Evidence map›Paper›PMID 41472288›Full record

ArticleViruses2025

Sequential Dengue Virus Infection in Marmosets: Histopathological and Immune Responses in the Liver.

Daniele Freitas Henriques, Livia M N Casseb, Milene S Ferreira, Larissa S Freitas, Hellen T Fuzii, Carla Pagliari, Luciane Kanashiro, Paulo H G Castro, Gilmara A Siva, Orlando Pereira Amador Neto and 5 more

Abstract read
In one paragraph

Article in Viruses, 2025. 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
–field-weighted citation impact
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

15 authors.

Daniele Freitas HenriquesDepartment of Arboviruses and Hemorrhagic Fevers, Evandro Chagas Institute, Ananindeua 67030-000, Brazil.ORCID 0000-0001-9576-6620
Livia M N CassebDepartment of Arboviruses and Hemorrhagic Fevers, Evandro Chagas Institute, Ananindeua 67030-000, Brazil.ORCID 0000-0001-8578-9984
Milene S FerreiraCenter of Tropical Medicine, Federal University of Pará, Belém 66055-240, Brazil.
Larissa S FreitasCenter of Tropical Medicine, Federal University of Pará, Belém 66055-240, Brazil.
Hellen T FuziiCenter of Tropical Medicine, Federal University of Pará, Belém 66055-240, Brazil.
Carla PagliariFaculty of Medicine, University of Sao Paulo, Sao Paulo 01246-903, Brazil.ORCID 0000-0001-6210-6917
Luciane KanashiroFaculty of Medicine, University of Sao Paulo, Sao Paulo 01246-903, Brazil.
Paulo H G CastroNational Center of Primates, Ananindeua 67030-000, Brazil.
Gilmara A SivaNational Center of Primates, Ananindeua 67030-000, Brazil.
Orlando Pereira Amador NetoDepartment of Pathology, Evandro Chagas Institute, Ananindeua 67030-000, Brazil.
Valter M CamposDepartment of Pathology, Evandro Chagas Institute, Ananindeua 67030-000, Brazil.
Beatriz C BelvisHospital Santa Virgínia, São Paulo 03014-000, Brazil.
Flavia B Dos SantosViral Immunology Laboratory, Oswaldo Cruz Institute, Rio de Janeiro 21040-360, Brazil.ORCID 0000-0002-1309-5366
Lilian R M de SáFaculty of Veterinary Medicine and zootechnics, University of São Paulo, São Paulo 05508-270, Brazil.ORCID 0000-0002-1909-1550
Pedro Fernando da Costa VasconcelosPostgraduate Program in Biology of Infectious and Parasitic Agents, Federal University of Pará, Belém 66075-110, Brazil.ORCID 0000-0002-6603-5527

Funding

by National Council for Scientific and Technological Development (CNPq) and National Institutes of Science and Technology: Viral Hemorrhagic Fevers INCT-FHV grant CNPq/CAPES/FAPESPA 573739/2008-0
6 · The paper itself

Abstract

This study evaluated hepatic pathological and phenotypic alterations, along with the inflammatory response, following sequential dengue virus (DENV) infection in Callithrix penicillata, a relevant model for human endemic scenarios. Twenty-six animals were initially infected subcutaneously with DENV-3. Thirteen were euthanized between 1 and 7 days post-infection (dpi) to assess the acute phase, and up to 60 dpi for the convalescent phase. The remaining animals received a secondary DENV-2 infection two months later. Liver samples underwent histopathological and immunohistochemical analysis. Viral antigens were identified in hepatocytes, Kupffer cells, and Councilman bodies. Observed liver changes included apoptosis, lytic necrosis, midzonal inflammation, Kupffer cell hyperplasia and hypertrophy, sinusoidal dilation, and hemosiderin deposition. Both primary and secondary infections increased activated macrophages, NK cells, S-100 protein, and B lymphocytes. Primary infection was associated with elevated CD4

Indexed as

DengueDengue VirusLiverAnimalsAntigens, ViralCallithrixCytokinesDisease Models, AnimalHepatocytesKupffer CellsMaleAntigens, ViralCytokinescallithrix penicillatadengue virus (DENV)immunohistochemistryliver pathologysequential infection

Identifiers

PMID41472288
PMCPMC12737778

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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.