Evidence map›Paper›PMID 33021470›Full record

ArticleeLife2020

Metabolic profiling during malaria reveals the role of the aryl hydrocarbon receptor in regulating kidney injury.

Michelle M Lissner, Katherine Cumnock, Nicole M Davis, José G Vilches-Moure, Priyanka Basak, Daniel J Navarrete, Jessica A Allen, David Schneider

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.5field-weighted citation impact, top 31% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. The role of the AHR in host-pathogen interactions.Nature reviews. Immunology · 2025
    Review
  6. IDO1-AhR axis increases T regulatory cells inFrontiers in immunology · 2025
    Article
  7. The intersection of hostMicrobiology and molecular biology reviews : MMBR · 2024
    Review
  8. Review
  9. Review
  10. Article
  11. Article
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

8 authors at 2 institutions in 1 country.

Michelle M LissnerDepartment of Microbiology and Immunology, Stanford University, Stanford, United States.ORCID 0000-0002-3854-2919
Katherine CumnockDepartment of Microbiology and Immunology, Stanford University, Stanford, United States.
Nicole M DavisDepartment of Microbiology and Immunology, Stanford University, Stanford, United States.
José G Vilches-MoureDepartment of Comparative Medicine, Stanford University, Stanford, United States.
Priyanka BasakDepartment of Microbiology and Immunology, Stanford University, Stanford, United States.ORCID 0000-0002-8550-7892
Daniel J NavarreteDepartment of Microbiology and Immunology, Stanford University, Stanford, United States.
Jessica A AllenDivision of Health, Mathematics and Science, Columbia College, Columbia, United States.
David SchneiderDepartment of Microbiology and Immunology, Stanford University, Stanford, United States.ORCID 0000-0002-2391-9963
Stanford University · USColumbia College - South Carolina · US

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Vittorio Sebastiano · 2007 to 2026
$71.4M
MOLECULAR BASIS OF HOST-PARASITE INTERACTIONT32AI007328 · NIAID · STANFORD UNIVERSITY · PI JUSTIN L SONNENBURG · 1987 to 2026
$11.9M
Mapping the road to recovery - Does the way we get better differ from the way weDP1AT007753 · NCCIH · STANFORD UNIVERSITY · PI SCHNEIDER, DAVID S. · 2012 to 2015
$3.1M
Using colloborative cross mice to monitor resilience to malariaR21AI145365 · NIAID · STANFORD UNIVERSITY · PI SCHNEIDER, DAVID S. · 2019 to 2020
$434k
Defense Advanced Research Projects Agency W911NF-16-0052National Science Foundation DGE-1656518NCCIH NIH HHS DP1 AT007753NCI NIH HHS P30 CA124435NIAID NIH HHS R21 AI145365NIAID NIH HHS T32 AI007328NIH HHS 1R21AI145365NIH HHS 5DP1AT007753
6 · The paper itself

Abstract

Systemic metabolic reprogramming induced by infection exerts profound, pathogen-specific effects on infection outcome. Here, we detail the host immune and metabolic response during sickness and recovery in a mouse model of malaria. We describe extensive alterations in metabolism during acute infection, and identify increases in host-derived metabolites that signal through the aryl hydrocarbon receptor (AHR), a transcription factor with immunomodulatory functions. We find that

Indexed as

Acute Kidney InjuryAnimalsBasic Helix-Loop-Helix ProteinsFemaleMalaria, FalciparumMaleMetabolomeMiceMice, Inbred C57BLPlasmodium falciparumReceptors, Aryl HydrocarbonAhr protein, mouseBasic Helix-Loop-Helix ProteinsReceptors, Aryl Hydrocarbonaryl hydrocarbon receptorinfectious diseasemalariametabolismmicrobiologymouse

Identifiers

PMID33021470
PMCPMC7538157
OpenAlexW3090429581

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.