Animal toxins and NETosis: A new frontier in innate immune modulation

Neutrophil extracellular traps are molecular structures that play a dual role in host defense and pathology. While NETs effectively capture and neutralize pathogens, excessive or dysregulated NET formation contributes to autoimmune and inflammatory disorders. Animal venoms contain bioactive molecules that can modulate neutrophil functions, including NETosis. They are capable of inducing, inhibiting, or degrading NETs through different mechanisms, such as signaling pathway modulation, or direct DNA hydrolysis. Such effects not only shape the course of envenomation but also reveal novel pathways of innate immune regulation. This review summarizes current knowledge on NET biogenesis, function, and pathological implications, and highlights how animal toxins influence NET formation. We further discuss the therapeutic and biotechnological potential of these molecules as tools to modulate neutrophil-driven inflammation in conditions such as sepsis, cancer, and autoimmunity. By integrating insights from immunology and toxinology, this work points to animal venoms as a promising frontier for the discovery of immunomodulatory agents targeting NETs.

Authors

Institutions

Publication Details

Journal
International Immunopharmacology
Published
2025-11-05
DOI
https://doi.org/10.1016/j.intimp.2025.115758
Primary Topic
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Animal toxins and NETosis: A new frontier in innate immune modulation

Ester Silveira Ramos, Beatriz Vieira, Beatriz de Cássia da Silva Jacob, Manuela B. Pucca et al.
International Immunopharmacology
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
article

Animal toxins and NETosis: A new frontier in innate immune modulation

Ester Silveira Ramos, Beatriz Vieira, Beatriz de Cássia da Silva Jacob, Manuela B. Pucca, Luciano Agati, Isabela Gobbo Ferreira, Isadora Sousa de Oliveira, Guilherme Melo-dos-Santos
article en

Abstract

Neutrophil extracellular traps are molecular structures that play a dual role in host defense and pathology. While NETs effectively capture and neutralize pathogens, excessive or dysregulated NET formation contributes to autoimmune and inflammatory disorders. Animal venoms contain bioactive molecules that can modulate neutrophil functions, including NETosis. They are capable of inducing, inhibiting, or degrading NETs through different mechanisms, such as signaling pathway modulation, or direct DNA hydrolysis. Such effects not only shape the course of envenomation but also reveal novel pathways of innate immune regulation. This review summarizes current knowledge on NET biogenesis, function, and pathological implications, and highlights how animal toxins influence NET formation. We further discuss the therapeutic and biotechnological potential of these molecules as tools to modulate neutrophil-driven inflammation in conditions such as sepsis, cancer, and autoimmunity. By integrating insights from immunology and toxinology, this work points to animal venoms as a promising frontier for the discovery of immunomodulatory agents targeting NETs.

International ImmunopharmacologyVol. 168(Pt 1)
Universidade de São Paulo (BR)
Openalex Percentile: Top 65%
Neutrophil, Myeloperoxidase and Oxidative Mechanisms
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Animal toxins and NETosis: A new frontier in innate immune modulation — Ester Silveira Ramos, Beatriz Vieira, et al. · International Immunopharmacology (2025) | TGRS Research Map | TGRS