Evidence map›Paper›PMID 42306974›Full record

ArticleThe Journal of infectious diseases2026

Molecular Phenotypes of Sex- and Age-Specific Differences Relating to Outcome in Patients With Ebola Virus Disease.

Xiaofeng Dong, Natasha Y Rickett, Piet Maes, Robert Orr, Tracy MacGill, Todd Myers, Tom Fletcher, Miles W Carroll, Julian A Hiscox

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Xiaofeng DongInstitute of Infection, Veterinary and Ecological Science, Faculty of Health and Life Science, University of Liverpool, UK.ORCID 0000-0003-1438-4079
Natasha Y RickettInstitute of Infection, Veterinary and Ecological Science, Faculty of Health and Life Science, University of Liverpool, UK.ORCID 0000-0002-3172-1877
Piet MaesEuropean Plotkin Institute for Vaccinology, Universite Libré de Bruxelles (ULB), Belgium.ORCID 0000-0002-4571-5232
Robert OrrOffice Regulatory and Emerging Science, Office of the Chief Scientist, US Food and Drug Administration, Silver Spring, Maryland, USA.
Tracy MacGillOffice Regulatory and Emerging Science, Office of the Chief Scientist, US Food and Drug Administration, Silver Spring, Maryland, USA.ORCID 0009-0007-9092-2680
Todd MyersOffice Regulatory and Emerging Science, Office of the Chief Scientist, US Food and Drug Administration, Silver Spring, Maryland, USA.
Tom FletcherDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Miles W CarrollWellcome Centre for Human Genetics.
Julian A HiscoxInstitute of Infection, Veterinary and Ecological Science, Faculty of Health and Life Science, University of Liverpool, UK.ORCID 0000-0002-6582-0275

Funding

FDA HHS HHSF223201510104CPandemic Institute
6 · The paper itself

Abstract

backgroundEbola virus causes a severe, potentially fatal disease with the outcome likely related to viral and host factors. There is a clear correlation between viral load and outcome (survival/death), and inflammatory and other cellular pathways are differentially activated in the acute stage between patients who survive and those who die. Age and sex may influence the course of Ebola virus disease with potential differences at the molecular level.

methodsTo investigate whether there were age- and/or sex-specific differences in patients with Ebola virus disease, previously published data from an RNA sequencing analysis of the blood transcriptome in patients from the 2013-2016 West African outbreak were stratified according to age and sex. This was correlated with the outcome of infection.

resultsSimilar to the previously published data, immune responses were downregulated during the acute phase in hospitalized survivors as compared with hospitalized fatal cases, regardless of the sex of the patient. However, aspects of the blood transcriptome/host response differed between females and males and certain age groups at the transcriptomic level. Genes associated with the lymphocyte differentiation pathway decreased in expression level with age in hospitalized fatal cases. However, this was the opposite in hospitalized survivors.

conclusionsFrom a medical countermeasure perspective, the work indicated that selection of animal models should consider age and sex, depending on the research question, and cellular pathways were identified that could be chemotherapeutically enhanced to promote survival.

Indexed as

EbolavirusHemorrhagic Fever, EbolaAdolescentAdultAfrica, WesternAge FactorsDisease OutbreaksFemaleHumansMaleMiddle AgedPhenotypeSex FactorsTranscriptomeViral LoadYoung AdultageEbola virusEbola virus diseasehemorrhagic feverRNA-seqsextranscriptomics

Identifiers

PMID42306974
PMCPMC13668345

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Registered trials

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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.