Francesco Corbo
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Francesco Corbo has a total of 9 co-authors. Here are the top co-authors by number of shared publications:
- Annunziata Dattola
Department of Clinical Sciences, Sapienza University of Rome, 00185 Rome, Italy
1 shared publication - Camilla Chello
Dermatology Unit, Department of Medical and Cardiovascular Sciences, University of “La Sapienza”, 00161 Rome, Italy
1 shared publication - Diletta Cordelli
Dermatology Unit, Department of Medical and Cardiovascular Sciences, University of “La Sapienza”, 00161 Rome, Italy
1 shared publication - Ester Del Duca
Dermatology Unit, Department of Medical and Cardiovascular Sciences, University of “La Sapienza”, 00161 Rome, Italy
1 shared publication - Fabiana Furci
Provincial Healthcare Unit, Section of Allergology, 89900 Vibo Valentia, Italy
1 shared publication - Giovanni Pellacani
Department of Clinical Sciences, Sapienza University of Rome, 00185 Rome, Italy
1 shared publication
Latest Publications
- Open Access
- 23 June 2026
- Published by MDPI AG in Applied Sciences
- Vol. 16 (13) , 6288
Emerging and Established Therapeutic Strategies for IgE-Mediated Food Allergy
Food allergy is an increasingly prevalent global health condition characterized by immune-mediated reactions to dietary antigens and a substantial clinical burden. Growing understanding of IgE-mediated mechanisms has highlighted the central role of type 2 inflammation, effector-cell activation, and impaired immune regulation. These advances have prompted the development of disease-modifying therapies beyond allergen avoidance. This narrative review summarizes recent advances in the therapeutic management of IgE-mediated food allergy. A structured PubMed search was performed to identify clinical trials, randomized studies, and meta-analyses published within the last five years. Both allergen-specific and non-allergen-specific interventions were evaluated. Current evidence supports oral immunotherapy as the most effective strategy for increasing reaction thresholds and inducing desensitization in peanut, milk, and egg allergies. However, safety concerns remain, and sustained unresponsiveness after treatment discontinuation is achieved inconsistently. Sublingual and epicutaneous immunotherapy show improved safety but lower efficacy. Modified allergen approaches, including baked milk and processed peanut products, may improve tolerability and facilitate immune modulation in selected patients. Biologic therapies, particularly anti-IgE agents, demonstrate efficacy both alone and when combined with immunotherapy. Emerging approaches include peptide vaccines, DNA immunization, microbiome-targeted interventions, and early dietary modulation. These strategies may improve durable immune tolerance through personalized, mechanism-based therapeutic approaches. Future progress will depend on optimizing safety, identifying predictive biomarkers, and integrating multimodal approaches to achieve durable immune tolerance.
- 23 June 2026
- Published by MDPI AG in Applied Sciences
- Vol. 16 (13) , 6288
Open AccessEmerging and Established Therapeutic Strategies for IgE-Mediated Food Allergy
Food allergy is an increasingly prevalent global health condition characterized by immune-mediated reactions to dietary antigens and a substantial clinical burden. Growing understanding of IgE-mediated mechanisms has highlighted the central role of type 2 inflammation, effector-cell activation, and impaired immune regulation. These advances have prompted the development of disease-modifying therapies beyond allergen avoidance. This narrative review summarizes recent advances in the therapeutic management of IgE-mediated food allergy. A structured PubMed search was performed to identify clinical trials, randomized studies, and meta-analyses published within the last five years. Both allergen-specific and non-allergen-specific interventions were evaluated. Current evidence supports oral immunotherapy as the most effective strategy for increasing reaction thresholds and inducing desensitization in peanut, milk, and egg allergies. However, safety concerns remain, and sustained unresponsiveness after treatment discontinuation is achieved inconsistently. Sublingual and epicutaneous immunotherapy show improved safety but lower efficacy. Modified allergen approaches, including baked milk and processed peanut products, may improve tolerability and facilitate immune modulation in selected patients. Biologic therapies, particularly anti-IgE agents, demonstrate efficacy both alone and when combined with immunotherapy. Emerging approaches include peptide vaccines, DNA immunization, microbiome-targeted interventions, and early dietary modulation. These strategies may improve durable immune tolerance through personalized, mechanism-based therapeutic approaches. Future progress will depend on optimizing safety, identifying predictive biomarkers, and integrating multimodal approaches to achieve durable immune tolerance.