Evidence map›Paper›PMID 24599360›Full record

ArticlePloS one2014

Neutrophils increase or reduce parasite burden in Trypanosoma cruzi-infected macrophages, depending on host strain: role of neutrophil elastase.

Tatiana Luna-Gomes, Alessandra A Filardy, Juliana Dutra B Rocha, Debora Decote-Ricardo, Isabel Ferreira LaRocque-de-Freitas, Alexandre Morrot, Patrícia T Bozza, Hugo C Castro-Faria-Neto, George A DosReis, Marise P Nunes and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Apoptosis: A Key Process ThatJournal of parasitology research · 2025
    Review
  3. Review
  4. IncreasedLife (Basel, Switzerland) · 2023
    Article
  5. Article
  6. Article
  7. The influence of parasitism byInternational journal for parasitology. Parasites and wildlife · 2019
    Article
  8. B-1 Cells May Drive Macrophages Susceptibility toFrontiers in microbiology · 2019
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. B-1 cells modulate the murine macrophage response toWorld journal of biological chemistry · 2017
    Article
  14. Article
  15. Review
  16. Unconventional Pro-inflammatory CD4Frontiers in immunology · 2017
    Article
  17. Article
  18. Review
  19. Article
  20. 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

11 authors at 3 institutions in 1 country.

Tatiana Luna-GomesInstituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Alessandra A FilardyInstituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Juliana Dutra B RochaInstituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Debora Decote-RicardoInstituto de Veterinária, Universidade Federal Rural do Rio de Janeiro, Seropédica, Rio de Janeiro, Brazil.
Isabel Ferreira LaRocque-de-FreitasInstituto de Veterinária, Universidade Federal Rural do Rio de Janeiro, Seropédica, Rio de Janeiro, Brazil.
Alexandre MorrotInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Patrícia T BozzaInstituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, Brazil.
Hugo C Castro-Faria-NetoInstituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, Brazil.
George A DosReisInstituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Marise P NunesInstituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, Brazil.
Célio G Freire-de-LimaInstituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Universidade Federal do Rio de Janeiro · BRFundação Oswaldo Cruz · BRUniversidade Federal Rural do Rio de Janeiro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neutrophils are involved in the initial steps of most responses to pathogens and are essential components of the innate immune response. Due to the ability to produce and release various soluble mediators, neutrophils may participate in the regulation of the inflammatory response. Little is known about the role of neutrophils during protozoan infections including infection by Trypanosoma cruzi. In the present study we investigated the importance of inflammatory neutrophils on macrophage activation and T. cruzi replication in vitro, in cells obtained from BALB/c mice and C57Bl/6 mice. Co-cultures of BALB/c apoptotic or live neutrophils with infected peritoneal macrophages resulted in increased replication of the parasites and in the production of TGF-β and PGE2. The treatment with anti-TGF-β neutralizing antibody and COX inhibitor blocked the parasite replication in vitro. On the other hand, co-cultures of T. cruzi infected macrophages with live neutrophils isolated from C57BL/6 mice resulted in decreased number of trypomastigotes in culture and increased production of TNF-α and NO. The addition of anti-TNF-α neutralizing antibody or elastase inhibitor resulted in the abolishment of macrophage microbicidal effect and increased parasite replication. Addition of elastase to infected macrophages reduced the replication of the parasites, and on the other hand, addition of a selective inhibitor of iNOS increased parasite growth, suggesting the role of NO in this system. Our findings reveal that neutrophils may regulate T. cruzi experimental infection and determine susceptibility and resistance to infection.

Indexed as

AnimalsApoptosisCells, CulturedChagas DiseaseCoculture TechniquesCytokinesDinoprostoneHost-Parasite InteractionsHost SpecificityLeukocyte ElastaseMacrophages, PeritonealMice, Inbred BALB CMice, Inbred C57BLNeutrophilsNitric OxideTrypanosoma cruziCytokinesDinoprostoneLeukocyte ElastaseNitric Oxide

Identifiers

PMID24599360
PMCPMC3944110
OpenAlexW2089266634

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.