TY - JOUR
T1 - Melittin in AllergoOncology
T2 - From Honey Bee Venom to Anti-Cancer Therapeutic Innovation—An EAACI Position Paper
AU - Jimenez-Rodriguez, Teodorikez Wilfox
AU - Ahmetaj, Luljeta
AU - Alfaya Arias, Teresa
AU - Boni, Elisa
AU - Bugadze, Lali
AU - Chauhan, Jitesh
AU - De Las Vecillas, Leticia
AU - Ferastraoaru, Denisa
AU - Izquierdo, Elena
AU - Karagiannis, Sophia N.
AU - Levi-Schaffer, Francesca
AU - Norelli, Francesca
AU - Nuñez-Borque, Emilio
AU - Pascal, Mariona
AU - Poli, Aurélie
AU - Vachová, Martina
AU - Vega Castro, Arantza
AU - Zurlo, Marco
AU - Breynaert, Christine
N1 - © 2026 European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd.
PY - 2026/6/23
Y1 - 2026/6/23
N2 - Honey bee venom (HBV) represents a unique interface between allergy and oncology, exemplifying how allergen-derived molecules can be repurposed as anti-cancer agents. Melittin, the principal component of HBV, accounts for 40%–50% of its dry weight and is responsible for most of its biological activity. Beyond its well-established role as a potent allergen and mast cell activator, melittin displays broad anti-tumour properties across multiple cancer models. Preclinical evidence demonstrates that melittin induces cancer cell death through membrane disruption, mitochondrial and death receptor–mediated apoptosis, ferroptosis, and inhibition of key oncogenic pathways, including PI3K/Akt/mTOR, NF-κB, and HIF-1α/VEGF signalling. Additional effects include suppression of angiogenesis, epithelial–mesenchymal transition, invasion, and metastatic dissemination, as well as modulation of the tumour immune microenvironment. However, the clinical translation of melittin is limited by its intrinsic haemolytic activity, systemic toxicity, and high allergenic potential. Advances in nanotechnology, targeted delivery systems, and venom-inspired peptide engineering are addressing these barriers, enabling tumour-selective delivery while reducing off-target effects. This EAACI Task Force Position Paper integrates current evidence on melittin within the emerging field of AllergoOncology. It highlights its dual relevance for allergists and oncologists and outlines the translational challenges to be overcome and opportunities to enable safe clinical application.
AB - Honey bee venom (HBV) represents a unique interface between allergy and oncology, exemplifying how allergen-derived molecules can be repurposed as anti-cancer agents. Melittin, the principal component of HBV, accounts for 40%–50% of its dry weight and is responsible for most of its biological activity. Beyond its well-established role as a potent allergen and mast cell activator, melittin displays broad anti-tumour properties across multiple cancer models. Preclinical evidence demonstrates that melittin induces cancer cell death through membrane disruption, mitochondrial and death receptor–mediated apoptosis, ferroptosis, and inhibition of key oncogenic pathways, including PI3K/Akt/mTOR, NF-κB, and HIF-1α/VEGF signalling. Additional effects include suppression of angiogenesis, epithelial–mesenchymal transition, invasion, and metastatic dissemination, as well as modulation of the tumour immune microenvironment. However, the clinical translation of melittin is limited by its intrinsic haemolytic activity, systemic toxicity, and high allergenic potential. Advances in nanotechnology, targeted delivery systems, and venom-inspired peptide engineering are addressing these barriers, enabling tumour-selective delivery while reducing off-target effects. This EAACI Task Force Position Paper integrates current evidence on melittin within the emerging field of AllergoOncology. It highlights its dual relevance for allergists and oncologists and outlines the translational challenges to be overcome and opportunities to enable safe clinical application.
KW - allergy
KW - bee venom
KW - cancer
KW - hypersensitivity
KW - melittin
UR - https://www.scopus.com/pages/publications/105042588385
UR - https://pubmed.ncbi.nlm.nih.gov/42337945/
U2 - 10.1111/all.70421
DO - 10.1111/all.70421
M3 - Article
C2 - 42337945
AN - SCOPUS:105042588385
SN - 0105-4538
JO - Allergy: European Journal of Allergy and Clinical Immunology
JF - Allergy: European Journal of Allergy and Clinical Immunology
ER -