Author

C. Fenwick

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Immunology· 2 Microbiology· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:host-pathogen & immune response· 4 Organism:human· 4 Assay:proteomics· 3 Research Focus:drug response / drug discovery· 1 Assay:flow cytometry· 1 Organism:non-human primate· 1 Approach:wet-lab / biochemical assay· 1

Frequent Co-Authors

G. Pantaleo· 4 shared c. raclot· 3 shared D. Trono· 3 shared P. Turelli· 3 shared A. Farina· 2 shared C. Herate· 2 shared C. S.-Y. Foo· 2 shared F. Fiscalini· 2 shared

Activity by Year

2018-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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4 shared papersMicrobiology

G. Pantaleo

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

ACE2 mimetic antibody potently neutralizes all SARS-CoV-2 variants and fully protects in XBB.1.5 challenged monkeys

C. Fenwick, P. Turelli, Y. Duhoo, K. Lau, C. Herate, R. Marlin, M. Lamrayah, J. Campos, L. Leuenberger, A. Farina, c. raclot, V. Genet, F. Fiscalini, J. Cesborn, L. Perez, , G. Pantaleo

bioRxiv · Jul 18, 2023 · PreprintMicrobiology

P2G3 human monoclonal antibody neutralizes SARS-CoV-2 Omicron subvariants including BA.4 and BA.5 and Bebtelovimab escape mutants

P. Turelli, C. Fenwick, C. Raclot, V. Genet, G. Pantaleo, D. Trono

bioRxiv · Jul 28, 2022 · PreprintMicrobiology

SARS-CoV-2 Omicron potently neutralized by a novel antibody with unique Spike binding properties

C. Fenwick, P. Turelli, D. Ni, L. Perez, K. Lau, E. Lana, C. Pellaton, C. Raclot, L. Esteves-Leuenberger, J. Campos, A. Farina, F. Fiscalini, C. Herate, R. Marlin, R. Abdelnabi, , G. Pantaleo

This paper identifies a potent human monoclonal antibody, P2G3, that neutralizes multiple SARS-CoV-2 variants including Omicron, and demonstrates its protective efficacy in a monkey model.

bioRxiv · Mar 18, 2022 · PreprintImmunology

CD32+ and PD-1+ Lymph Node CD4 T Cells Support Persistent HIV-1 Transcription in Treated Aviremic Individuals

A. Noto, F. Procopio, R. Banga, M. Suffiotti, J.-M. Corpataux, M. Cavassini, C. Fenwick, R. Gottardo, M. Perreau, G. Pantaleo

This study identifies CD32+ CD4 T cells in lymph nodes as a population with persistent HIV-1 transcription, with CD32+PD-1+ cells showing the highest levels in both viremic and treated individuals.

bioRxiv · May 24, 2018Immunology