Evidence map›Paper›PMID 27837016›Full record

ArticleJournal of leukocyte biology2017

Chronic alcohol consumption inhibits peripheral NK cell development and maturation by decreasing the availability of IL-15.

Faya Zhang, Alex Little, Hui Zhang

Open access · greenAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

28 citing papers in PubMed, 37 citations in OpenAlex.

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  15. Tissue-Resident Memory CD4Journal of immunology (Baltimore, Md. : 1950) · 2022
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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.

Faya ZhangDepartment of Pharmaceutical Sciences, College of Pharmacy, Washington State University, Spokane, Washington, USA.
Alex LittleDepartment of Pharmaceutical Sciences, College of Pharmacy, Washington State University, Spokane, Washington, USA.
Hui ZhangDepartment of Pharmaceutical Sciences, College of Pharmacy, Washington State University, Spokane, Washington, USA hzhang@wsu.edu.
Washington State University Spokane · US

Funding

Immunotherapy to Mitigate the Negative Effects of Alcohol on Cancer ProgressionR21AA022098 · NIAAA · WASHINGTON STATE UNIVERSITY · PI ZHANG, HUI · 2014 to 2015
$391k
NIAAA NIH HHS R21 AA022098
6 · The paper itself

Abstract

NK cells are innate immune cells and have important roles in antiviral and antitumor immunity. Based on the transcriptional regulation, organ distribution, and cell function, NK cells have recently been further divided into cytotoxic conventional NK cells (cNK) and noncytotoxic helper-like group 1 innate lymphoid cells (ILC1s). It is well known that chronic alcohol consumption decreases peripheral NK cell number and cytolytic activity; however, the underlying mechanism remains to be elucidated. How chronic alcohol consumption affects ILC1s is, to our knowledge, completely unexplored. Herein, we used a well-established mouse model of chronic alcohol consumption to study the effects of alcohol on transcription factor expression, maturation, and cytokine production of cNK cells and ILC1s in various organs. We found that alcohol consumption significantly decreased Eomes-expressing cNK cells in all the examined organs, except BM, but did not significantly affect ILC1s. Alcohol consumption compromised cNK cell development and maturation. Exogenous IL-15/IL-15Rα treatment caused full recovery of Eomes-expressing cNK cell number and maturation. Taken together, our data indicated that chronic alcohol consumption decreases cNK cell number and cytolytic activity by arresting cNK cell development at the CD27

Indexed as

Cell DifferentiationAlcohol DrinkingAnimalsBone MarrowCell CountCell ProliferationChronic DiseaseFemaleGranzymesInterleukin-15Interleukin-15 Receptor alpha SubunitKiller Cells, NaturalLectins, C-TypeMice, Inbred C57BLNK Cell Lectin-Like Receptor Subfamily AReceptors, ImmunologicEomes protein, mouseGranzymesInterleukin-15Interleukin-15 Receptor alpha SubunitKlrg1 protein, mouseLectins, C-TypeNK Cell Lectin-Like Receptor Subfamily AReceptors, ImmunologicT-Box Domain ProteinsEomesinnate immune cellsT-bet

Identifiers

PMID27837016
PMCPMC5346179
OpenAlexW2554583968

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.