NK cells contribute to the resolution of experimental malaria-associated acute respiratory distress syndrome after antimalarial treatment
In both humans and mice, natural killer (NK) cells are important lymphocytes of the innate immune system. They are often considered pro-inflammatory effector cells but may also have a regulatory or pro-resolving function by switching their cytokine profile towards the production of anti-inflammatory cytokines, including interleukin-10 (IL-10) and transforming growth factor-β, and by killing pro-inflammatory immune cells. Here, the role of NK cells in the resolution of malaria lung pathology was studied. Malaria complications, such as malaria-associated acute respiratory distress syndrome (MA-ARDS), are often lethal despite the rapid and efficient killing of <i>Plasmodium</i> parasites with antimalarial drugs. Hence, studying the resolution and healing mechanisms involved in the recovery from these complications could be useful to develop adjunctive treatments. Treatment of <i>Plasmodium berghei NK65</i>-infected C57BL/6 mice with a combination of artesunate and chloroquine starting at the appearance of symptoms was used as a model to study the resolution of MA-ARDS. The role of NK cells was studied using anti-NK1.1 depletion antibodies and NK cell-deficient mice. Using both methods, NK cells were found to be dispensable in the development of MA-ARDS, as shown previously. In contrast, NK cells were crucial in the initiation of resolution upon antimalarial treatment, as survival was significantly decreased in the absence of NK cells. Considerably increased IL-10 expression by NK cells suggested an anti-inflammatory and pro-resolving phenotype. Despite the increase in <i>Il10</i> expression in the NK cells, inhibition of the IL-10/IL-10R axis using anti-IL10R antibodies had no effect on the resolution for MA-ARDS, suggesting that the pro-resolving effect of NK cells cannot solely be attributed to their IL-10 production. In conclusion, NK cells contribute to the resolution of experimental MA-ARDS.
Authors
- Emilie Pollenus (ORCID: https://orcid.org/0000-0002-2706-6259)
- Hendrik Possemiers (ORCID: https://orcid.org/0000-0001-7565-9668)
- Fran Prenen (ORCID: https://orcid.org/0000-0002-5431-1715)
- Philippe E. Van den Steen (ORCID: https://orcid.org/0000-0002-7334-9145)
- Leen Vandermosten (ORCID: https://orcid.org/0000-0001-6355-3129)
- Thao‐Thy Pham (ORCID: https://orcid.org/0000-0003-3728-6455)
- Patrick Matthys (ORCID: https://orcid.org/0000-0002-9685-6836)
- Laura Buysrogge
- Sofie Knoops
Institutions
- Rega Institute for Medical Research (BE)
- Instituut voor Tropische Geneeskunde (BE)
- KU Leuven (BE)
Publication Details
- Journal
- Frontiers in Immunology
- Published
- 2024-09-17
- DOI
- https://doi.org/10.3389/fimmu.2024.1433904
- Citations
- 1
- Primary Topic
- Immune Cell Function and Interaction
- Type
- article
- Field-Weighted Citation Impact
- 0.24
Funders
- Fonds Wetenschappelijk Onderzoek
- KU Leuven
- Vlaamse regering