Evidence map›Paper›PMID 29559978›Full record

ArticleFrontiers in immunology2018

Human Body Composition and Immunity: Visceral Adipose Tissue Produces IL-15 and Muscle Strength Inversely Correlates with NK Cell Function in Elderly Humans.

Ahmad Al-Attar, Steven R Presnell, Jody L Clasey, Douglas E Long, R Grace Walton, Morgan Sexton, Marlene E Starr, Philip A Kern, Charlotte A Peterson, Charles T Lutz

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

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  8. Crosstalk between Metabolic Disorders and Immune Cells.International journal of molecular sciences · 2021
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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

10 authors at 1 institution in 1 country.

Ahmad Al-AttarDepartment of Pathology and Laboratory Medicine, College of Medicine, University of Kentucky, Lexington, KY, United States.
Steven R PresnellDepartment of Pathology and Laboratory Medicine, College of Medicine, University of Kentucky, Lexington, KY, United States.
Jody L ClaseyDepartment of Kinesiology and Health Promotion, College of Education, University of Kentucky, Lexington, KY, United States.
Douglas E LongDepartment of Rehabilitation Sciences, College of Health Sciences, University of Kentucky, Lexington, KY, United States.
R Grace WaltonDepartment of Rehabilitation Sciences, College of Health Sciences, University of Kentucky, Lexington, KY, United States.
Morgan SextonDepartment of Pathology and Laboratory Medicine, College of Medicine, University of Kentucky, Lexington, KY, United States.
Marlene E StarrDepartment of Surgery, College of Medicine, University of Kentucky, Lexington, KY, United States.
Philip A KernDivision of Endocrinology, Department of Medicine, College of Medicine, University of Kentucky, Lexington, KY, United States.
Charlotte A PetersonDepartment of Rehabilitation Sciences, College of Health Sciences, University of Kentucky, Lexington, KY, United States.
Charles T LutzDepartment of Pathology and Laboratory Medicine, College of Medicine, University of Kentucky, Lexington, KY, United States.
University of Kentucky · US

Funding

Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
Appalachian Career Training in Oncology (ACTION) ProgramR25CA221765 · NCI · UNIVERSITY OF KENTUCKY · PI Nathan Lane Vanderford · 2018 to 2026
$3.7M
Mechanisms Underlying Metabolic Syndrome in ObesityR01DK071349 · NIDDK · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A, PETERSON, CHARLOTTE A. · 2005 to 2013
$2.3M
The effects of exercise on satellite cell dynamics during agingR01AG049806 · NIA · UNIVERSITY OF KENTUCKY · PI MCCARTHY, JOHN JOSEPH, PETERSON, CHARLOTTE A. · 2016 to 2020
$1.8M
Cold Induced Changed in Human Subcutaneous White AdiposeR01DK107646 · NIDDK · UNIVERSITY OF KENTUCKY · PI KERN, PHILIP A · 2015 to 2017
$1.5M
Muscle, Fat and NK Lymphocytes in AgingR21AG040542 · NIA · UNIVERSITY OF KENTUCKY · PI LUTZ, CHARLES T. · 2012 to 2013
$398k
NCATS NIH HHS UL1 TR001998NCI NIH HHS R25 CA221765NIA NIH HHS R01 AG049806NIA NIH HHS R21 AG040542NIDDK NIH HHS R01 DK071349NIDDK NIH HHS R01 DK107646
6 · The paper itself

Abstract

Natural killer (NK) lymphocyte-mediated cytotoxicity and cytokine secretion control infections and cancers, but these crucial activities decline with age. NK cell development, homeostasis, and function require IL-15 and its chaperone, IL-15 receptor alpha (IL-15Rα). Macrophages and dendritic cells (DC) are major sources of these proteins. We had previously postulated that additional IL-15 and IL-15Rα is made by skeletal muscle and adipose tissue. These sources may be important in aging, when IL-15-producing immune cells decline. NK cells circulate through adipose tissue, where they may be exposed to local IL-15. The objectives of this work were to determine (1) if human muscle, subcutaneous adipose tissue (SAT), and visceral adipose tissue (VAT) are sources of IL-15 and IL-15 Rα, and (2) whether any of these tissues correlate with NK cell activity in elderly humans. We first investigated IL-15 and IL-15Rα RNA expression in paired muscle and SAT biopsies from healthy human subjects. Both tissues expressed these transcripts, but IL-15Rα RNA levels were higher in SAT than in skeletal muscle. We also investigated tissue obtained from surgeries and found that SAT and VAT expressed equivalent amounts of IL-15 and IL-15Rα RNA, respectively. Furthermore, stromal vascular fraction cells expressed more IL-15 RNA than did adipocytes. To test if these findings related to circulating IL-15 protein and NK cell function, we tested 50 healthy adults aged > 70 years old. Plasma IL-15 levels significantly correlated with abdominal VAT mass in the entire cohort and in non-obese subjects. However, plasma IL-15 levels did not correlate with skeletal muscle cross-sectional area and correlated inversely with muscle strength. Plasma IL-15 did correlate with NK cell cytotoxic granule exocytosis and with CCL4 (MIP-1β) production in response to NKp46-crosslinking. Additionally, NK cell responses to K562 leukemia cells correlated inversely with muscle strength. With aging, immune function declines while infections, cancers, and deaths increase. We propose that VAT-derived IL-15 and IL-15Rα is a compensatory NK cell support mechanism in elderly humans.

Indexed as

AdultAgedAgingBody CompositionCohort StudiesCytotoxicity, ImmunologicFemaleGene Expression RegulationHumansImmunityInterleukin-15Interleukin-15 Receptor alpha SubunitIntra-Abdominal FatK562 CellsKiller Cells, NaturalMaleInterleukin-15Interleukin-15 Receptor alpha SubunitNatural Cytotoxicity Triggering Receptor 1NCR1 protein, humanadipose tissueagingIL-15natural killer cellskeletal muscle strength

Identifiers

PMID29559978
PMCPMC5845694
OpenAlexW2790290227

What OpenQuestion holds

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LicenceCC BY
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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.