Evidence map›Paper›PMID 29212951›Full record

ArticleJCI insight2017

Glycolytic requirement for NK cell cytotoxicity and cytomegalovirus control.

Annelise Y Mah, Armin Rashidi, Molly P Keppel, Nermina Saucier, Emily K Moore, Joshua B Alinger, Sandeep K Tripathy, Sandeep K Agarwal, Emily K Jeng, Hing C Wong and 5 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in JCI insight, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
4.0field-weighted citation impact, top 5% 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

93 citing papers in PubMed, 132 citations in OpenAlex.

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

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

15 authors at 3 institutions in 1 country.

Annelise Y MahDepartment of Pediatrics, Division of Rheumatology, Washington University School of Medicine, St. Louis, Missouri, USA.
Armin RashidiDepartment of Medicine, Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, Minnesota, USA.
Molly P KeppelDepartment of Pediatrics, Division of Rheumatology, Washington University School of Medicine, St. Louis, Missouri, USA.
Nermina SaucierDepartment of Pediatrics, Division of Rheumatology, Washington University School of Medicine, St. Louis, Missouri, USA.
Emily K MooreDepartment of Pediatrics, Division of Rheumatology, Washington University School of Medicine, St. Louis, Missouri, USA.
Joshua B AlingerDepartment of Pediatrics, Division of Rheumatology, Washington University School of Medicine, St. Louis, Missouri, USA.
Sandeep K TripathyDepartment of Medicine, Division of Gastroenterology, Washington University School of Medicine, St. Louis, Missouri, USA.
Sandeep K AgarwalDepartment of Medicine, Division of Immunology, Allergy, and Rheumatology, Baylor College of Medicine, Houston, Texas, USA.
Emily K JengAltor BioScience, Miramar, Florida, USA.
Hing C WongAltor BioScience, Miramar, Florida, USA.
Jeffrey S MillerDepartment of Medicine, Division of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, Minnesota, USA.
Todd A FehnigerDepartment of Medicine, Division of Oncology, Washington University School of Medicine, St. Louis, Missouri, USA.
Emily M MaceCenter for Human Immunobiology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, USA.
Anthony R FrenchDepartment of Pediatrics, Division of Rheumatology, Washington University School of Medicine, St. Louis, Missouri, USA.
Megan A CooperDepartment of Pediatrics, Division of Rheumatology, Washington University School of Medicine, St. Louis, Missouri, USA.
Altor BioScience (United States) · USUniversity of Minnesota · USWashington University in St. Louis · US

Funding

NATIONAL RESEARCH SERVICE AWARD-MEDICAL SCIENTISTT32GM007200 · NIGMS · WASHINGTON UNIVERSITY · PI YOKOYAMA, WAYNE M. · 1985 to 2024
$59.8M
Trial Design and Biostatistical Support CoreP01CA065493 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI John E. Wagner · 1995 to 2026
$48.2M
Therapeutic Potential of Adaptive NK Cells in Cancer and TransplantationP01CA111412 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MILLER, JEFFREY S. · 2005 to 2025
$38.2M
REGULATION OF VIRAL-INDUCED NK CELL PROLIFERATION DURING MURINE CMV INFECTIONR01AI078994 · NIAID · WASHINGTON UNIVERSITY · PI FRENCH, ANTHONY R · 2009 to 2019
$3.8M
METABOLIC REGULATION OF NATURAL KILLER CELL ACTIVATIONR01AI127752 · NIAID · WASHINGTON UNIVERSITY · PI COOPER, MEGAN ANNE · 2017 to 2021
$1.9M
INNATE IMMUNE RECEPTOR ANTAGONISM BY ORTHOPOXVIRUS PROTEINSR01AI073552 · NIAID · WASHINGTON UNIVERSITY · PI FRENCH, ANTHONY R · 2008 to 2011
$1.5M
MICRORNA REGULATION OF NK CELL DEVELOPMENT AND FUNCTIONR01AI102924 · NIAID · WASHINGTON UNIVERSITY · PI FEHNIGER, TODD A · 2013 to 2016
$1.5M
Mechanisms of Innate Immune MemoryK08AI085030 · NIAID · WASHINGTON UNIVERSITY · PI COOPER, MEGAN ANNE · 2010 to 2014
$600k
Metabolic requirements of NK cell responses to viral infectionF30AI129110 · NIAID · WASHINGTON UNIVERSITY · PI MAH-SOM, ANNELISE YOO · 2017 to 2019
$103k
NCI NIH HHS P01 CA065493NCI NIH HHS P01 CA111412NIAID NIH HHS F30 AI129110NIAID NIH HHS K08 AI085030NIAID NIH HHS R01 AI073552NIAID NIH HHS R01 AI078994NIAID NIH HHS R01 AI102924NIAID NIH HHS R01 AI127752NIGMS NIH HHS T32 GM007200
6 · The paper itself

Abstract

NK cell activation has been shown to be metabolically regulated in vitro; however, the role of metabolism during in vivo NK cell responses to infection is unknown. We examined the role of glycolysis in NK cell function during murine cytomegalovirus (MCMV) infection and the ability of IL-15 to prime NK cells during CMV infection. The glucose metabolism inhibitor 2-deoxy-ᴅ-glucose (2DG) impaired both mouse and human NK cell cytotoxicity following priming in vitro. Similarly, MCMV-infected mice treated with 2DG had impaired clearance of NK-specific targets in vivo, which was associated with higher viral burden and susceptibility to infection on the C57BL/6 background. IL-15 priming is known to alter NK cell metabolism and metabolic requirements for activation. Treatment with the IL-15 superagonist ALT-803 rescued mice from otherwise lethal infection in an NK-dependent manner. Consistent with this, treatment of a patient with ALT-803 for recurrent CMV reactivation after hematopoietic cell transplant was associated with clearance of viremia. These studies demonstrate that NK cell-mediated control of viral infection requires glucose metabolism and that IL-15 treatment in vivo can reduce this requirement and may be effective as an antiviral therapy.

Indexed as

ActinsAnimalsAntiviral AgentsBlood GlucoseCell ProliferationCells, CulturedCytomegalovirusCytomegalovirus InfectionsCytotoxicity, ImmunologicDeoxyglucoseFemaleGlycolysisGranzymesHerpesviridae InfectionsHumansInterferon-gammaActinsALT-803Antiviral AgentsBlood GlucoseDeoxyglucoseGranzymesGzmb protein, mouseInterferon-gammaInterleukin-15ProteinsRecombinant Fusion ProteinsImmunologyNK cells

Identifiers

PMID29212951
PMCPMC5752285
OpenAlexW2772960486

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.