ORIGINAL RESEARCH article
Front. Immunol.
Sec. Inflammation
Complement-Mediated and Direct Activation of Human Neutrophils Induced by Premolis semirufa Caterpillar Toxins
Provisionally accepted
- 1Laboratory of Immunochemistry, Butantan Institute, São Paulo, Brazil
- 2School of Biomedical Sciences, University of Queensland, Queensland, Australia
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Pararamosis is an occupational inflammatory disease caused by contact with hairs of the caterpillar Premolis semirufa, endemic to the Brazilian Amazon and primarily affecting rubber tree workers. Exposure to pararama hairs induces acute pruritic dermatitis and, in some cases, chronic joint inflammation resembling rheumatoid arthritis and osteoarthritis. Previous studies demonstrated that pararama hair extract activates the complement system and induces a robust inflammatory response in mouse models, characterized by cytokine production and immune cell recruitment. Given the critical role of neutrophils in inflammation and their activation by complement components, this study investigated the effects of pararama hair extract on human peripheral blood neutrophils. Neutrophils isolated from healthy donors were directly stimulated with the extract or incubated with plasma derived from whole blood treated with the extract, in the presence or absence of compstatin, a C3 inhibitor that blocks complement activation, and PMX205, a selective C5aR1 antagonist applied directly to neutrophils. We assessed neutrophil activation by measuring cytokine and chemokine secretion, myeloperoxidase and elastase release, and neutrophil extracellular trap (NET) formation. Our results reveal that pararama hair extract directly activates neutrophils, enhancing pro-inflammatory mediator release and degranulation. Moreover, plasma from extract-treated human whole blood samples further potentiated neutrophil activation, which was significantly reduced by compstatin, through inhibition of C3, and by selective blockade of the C5a receptor (C5aR1). These findings highlight the integrated role of complement in neutrophil activation, as compstatin broadly inhibited complement-dependent effects, while PMX205 demonstrated the specific contribution of the C5a–C5aR1 axis. Targeting complement thus emerges as a promising strategy to mitigate inflammation and tissue damage in affected individuals.
Keywords: Pararamosis1, Joint disease2, innate immunity3, Complement4, Neutrophils5, inflammation6, Complement-targeted therapy7
Received: 15 Sep 2025; Accepted: 30 Nov 2025.
Copyright: © 2025 Gabrili, Megale, Pidde, Woodruff and Tambourgi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence: Denise V. Tambourgi
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