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The Journal of Immunology, 2004, 173: 5445-5450.
Copyright © 2004 by The American Association of Immunologists

B7-H3 Enhances Tumor Immunity In Vivo by Costimulating Rapid Clonal Expansion of Antigen-Specific CD8+ Cytolytic T Cells1

Liqun Luo*, Andrei I. Chapoval*, Dallas B. Flies*, Gefeng Zhu*, Fumiya Hirano*, Shengdian Wang*, Julie S. Lau*, Haidong Dong*, Koji Tamada*, Andrew S. Flies*, Yang Liu{dagger} and Lieping Chen2,*

* Department of Immunology, Mayo Clinic, Rochester, MN 55905; and {dagger} Department of Pathology, Ohio State University Medical Center, Columbus, OH 43210

B7-H3 is a B7 family molecule with T cell costimulatory function in vitro. The in vivo role of B7-H3 in the stimulation of tumor immunity is unclear. We report here that expression of B7-H3 by transfection of the mouse P815 tumor line enhances its immunogenicity, leading to the regression of tumors and amplification of a tumor-specific CD8+ CTL response in syngeneic mice. Tumor cells engineered to express B7-H3 elicit a rapid clonal expansion of P1A tumor Ag-specific CD8+ CTL in lymphoid organs in vivo and acquire the ability to directly stimulate T cell growth, division, and development of cytolytic activity in vitro. Our results thus establish a role for B7-H3 in the costimulation of T cell immune responses in vivo.




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