Evidence map›Paper›PMID 28483582›Full record

ArticleEBioMedicine2017

The Role of Heterotypic DENV-specific CD8

Laura B Talarico, Juan P Batalle, Alana B Byrne, Jorge M Brahamian, Adrián Ferretti, Ayelén G García, Aldana Mauri, Carla Simonetto, Diego R Hijano, Andrea Lawrence and 9 more

Abstract read
In one paragraph

Article in EBioMedicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Dengue Dilemma: Navigating Cross-Reactivity and Immune Challenges.Current topics in microbiology and immunology · 2026
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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

19 authors.

Laura B TalaricoFundación INFANT, Buenos Aires, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina. Electronic address: ltalarico@infant.org.ar.
Juan P BatalleFundación INFANT, Buenos Aires, Argentina.
Alana B ByrneFundación INFANT, Buenos Aires, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina.
Jorge M BrahamianFundación INFANT, Buenos Aires, Argentina.
Adrián FerrettiFundación INFANT, Buenos Aires, Argentina.
Ayelén G GarcíaFundación INFANT, Buenos Aires, Argentina.
Aldana MauriFundación INFANT, Buenos Aires, Argentina.
Carla SimonettoFundación INFANT, Buenos Aires, Argentina.
Diego R HijanoFundación INFANT, Buenos Aires, Argentina; Department of Pediatrics, Vaccine Center, Vanderbilt University, Nashville, TN, USA.
Andrea LawrenceDepartment of Pediatrics, Vaccine Center, Vanderbilt University, Nashville, TN, USA.
Patricio L AcostaFundación INFANT, Buenos Aires, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina.
Mauricio T CaballeroFundación INFANT, Buenos Aires, Argentina.
Yésica Paredes RojasConsejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina; Centro de Virología Animal (CEVAN), Instituto de Ciencia y Tecnología Dr. César Milstein, CONICET, Buenos Aires, Argentina.
Lorena I IbañezConsejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina; Centro de Virología Animal (CEVAN), Instituto de Ciencia y Tecnología Dr. César Milstein, CONICET, Buenos Aires, Argentina.
Guillermina A MelendiFundación INFANT, Buenos Aires, Argentina.
Félix A ReyDépartement de Virologie, Institut Pasteur, Unité de Virologie Structurale, Paris, France.
Elsa B DamonteLaboratorio de Virología, Departamento de Química Biológica-IQUIBICEN (CONICET-UBA), Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina.
Eva HarrisDivision of Infectious Diseases and Vaccinology, School of Public Health, University of California, Berkeley, Berkeley, CA, USA.
Fernando P PolackFundación INFANT, Buenos Aires, Argentina; Department of Pediatrics, Vaccine Center, Vanderbilt University, Nashville, TN, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dengue is the most prevalent arthropod-borne viral disease worldwide and is caused by the four dengue virus serotypes (DENV-1-4). Sequential heterologous DENV infections can be associated with severe disease manifestations. Here, we present an immunocompetent mouse model of secondary DENV infection using non mouse-adapted DENV strains to investigate the pathogenesis of severe dengue disease. C57BL/6 mice infected sequentially with DENV-1 (strain Puerto Rico/94) and DENV-2 (strain Tonga/74) developed low platelet counts, internal hemorrhages, and increase of liver enzymes. Cross-reactive CD8

Indexed as

AnimalsAntibodies, NeutralizingAntibodies, ViralCD8-Positive T-LymphocytesCell LineCross ReactionsDengueDengue VirusDisease Models, AnimalImmunoglobulin GLymphocyte DepletionMiceMice, KnockoutSerogroupSeverity of Illness IndexT-Cell Antigen Receptor SpecificityAntibodies, NeutralizingAntibodies, ViralImmunoglobulin GCD8(+) T lymphocytesDengue virusImmune responseImmunocompetent mouse modelSecondary infection

Identifiers

PMID28483582
PMCPMC5478214

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.