DNA vaccination as a tool to identify subdominant CD8 T cell epitopes

DNA vaccination is highly efficient at inducing CD8(+) T cell responses in animal models. Here we investigated whether DNA vaccine technology could be exploited to identify subdominant cytotoxic T lymphocytes (CTL) epitopes. Previous studies have shown that the Sendai virus HN protein does not induc e a CD8(+) T cell response in C57BL/6 mice. Thus, we vaccinated C57BL/6 mic e with a DNA vaccine encoding Sendai virus hemagglutinin neuraminidase (HN) protein. The data show that this strategy elicited a potent D-b-restricted CD8(+) CTL response against at least one subdominant HN-derived epitope. T hese CTL were able to lyse Sendai virus-infected target cells, demonstratin g that the epitope was appropriately processed and present at sufficient le vels for T cell recognition. However, these cells did not confer protection against lethal challenge with Sendai virus. These data demonstrate the cap acity of DNA vaccine to raise CTL responses to subdominant epitopes, but sh ow that such responses may be limited in their efficacy against non-persist ent viruses. (C) 1999 Elsevier Science Ltd. All rights reserved.