Evidence map›Paper›PMID 34168651›Full record

ArticleFrontiers in immunology2021

Immunological and Pathological Landscape of Dengue Serotypes 1-4 Infections in Immune-Competent Mice.

Abhay P S Rathore, Chinmay K Mantri, Meredith W Tan, Roksana Shirazi, Andrew Nishida, Siti A B Aman, Juliet Morrison, Ashley L St John

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
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  9. Dengue virus infection modifies mosquito blood-feeding behavior to increase transmission to the host.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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

8 authors at 4 institutions in 2 countries.

Abhay P S RathoreProgram in Emerging Infectious Diseases, Duke-National University of Singapore, Singapore, Singapore.
Chinmay K MantriProgram in Emerging Infectious Diseases, Duke-National University of Singapore, Singapore, Singapore.
Meredith W TanProgram in Emerging Infectious Diseases, Duke-National University of Singapore, Singapore, Singapore.
Roksana ShiraziDepartment of Microbiology and Plant Pathology, University of California, Riverside, CA, United States.
Andrew NishidaDepartment of Microbiology, University of Washington, Seattle, WA, United States.
Siti A B AmanProgram in Emerging Infectious Diseases, Duke-National University of Singapore, Singapore, Singapore.
Juliet MorrisonDepartment of Microbiology and Plant Pathology, University of California, Riverside, CA, United States.
Ashley L St JohnProgram in Emerging Infectious Diseases, Duke-National University of Singapore, Singapore, Singapore.
National University of Singapore · SGUniversity of California, Riverside · USDuke Medical Center · USUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dengue virus (DENV), a Flavivirus, causes a broad spectrum of disease in humans with key clinical signs including thrombocytopenia, vascular leakage and hemorrhaging. A major obstacle to understanding DENV immunity has been the lack of a validated immune-competent mouse model. Here, we report the infection profiles of human clinical isolates of DENV serotypes 1-4 in an immune-competent mouse model. We detected replicating DENV in the peritoneal cells, liver and the spleen that was generally resolved within 2 weeks. The DENV target cell types for infection were monocytes/macrophages, dendritic cells, endothelial cells, and we identified a novel DENV cellular target, fibroblast reticular cells of the spleen. We observed gross pathologies in the spleen and liver that are consistent with dengue disease, including hemorrhaging as well as transcriptional patterns suggesting that antiviral responses and tissue damage were induced. Key clinical blood parameters that define human DENV disease such as hemoconcentration, leukopenia and reduced number of platelets were also observed. Thus, immune-competent mice sustain replicating infection and experience signs, such as hemorrhaging, that define DENV disease in humans. This study thoroughly characterizes DENV1-4 infection in immune-competent mice and confirms the wild-type mouse model as a valid and reproducible system for investigating the mechanisms of DENV pathogenesis.

Indexed as

AnimalsBiopsyDengueDengue VirusDisease Models, AnimalDisease SusceptibilityFemaleGene Expression RegulationHost-Pathogen InteractionsImmunocompromised HostMiceOrgan SpecificitySerogroupdengueDENV 1-4fibroblast reticular cellflow cytometryhistologyliverspleentranscriptomics

Identifiers

PMID34168651
PMCPMC8219075
OpenAlexW3169943263

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.