Abstract
Malaria, caused by infection with Plasmodium parasites, drives multiple regulatory responses across the immune landscape. These regulatory responses help to protect against inflammatory disease but may in some situations hamper the acquisition of adaptive immune responses that clear parasites. In addition, the regulatory responses that occur during Plasmodium infection may negatively affect malaria vaccine efficacy in the most at-risk populations. Here, we discuss the specific cellular mechanisms of immunoregulatory networks that develop during malaria, with a focus on knowledge gained from human studies and studies that involve the main malaria parasite to affect humans, Plasmodium falciparum. Leveraging this knowledge may lead to the development of new therapeutic approaches to increase protective immunity to malaria during infection or after vaccination.
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References
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Acknowledgements
M.J.B. is supported by a Snow Medical Fellowship and CSL Centenary Fellowship. P.J. is supported by the NIH (U01 AI15532, U01 AI150741, R01 AI 177377), the Bill and Melinda Gates Foundation (OPP 052649) and the Stanford Maternal and Child Health Faculty Scholars Program. C.R.E. has been supported by funding from the Australian National Health and Medical Research Council (1132975, 1154265).
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Boyle, M.J., Engwerda, C.R. & Jagannathan, P. The impact of Plasmodium-driven immunoregulatory networks on immunity to malaria. Nat Rev Immunol 24, 637–653 (2024). https://doi.org/10.1038/s41577-024-01041-5
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DOI: https://doi.org/10.1038/s41577-024-01041-5
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