Evidence map›Paper›PMID 25716232›Full record

ArticleClinical and vaccine immunology : CVI2015

Coinfection with Blood-Stage Plasmodium Promotes Systemic Type I Interferon Production during Pneumovirus Infection but Impairs Inflammation and Viral Control in the Lung.

Chelsea L Edwards, Vivian Zhang, Rhiannon B Werder, Shannon E Best, Ismail Sebina, Kylie R James, Rebecca J Faleiro, Fabian de Labastida Rivera, Fiona H Amante, Christian R Engwerda and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 28% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Investigation of Parasitic Infection in Crocodile Lizards (Animals : an open access journal from MDPI · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Malaria and Parasitic Neglected Tropical Diseases: Potential Syndemics with COVID-19?The American journal of tropical medicine and hygiene · 2020
    Article
  13. Review
  14. Article
  15. Rapid loss of group 1 innate lymphoid cells during blood stageClinical & translational immunology · 2018
    Article
  16. Plasmodium Parasitemia Associated With Increased Survival in Ebola Virus-Infected Patients.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2016
    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

12 authors at 2 institutions in 1 country.

Chelsea L EdwardsMalaria Immunology Lab, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Vivian ZhangLaboratory for Respiratory Mucosal Immunity, School of Biomedical Sciences, The University of Queensland, Queensland, Australia.
Rhiannon B WerderLaboratory for Respiratory Mucosal Immunity, School of Biomedical Sciences, The University of Queensland, Queensland, Australia.
Shannon E BestMalaria Immunology Lab, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Ismail SebinaMalaria Immunology Lab, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Kylie R JamesMalaria Immunology Lab, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Rebecca J FaleiroImmunology and Infection Lab, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Fabian de Labastida RiveraImmunology and Infection Lab, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Fiona H AmanteImmunology and Infection Lab, QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Christian R EngwerdaImmunology and Infection Lab, QIMR Berghofer Medical Research Institute, Brisbane, Australia Australian Infectious Diseases Research Centre, The University of Queensland, Queensland, Australia.
Simon PhippsLaboratory for Respiratory Mucosal Immunity, School of Biomedical Sciences, The University of Queensland, Queensland, Australia Australian Infectious Diseases Research Centre, The University of Queensland, Queensland, Australia.
Ashraful HaqueMalaria Immunology Lab, QIMR Berghofer Medical Research Institute, Brisbane, Australia Australian Infectious Diseases Research Centre, The University of Queensland, Queensland, Australia ashraful.haque@qimrbergofer.edu.au.
University of Queensland · AUQIMR Berghofer Medical Research Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute lower respiratory tract infections (ALRTI) are the leading cause of global childhood mortality, with human respiratory syncytial virus (hRSV) being a major cause of viral ALRTI in young children worldwide. In sub-Saharan Africa, many young children experience severe illnesses due to hRSV or Plasmodium infection. Although the incidence of malaria in this region has decreased in recent years, there remains a significant opportunity for coinfection. Recent data show that febrile young children infected with Plasmodium are often concurrently infected with respiratory viral pathogens but are less likely to suffer from pneumonia than are non-Plasmodium-infected children. Here, we hypothesized that blood-stage Plasmodium infection modulates pulmonary inflammatory responses to a viral pathogen but does not aid its control in the lung. To test this, we established a novel coinfection model in which mice were simultaneously infected with pneumovirus of mice (PVM) (to model hRSV) and blood-stage Plasmodium chabaudi chabaudi AS (PcAS) parasites. We found that PcAS infection was unaffected by coinfection with PVM. In contrast, PVM-associated weight loss, pulmonary cytokine responses, and immune cell recruitment to the airways were substantially reduced by coinfection with PcAS. Importantly, PcAS coinfection facilitated greater viral dissemination throughout the lung. Although Plasmodium coinfection induced low levels of systemic interleukin-10 (IL-10), this regulatory cytokine played no role in the modulation of lung inflammation or viral dissemination. Instead, we found that Plasmodium coinfection drove an early systemic beta interferon (IFN-β) response. Therefore, we propose that blood-stage Plasmodium coinfection may exacerbate viral dissemination and impair inflammation in the lung by dysregulating type I IFN-dependent responses to respiratory viruses.

Indexed as

CoinfectionAnimalsBronchiolitis, ViralDisease Models, AnimalFemaleInflammationInterferon-betaInterleukin-10LungMalariaPlasmodium chabaudiPneumovirusPneumovirus InfectionsRespiratory Syncytial Virus, HumanViral LoadWeight LossIL10 protein, mouseInterferon-betaInterleukin-10

Identifiers

PMID25716232
PMCPMC4412948
OpenAlexW2048756230

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.