Our studies in mice show that DNA vaccines, initially designed to prevent i
nfection, can have a dramatic therapeutic action too. In heavily infected m
ice, simply by giving DNA vaccination, the immune response can be caused to
switch from one that is relatively inefficient and gives bacterial stasis
to one that kills the bacteria, and persistent bacteria can be eliminated.
Adoptive transfer of protection with I cell clones and in vitro tests of cl
one function indicate that the effects are probably mainly mediated by anti
gen specific CD8+/CD4-/CD44hi T cells that both produce gamma-interferon an
d kill the bacteria during granule-dependent lysis of infected macrophages.
We can speculate that application of such immunotherapy in conjunction wit
h conventional chemotherapeutic antibacterial drugs might result in faster
or more certain cure of the disease in man. Furthermore, similar vaccines u
sed prophylactically and therapeutically might be able to both prevent esta
blishment of this persistent state and eliminate it if it is already establ
ished. (C) 2000 Elsevier Science Ltd. All rights reserved.