Over the last few years, some of our experiments in which mycobacterial ant
igens were presented to the immune system as if they were viral antigens ha
ve had a significant impact on our understanding of protective immunity aga
inst tuberculosis. They have also markedly enhanced the prospects for new v
accines. We now know that individual mycobacterial protein antigens can con
fer protection equal to that from live BCG vaccine in mice. A critical dete
rminant of the outcome of immunization appears to be the degree to which an
tigen-specific cytotoxic T cells are generated by the immune response. Our
most recent studies indicate that DNA vaccination is an effective way to es
tablish long-lasting cytotoxic T cell memory and protection against tubercu
losis.