In this article, we describe several never genetic vaccination strategies d
esigned to facilitate the development of different types of immune response
s. These include: i) the consecutive use of DNA and fowlpoxvirus vectors in
"prime-boost" strategies which induce greatly enhanced and sustained level
s of both cell-mediated immunity and humoral immunity, including mucosal re
sponses; ii) the co-expression of genes encoding cytokines and cell-surface
receptors, and the use of immunogenic carrier molecules, for immune modula
tion and/or improved targeting of vector-expressed vaccine antigens; and ii
i) the expression of minimal immunogenic amino add sequences, particularly
cytotoxic CD8(+) T-cell determinants, in "polytope" vector vaccines. The ca
pacity to modulate and enhance specific immune responses by the use of appr
oaches such as these may underpin the development of vaccines against disea
ses for which no effective strategies are currently available.