Evidence map›Paper›PMID 31229914›Full record

ReviewCurrent opinion in immunology2019

HIF-1α as a central mediator of cellular resistance to intracellular pathogens.

Matthew Knight, Sarah Stanley

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 9% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 83 citations in OpenAlex.

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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

2 authors at 1 institution in 1 country.

Matthew KnightDepartment of Plant and Microbial Biology, University of California, Berkeley, CA, United States.
Sarah StanleyDepartment of Molecular and Cell Biology, Division of Immunology and Pathogenesis, University of California, Berkeley, CA, United States; School of Public Health, Division of Infectious Diseases and Vaccinology, University of California, Berkeley, CA, United States. Electronic address: sastanley@berkeley.edu.
University of California, Berkeley · US

Funding

Metabolic regulation of macrophage function during M. tuberculosis infectionR01AI113270 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI STANLEY, SARAH A · 2015 to 2024
$3.8M
NIAID NIH HHS R01 AI113270
6 · The paper itself

Abstract

Hypoxia-inducible transcription factor-1α (HIF-1α) was originally identified as a master regulator of cellular responses to hypoxia. More recently, HIF-1α has emerged as a critical regulator of immune cell function that couples shifts in cellular metabolism to cell type-specific transcriptional outputs. Activation of macrophages with inflammatory stimuli leads to induction of the metabolic program aerobic glycolysis and to HIF-1α stabilization, which reinforce one another in a positive feedback loop that helps drive macrophage activation. This activation of aerobic glycolysis and HIF-1α is important both for production of inflammatory cytokines, such as IL-1β, and for cell intrinsic control of infection. Here, we review the importance of HIF-1α for control of bacterial, fungal, and protozoan intracellular pathogens, highlighting recent findings that reveal mechanisms by which HIF-1α is activated during infection and how HIF-1α coordinates antimicrobial responses of macrophages.

Indexed as

BiomarkersDisease ResistanceHost-Pathogen InteractionsAnimalsEnergy MetabolismGene Expression RegulationHumansHypoxia-Inducible Factor 1, alpha SubunitImmunity, InnateIntracellular SpaceMacrophage ActivationMacrophagesPhagocytosisSignal TransductionTranscription FactorsBiomarkersHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitTranscription Factors

Identifiers

PMID31229914
PMCPMC8592400
OpenAlexW2950262061

What OpenQuestion holds

Textmetadata
LicenceTDM
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.