The 'Bacille Calmette-Guerin' (BCG) vaccine has been used throughout most p
arts of the world for the majority of the century. It is safe to use and ch
eap to produce, but there have been increasing doubts about its effectivene
ss. These doubts could not come at a worse time, as tuberculosis (TB) rates
continue to rise, compounded by the AIDS epidemic, and outbreaks of tuberc
ulosis caused by multidrug-resistant strains are more common even in advanc
ed countries. As a result, there is now a concerted research effort to prod
uce new TB vaccine candidates. These include DNA vaccines, recombinant and
auxotrophic vaccines and subunit vaccines, all of which hold promise, The r
eal difficulty will probably arise at the clinical trial level, when a deci
sion must be made either to replace BCG or to boost existing BCG-induced im
munity using these new-generation vaccines.