more palatable to the monkeys than was a dry ration. The ration was offered in small amounts, about 50 g, 3 times daily. Control animals received the 18% casein basal ( 7). I n the first experiment, a group of 9 monkeys was placed on the basal ration containing 2 % 6-R4T and 0.05% dl-tryptophan for 7 days: and on the 8th, 9th-and 10th days this group and a control group of 9 monkeys were fed a total of 120 ml of 10% virus suspension (about 1,200,000 intracerebral LD50) in 6 doses of 20 ml each. Temperatures were recorded daily and the animals were observed for signs of disease twice daily. Three weeks after the first virus feeding the surviving animals were placed on the 18% casein basal diet. The results are recorded in Table I. Exp. 2 and 3 (Table I) were similar except that 1) the 2% 6-MT ration was not supplemented with tryptophan and 2 ) the monkeys received two feedings of 20 ml of a 1:400 dilution (approximately 1 0,000 intracerebral LDS0) from the same pool of Wisconsin '45 virus on the eighth day of the experiment. The surviving animals of all 3 experiments were challenged intracerebrally with 500 LDZo IVisconsin '45 virus 6-9 weeks after their oral exposure.In Exp. 1, there was a suggestion of protection against the virus in the 6-MT group, i.e., incubation periods were longer, febrile prodromata less pronounced and two animals escaped paralytic infection. These 2 animals, KO. 3 and 4, apparently did experience an inapparent infection for they resisted a large intracerebral challenge 9 weeks later, I n the second and third experiments, the smaller inoculum resulted in a lower incidence of paralytic infection in the controls, 8/10 and 4/9 respectively, while only one of the 20 animals receiving 6-MT became paralyzed. The surviving animals in the latter experiment succumbed to intracerebral challenge.Summary. These experiments are obviously of a preliminary nature but they do show that the susceptibility of a primate to poliomyelitis via a natural portal of entry may be altered and they suggest that this approach to the modification of susceptibility to poliomyelitis should be explored further.