Evidence map›Paper›PMID 29867949›Full record

ArticleFrontiers in immunology2018

NH36 and F3 Antigen-Primed Dendritic Cells Show Preserved Migrating Capabilities and CCR7 Expression and F3 Is Effective in Immunotherapy of Visceral Leishmaniasis.

Dirlei Nico, Fernanda Martins Almeida, Juliana Maria Motta, Fellipe Soares Dos Santos Cardoso, Celio Geraldo Freire-de-Lima, Leonardo Freire-de-Lima, Paula Melo de Luca, Ana Maria Blanco Martinez, Alexandre Morrot, Clarisa Beatriz Palatnik-de-Sousa

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-weighted citation impact, top 13% 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, 12 citations in OpenAlex.

  1. A review of vaccinology andHuman vaccines & immunotherapeutics · 2025
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  9. The F1F3 Recombinant Chimera ofFrontiers in immunology · 2019
    Article
  10. Biomarkers Associated WithFrontiers in cellular and infection microbiology · 2018
    Review
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

10 authors at 3 institutions in 1 country.

Dirlei NicoDepartamento de Microbiologia Geral, Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Fernanda Martins AlmeidaPrograma de Pós Graduação em Anatomia Patológica, HUCFF, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Juliana Maria MottaPrograma de Glicobiologia, Instituto de Bioquímica Médica Leopoldo De Meis, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Fellipe Soares Dos Santos CardosoPrograma de Pós Graduação em Anatomia Patológica, HUCFF, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Celio Geraldo Freire-de-LimaPrograma de Imunobiologia, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Leonardo Freire-de-LimaPrograma de Medicina Regenerativa, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Paula Melo de LucaLaboratório de Imunoparasitologia, Instituto Oswaldo Cruz (IOC), Rio de Janeiro, Brazil.
Ana Maria Blanco MartinezPrograma de Pós Graduação em Anatomia Patológica, HUCFF, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Alexandre MorrotLaboratório de Imunoparasitologia, Instituto Oswaldo Cruz (IOC), Rio de Janeiro, Brazil.
Clarisa Beatriz Palatnik-de-SousaDepartamento de Microbiologia Geral, Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Universidade Federal do Rio de Janeiro · BRHospital Universitário Clementino Fraga Filho · BRFundação Oswaldo Cruz · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Physical contact between dendritic cells (DCs) and T cell lymphocytes is necessary to trigger the immune cell response. CCL19 and CCL21 chemokines bind to the CCR7 receptor of mature DCs, and of T cells and regulate DCs migration to the white pulp (wp) of the spleen, where they encounter lymphocytes. In visceral leishmaniasis (VL), cellular immunosuppression is mediated by impaired DC migration due to the decreased chemokine secretion by endothelium and to the reduced DCs CCR7 expression. The

Indexed as

ImmunotherapyAnimalsAntigens, ProtozoanCell MovementCytokinesDendritic CellsEpitopes, T-LymphocyteFemaleImmunity, CellularLeishmania donovaniLeishmaniasis VaccinesLeishmaniasis, VisceralMiceMice, Inbred BALB CMice, Inbred C57BLN-Glycosyl HydrolasesAntigens, ProtozoanCcr7 protein, mouseCytokinesEpitopes, T-LymphocyteLeishmaniasis VaccinesN-Glycosyl HydrolasesReceptors, CCR7CCR7 expressiondendritic cells defective migrationF3 domainLeishmania donovaniLeishmania infantum chagasiNH36nucleoside hydrolasevisceral leishmaniasis

Identifiers

PMID29867949
PMCPMC5949526
OpenAlexW2802344636

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.