Evidence map›Paper›PMID 30866943›Full record

Trial reportMalaria journal2019

Longitudinal analysis of gamma delta T cell subsets during malaria infections in Malian adults.

Hama Diallo, Abdoulaye Katile, Jennifer L Kwan, Mahamadou S Sissoko, Sara A Healy, Ogobara K Doumbo, Patrick E Duffy, Irfan Zaidi

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Malaria journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. 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

8 authors at 2 institutions in 2 countries.

Hama DialloMalaria Research Training Center, International Center of Excellence in Research, Faculty of Medicine and Pharmacy of the University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Abdoulaye KatileMalaria Research Training Center, International Center of Excellence in Research, Faculty of Medicine and Pharmacy of the University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Jennifer L KwanLaboratory for Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA.
Mahamadou S SissokoMalaria Research Training Center, International Center of Excellence in Research, Faculty of Medicine and Pharmacy of the University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Sara A HealyLaboratory for Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA.
Ogobara K DoumboMalaria Research Training Center, International Center of Excellence in Research, Faculty of Medicine and Pharmacy of the University of Sciences, Techniques and Technologies of Bamako, Bamako, Mali.
Patrick E DuffyLaboratory for Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA. patrick.duffy@nih.gov.ORCID http://orcid.org/0000-0002-4483-5005
Irfan ZaidiLaboratory for Malaria Immunology and Vaccinology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD, USA.
National Institutes of Health · USUniversité des Sciences, des Techniques et des Technologies de Bamako · ML

Funding

Malaria Pathogenesis in young children and vaccine discoveryZIAAI001134 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI DUFFY, PATRICK · 2010 to 2025
$11.3M
The Role of T Cell Regulatory Mechanisms in Protection from Severe MalariaZIAAI001147 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI DUFFY, PATRICK · 2011 to 2025
$2.3M
6 · The paper itself

Abstract

backgroundImmunity that limits malarial disease is acquired over time, but adults living in endemic areas continue to become infected and can require treatment for clinical illness. Gamma delta (γδ) T cells, particularly the Vδ2+ subset, have been associated with development of clinical malaria in children. In this study, the dynamics of total γδ T cells, Vδ2+ and Vδ2- T cells were measured during a malaria transmission season in Malian adults.

methodsThis study explored γδ T cell dynamics and Plasmodium falciparum infection outcomes over the course of the malaria transmission season in Malian adults enrolled in the placebo arm of a double-blind randomized vaccine trial. All volunteers were treated with anti-malarial drugs prior to the start of the transmission season and blood smears were assessed for P. falciparum infection every 2 weeks from July 2014 to January 2015. The study participants were stratified as either asymptomatic infections or clinical malaria cases. Vδ2+ and Vδ2- γδ T cell frequencies and activation (as measured by CD38 expression) were measured in all study participants at baseline and then every 2 months using a whole blood flow cytometry assay.

resultsForty of the forty-three subjects became infected with P. falciparum and, of those, 21 individuals were diagnosed with clinical malaria at least once during the season. The γδ T cell percentage and activation increased over the duration of the transmission season. Both the Vδ2+ and Vδ2- γδ T cells were activated by P. falciparum infection.

conclusionγδ T cells increased during a malaria transmission season and this expansion was noted in both the Vδ2+ and Vδ2- γδ T cells. However, neither expansion or activation of either γδ T cell subsets discriminated study participants that had asymptomatic infections from those that had clinical malaria cases.

Indexed as

AdolescentAdultBlood CellsFemaleHumansIntraepithelial LymphocytesLongitudinal StudiesMalaria, FalciparumMaleMaliPlasmodium falciparumT-Lymphocyte SubsetsYoung AdultClinical malariaLongitudinal analysisPlasmodium falciparumγδ T cells

Identifiers

PMID30866943
PMCPMC6416881
OpenAlexW2947416429

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.