Evidence map›Paper›PMID 36310868›Full record

ReviewFrontiers in cellular and infection microbiology2022

Macrophage infection, activation, and histopathological findings in ebolavirus infection.

Timothy G Wanninger, Daniel E Millian, Omar A Saldarriaga, Junki Maruyama, Takeshi Saito, Rachel A Reyna, Satoshi Taniguchi, Esteban Arroyave, Melanie E Connolly, Heather L Stevenson and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cellular and infection microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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 1 institution in 1 country.

Timothy G WanningerDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
Daniel E MillianDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
Omar A SaldarriagaDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
Junki MaruyamaDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
Takeshi SaitoDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
Rachel A ReynaDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
Satoshi TaniguchiDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
Esteban ArroyaveDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
Melanie E ConnollyDepartment of Surgery, University of Texas Medical Branch, Galveston, TX, United States.
Heather L StevensonDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
Slobodan PaesslerDepartment of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
The University of Texas Medical Branch at Galveston · US

Funding

UTMB Clinical and Translational Science AwardTL1TR001440 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI HOMMEL, JONATHAN DEAN · 2015 to 2024
$3.4M
Viral factors responsible for Lassa virus pathogenicityK99AI156012 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI MARUYAMA, JUNKI · 2021 to 2022
$177k
NCATS NIH HHS TL1 TR001440NIAID NIH HHS K99 AI156012
6 · The paper itself

Abstract

Macrophages contribute to Ebola virus disease through their susceptibility to direct infection, their multi-faceted response to ebolaviruses, and their association with pathological findings in tissues throughout the body. Viral attachment and entry factors, as well as the more recently described influence of cell polarization, shape macrophage susceptibility to direct infection. Moreover, the study of Toll-like receptor 4 and the RIG-I-like receptor pathway in the macrophage response to ebolaviruses highlight important immune signaling pathways contributing to the breadth of macrophage responses. Lastly, the deep histopathological catalogue of macrophage involvement across numerous tissues during infection has been enriched by descriptions of tissues involved in sequelae following acute infection, including: the eye, joints, and the nervous system. Building upon this knowledge base, future opportunities include characterization of macrophage phenotypes beneficial or deleterious to survival, delineation of the specific roles macrophages play in pathological lesion development in affected tissues, and the creation of macrophage-specific therapeutics enhancing the beneficial activities and reducing the deleterious contributions of macrophages to the outcome of Ebola virus disease.

Indexed as

EbolavirusHemorrhagic Fever, EbolaHumansMacrophagesfilovirushistologyhumanimmunitylivermacaquepathology

Identifiers

PMID36310868
PMCPMC9597316
OpenAlexW4304789133

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.