INTRODUCTION Monoclonal antibodies (mAbs) have recently gained prominence as protein drugs in the treatment of different kinds of cancer. Because of their protein nature, they can be unstable to some stressors during manufacturing, transportation, storage, handling/dilution, and administration. Light can induce chemico-physical changes which can be relevant when amino acids are in the CDRs, as efficacy and safety could be compromised. AIM Chemico-physical stability of Bevacizumab-Avastin® and Durvalumab- Imfinzi®, and their biological activity were evaluated under light doses close to the exposure of mAbs in their real-life. RESULTS Exposure of the diluted mAbs to a dose of sunlight experienced in their real life did not affect their conformation. On the other hand, light was able to induce mAb aggregation, at a higher extent in Bevacizumab than in Durvalumab. The chemical modifications detected on both mAbs revealed low oxidative damage plus deamidations. Chemico-physical modifications on both Bevacizumab and Durvalumab had little effect on their target recognition (VEGF and PDL1, respectively). Furthermore, immunogenic potential in dendritic cells from differentiated monocytes seems absent. CONCLUSIONS The chemico-physical changes induced by real-life doses of light on the tested mAbs are not crucial for the overall protein structure and very low chemical modifications involve amino acids located in the CDRs. Consequently, in vitro target recognition barely decreases. Moreover, the detected aggregation does not seem to induce immunogenicity. AKNOWLEDGEMENTS This project has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement N° 101007939 (RealHOPE).

Impact of light on the chemico-physical and biological properties of two monoclonal antibodies, Bevacizumab (Avastin®) and Durvalumab (Imfinzi®)

Luca Menilli;Patrizia Polverino De Laureto;Giorgia Miolo
Project Administration
2025

Abstract

INTRODUCTION Monoclonal antibodies (mAbs) have recently gained prominence as protein drugs in the treatment of different kinds of cancer. Because of their protein nature, they can be unstable to some stressors during manufacturing, transportation, storage, handling/dilution, and administration. Light can induce chemico-physical changes which can be relevant when amino acids are in the CDRs, as efficacy and safety could be compromised. AIM Chemico-physical stability of Bevacizumab-Avastin® and Durvalumab- Imfinzi®, and their biological activity were evaluated under light doses close to the exposure of mAbs in their real-life. RESULTS Exposure of the diluted mAbs to a dose of sunlight experienced in their real life did not affect their conformation. On the other hand, light was able to induce mAb aggregation, at a higher extent in Bevacizumab than in Durvalumab. The chemical modifications detected on both mAbs revealed low oxidative damage plus deamidations. Chemico-physical modifications on both Bevacizumab and Durvalumab had little effect on their target recognition (VEGF and PDL1, respectively). Furthermore, immunogenic potential in dendritic cells from differentiated monocytes seems absent. CONCLUSIONS The chemico-physical changes induced by real-life doses of light on the tested mAbs are not crucial for the overall protein structure and very low chemical modifications involve amino acids located in the CDRs. Consequently, in vitro target recognition barely decreases. Moreover, the detected aggregation does not seem to induce immunogenicity. AKNOWLEDGEMENTS This project has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement N° 101007939 (RealHOPE).
2025
BOOK OF ABSTRACTS International conference on protein stability – The gap between industry and administration
International conference on protein stability – The gap between industry and administration
   Real World Handling of Protein Drugs-Exploration, Evaluation and Education
   RealHOPE
   -Innovative Medicine Initiative
   -H2020
   -101007939
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/3575337
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