Characterization of anti-self CD8 T-cell responses stimulated by recombinant Listeria monocytogenes expressing the melanoma antigen TRP-2

KW Bruhn, N Craft, BD Nguyen, J Yip, JF Miller - Vaccine, 2005 - Elsevier
KW Bruhn, N Craft, BD Nguyen, J Yip, JF Miller
Vaccine, 2005Elsevier
A potential approach to activate tumor-specific T cells is to use live bacterial vectors to
deliver appropriate antigens in a highly immunostimulatory context. We constructed a
recombinant strain of Listeria monocytogenes (rLM) expressing murine tyrosinase-related
protein-2 (TRP-2), a nonmutated melanocyte-derived differentiation antigen highly
expressed in melanomas. Immunization of C57Bl/6 mice with this rLM strain efficiently
primed CD8 T cells to recognize the MHC class I-restricted TRP-2180–188 epitope and …
A potential approach to activate tumor-specific T cells is to use live bacterial vectors to deliver appropriate antigens in a highly immunostimulatory context. We constructed a recombinant strain of Listeria monocytogenes (rLM) expressing murine tyrosinase-related protein-2 (TRP-2), a nonmutated melanocyte-derived differentiation antigen highly expressed in melanomas. Immunization of C57Bl/6 mice with this rLM strain efficiently primed CD8 T cells to recognize the MHC class I-restricted TRP-2180–188 epitope and express IFN-γ upon in vitro peptide stimulation. Peptide-loaded target cells were lysed in vitro by TRP-2-specific T cells in cytotoxicity assays, and mice immunized and boosted with rLM expressing TRP-2 were functionally protected from subcutaneous challenge with B16 melanoma cells. These results identify and characterize the anti-“self” T-cell responses induced by recombinant L. monocytogenes expressing an endogenous, nonmutated tumor antigen.
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