Tissue invasion and pathology by Trypanosoma cruzi result from an interacti
on between parasite virulence and host immunity. Successive in vivo generat
ions of the parasite select populations with increasing ability to invade t
he host. Conversely, prolonged in vitro selection of the parasite produces
attenuated sublines with low infectivity for mammals. One such subline (TCC
clone) has been extensively used in our laboratory as experimental vaccine
and tested in comparative experiments with its virulent ancestor (TUL). Th
e experiments here reviewed aimed at the use of immunodeficient mice for te
sting the infectivity of TCC parasites. It has not been possible to obtain
virulent, revertant sublines by prolonged passaged in such mice.