Evidence map›Paper›PMID 41491654›Full record

ArticleImmunoHorizons2026

Altered natural killer cell function in children with severe malaria.

Grace Turyasingura, Kagan A Mellencamp, Ruth Namazzi, Robert O Opoka, Chandy C John, Geoffrey T Hart

Abstract read
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Article in ImmunoHorizons, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Grace TuryasinguraDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN, United States.
Kagan A MellencampRyan White Center for Pediatric Infectious Diseases and Global Health, Indiana University School of Medicine, Indianapolis, IN, United States.
Ruth NamazziDepartment of Paediatrics and Child Health, Makerere University, Kampala, Uganda.
Robert O OpokaDepartment of Paediatrics and Child Health, Makerere University, Kampala, Uganda.
Chandy C JohnDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN, United States.
Geoffrey T HartDivision of Infectious Disease and International Medicine, Department of Medicine, University of Minnesota, Minneapolis, MN, United States.

Funding

Severe Malaria And Risk to The Brain (SMART Brain)R01NS055349 · NINDS · UNIVERSITY OF MINNESOTA · PI Chandy C. John, Ruth Namazzi · 2008 to 2026
$11.2M
The role of natural killer cells and antibodies in protection from malariaR01AI146031 · NIAID · UNIVERSITY OF MINNESOTA · PI HART, GEOFFREY T · 2020 to 2024
$2.7M
Research training in infection, nutrition and neurodevelopment in UgandaD43TW010928 · FIC · INDIANA UNIVERSITY INDIANAPOLIS · PI Chandy C. John · 2018 to 2026
$1.9M
FIC NIH HHS D43 TW010928NIAID NIH HHS R01 AI146031NINDS NIH HHS R01 NS055349
6 · The paper itself

Abstract

Memory-like natural killer (NK) cells with enhanced antibody-dependent cellular cytotoxicity (ADCC) have correlated with protection from uncomplicated malaria in prior studies. However, the role of NK cells in severe malaria (SM) has not been characterized. In Ugandan sites with moderate and low malaria transmission, we evaluated NK cell (CD56bright, CD56dim, CD56neg) phenotype and ADCC function by flow cytometry in children <5 years of age with SM (n = 21) and control community children (CC, n = 19). Children with SM had similar total NK cell counts to CC. Children with SM had a higher proportion of LILRB1+ NK cells than CC. The level of malaria transmission in an area was related to NK cell function. In the low malaria transmission area only, children with SM had a higher proportion than CC of NK cells that degranulated, whereas children with SM from both low and moderate malaria transmission areas had lower IFN-γ production than CC. We next evaluated functional Boolean gating for degranulation and IFN-γ production (CD107a+/IFN-γ-, CD107a-/IFN-γ+, and CD107a+/IFN-γ+) in relation to memory-like and checkpoint/exhaustion NK cell markers in low and moderate malaria transmission SM and CC groups. We found there was a significant increase in degranulating only NK cells (CD107a+, IFN-γ-) in children with SM compared to CC solely in the low malaria transmission area. However, there was a significant decrease in NK cells that produced IFN-γ but did not degranulate (CD107a-, IFN-γ+) in children with SM compared to CC in both low and moderate transmission areas. Our data reveal compound functional differences in NK cells among children with SM living in areas of low versus moderate malaria transmission; however, a consistent finding is reduced NK cell IFN-γ production in SM, regardless of transmission intensity.

Indexed as

Killer Cells, NaturalMalariaMalaria, FalciparumAntibody-Dependent Cell CytotoxicityCD56 AntigenCell DegranulationChild, PreschoolFemaleFlow CytometryHumansInfantInterferon-gammaMaleUgandaCD56 AntigenInterferon-gammacerebral malarianatural killer cellsPlasmodium falciparumsevere malariasevere malarial anemia

Identifiers

PMID41491654
PMCPMC12768885

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LicenceCC BY-NC
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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.