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Published online first on November 10, 2009
[Cancer Research, 10.1158/0008-5472.CAN-09-2687]
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Recognition and Killing of Brain Tumor Stem-Like Initiating Cells by CD8+ Cytolytic T Cells

Christine E. Brown1, Renate Starr1, Catalina Martinez1, Brenda Aguilar1, Massimo D'Apuzzo2, Ivan Todorov3, Chu-Chih Shih4, Behnam Badie1,5, Michael Hudecek6, Stanley R. Riddell6 and Michael C. Jensen1

Departments of 1 Cancer Immunotherapeutics & Tumor Immunology, 2 Pathology, 3 Diabetes, Endocrinology and Metabolism, and 4 Hematology and Hematopoietic Cell Transplantation and 5 Division of Neurosurgery, Beckman Research Institute, City of Hope National Medical Center, Duarte, California and 6 Program in Immunology, Fred Hutchinson Cancer Research Center, Seattle, Washington

Requests for reprints: Michael C. Jensen, Department of Cancer Immunotherapeutics & Tumor Immunology, City of Hope National Medical Center, Duarte, CA 91010. Phone: 626-256-4673, ext. 68993; Fax: 626-301-8978; E-mail: mjensen{at}coh.org.

Solid tumors contain a subset of stem-like cells that are resistant to the cytotoxic effects of chemotherapy/radiotherapy, but their susceptibility to cytolytic T lymphocyte (CTL) effector mechanisms has not been well characterized. Using a panel of early-passage human brain tumor stem/initiating cell (BTSC) lines derived from high-grade gliomas, we show that BTSCs are subject to immunologic recognition and elimination by CD8+ CTLs. Compared with serum-differentiated CD133low tumor cells and established glioma cell lines, BTSCs are equivalent with respect to expression levels of HLA class I and ICAM-1, similar in their ability to trigger degranulation and cytokine synthesis by antigen-specific CTLs, and equally susceptible to perforin-dependent CTL-mediated cytolysis. BTSCs are also competent in the processing and presentation of antigens as evidenced by the killing of these cells by CTL when antigen is endogenously expressed. Moreover, we show that CTLs can eliminate all BTSCs with tumor-initiating activity in an antigen-specific manner in vivo. Current models predict that curative therapies for many cancers will require the elimination of the stem/initiating population, and these studies lay the foundation for developing immunotherapeutic approaches to eradicate this tumor population. [Cancer Res 2009;69(23):OF1–8]

Key Words: cancer stem cell • brain tumor stem/initiating cell • tumor sphere • CD133 • CD8+ cytolytic T lymphocyte







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Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2009 by the American Association for Cancer Research.