASHKOOR A · 2002 to 2021
$4.4M
Alcohol Intoxication and Postburn Intestinal ImmunityR01AA015731 · NIAAA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CHOUDHRY, MASHKOOR A · 2007 to 2017
$3.8M
Effects of acute ethanol exposure on post burn intestinal immunity: role of IL-23F30AA020167 · NIAAA · LOYOLA UNIVERSITY CHICAGO · PI RENDON, JUAN LUIS · 2010 to 2014
$139k
NIAAA NIH HHS F30 AA020167NIAAA NIH HHS F30AA020167NIAAA NIH HHS R01AA015731NIAAA NIH HHS R01AA015731-04S1NIAAA NIH HHS T32AA013527
6 · The paper itself

Abstract

Acute alcohol (ethanol) exposure is linked with increased susceptibility to infection and increased mortality in trauma and burn patients. Dendritic cells (DCs) are central mediators in innate and adaptive immune responses, and they play a role in the presentation of pathogens to adaptive immune cells. We investigated the effects of acute ethanol exposure on bone marrow-derived DC (BM-DC) responses. Total bone marrow cells, obtained from 8 to 10 week old C57BL/6 male mice, were cultured in the presence of granulocyte/monocyte-colony stimulating factor and interleukin (IL)-4 for 7 days. BM-DCs were harvested and treated with increasing doses of ethanol (50, 100, and 250 mM) at the time of, or 3 h before, lipopolysaccharide (LPS). After LPS, supernatants were collected for cytokine measurement, and cells were harvested for flow cytometry. Concurrent acute ethanol exposure and LPS treatment resulted in a dose-dependent suppression of IL-6, IL-12p40, IL-23, and IL-10. In addition, ethanol exposure before LPS dysregulated the IL-12p40/IL-23 balance and more profoundly suppressed IL-6 and IL-10 secretion by BM-DCs, as compared with cells concurrently treated with ethanol and LPS. Ethanol treatment did not affect either toll-like receptor (TLR)4 or TLR2 expression. In summary, our study demonstrates that acute ethanol exposure suppresses BM-DC LPS-induced responses, irrespective of affecting TLR4 or TLR2 expression.

Indexed as

AnimalsBone Marrow CellsCentral Nervous System DepressantsDendritic CellsEthanolGene Expression RegulationInflammationInterleukin-4LipopolysaccharidesMaleMiceToll-Like Receptor 2Toll-Like Receptor 4Central Nervous System DepressantsEthanolInterleukin-4LipopolysaccharidesTlr2 protein, mouseTlr4 protein, mouseToll-Like Receptor 2Toll-Like Receptor 4

Identifiers

PMID22812678
PMCPMC3438840
OpenAlexW2084666176

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.