2013
DOI: 10.1016/j.bbmt.2012.11.541
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Fully Automated Clinical-Scale Separation of CD133 + Cells From Bone Marrow Aspirate

Abstract: than targeting either alone. Erythropoietin-producing hepatocellular carcinoma-A2 (EphA2)-specific CAR T cells were used to target the A549 tumor cells. EphA2-specific T cells when administered together with FAP-specific T cells, resulted in a significant decrease in tumor growth and increased survival compared to mice that received either EphA2-or FAPspecific T cells alone. Our study underscores the value of cotargeting both CAFs and cancer cells to increase the benefits of T-cell immunotherapy for solid tumo… Show more

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“…On the other hand, BM constitute a rich source of EPC (Hristov et al, 2003). EPCs can initiate neovascularization (Asahara et al, 1997(Asahara et al, , 1999Schatteman and Awad, 2004) and their intraoperative isolation at high yields from BMAC is feasible (Kolvenbach et al, 2010;Essl et al, 2013). In addition, BMAC promotes in vivo bone regeneration by bringing platelets and growth factors such as PDGF-BB and VEGF to the injury site (Hernigou et al, 2005;Holmes et al, 2007;Zhong et al, 2012;Gary et al, 2013).…”
Section: Discussionmentioning
confidence: 99%
“…On the other hand, BM constitute a rich source of EPC (Hristov et al, 2003). EPCs can initiate neovascularization (Asahara et al, 1997(Asahara et al, , 1999Schatteman and Awad, 2004) and their intraoperative isolation at high yields from BMAC is feasible (Kolvenbach et al, 2010;Essl et al, 2013). In addition, BMAC promotes in vivo bone regeneration by bringing platelets and growth factors such as PDGF-BB and VEGF to the injury site (Hernigou et al, 2005;Holmes et al, 2007;Zhong et al, 2012;Gary et al, 2013).…”
Section: Discussionmentioning
confidence: 99%