@article{gareau_sekiguchi_warry_ripoll_sullivan_westfall_chretin_fulton_harkey_storb_et al._2022, title={Allogeneic peripheral blood haematopoietic stem cell transplantation for the treatment of dogs with high-grade B-cell lymphoma}, ISSN={["1476-5829"]}, DOI={10.1111/vco.12847}, abstractNote={Abstract}, journal={VETERINARY AND COMPARATIVE ONCOLOGY}, author={Gareau, Alexandra and Sekiguchi, Toko and Warry, Emma and Ripoll, Alexandra Z. and Sullivan, Edmund and Westfall, Theresa and Chretin, John and Fulton, Lisa M. and Harkey, Michael and Storb, Rainer and et al.}, year={2022}, month={Jul} }
 @article{culler_vigani_ripoll_gareau_suter_2022, title={Centrifugal therapeutic plasma exchange in dogs with immune-mediated hemolytic anemia (2016-2018): 7 cases}, ISSN={["1476-4431"]}, DOI={10.1111/vec.13196}, abstractNote={Abstract}, journal={JOURNAL OF VETERINARY EMERGENCY AND CRITICAL CARE}, author={Culler, Christine A. and Vigani, Alessio and Ripoll, Alexandra Z. and Gareau, Alexandra and Suter, Steven E.}, year={2022}, month={May} }
 @article{gareau_ripoll_suter_2021, title={A Retrospective Analysis: Autologous Peripheral Blood Hematopoietic Stem Cell Transplant Combined With Adoptive T-Cell Therapy for the Treatment of High-Grade B-Cell Lymphoma in Ten Dogs}, volume={8}, ISSN={["2297-1769"]}, DOI={10.3389/fvets.2021.787373}, abstractNote={In humans, a type of cellular immunotherapy, called adoptive T cell transfer (ACT), can elicit curative responses against hematological malignancies and melanoma. ACT using ex vivo expanded peripheral blood T-cells after multiagent chemotherapy enhances tumor-free survival of dogs with B-cell lymphoma (LSA). Since 2008, our group has been performing autologous peripheral blood hematopoietic stem cell transplants (autoPBHSCT) for the treatment of canine high-grade B-cell LSA, although relapse of residual disease is a common cause of reduced survival in ~70% of treated dogs. We reasoned that a more aggressive treatment protocol combining CHOP (cyclophosphamide, doxorubicin, vincristine, prednisone) chemotherapy, autoPBHSCT, and ACT to treat 10 dogs with B-cell LSA could lead to better outcomes when compared to dogs treated with CHOP chemotherapy and autoPBHSCT alone. Using this protocol, once dogs achieved complete hematologic reconstitution post-autoPBHSCT, CD3+ CD8+ and CD3+CD4+ T-cells were expanded from the peripheral blood at a commercial laboratory. Two to four ACT infusions were given to each dog, with a total of 23 infusions given. Infusions were administered with no complications or adverse events. The median cell dose for all infusions was 5.62 x 106 cells/kg (range: 2.59 x 106-8.55 x 106 cells/kg). 4/10 (40%) of dogs were cured of their disease (defined as disease-free for ≥2 years post-autoPBHSCT). Our results confirm that the autoPBHSCT protocol did not hinder the in vitro expansion of autologous peripheral blood T-cells and that the final product could be administered safely, with no adverse events recorded. Finally, since only ten dogs were treated, our results can only suggest that the administration of ACT to dogs after multiagent chemotherapy and autoPHSCT did not lead to a statistically significant increase in median disease-free interval and overall survival when compared to dogs who received CHOP chemotherapy and autoPHSCT alone.}, journal={FRONTIERS IN VETERINARY SCIENCE}, author={Gareau, Alexandra and Ripoll, Alexandra Z. and Suter, Steven E.}, year={2021}, month={Dec} }