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Caroline Costa

In vivo generation of human CD19‐CAR T cells results in B‐cell depletion and signs of cytokine release syndrome
2018 · Anett Pfeiffer, Frederic B Thalheimer, et al. · EMBO Molecular Medicine · 212
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Mystery solved: VSV-G-LVs do not allow efficient gene transfer into unstimulated T cells, B cells, and HSCs because they lack the LDL receptor
2014 · Fouzia Amirache, Camille Lévy, et al. · Blood · 197
Baboon envelope pseudotyped LVs outperform VSV-G-LVs for gene transfer into early-cytokine-stimulated and resting HSCs
2014 · Anais Girard-Gagnepain, Fouzia Amirache, et al. · Blood · 179
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Stable transduction of quiescent T cells without induction of cycle progression by a novel lentiviral vector pseudotyped with measles virus glycoproteins
2008 · Cecilia Frecha, Caroline Costa, et al. · Blood · 165
Glut1-mediated glucose transport regulates HIV infection
2012 · Séverine Loisel-Meyer, Louise Swainson, et al. · Proceedings of the National Academy of Sciences · 162
Efficient and stable transduction of resting B lymphocytes and primary chronic lymphocyte leukemia cells using measles virus gp displaying lentiviral vectors
2009 · Cecilia Frecha, Caroline Costa, et al. · Blood · 92
Measles Virus Glycoprotein-Pseudotyped Lentiviral Vector-Mediated Gene Transfer into Quiescent Lymphocytes Requires Binding to both SLAM and CD46 Entry Receptors
2011 · Cecilia Frecha, Camille Lévy, et al. · Journal of Virology · 76
Baboon envelope pseudotyped lentiviral vectors efficiently transduce human B cells and allow active factor IX B cell secretion in vivo in NOD/SCIDγc‐/‐ mice
2016 · C. Levy, F. Fusil, et al. · Journal of Thrombosis and Haemostasis · 66
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Expression and Regulation of INTELECTIN1 in Human Granulosa-Lutein Cells: Role in IGF-1-Induced Steroidogenesis Through NAMPT1
2014 · Lucie Cloix, Maxime Reverchon, et al. · Biology of Reproduction · 59
Measles virus envelope pseudotyped lentiviral vectors transduce quiescent human HSCs at an efficiency without precedent
2017 · Camille Lévy, Fouzia Amirache, et al. · Blood Advances · 56
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Baboon Envelope Pseudotyped “Nanoblades” Carrying Cas9/gRNA Complexes Allow Efficient Genome Editing in Human T, B, and CD34+ Cells and Knock-in of AAV6-Encoded Donor DNA in CD34+ Cells
2021 · Alejandra Gutierrez-Guerrero, Maria Jimena Abrey Recalde, et al. · Frontiers in Genome Editing · 51
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Disruption of HIV-1 co-receptors CCR5 and CXCR4 in primary human T cells and hematopoietic stem and progenitor cells using base editing
2021 · Friederike Knipping, Gregory A. Newby, et al. · Molecular Therapy · 48
A Lentiviral Vector Allowing Physiologically Regulated Membrane-anchored and Secreted Antibody Expression Depending on B-cell Maturation Status
2015 · Floriane Fusil, Sara Calattini, et al. · Molecular Therapy · 47
Baboon envelope LVs efficiently transduced human adult, fetal, and progenitor T cells and corrected SCID-X1 T-cell deficiency
2019 · Ornellie Bernadin, Fouzia Amirache, et al. · Blood Advances · 44
Lentiviral Vectors Displaying Modified Measles Virus gp Overcome Pre-existing Immunity in In Vivo-like Transduction of Human T and B Cells
2012 · Camille Lévy, Fouzia Amirache, et al. · Molecular Therapy · 42
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A novel lentiviral vector targets gene transfer into human hematopoietic stem cells in marrow from patients with bone marrow failure syndrome and in vivo in humanized mice
2011 · Cecilia Frecha, Caroline Costa, et al. · Blood · 42
Lentiviral Vector Gene Transfer into Human T Cells
2009 · Els Verhoeyen, Caroline Costa, et al. · Methods in molecular biology · 34
Improved lentiviral vectors for Wiskott–Aldrich syndrome gene therapy mimic endogenous expression profiles throughout haematopoiesis
2008 · C Frecha, M G Toscano, et al. · Gene Therapy · 33
Lentiviral vectors and transduction of human cancer B cells
2010 · Camille Lévy, Cecilia Frecha, et al. · Blood · 19
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Viability and stress protection of chronic lymphoid leukemia cells involves overactivation of mitochondrial phosphoSTAT3Ser727
2014 · C Capron, K Jondeau, et al. · Cell Death and Disease · 17
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Baboon envelope pseudotyped lentiviral vectors: a highly efficient new tool to genetically manipulate T-cell acute lymphoblastic leukaemia-initiating cells
2016 · C Costa, G Hypolite, et al. · Leukemia · 13
A Novel BaEVRless-Pseudotyped γ-Globin Lentiviral Vector Drives High and Stable Fetal Hemoglobin Expression and Improves Thalassemic Erythropoiesis In Vitro
2018 · Ekati Drakopoulou, Maria Georgomanoli, et al. · Human Gene Therapy · 12
Stem Cell Factor-Displaying Simian Immunodeficiency Viral Vectors Together with a Low Conditioning Regimen Allow for Long-Term Engraftment of Gene-Marked Autologous Hematopoietic Stem Cells in Macaques
2012 · Els Verhoeyen, Francis Relouzat, et al. · Human Gene Therapy · 10
Efficient adoptive transfer of autologous modified B cells: a new humanized platform mouse model for testing B cells reprogramming therapies
2021 · Audrey Page, Emilie Laurent, et al. · Cancer Immunology Immunotherapy · 8
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Ligand-modified rAAV6 vectors with nanoblades allow high-level gene knockin in HSPCs without compromising cell survival
2025 · Alejandra Gutierrez-Guerrero, Séverine Périan, et al. · Molecular Therapy — Nucleic Acids · 7
Works count: 41
Citation count: 1,710
H-index: 19
I10-index: 23
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