An Inducible Caspase 9 Safety Switch Can Halt Cell Therapy-Induced Autoimmune Disease
Author(s) -
Moniek A. de Witte,
Annelies Jorritsma,
Erwin Swart,
Karin Straathof,
Karin de Punder,
John B.A.G. Haanen,
Cliona M. Rooney,
Ton N. Schumacher
Publication year - 2008
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.180.9.6365
Subject(s) - adoptive cell transfer , cell therapy , effector , immunology , t cell , cell , disease , cancer research , medicine , biology , immune system , genetics
Transfer of either allogeneic or genetically modified T cells as a therapy for malignancies can be accompanied by T cell-mediated tissue destruction. The introduction of an efficient "safety switch" can potentially be used to control the survival of adoptively transferred cell populations and as such reduce the risk of severe graft-vs-host disease. In this study, we have tested the value of an inducible caspase 9-based safety switch to halt an ongoing immune attack in a murine model for cell therapy-induced type I diabetes. The data obtained in this model indicate that self-reactive T cells expressing this conditional safety switch show unimpaired lymphopenia- and vaccine-induced proliferation and effector function in vivo, but can be specifically and rapidly eliminated upon triggering. These data provide strong support for the evaluation of this conditional safety switch in clinical trials of adoptive cell therapy.
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