Tolerance or immunity to a tumor antigen expressed in somatic cells can be determined by systemic proinflammatory signals at the time of first antigen exposure

IH Frazer, RD Kluyver, GR Leggatt… - The Journal of …, 2001 - journals.aai.org
IH Frazer, RD Kluyver, GR Leggatt, H Yang Guo, L Dunn, O White, C Harris, A Liem…
The Journal of Immunology, 2001journals.aai.org
Mice transgenic for the E7 tumor Ag of human papillomavirus type 16, driven from a keratin
14 promoter, express E7 in keratinocytes but not dendritic cells. Grafted E7-transgenic skin
is not rejected by E7-immunized mice that reject E7-transduced transplantable tumors.
Rejection of recently transplanted E7-transgenic skin grafts, but not of control nontransgenic
grafts or of established E7-transgenic grafts, is induced by systemic administration of live or
killed Listeria monocytogenes or of endotoxin. Graft recipients that reject an E7 graft reject a …
Abstract
Mice transgenic for the E7 tumor Ag of human papillomavirus type 16, driven from a keratin 14 promoter, express E7 in keratinocytes but not dendritic cells. Grafted E7-transgenic skin is not rejected by E7-immunized mice that reject E7-transduced transplantable tumors. Rejection of recently transplanted E7-transgenic skin grafts, but not of control nontransgenic grafts or of established E7-transgenic grafts, is induced by systemic administration of live or killed Listeria monocytogenes or of endotoxin. Graft recipients that reject an E7 graft reject a subsequent E7 graft more rapidly and without further L. monocytogenes exposure, whereas recipients of an E7 graft given without L. monocytogenes do not reject a second graft, even if given with L. monocytogenes. Thus, cross-presentation of E7 from keratinocytes to the adaptive immune system occurs with or without a proinflammatory stimulus, but proinflammatory stimuli at the time of first cross-presentation of Ag can determine the nature of the immune response to the Ag. Furthermore, immune effector mechanisms responsible for rejection of epithelium expressing a tumor Ag in keratinocytes are different from those that reject an E7-expressing transplantable tumor. These observations have implications for immunotherapy for epithelial cancers.
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