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Olivier HenryDépartement de génie chimique
Voir sa fiche dans le Répertoire des Expertises de Polytechnique Montréal
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Ansorge, S., Lanthier, S., Transfiguracion, J., Henry, O., & Kamen, A. A. (2011). Monitoring lentiviral vector production kinetics using online permittivity measurements. Biochemical Engineering Journal, 54(1), 16-25. Lien externe
Ansorge, S., Henry, O., Aucoin, M., Voyer, R., Carvell, J. P., & Kamen, A. (juin 2007). Monitoring the Cell Size Distribution of Mammalian Cell Cultures Using On-Line Capacitance Measurements [Communication écrite]. 20th ESACT Meeting, Dresden, Germany. Lien externe
Ansorge, S., Henry, O., & Kamen, A. A. (2010). Recent progress in lentiviral vector mass production. Biochemical Engineering Journal, 48(3), 362-377. Lien externe
Ansorge, S., Lanthier, S., Transfiguracion, J., Durocher, Y., Henry, O., & Kamen, A. (2009). Development of a Scalable Process for High-Yield Lentiviral Vector Production by Transient Transfection of Hek293 Suspension Cultures. Journal of Gene Medicine, 11(10), 868-876. Lien externe
Cambay, F., Forest-Nault, C., Dumoulin, L., Seguin, A., Henry, O., Durocher, Y., & De Crescenzo, G. (2020). Glycosylation of Fcγ receptors influences their interaction with various IgG1 glycoforms. Molecular Immunology, 121, 144-158. Lien externe
Cambay, F., Raymond, C., Brochu, D., Gilbert, M., Tu, T. M., Cantin, C., Lenferink, A., Grail, M., Henry, O., De Crescenzo, G., & Durocher, Y. (2020). Impact of IgG1 N-glycosylation on their interaction with Fc gamma receptors. Current Research in Immunology, 1, 23-37. Lien externe
Cambay, F., Henry, O., Durocher, Y., & De Crescenzo, G. (2019). Impact of N-glycosylation on Fcγ receptor / IgG interactions: unravelling differences with an enhanced surface plasmon resonance biosensor assay based on coiled-coil interactions. mAbs, 11(3), 435-452. Lien externe
Dégardin, M., Liberelle, B., Oliverio, R., Baniahmad, S. F., Darviot, C., Largillière, I., Henry, O., Durocher, Y., Banquy, X., Meunier, M., & De Crescenzo, G. (2023). Coiled-coil-based biofunctionalization of 100 nm gold nanoparticles with the trastuzumab antibody for the detection of HER2-positive cancer cells. Langmuir, 39(34), 12235-12247. Lien externe
Durocher, Y., Toussaint, C., & Henry, O. (mai 2018). Regulation of recombinant protein expression during CHO pool selection enhances high producer frequency [Communication écrite]. Cell Culture Engineering XVI, Tampa, FL. Non disponible
Forest-Nault, C., Koyuturk, I., Gaudreault, J., Pelletier, A., L'Abbé, D., Cass, B., Bisson, L., Burlacu, A., Delafosse, L., Stuible, M., Henry, O., De Crescenzo, G., & Durocher, Y. (2024). A Biosensor Assay Based on Coiled-Coil-Mediated Human ACE2 Receptor Capture for the Analysis of Its Interactions with the SARS-CoV-2 Receptor Binding Domain. Dans Bradfute, S. B. (édit.), Recombinant Glycoproteins: Methods and Protocols (p. 89-105). Lien externe
Forest-Nault, C., Koyuturk, I., Gaudreault, J., Pelletier, A., L'Abbé, D., Cass, B., Bisson, L., Burlacu, A., Delafosse, L., Stuible, M., Henry, O., De Crescenzo, G., & Durocher, Y. (2022). Impact of the temperature on the interactions between common variants of the SARS-CoV-2 receptor binding domain and the human ACE2. Scientific Reports, 12(1), 11520 (11 pages). Lien externe
Forest-Nault, C., Gaudreault, J., Henry, O., Durocher, Y., & De Crescenzo, G. (2021). On the use of surface plasmon resonance biosensing to understand IgG-FcγR interactions. International Journal of Molecular Sciences, 22(12), 6616 (27 pages). Disponible
Gaudreault, J., Forest‐Nault, C., Gilbert, M., Durocher, Y., Henry, O., & De Crescenzo, G. (2024). A low‐temperature SPR‐based assay for monoclonal antibody galactosylation and fucosylation assessment using FcγRIIA/B. Biotechnology and Bioengineering, 121(5), 1659-1673. Disponible
Gaudreault, J., Durocher, Y., Henry, O., & De Crescenzo, G. (2022). Multi-temperature experiments to ease analysis of heterogeneous binder solutions by surface plasmon resonance biosensing. Scientific Reports, 12(1), 14401 (25 pages). Lien externe
Gaudreault, J., Liberelle, B., Durocher, Y., Henry, O., & De Crescenzo, G. (2021). Determination of the composition of heterogeneous binder solutions by surface plasmon resonance biosensing. Scientific Reports, 11(1), 3685 (16 pages). Disponible
Gaudreault, J., Forest-Nault, C., De Crescenzo, G., Durocher, Y., & Henry, O. (2021). On the Use of Surface Plasmon Resonance-Based Biosensors for Advanced Bioprocess Monitoring. Processes, 9(11), 1996 (28 pages). Lien externe
Ghorbaniaghdam, A., Chen, J., Henry, O., & Jolicoeur, M. (2014). Analyzing Clonal Variation of Monoclonal Antibody-Producing CHO Cell Lines Using an In Silico Metabolomic Platform. PLOS One, 9(3). Disponible
Ghorbaniaghdam, A., Henry, O., & Jolicoeur, M. (2014). An in-silico study of the regulation of CHO cells glycolysis. Journal of Theoretical Biology, 357, 112-122. Lien externe
Ghorbaniaghdam, A., Henry, O., & Jolicoeur, M. (2013). A kinetic-metabolic model based on cell energetic state: study of CHO cells behaviour under Na-butyrate stimulation. Bioprocess and Biosystems Engineering, 36(4), 469-487. Lien externe
Ghorbaniaghdam, A., Henry, O., & Jolicoeur, M. (juillet 2010). A kinetic modelling approach to study the role of energy regulatory pathways in CHO cells [Communication écrite]. 11th IFAC Symposium on Computer Applications in Biotechnology, Leuven, Belgium. Publié dans IFAC Proceedings Volumes, 43(6). Lien externe
Henry, O., Karengera, E., Cambay, F., & De Crescenzo, G. (2020). Surface Plasmon Resonance-Based Method for Rapid Product Sialylation Assessment in Cell Culture. Dans Pörtner, R. (édit.), Animal Cell Biotechnology: Methods and Protocols (Vol. 2095, p. 285-293). Lien externe
Henry, O., & Durocher, Y. (2011). Enhanced glycoprotein production in HEK-293 cells expressing pyruvate carboxylase. Metabolic Engineering, 13(5), 499-507. Lien externe
Henry, O., Jolicoeur, M., & Kamen, A. A. (2011). Unraveling the metabolism of HEK-293 cells using lactate isotopomer analysis. Bioprocess and Biosystems Engineering, 34(3), 263-73. Lien externe
Henry, O., & Durocher, Y. (juillet 2010). Engineering of the Human Cell Line HEK-293 to Enhance Recombinant Protein Production [Communication écrite]. 11th IFAC Symposium on Computer Applications in Biotechnology (CAB 2020), Leuven, Belgium. Publié dans IFAC Proceedings Volumes, 43(6). Lien externe
Henry, O., Kwok, E., & Piret, J. M. (2008). Simpler Noninstrumented Batch and Semicontinuous Cultures Provide Mammalian Cell Kinetic Data Comparable to Continuous and Perfusion Cultures. Biotechnology Progress, 24(4), 921-931. Lien externe
Henry, O., Kamen, A., & Perrier, M. (avril 2006). Monitoring the Physiological State of Mammalian Cell Perfusion Processes by on-Line Estimation of Intracellular Fluxes [Communication écrite]. ADCHEM 2006 Symposium, Gramado, Brazil. Publié dans Journal of Process Control, 17(3). Lien externe
Henry, O., Ansorge, S., Aucoin, M., Voyer, R., & Kamen, A. (juin 2007). On-line monitoring of cell size distribution in mammalian cell culture processes [Communication écrite]. 10th IFAC Symposium on Computer Applications in Biotechnology, Cancun, Mexico. Publié dans IFAC Proceedings Volumes, 40(4). Lien externe
Henry, O., Perrier, M., & Kamen, A. (avril 2006). Monitoring the physiological state of mammalian cell perfusion processes by on-line estimation of intracellular fluxes [Communication écrite]. International Symposium on Advanced Control of Chemical Processes, Gramado, Brazil. Lien externe
Henry, O., Perrier, M., & Kamen, A. (2005). Metabolic Flux Analysis of Hek-293 Cells in Perfusion Cultures for the Production of Adenoviral Vectors. Metabolic Engineering, 7(5-6), 467-476. Lien externe
Henry, O. (2004). Caractérisation et modélisation de la production de vecteurs adénoviraux dans un bioréacteur opérant en mode perfusion [Thèse de doctorat, École Polytechnique de Montréal]. Disponible
Henry, O., Dormond, E., Perrier, M., & Kamen, A. (2004). Insights into adenoviral vector production kinetics in acoustic filter-based perfusion cultures. Biotechnology and Bioengineering, 86(7), 765-774. Lien externe
Henry, O., Perrier, M., & Kamen, A. (mars 2004). On-line monitoring of adenovirus production in perfusion cultures [Communication écrite]. 9th International Symposium on Computer Applications in Biotechnology (CAB9), Nancy, France. Lien externe
Henry, O., Perrier, M., & Kamen, A. (septembre 2003). Optimization of adenovirus production in perfusion cultures using an ultrasonic retention device [Communication écrite]. 6th Conference on Protein Expression in Animal Cells, Mont-Tremblant. Non disponible
Karengera, E., Robotham, A., Kelly, J., Durocher, Y., De Crescenzo, G., & Henry, O. (2018). Concomitant reduction of lactate and ammonia accumulation in fed-batch cultures: Impact on glycoprotein production and quality. Biotechnology Progress, 34(2), 494-504. Lien externe
Karengera, E., Robotham, A., Kelly, J., Durocher, Y., De Crescenzo, G., & Henry, O. (2017). Altering the central carbon metabolism of HEK293 cells: Impact on recombinant glycoprotein quality. Journal of Biotechnology, 242, 73-82. Lien externe
Karengera, E., Durocher, Y., De Crescenzo, G., & Henry, O. (2017). Combining metabolic and process engineering strategies to improve recombinant glycoprotein production and quality. Applied Microbiology and Biotechnology, 101(21), 7837-7851. Lien externe
Karengera, E., De Crescenzo, G., Durocher, Y., & Henry, O. (mai 2016). Improving the metabolic efficiency of mammalian cells and its impact on glycoproteins quality [Affiche]. Cell Culture Engineering XV, Palm Spring (CA). Non disponible
Kamen, A., & Henry, O. (2004). Development and optimization of an adenovirus production process. Journal of Gene Medicine, 6(S1), S184-S192. Lien externe
Kamen, A., Henry, O., Jacob, D., & Bernier, A. (mai 2003). Successful development of a robust adenovirus production process primarily relies on a better understanding of packaging cell line physiology and vector replication kinetics [Communication écrite]. 18th ESACT Meeting, Granada, Spain. Lien externe
Lemire, L., Pham, P. L., Durocher, Y., & Henry, O. (2021). Practical Considerations for the Scale-Up of Chinese Hamster Ovary (CHO) Cell Cultures. Dans Cell Culture Engineering and Technology: In appreciation to Professor Mohamed Al-Rubeai (Vol. 10, p. 367-400). Lien externe
Le Ru, A., Jacob, D., Transfiguracion, J., Ansorge, S., Henry, O., & Kamen, A. A. (2010). Scalable Production of Influenza Virus in Hek-293 Cells for Efficient Vaccine Manufacturing. Vaccine, 28(21), 3661-3671. Lien externe
Mellahi, K., Brochu, D., Gilbert, M., Perrier, M., Ansorge, S., Durocher, Y., & Henry, O. (2019). Assessment of fed-batch cultivation strategies for an inducible CHO cell line. Journal of Biotechnology, 298, 45-56. Lien externe
Mellahi, K., Cambay, F., Brochu, D., Gilbert, M., Perrier, M., Ansorge, S., Durocher, Y., & Henry, O. (2019). Process development for an inducible rituximab-expressing Chinese hamster ovary cell line. Biotechnology Progress, 35(1), e2742. Lien externe
Mellahi, K., Brochu, D., Gilbert, M., Perrier, M., Ansorge, S., Durocher, Y., & Henry, O. (2019). Process intensification for the production of rituximab by an inducible CHO cell line. Bioprocess and Biosystems Engineering, 42(5), 711-725. Lien externe
Nadeau, I., Henry, O., Jacob, D., Perrier, M., & Kamen, A. (juin 2001). Effect of Medium Composition on the 293SF Central Metabolic Fluxes during Growth and Infection with Adenovirus [Communication écrite]. 8th International Symposium on Computer Applications in Biotechnology (CAB8), Québec City, Qc. Non disponible
Reyes, S.‐J., Pham, P. L., Durocher, Y., & Henry, O. (2024). CHO stable pool fed-batch process development of SARS-CoV-2 spike protein production: Impact of aeration conditionsand feeding strategies. Biotechnology Progress, 3507 (20 pages). Disponible
Reyes, S.‐J., Lemire, L., Roy, M., LʹÉcuyer-Coelho, H., Martynova, Y., Cass, B., Voyer, R., Durocher, Y., Henry, O., Pham, P. L., & Molina, R.-S. (2024). Multivariate data analysis of process parameters affecting the growth and productivity of stable Chinese hamster ovary cell pools expressing SARS‐CoV‐2 spike protein as vaccine antigen in early process development. Biotechnology Progress, e3467 (19 pages). Disponible
Reyes, S. J., Durocher, Y., Pham, P. L., & Henry, O. (2022). Modern Sensor Tools and Techniques for Monitoring, Controlling, and Improving Cell Culture Processes. Processes, 10(2), 189 (36 pages). Lien externe
Riahi, N., Murschel, F., Lerouge, S., Durocher, Y., Henry, O., & De Crescenzo, G. (2017). Bioavailability of immobilized epidermal growth factor: Covalent versus noncovalent grafting. Biointerphases, 12(1), 010501 (8 pages). Lien externe
Riahi, N., Liberelle, B., Henry, O., & De Crescenzo, G. (2017). Impact of RGD amount in dextran-based hydrogels for cell delivery. Carbohydrate Polymers, 161, 219-227. Lien externe
Riahi, N., Cappadocia, L., Henry, O., Omichinski, J., & De Crescenzo, G. (2016). Soluble expression, purification and functional characterization of a coil peptide composed of a positively charged and hydrophobic motif. Amino Acids, 48(2), 567-577. Lien externe
Serafin, B., Kamen, A., De Crescenzo, G., & Henry, O. (2024). Impact of Lectin Biotinylation for Surface Plasmon Resonance and Enzyme-Linked Lectin Assays for Protein Glycosylation. Analytical Biochemistry, 115693 (9 pages). Lien externe
Silva, C. A. T., Kamen, A., & Henry, O. (2024). Fed-batch strategies for intensified rVSV vector production in high cell density cultures of suspension HEK293 cells. Biotechnology Progress, 3506 (9 pages). Disponible
Serafin, B., Kamen, A., De Crescenzo, G., & Henry, O. (2024). Antibody-independent surface plasmon resonance assays for influenza vaccine quality control. Applied Microbiology and Biotechnology, 108(1), 307 (10 pages). Disponible
Silva, C. A. T., Kamen, A. A., & Henry, O. Intensified Influenza Virus Production in Suspension HEK293SF Cell Cultures Operated in Fed-Batch or Perfusion with Continuous Harvest [Communication écrite]. Non spécifié (19 pages). Lien externe
Silva, C. A. T., Kamen, A. A., & Henry, O. (juin 2022). Intensification of influenza virus production in fed-batch and perfusion cultures of HEK293SF cells [Communication écrite]. Vaccine Technology VIII, Stiges, Spain. Lien externe
Silva, C. A. T., Kamen, A. A., & Henry, O. (2021). Recent advances and current challenges in process intensification of cell culture-based influenza virus vaccine manufacturing. Canadian Journal of Chemical Engineering, 99(11), 2525-2535. Lien externe
Sheikholeslami, Z., Jolicoeur, M., & Henry, O. (2014). Elucidating the effects of postinduction glutamine feeding on the growth and productivity of CHO cells. Biotechnology Progress, 30(3), 535-546. Lien externe
Sheikholeslami, Z., Jolicoeur, M., & Henry, O. (2013). The impact of the timing of induction on the metabolism and productivity of CHO cells in culture. Biochemical Engineering Journal, 79, 162-171. Lien externe
Sheikholeslami, Z., Jolicoeur, M., & Henry, O. (2013). Probing the metabolism of an inducible mammalian expression system using extracellular isotopomer analysis. Journal of Biotechnology, 164(4), 469-478. Lien externe
Toussaint, C., Henry, O., & Durocher, Y. (2016). Metabolic engineering of CHO cells to alter lactate metabolism during fed-batch cultures. Journal of Biotechnology, 217(C), 122-131. Disponible
Thompson, C. M., Petiot, E., Mullick, A., Aucoin, M. G., Henry, O., & Kamen, A. A. (2015). Critical assessment of influenza VLP production in Sf9 and HEK293 expression systems. BMC Biotechnology, 15(1). Disponible
Thompson, C. M., Petiot, E., Aucoin, M. G., Henry, O., & Kamen, A. A. (juin 2013). Developing a production process for influenza VLPs: a comparison between HEK 293SF and Sf9 production platforms [Affiche]. 23rd European Society for Animal Cell Technology Meeting (ESACT 2013), Lille, France (2 pages). Publié dans BMC Proceedings, 7(S6). Disponible
Thompson, C. M., Petiot, E., Lennaertz, A., Henry, O., & Kamen, A. A. (2013). Analytical technologies for influenza virus-like particle candidate vaccines: challenges and emerging approaches. Virology Journal, 10(1). Disponible
Venereo-Sanchez, A., Fulton, K., Koczka, K., Twine, S., Chahal, P., Ansorge, S., Gilbert, R., Henry, O., & Kamen, A. (2019). Characterization of influenza H1N1 Gag virus-like particles and extracellular vesicles co-produced in HEK-293SF. Vaccine, 37(47), 7100-7107. Lien externe
Venereo-Sanchez, A., Simoneau, M., Lanthier, S., Chahal, P., Bourget, L., Ansorge, S., Gilbert, R., Henry, O., & Kamen, A. (2017). Process intensification for high yield production of influenza H1N1 Gag virus-like particles using an inducible HEK-293 stable cell line. Vaccine, 35(33), 4220-4228. Lien externe
Venereo-Sanchez, A., Gilbert, R., Simoneau, M., Caron, A., Chahal, P., Chen, W., Ansorge, S., Li, X., Henry, O., & Kamen, A. (2016). Hemagglutinin and neuraminidase containing virus-like particles produced in HEK-293 suspension culture: An effective influenza vaccine candidate. Vaccine, 34(29), 3371-3380. Lien externe
Vallee, C., Durocher, Y., & Henry, O. (2014). Exploiting the metabolism of PYC expressing HEK293 cells in fed-batch cultures. Journal of Biotechnology, 169(1), 63-70. Lien externe
Yang, Z., Xu, X., Silva, C. A. T., Farnos, O., Venereo-Sanchez, A., Toussaint, C., Dash, S., Gonzalez-Dominguez, I., Bernier, A., Henry, O., & Kamen, A. (2022). Membrane chromatography-based downstream processing for cell-culture produced influenza vaccines. Vaccines, 10(8), 1310 (13 pages). Lien externe
