Research Topics
Species | Gavin M BendleSummaryAffiliation: The Netherlands Cancer Institute Country: The Netherlands Publications
| Collaborators
|
Detail Information
Publications
Preclinical development of T cell receptor gene therapyGavin M Bendle
Division of Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands
Curr Opin Immunol 21:209-14. 2009..Here we discuss in which areas preclinical studies in mouse models can or cannot be expected to be of value to guide clinical trial design, and how the available data from preclinical studies should influence forthcoming clinical trials...
Lethal graft-versus-host disease in mouse models of T cell receptor gene therapyGavin M Bendle
Division of Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands
Nat Med 16:565-70, 1p following 570. 2010..Furthermore, we demonstrate that adjustments in the design of gene therapy vectors and target T cell populations can be used to reduce the risk of TCR gene therapy-induced autoimmune pathology...
Requirements for effective antitumor responses of TCR transduced T cellsMoniek A de Witte
Division of Immunology, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, The Netherlands
J Immunol 181:5128-36. 2008..The strategies outlined in this study should be of value to enhance the antitumor activity of TCR-modified T cells in clinical trials...
T-cell receptor gene therapy: critical parameters for clinical successCarsten Linnemann
Division of Immunology, The Netherlands Cancer Institute, Amsterdam, The Netherlands
J Invest Dermatol 131:1806-16. 2011..This review highlights those strategies that can be followed to develop TCR gene therapy into a clinically relevant treatment option for cancer patients...
TCR gene therapy of spontaneous prostate carcinoma requires in vivo T cell activationMoniek A de Witte
Division of Immunology, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, The Netherlands
J Immunol 181:2563-71. 2008..These results demonstrate the value of TCR gene transfer to target otherwise nonimmunogenic tumor-associated self-Ags provided that adoptive transfer occurs under conditions that allow in vivo expansion of the TCR-modified T cells...
