Mona O. Mohsen
University of Bern, University of Oxford, Qatar University
Research areas: Medicine · Infectious Diseases · Immunotherapy and Immune Responses · vaccines and immunoinformatics approaches · SARS-CoV-2 and COVID-19 Research
About
My research interest is focused on cancer immunology/immunotherapy. Specifically, I work on developing therapeutic cancer vaccines, immune-enhancers, checkpoint-inhibitors and other immunotherapeutic approaches for different solid tumours such as breast cancer, melanoma and head/neck carcinoma. I work with virus-like nanoparticles (VLPs) as an efficient platform for vaccine development. Designing and developing universal and also personalised cancer vaccines are of high-interest. I have provided proof-of-concepts (PoCs) for effective therapeutic cancer vaccines and immune-enhancers in different preclinical murine models. I have been awarded several funding grants allowing to finance my own research group. I have also worked during my postdoc period on developing vaccines against infectious diseases such as MERS, Dengue and SARS-CoV-2. During the COVID-19 pandemic, I have been appointed as the head of corona-preclinical development team in Prof. Bachmann's lab where I worked and led the group with great enthusiasm and published several papers, several of them as corresponding author.
Employment
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University of Bern Group Leader2019 - Present
Education
- 2015 - 2018
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Qatar University Master in Biomedical Research2013 - 2015
Projects & Funding
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Personalized, antigen-directed immunotherapy delivered to lymph nodes National Institutes of Health2023 - 2027
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Preclinical efficacy of a personalized therapeutic vaccine to prevent postoperative metastases in mammary carcinoma Jubiläumsstiftung von Swiss Life2023 - 2024
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Nanoparticle Trafficking in Trees Visualized by Virus-Like Particles Swiss Federal Institute for Forest, Snow and Landscape Research2023 - 2025
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Intratumor immunotherapy using TLR7/8 loaded nanoparticles formulated with an inflammasome activating micron-sized particulate adjuvant (MCT) in solid murine tumor models Swiss Cancer League2021 - 2024
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Development and exploration of a novel personalized breast-cancer vaccine based on virus-like particles by incorporating tumor- specific T-cell epitopes Qatar Foundation2019 - 2021
Publications (70)
- Probing novel epitopes on the Plasmodium falciparum circumsporozoite protein for vaccine development Save
- Correction: Rothen et al. Preclinical Evaluation of Novel Sterically Optimized VLP-Based Vaccines against All Four DENV Serotypes. Vaccines 2024, 12, 874 Save
- Preclinical Evaluation of Novel Sterically Optimized VLP-Based Vaccines against All Four DENV Serotypes Save
- Green Routes: Exploring Protein-Based Virus-like Nanoparticle Transport and Immune Activation in Nicotiana benthamiana for Biotechnological Applications Save
- Regulation of pulmonary plasma cell responses during secondary infection with influenza virus Save
- Identifying Key Drivers of Efficient B Cell Responses: On the Role of T Help, Antigen-Organization, and Toll-like Receptor Stimulation for Generating a Neutralizing Anti-Dengue Virus Response Save
- A tetravalent nanovaccine that inhibits growth of HPV-associated head and neck carcinoma via dendritic and T cell activation Save
- Intranodal Injection of Immune Activator Demonstrates Antitumor Efficacy in an Adjuvant Approach Save
- On the role of antibody affinity in the IgE mediated allergic response Save
- The next generation virus-like particle platform for the treatment of peanut allergy. Save
- Alzheimer's Disease: A Brief History of Immunotherapies Targeting Amyloid β. Save
- Vaccination using mutated receptor binding domains of SARS-CoV-2: Evidence for partial immune escape but not serotype formation. Save
- Emerging COVID-19 variants and their impact on SARS-CoV-2 diagnosis, therapeutics and vaccines. Save
- In situ delivery of nanoparticles formulated with micron-sized crystals protects from murine melanoma. Save
- Virus-like particle vaccinology, from bench to bedside. Save
- Virus-Like Particles Are Efficient Tools for Boosting mRNA-Induced Antibodies. Save
- Increased Receptor Affinity and Reduced Recognition by Specific Antibodies Contribute to Immune Escape of SARS-CoV-2 Variant Omicron. Save
- Increased receptor affinity of SARS-CoV-2: a new immune escape mechanism. Save
- Intranasal administration of a virus like particles-based vaccine induces neutralizing antibodies against SARS-CoV-2 and variants of concern. Save
- Increased receptor affinity and reduced recognition by specific antibodies contribute to immune escape of SARS-CoV-2 variant Omicron Save