Evidence map›Paper›PMID 28256637›Full record

ArticleScientific reports2017

Ebola virus infection kinetics in chimeric mice reveal a key role of T cells as barriers for virus dissemination.

Anja Lüdtke, Paula Ruibal, David M Wozniak, Elisa Pallasch, Stephanie Wurr, Sabrina Bockholt, Sergio Gómez-Medina, Xiangguo Qiu, Gary P Kobinger, Estefanía Rodríguez and 5 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. CD4Nature immunology · 2026
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  18. Dendritic Cells Generated FromFrontiers in immunology · 2019
    Article
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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

15 authors at 7 institutions in 3 countries.

Anja LüdtkeHeinrich Pette Institute, Leibniz Institute For Experimental Virology, Martinistrasse 52 20251 Hamburg, Germany.
Paula RuibalHeinrich Pette Institute, Leibniz Institute For Experimental Virology, Martinistrasse 52 20251 Hamburg, Germany.
David M WozniakDepartment of Virology, Bernhard Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Elisa PallaschDepartment of Virology, Bernhard Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Stephanie WurrDepartment of Virology, Bernhard Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Sabrina BockholtDepartment of Virology, Bernhard Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Sergio Gómez-MedinaHeinrich Pette Institute, Leibniz Institute For Experimental Virology, Martinistrasse 52 20251 Hamburg, Germany.
Xiangguo QiuSpecial Pathogens Program, National Microbiology Laboratory, Public Health Agency of Canada, Winnipeg, MB R3E 3R2, Canada.
Gary P KobingerDepartment of Microbiology, Immunology &Infectious Diseases, Université Laval, Quebec City, Canada.
Estefanía RodríguezHeinrich Pette Institute, Leibniz Institute For Experimental Virology, Martinistrasse 52 20251 Hamburg, Germany.
Stephan GüntherDepartment of Virology, Bernhard Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
Susanne KrasemannInstitute for Neuropathology, University Medical Center Hamburg-Eppendorf, 20251 Hamburg, Germany.
Juliana IdoyagaDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Lisa OestereichDepartment of Virology, Bernhard Nocht Institute for Tropical Medicine, 20359 Hamburg, Germany.
César Muñoz-FontelaHeinrich Pette Institute, Leibniz Institute For Experimental Virology, Martinistrasse 52 20251 Hamburg, Germany.
German Center for Infection Research · DELeibniz Institute of Virology (LIV) · DEBernhard Nocht Institute for Tropical Medicine · DEPublic Health Agency of Canada · CAStanford University · USUniversität Hamburg · DEUniversité Laval · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ebola virus (EBOV) causes severe systemic disease in humans and non-human primates characterized by high levels of viremia and virus titers in peripheral organs. The natural portals of virus entry are the mucosal surfaces and the skin where macrophages and dendritic cells (DCs) are primary EBOV targets. Due to the migratory properties of DCs, EBOV infection of these cells has been proposed as a necessary step for virus dissemination via draining lymph nodes and blood. Here we utilize chimeric mice with competent hematopoietic-driven immunity, to show that EBOV primarily infects CD11b

Indexed as

AnimalsAntigens, CDCD11b AntigenCross-PrimingDendritic CellsEbolavirusHemorrhagic Fever, EbolaHost-Pathogen InteractionsIntegrin alpha ChainsKineticsLymphoid TissueMice, Inbred C57BLMice, KnockoutT-LymphocytesViremiaVirus Replicationalpha E integrinsAntigens, CDCD11b AntigenIntegrin alpha Chains

Identifiers

PMID28256637
PMCPMC5335601
OpenAlexW2594418734

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.