Evidence map›Paper›PMID 26582961›Full record

ArticleThe Journal of infectious diseases2016

Humanized Mouse Model of Ebola Virus Disease Mimics the Immune Responses in Human Disease.

Brian H Bird, Jessica R Spengler, Ayan K Chakrabarti, Marina L Khristova, Tara K Sealy, JoAnn D Coleman-McCray, Brock E Martin, Kimberly A Dodd, Cynthia S Goldsmith, Jeanine Sanders and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Review
  3. Filovirus Infection in Humanized Mouse Models.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  4. Article
  5. Review
  6. Emerging microbes & infections · 2023
    Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Animal Models of Hepatitis C Virus Infection.Cold Spring Harbor perspectives in medicine · 2020
    Review
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Brian H BirdViral Special Pathogens Branch.
Jessica R SpenglerViral Special Pathogens Branch.
Ayan K ChakrabartiViral Special Pathogens Branch.
Marina L KhristovaBiotechnology Core Facility.
Tara K SealyViral Special Pathogens Branch.
JoAnn D Coleman-McCrayViral Special Pathogens Branch.
Brock E MartinViral Special Pathogens Branch.
Kimberly A DoddViral Special Pathogens Branch.
Cynthia S GoldsmithInfectious Diseases Pathology Branch, Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
Jeanine SandersInfectious Diseases Pathology Branch, Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
Sherif R ZakiInfectious Diseases Pathology Branch, Division of High-Consequence Pathogens and Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia.
Stuart T NicholViral Special Pathogens Branch.
Christina F SpiropoulouViral Special Pathogens Branch.
Global Viral · USCenters for Disease Control and Prevention · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Animal models recapitulating human Ebola virus disease (EVD) are critical for insights into virus pathogenesis. Ebola virus (EBOV) isolates derived directly from human specimens do not, without adaptation, cause disease in immunocompetent adult rodents. Here, we describe EVD in mice engrafted with human immune cells (hu-BLT). hu-BLT mice developed EVD following wild-type EBOV infection. Infection with high-dose EBOV resulted in rapid, lethal EVD with high viral loads, alterations in key human antiviral immune cytokines and chemokines, and severe histopathologic findings similar to those shown in the limited human postmortem data available. A dose- and donor-dependent clinical course was observed in hu-BLT mice infected with lower doses of either Mayinga (1976) or Makona (2014) isolates derived from human EBOV cases. Engraftment of the human cellular immune system appeared to be essential for the observed virulence, as nonengrafted mice did not support productive EBOV replication or develop lethal disease. hu-BLT mice offer a unique model for investigating the human immune response in EVD and an alternative animal model for EVD pathogenesis studies and therapeutic screening.

Indexed as

AnimalsBrainCytokinesEbolavirusGene Expression RegulationHemorrhagic Fever, EbolaHumansKidneyLiverLungMaleMiceMice, TransgenicRNA, ViralSpleenTestisCytokinesRNA, Viralanimal modelcytokine profileEbola virus diseasehumanized miceviral hemorrhagic fevervirus pathogenesis

Identifiers

PMID26582961
PMCPMC4747627
OpenAlexW2328924450

What OpenQuestion holds

Textmetadata
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.