Evidence map›Paper›PMID 28133423›Full record

ArticleCurrent trends in immunology2016

Therapeutic potential of the heme oxygenase-1 inducer hemin against Ebola virus infection.

Hanxia Huang, Krishnamurthy Konduru, Veronica Solovena, Zhao-Hua Zhou, Namita Kumari, Kazuyo Takeda, Sergei Nekhai, Sina Bavari, Gerardo G Kaplan, Kenneth M Yamada and 1 more

Open access · greenAbstract read
In one paragraph

Article in Current trends in immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. NRF2 in Viral Infection.Antioxidants (Basel, Switzerland) · 2021
    Review
  6. Heme oxygenase-1 inducer hemin does not inhibit SARS-CoV-2 virus infection.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2021
    Article
  7. 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

11 authors at 3 institutions in 1 country.

Hanxia HuangFood and Drug Administration, Silver Spring, Maryland.
Krishnamurthy KonduruFood and Drug Administration, Silver Spring, Maryland.
Veronica SolovenaMolecular and Translational Sciences Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, Maryland.
Zhao-Hua ZhouFood and Drug Administration, Silver Spring, Maryland.
Namita KumariCenter for Sickle Cell Disease, Department of Medicine, Howard University, Washington DC.
Kazuyo TakedaFood and Drug Administration, Silver Spring, Maryland.
Sergei NekhaiCenter for Sickle Cell Disease, Department of Medicine, Howard University, Washington DC.
Sina BavariMolecular and Translational Sciences Division, United States Army Medical Research Institute of Infectious Diseases, Frederick, Maryland.
Gerardo G KaplanFood and Drug Administration, Silver Spring, Maryland.
Kenneth M YamadaLaboratory of Cell and Developmental Biology, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, Maryland, USA.
Subhash DhawanFood and Drug Administration, Silver Spring, Maryland.
United States Food and Drug Administration · USHoward University · USNational Institute of Dental and Craniofacial Research · US

Funding

SWG 2: Cure Research Scientific Working GroupP30AI117970 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI MICHAEL Ilya BUKRINSKY · 2015 to 2026
$29.6M
PROTEOMICS CORE FACILITYG12MD007597 · NIMHD · HOWARD UNIVERSITY · PI SOUTHERLAND, WILLIAM M. · 2012 to 2018
$14.8M
Craniofacial Developmental DynamicsZIADE000525 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI YAMADA, KENNETH · 2009 to 2025
$14.5M
Cell-Surface Interactions in PathogenesisZIADE000719 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI YAMADA, KENNETH · 2009 to 2025
$13.5M
Cell-Matrix Interactions and MigrationZIADE000524 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI YAMADA, KENNETH · 2009 to 2025
$10.2M
Center for Hemoglobin Research in Minorities (CHaRM)P50HL118006 · NHLBI · HOWARD UNIVERSITY · PI NEKHAI, SERGEI · 2013 to 2017
$7.0M
Sickle Cell Disease and Sickle Cell Trait Protection Against HIV-1-infection in Africans and African AmericansR01HL125005 · NHLBI · HOWARD UNIVERSITY · PI MARINA A JEREBTSOVA, SERGEI NEKHAI · 2014 to 2026
$6.7M
Second Generation Small Molecule Inhibitors of Botulinum NeurotoxinsU01AI082051 · NIAID · GENEVA FOUNDATION · PI BAVARI, SINA · 2009 to 2013
$4.5M
REGULATION OF CELL ADHESION, MIGRATION, AND MORPHOGENESISZ01DE000525 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI YAMADA, KENNETH MANAO · 1991 to 2008
$1.5M
INTEGRIN RECEPTOR FUNCTION AND SIGNALINGZ01DE000524 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI YAMADA, KENNETH MANAO · 1991 to 2008
$1.5M
Targeting Cellular Processes to Counter the Effects of BoNT IntoxicationR33AI101387 · NIAID · GENEVA FOUNDATION · PI BAVARI, SINA · 2014 to 2016
$1.1M
Targeting Cellular Processes to Counter the Effects of BoNT IntoxicationR21AI101387 · NIAID · GENEVA FOUNDATION · PI BAVARI, SINA · 2012 to 2013
$339k
Intramural FDA HHS FD999999Intramural NIH HHS Z01 DE000524Intramural NIH HHS Z01 DE000525NHLBI NIH HHS P50 HL118006NHLBI NIH HHS R01 HL125005NIAID NIH HHS P30 AI117970NIAID NIH HHS R21 AI101387NIAID NIH HHS U01 AI082051NIMHD NIH HHS G12 MD007597
6 · The paper itself

Abstract

Promising drugs to treat Ebola virus (EBOV) infection are currently being developed, but so far none has shown efficacy in clinical trials. Drugs that can stimulate host innate defense responses may retard the progression of EBOV disease. We report here the dramatic effect of hemin, the natural inducer of the heme catabolic enzyme heme oxygenase-1 (HO-1), in the reduction of EBOV replication. Treatment of primary monocyte-derived macrophages (MDM), Vero E6 cells, HeLa cells, and human foreskin fibroblasts (HFF1) with hemin reduced EBOV infection by >90%, and showed minimal toxicity to infected cells. Inhibition of HO-1 enzymatic activity and silencing HO-1 expression prevented the hemin-mediated suppression of EBOV infection, suggesting an important role for induction of this intracellular mediator in restricting EBOV replication. The inverse correlation between hemin-induced HO-1 and EBOV replication provides a potentially useful therapeutic modality based on the stimulation of an innate cellular response against Ebola infection.

Indexed as

Ebolaheme oxygenase-1heminmonocytes/macrophages

Identifiers

PMID28133423
PMCPMC5267496
OpenAlexW2585697213

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.