DNA-Containing Immunocomplexes Promote Inflammasome Assembly and Release of Pyrogenic Cytokines by CD14<sup>+</sup> CD16<sup>+</sup> CD64<sup>high</sup> CD32<sup>low</sup> Inflammatory Monocytes from Malaria Patients

ABSTRACT High levels of circulating immunocomplexes (ICs) are found in patients with either infectious or sterile inflammation. We report that patients with either Plasmodium falciparum or Plasmodium vivax malaria have increased levels of circulating anti-DNA antibodies and ICs containing parasite D...

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Autores principales: Isabella C. Hirako, Carolina Gallego-Marin, Marco A. Ataide, Warrison A. Andrade, Humberto Gravina, Bruno C. Rocha, Rosane B. de Oliveira, Dhelio B. Pereira, Joseph Vinetz, Betty Diamond, Sanjay Ram, Douglas T. Golenbock, Ricardo T. Gazzinelli
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Publicado: American Society for Microbiology 2015
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spelling oai:doaj.org-article:33ef047a24c34bcc87c54300905ab7702021-11-15T15:41:24ZDNA-Containing Immunocomplexes Promote Inflammasome Assembly and Release of Pyrogenic Cytokines by CD14<sup>+</sup> CD16<sup>+</sup> CD64<sup>high</sup> CD32<sup>low</sup> Inflammatory Monocytes from Malaria Patients10.1128/mBio.01605-152150-7511https://doaj.org/article/33ef047a24c34bcc87c54300905ab7702015-12-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.01605-15https://doaj.org/toc/2150-7511ABSTRACT High levels of circulating immunocomplexes (ICs) are found in patients with either infectious or sterile inflammation. We report that patients with either Plasmodium falciparum or Plasmodium vivax malaria have increased levels of circulating anti-DNA antibodies and ICs containing parasite DNA. Upon stimulation with malaria-induced ICs, monocytes express an NF-κB transcriptional signature. The main source of IC-induced proinflammatory cytokines (i.e., tumor necrosis factor alpha [TNF-α] and interleukin-1β [IL-1β])in peripheral blood mononuclear cells from acute malaria patients was found to be a CD14+ CD16 (FcγRIIIA)+ CD64 (FcγRI)high CD32 (FcγRIIB)low monocyte subset. Monocytes from convalescent patients were predominantly of the classical phenotype (CD14+ CD16−) that produces high levels of IL-10 and lower levels of TNF-α and IL-1β in response to ICs. Finally, we report a novel role for the proinflammatory activity of ICs by demonstrating their ability to induce inflammasome assembly and caspase-1 activation in human monocytes. These findings illuminate our understanding of the pathogenic role of ICs and monocyte subsets and may be relevant for future development of immunity-based interventions with broad applications to systemic inflammatory diseases. IMPORTANCE Every year, there are approximately 200 million cases of Plasmodium falciparum and P. vivax malaria, resulting in nearly 1 million deaths, most of which are children. Decades of research on malaria pathogenesis have established that the clinical manifestations are often a consequence of the systemic inflammation elicited by the parasite. Recent studies indicate that parasite DNA is a main proinflammatory component during infection with different Plasmodium species. This finding resembles the mechanism of disease in systemic lupus erythematosus, where host DNA plays a central role in stimulating an inflammatory process and self-damaging reactions. In this study, we disclose the mechanism by which ICs containing Plasmodium DNA activate innate immune cells and consequently stimulate systemic inflammation during acute episodes of malaria. Our results further suggest that Toll-like receptors and inflammasomes have a central role in malaria pathogenesis and provide new insights toward developing novel therapeutic interventions for this devastating disease.Isabella C. HirakoCarolina Gallego-MarinMarco A. AtaideWarrison A. AndradeHumberto GravinaBruno C. RochaRosane B. de OliveiraDhelio B. PereiraJoseph VinetzBetty DiamondSanjay RamDouglas T. GolenbockRicardo T. GazzinelliAmerican Society for MicrobiologyarticleMicrobiologyQR1-502ENmBio, Vol 6, Iss 6 (2015)
institution DOAJ
collection DOAJ
language EN
topic Microbiology
QR1-502
spellingShingle Microbiology
QR1-502
Isabella C. Hirako
Carolina Gallego-Marin
Marco A. Ataide
Warrison A. Andrade
Humberto Gravina
Bruno C. Rocha
Rosane B. de Oliveira
Dhelio B. Pereira
Joseph Vinetz
Betty Diamond
Sanjay Ram
Douglas T. Golenbock
Ricardo T. Gazzinelli
DNA-Containing Immunocomplexes Promote Inflammasome Assembly and Release of Pyrogenic Cytokines by CD14<sup>+</sup> CD16<sup>+</sup> CD64<sup>high</sup> CD32<sup>low</sup> Inflammatory Monocytes from Malaria Patients
description ABSTRACT High levels of circulating immunocomplexes (ICs) are found in patients with either infectious or sterile inflammation. We report that patients with either Plasmodium falciparum or Plasmodium vivax malaria have increased levels of circulating anti-DNA antibodies and ICs containing parasite DNA. Upon stimulation with malaria-induced ICs, monocytes express an NF-κB transcriptional signature. The main source of IC-induced proinflammatory cytokines (i.e., tumor necrosis factor alpha [TNF-α] and interleukin-1β [IL-1β])in peripheral blood mononuclear cells from acute malaria patients was found to be a CD14+ CD16 (FcγRIIIA)+ CD64 (FcγRI)high CD32 (FcγRIIB)low monocyte subset. Monocytes from convalescent patients were predominantly of the classical phenotype (CD14+ CD16−) that produces high levels of IL-10 and lower levels of TNF-α and IL-1β in response to ICs. Finally, we report a novel role for the proinflammatory activity of ICs by demonstrating their ability to induce inflammasome assembly and caspase-1 activation in human monocytes. These findings illuminate our understanding of the pathogenic role of ICs and monocyte subsets and may be relevant for future development of immunity-based interventions with broad applications to systemic inflammatory diseases. IMPORTANCE Every year, there are approximately 200 million cases of Plasmodium falciparum and P. vivax malaria, resulting in nearly 1 million deaths, most of which are children. Decades of research on malaria pathogenesis have established that the clinical manifestations are often a consequence of the systemic inflammation elicited by the parasite. Recent studies indicate that parasite DNA is a main proinflammatory component during infection with different Plasmodium species. This finding resembles the mechanism of disease in systemic lupus erythematosus, where host DNA plays a central role in stimulating an inflammatory process and self-damaging reactions. In this study, we disclose the mechanism by which ICs containing Plasmodium DNA activate innate immune cells and consequently stimulate systemic inflammation during acute episodes of malaria. Our results further suggest that Toll-like receptors and inflammasomes have a central role in malaria pathogenesis and provide new insights toward developing novel therapeutic interventions for this devastating disease.
format article
author Isabella C. Hirako
Carolina Gallego-Marin
Marco A. Ataide
Warrison A. Andrade
Humberto Gravina
Bruno C. Rocha
Rosane B. de Oliveira
Dhelio B. Pereira
Joseph Vinetz
Betty Diamond
Sanjay Ram
Douglas T. Golenbock
Ricardo T. Gazzinelli
author_facet Isabella C. Hirako
Carolina Gallego-Marin
Marco A. Ataide
Warrison A. Andrade
Humberto Gravina
Bruno C. Rocha
Rosane B. de Oliveira
Dhelio B. Pereira
Joseph Vinetz
Betty Diamond
Sanjay Ram
Douglas T. Golenbock
Ricardo T. Gazzinelli
author_sort Isabella C. Hirako
title DNA-Containing Immunocomplexes Promote Inflammasome Assembly and Release of Pyrogenic Cytokines by CD14<sup>+</sup> CD16<sup>+</sup> CD64<sup>high</sup> CD32<sup>low</sup> Inflammatory Monocytes from Malaria Patients
title_short DNA-Containing Immunocomplexes Promote Inflammasome Assembly and Release of Pyrogenic Cytokines by CD14<sup>+</sup> CD16<sup>+</sup> CD64<sup>high</sup> CD32<sup>low</sup> Inflammatory Monocytes from Malaria Patients
title_full DNA-Containing Immunocomplexes Promote Inflammasome Assembly and Release of Pyrogenic Cytokines by CD14<sup>+</sup> CD16<sup>+</sup> CD64<sup>high</sup> CD32<sup>low</sup> Inflammatory Monocytes from Malaria Patients
title_fullStr DNA-Containing Immunocomplexes Promote Inflammasome Assembly and Release of Pyrogenic Cytokines by CD14<sup>+</sup> CD16<sup>+</sup> CD64<sup>high</sup> CD32<sup>low</sup> Inflammatory Monocytes from Malaria Patients
title_full_unstemmed DNA-Containing Immunocomplexes Promote Inflammasome Assembly and Release of Pyrogenic Cytokines by CD14<sup>+</sup> CD16<sup>+</sup> CD64<sup>high</sup> CD32<sup>low</sup> Inflammatory Monocytes from Malaria Patients
title_sort dna-containing immunocomplexes promote inflammasome assembly and release of pyrogenic cytokines by cd14<sup>+</sup> cd16<sup>+</sup> cd64<sup>high</sup> cd32<sup>low</sup> inflammatory monocytes from malaria patients
publisher American Society for Microbiology
publishDate 2015
url https://doaj.org/article/33ef047a24c34bcc87c54300905ab770
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