Evidence map›Paper›PMID 26302057›Full record

ArticleImmunology2015

Protection against Paracoccidioides brasiliensis infection in mice treated with modulated dendritic cells relies on inhibition of interleukin-10 production by CD8+ T cells.

Thiago Alves da Costa, Rosária Di Gangi, Paula Martins, Ana Leda Figueiredo Longhini, Fábio Zanucoli, Alexandre Leite Rodrigues de Oliveira, Dagmar Ruth Stach-Machado, Eva Burger, Liana Verinaud, Rodolfo Thomé

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Thiago Alves da CostaDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Rosária Di GangiDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Paula MartinsDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Ana Leda Figueiredo LonghiniDepartment of Haematology, Faculdade de Ciências Médicas, University of Campinas, Campinas, SP, Brazil.
Fábio ZanucoliDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Alexandre Leite Rodrigues de OliveiraDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Dagmar Ruth Stach-MachadoDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Eva BurgerInstituto de Biociências, Universidade Federal de Alfenas, Alfenas, MG, Brazil.
Liana VerinaudDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Rodolfo ThoméDepartment of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Universidade Estadual de Campinas (UNICAMP) · BRUniversidade Federal de Alfenas · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paracoccidioidomycosis is a systemic infection prevalent in Latin American countries. Disease develops after inhalation of Paracoccidioides brasiliensis conidia followed by an improper immune activation by the host leucocytes. Dendritic cells (DCs) are antigen-presenting cells with the unique ability to direct the adaptive immune response by the time of activation of naive T cells. This study was conducted to test whether extracts of P. brasiliensis would induce maturation of DCs. We found that DCs treated with extracts acquired an inflammatory phenotype and upon adoptive transfer conferred protection to infection. Interestingly, interleukin-10 production by CD8(+) T cells was ablated following DC transfer. Further analyses showed that lymphocytes from infected mice were high producers of interleukin-10, with CD8(+) T cells being the main source. Blockage of cross-presentation to CD8(+) T cells by modulated DCs abolished the protective effect of adoptive transfer. Collectively, our data show that adoptive transfer of P. brasiliensis-modulated DCs is an interesting approach for the control of infection in paracoccidioidomycosis.

Indexed as

Adoptive TransferAnimalsAntigens, FungalCD8-Positive T-LymphocytesCell DifferentiationCross-PrimingCytokinesDendritic CellsFemaleFungal VaccinesInflammation MediatorsInterleukin-10MaleMiceMice, Inbred BALB CMice, Inbred C57BLAntigens, FungalCytokinesFungal VaccinesIL10 protein, mouseInflammation MediatorsInterleukin-10cell-based vaccinedendritic cellsfungal infectionimmunoregulationParacoccidioides brasiliensisparacoccidioidomycosis

Identifiers

PMID26302057
PMCPMC4610636
OpenAlexW2136917827

What OpenQuestion holds

Textmetadata
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.