Age is an intrinsic driver of inflammatory responses to malaria

Age is a critical factor in immune responses to infection. In malaria, severe disease risk increases with age in non-immune individuals. Malaria severity is in part driven by inflammation, but mechanisms contributing to age-dependent disease risk are incompletely understood. We assessed inflammatory cytokines during malaria in non-immune children and adults, and innate cell responses in vitro to malaria parasites in naive children and adults. We show during malaria age is associated with increased inflammatory chemokines CCL2, CCL3, CXCL8, CXCL9, along with CRP, and IDO, which associate with symptoms. In naive individuals, classical monocyte and Vδ2<sup>+</sup> γδ T cells from adults have higher inflammatory cytokine production, and transcriptional activation following stimulation with parasites. Classical monocyte responses in adults are dominated by CCL2, while in children increased IL10 and enrichment of IL10 signaling pathways is detected. Findings identify age-dependent cellular mechanisms that play crucial roles in driving inflammatory responses in malaria.

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Publication Details

Journal
Nature Communications
Published
2025-09-30
DOI
https://doi.org/10.1038/s41467-025-63638-1
Citations
4
Primary Topic
Immune responses and vaccinations
Type
article
Field-Weighted Citation Impact
3.19

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article

Age is an intrinsic driver of inflammatory responses to malaria

Christian Engwerda, Gabriela Minigo, Peter Bourke, Jessica R. Loughland et al.
4 citations
Nature Communications
Immune responses and vaccinations
3.19
article

Age is an intrinsic driver of inflammatory responses to malaria

Christian Engwerda, Gabriela Minigo, Peter Bourke, Jessica R. Loughland, Nicholas M. Anstey, Timothy William, Matthew J. Grigg, Bridget E. Barber, Nicholas L. Dooley, José Alejandro López, Peta Tipping, Arya SheelaNair, Kim A. Piera, Zuleima Pava, Dean W. Andrew, Michelle J. Boyle
article en
4 citations

Abstract

Age is a critical factor in immune responses to infection. In malaria, severe disease risk increases with age in non-immune individuals. Malaria severity is in part driven by inflammation, but mechanisms contributing to age-dependent disease risk are incompletely understood. We assessed inflammatory cytokines during malaria in non-immune children and adults, and innate cell responses in vitro to malaria parasites in naive children and adults. We show during malaria age is associated with increased inflammatory chemokines CCL2, CCL3, CXCL8, CXCL9, along with CRP, and IDO, which associate with symptoms. In naive individuals, classical monocyte and Vδ2<sup>+</sup> γδ T cells from adults have higher inflammatory cytokine production, and transcriptional activation following stimulation with parasites. Classical monocyte responses in adults are dominated by CCL2, while in children increased IL10 and enrichment of IL10 signaling pathways is detected. Findings identify age-dependent cellular mechanisms that play crucial roles in driving inflammatory responses in malaria.

Nature CommunicationsVol. 16(1)
Griffith University (AU), Burnet Institute (AU), QIMR Berghofer Medical Research Institute (AU), Cairns Hospital (AU), Charles Darwin University (AU), Menzies School of Health Research (AU), Subang Jaya Medical Centre (MY)
Burnet Institute, Snow Medical, Medical Research Council, National Health and Medical Research Council
Openalex Percentile: Top 7%
Immune responses and vaccinations
3.19
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