Evidence map›Paper›PMID 31234875›Full record

ArticleMalaria journal2019

Signatures of divergent anti-malarial treatment responses in peripheral blood from adults and young children in Malawi.

Paul L Maurizio, Hubaida Fuseini, Gerald Tegha, Mina Hosseinipour, Kristina De Paris

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 38% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

5 authors at 2 institutions in 2 countries.

Paul L MaurizioDepartment of Medicine, Section of Genetic Medicine, The University of Chicago, Chicago, IL, 60637, USA. maurizio@uchicago.edu.ORCID http://orcid.org/0000-0002-5859-6260
Hubaida FuseiniDepartment of Pathology, Microbiology & Immunology, Vanderbilt University, Nashville, TN, USA.
Gerald TeghaDivision of Infectious Diseases, Department of Medicine, University of North Carolina, 130 Mason Farm Rd, Bioinformatics Bldg, Chapel Hill, NC, 27599, USA.
Mina HosseinipourDivision of Infectious Diseases, Department of Medicine, University of North Carolina, 130 Mason Farm Rd, Bioinformatics Bldg, Chapel Hill, NC, 27599, USA.
Kristina De ParisDepartment of Microbiology and Immunology, University of North Carolina, Chapel Hill, NC, 27599, USA.
University of North Carolina at Chapel Hill · USVanderbilt University · US

Funding

Virology, Immunology, and Microbiology CoreP30AI050410 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2001 to 2026
$76.9M
Molecular Biology of Viral Diseases Predoctoral Training GrantT32AI007419 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Mark T Heise, CARY A MOODY · 1993 to 2026
$4.7M
Molecular Mechanisms Associated with Immune Maturation in InfantsR01AI100067 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DE PARIS, KRISTINA · 2012 to 2015
$1.8M
Center for AIDS Research, University of North Carolina at Chapel Hill 5P30AI050410National Institute of Allergy and Infectious Diseases 5T32AI007419-23National Institute of Allergy and Infectious Diseases AI100067NIAID NIH HHS P30 AI050410NIAID NIH HHS R01 AI100067NIAID NIH HHS T32 AI007419
6 · The paper itself

Abstract

backgroundHeterogeneity in the immune response to parasite infection is mediated in part by differences in host genetics, gender, and age group. In infants and young children, ongoing immunological maturation often results in increased susceptibility to infection and variable responses to drug treatment, increasing the risk of complications. Even though significant age-associated effects on host cytokine responses to Plasmodium falciparum infection have been identified, age-associated effects on uncomplicated malaria infection and anti-malarial treatment remain poorly understood.

methodsIn samples of whole blood from a cohort of naturally infected malaria-positive individuals with non-severe falciparum malaria in Malawi (n = 63 total; 34 infants and young children < 2 years old, 29 adults > 18 years old), blood cytokine levels and monocyte and dendritic cell frequencies were assessed at two timepoints: acute infection, and 4 weeks post anti-malarial treatment. The effects of age group, gender, and timepoint were modeled, and the role of these factors on infection and treatment outcomes was evaluated.

resultsRegardless of treatment timepoint, in this population age was significantly associated with overall blood haemoglobin, which was higher in adults, and plasma nitric oxide metabolites, IL-10, and TNF levels, which were higher in young children. There was a significant effect of age on the haemoglobin treatment response, whereby after treatment, levels increased in young children and decreased in adults. Furthermore, there were significant age-associated effects on treatment response for overall parasite load, IFN-γ, and IL-12(p40), and these effects were gender-dependent. Significant age effects on the overall levels and treatment response of myeloid dendritic cell frequencies were observed. In addition, within each age group, results showed continuous age effects on gametocyte levels (Pfs16), TNF, and nitric oxide metabolites.

conclusionsIn a clinical study of young children and adults experiencing natural falciparum malaria infection and receiving anti-malarial treatment, age-associated signatures of infection and treatment responses in peripheral blood were identified. This study describes host markers that may indicate, and potentially contribute to, differential post-treatment outcomes for malaria in young children versus adults.

Indexed as

Models, BiologicalAdultAge FactorsAntimalarialsBiomarkersBlood Cell CountCytokinesFemaleHumansInfantMalaria, FalciparumMalawiMaleParasite LoadSex FactorsAntimalarialsBiomarkersCytokinesCytokinesHeterogeneityPaediatricPlasmodium falciparumUncomplicated malaria

Identifiers

PMID31234875
PMCPMC6591936
OpenAlexW2954531424

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.