Sophie Viaud
Affiliations: | California Institute for Biomedical Research |
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Parents
Sign in to add mentorTravis S. Young | post-doc | 2015- | California Institute for Biomedical Research |
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Publications
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Pennell CA, Campbell H, Storlie MD, et al. (2022) Human CD19-specific switchable CAR T-cells are efficacious as constitutively active CAR T-cells but cause less morbidity in a mouse model of human CD19 malignancy. Journal For Immunotherapy of Cancer. 10 |
Viaud S, Ma JSY, Hardy IR, et al. (2018) Switchable control over in vivo CAR T expansion, B cell depletion, and induction of memory. Proceedings of the National Academy of Sciences of the United States of America |
Huang H, Viaud S, Theofilopoulos AN, et al. (2018) AI-04 Immunotherapy for lupus in a mouse model to define pathogenesis and therapeutic targeting Lupus Science & Medicine. 5 |
Besse B, Charrier M, Lapierre V, et al. (2016) Dendritic cell-derived exosomes as maintenance immunotherapy after first line chemotherapy in NSCLC. Oncoimmunology. 5: e1071008 |
Pitt JM, Charrier M, Viaud S, et al. (2014) Dendritic cell-derived exosomes as immunotherapies in the fight against cancer. Journal of Immunology (Baltimore, Md. : 1950). 193: 1006-11 |
Viaud S, Daillère R, Boneca IG, et al. (2014) Gut microbiome and anticancer immune response: really hot Sh*t! Cell Death and Differentiation. 22: 199-214 |
Viaud S, Daillère R, Yamazaki T, et al. (2014) Why should we need the gut microbiota to respond to cancer therapies? Oncoimmunology. 3: e27574 |
Viaud S, Saccheri F, Mignot G, et al. (2013) The intestinal microbiota modulates the anticancer immune effects of cyclophosphamide. Science (New York, N.Y.). 342: 971-6 |
Hannani D, Locher C, Yamazaki T, et al. (2013) Contribution of humoral immune responses to the antitumor effects mediated by anthracyclines. Cell Death and Differentiation. 21: 50-8 |
Viaud S, Ploix S, Lapierre V, et al. (2011) Updated technology to produce highly immunogenic dendritic cell-derived exosomes of clinical grade: a critical role of interferon-γ. Journal of Immunotherapy (Hagerstown, Md. : 1997). 34: 65-75 |