Nonhuman primates appear to have significant advantages over conventional l
aboratory animals in terms of modeling pulmonary tuberculosis for purposes
of vaccine evaluation. Primates are quite susceptible to infection by the a
erosol route, develop a humanlike disease, exhibit antigen-induced T lympho
cyte reactivity both in vitro and in vivo, and can be protected quite effec
tively by bacille Calmette-Guerin vaccination. There are fewer than a dozen
published studies of experimental tuberculosis in primates, and all of the
available data on the response of primates to vaccination have been genera
ted in rhesus monkeys (Macaca mulatta). There have been no modern immunolog
ic studies of primate tuberculosis. Thus, responses to tuberculosis vaccine
s in primates are only minimally characterized, and much additional baselin
e work remains to be done before the responses to new vaccines can be place
d in the proper biological context.