Cutting Edge: Tumor Secreted Heat Shock-Fusion Protein Elicits CD8 Cells for Rejection

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  • Koichi Yamazaki
    Department of Microbiology and Immunology, University of Miami School of Medicine, Miami, FL 33101
  • Timmy Nguyen
    Department of Microbiology and Immunology, University of Miami School of Medicine, Miami, FL 33101
  • Eckhard R. Podack
    Department of Microbiology and Immunology, University of Miami School of Medicine, Miami, FL 33101

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<jats:title>Abstract</jats:title><jats:p>The endoplasmic reticulum resident heat shock protein gp96 chaperons peptides, including those derived from tumor Ags, on their way to presentation by MHC class I. Replacement of the endoplasmic reticulum retention signal of gp96 with the Fc portion of murine IgG1 generated a secretory form of gp96, gp96-Ig. Tumor cells secreting gp96-Ig exhibited decreased tumorigenicity and increased immunogenicity in vivo and were rejected after initial growth. Rejection required CD8 T cells during the priming and effector phase. CD4 T cells were not required for rejection in either phase. Carrageenan, a compound known to inactivate macrophages in vivo, did not diminish CD8-mediated tumor rejection. Therefore, immunization with tumors secreting gp96-Ig generates efficient tumor-rejecting CD8 CTL without requirement for CD4 or macrophage help. In contrast, immunization with purified, tumor-derived gp96 or with irradiated tumor cells requires both.</jats:p>

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