Evidence map›Paper›PMID 40831704›Full record

ArticleFrontiers in cellular and infection microbiology2025

Fabiane Dos Santos Ferreira, Wandrey Roberto Dos Santos Brito, Emmanuelle Giuliana Mendes Santana, Aline Kelly Alves Oliveira, Aline Cecy Rocha de Lima, Ednelza da Silva Graça Amoras, Carlos Araujo da Costa, Maísa Silva Souza, Sandra Souza Lima, Ricardo Ishak and 3 more

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

13 authors.

Fabiane Dos Santos FerreiraLaboratory of Virology, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Wandrey Roberto Dos Santos BritoLaboratory of Virology, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Emmanuelle Giuliana Mendes SantanaLaboratory of Virology, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Aline Kelly Alves OliveiraLaboratory of Virology, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Aline Cecy Rocha de LimaLaboratory of Virology, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Ednelza da Silva Graça AmorasLaboratory of Virology, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Carlos Araujo da CostaLaboratory of Cellular and Molecular Biology, Tropical Medicine Center, Federal University of Pará, Belém, Brazil.
Maísa Silva SouzaLaboratory of Cellular and Molecular Biology, Tropical Medicine Center, Federal University of Pará, Belém, Brazil.
Sandra Souza LimaLaboratory of Virology, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Ricardo IshakLaboratory of Virology, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Izaura Maria Vieira Cayres-VallinotoLaboratory of Virology, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Antonio Carlos Rosário VallinotoLaboratory of Virology, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.
Maria Alice Freitas QueirozLaboratory of Virology, Institute of Biological Sciences, Federal University of Pará, Belém, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Alterations in the immune response may influence the development of HTLV-1-associated diseases. TLR3 detects viral nucleic acids, including HTLV-1, and triggers the production of IFN-I and other cytokines. Genetic variations in Methods: Blood samples were collected from 179 individuals with HTLV-1 infection (82 with inflammatory diseases and 97 asymptomatic individuals) and 179 controls. Genotyping of polymorphisms, analysis of Results: The polymorphisms showed no correlation with susceptibility to HTLV-1 infection, or the occurrence of disease symptoms linked to the infection. The presence of disease symptoms was associated with higher TNF-α levels and proviral load. Conclusion: Although polymorphisms in the TLR3 gene have not been associated with the presence of symptoms of HTLV-1-related inflammatory diseases, the

Indexed as

Asymptomatic InfectionsHTLV-I InfectionsHuman T-lymphotropic virus 1Interferon-alphaPolymorphism, Single NucleotideToll-Like Receptor 3AdultAgedCytokinesFemaleGenetic Predisposition to DiseaseGenotypeHumansMaleMiddle AgedViral LoadCytokinesInterferon-alphaTLR3 protein, humanToll-Like Receptor 3cytokinesHTLV-I infectioninflammatory diseasespolymorphism genetictoll-like receptor 3

Identifiers

PMID40831704
PMCPMC12358490

What Socratic 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 Socratic graph.