Evidence map›Paper›PMID 27191716›Full record

ArticlePLoS pathogens2016

Chimeric Mice with Competent Hematopoietic Immunity Reproduce Key Features of Severe Lassa Fever.

Lisa Oestereich, Anja Lüdtke, Paula Ruibal, Elisa Pallasch, Romy Kerber, Toni Rieger, Stephanie Wurr, Sabrina Bockholt, José V Pérez-Girón, Susanne Krasemann and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

38 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Observational
  17. Review
  18. Article
  19. Article
  20. 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

12 authors at 4 institutions in 1 country.

Lisa OestereichBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Anja LüdtkeBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Paula RuibalBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Elisa PallaschBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Romy KerberBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Toni RiegerBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Stephanie WurrBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
Sabrina BockholtBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
José V Pérez-GirónHeinrich Pette Institute, Leibniz Institute For Experimental Virology, Hamburg, Germany.
Susanne KrasemannInstitute for Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Stephan GüntherBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
César Muñoz-FontelaBernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
German Center for Infection Research · DEBernhard Nocht Institute for Tropical Medicine · DELeibniz Institute of Virology (LIV) · DEUniversität Hamburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lassa fever (LASF) is a highly severe viral syndrome endemic to West African countries. Despite the annual high morbidity and mortality caused by LASF, very little is known about the pathophysiology of the disease. Basic research on LASF has been precluded due to the lack of relevant small animal models that reproduce the human disease. Immunocompetent laboratory mice are resistant to infection with Lassa virus (LASV) and, to date, only immunodeficient mice, or mice expressing human HLA, have shown some degree of susceptibility to experimental infection. Here, transplantation of wild-type bone marrow cells into irradiated type I interferon receptor knockout mice (IFNAR-/-) was used to generate chimeric mice that reproduced important features of severe LASF in humans. This included high lethality, liver damage, vascular leakage and systemic virus dissemination. In addition, this model indicated that T cell-mediated immunopathology was an important component of LASF pathogenesis that was directly correlated with vascular leakage. Our strategy allows easy generation of a suitable small animal model to test new vaccines and antivirals and to dissect the basic components of LASF pathophysiology.

Indexed as

Disease Models, AnimalAnimalsFlow CytometryImmunohistochemistryLassa FeverMiceMice, Inbred C57BLMice, KnockoutRadiation Chimera

Identifiers

PMID27191716
PMCPMC4871546
OpenAlexW2401484307

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.