A study was done to investigate possible late central nervous system (CNS) complications of latent measles infection in hamsters. Signs of CNS disease, consisting of myoclonus and paralysis, occurred in some weanling hamsters inoculated intraperitoneally at 3 or 9 days of age with antithymocyte serum (ATS) and measles virus, but no late complications in adult life attributable to measles virus were seen. A single series of ATS injections plus an injection of measles virus resulted in sustained antibody formation postulated due to establishment of a latent viral infection, whereas similar treatment with normal rabbit serum plus virus caused no or minimal antibody response. The majority of hamsters receiving ATS as newborns and ATS plus virus as weanlings also did not produce antibody. This differential effect of ATS may be due to combined elimination of suppressor and helper cells in the latter ATS-treated group and of suppressor cells only in the former ATS-treated group. Cellular immunity could not be evaluated since lymphocytes from inoculated and uninoculated hamsters released equal and variable amounts of 5'Cr for both infected and noninfected labeled, allogeneic hamster target cells.The immunological implications in the pathogenesis of subacute sclerosing panencephalitis (SSPE) induced by latent measles virus infection of the central nervous system (CNS) are not clear at present. Antibody titers to measles virus in serum and cerebrospinal fluid at the time of recognized CNS disease are elevated by all criteria tested. There is less unanimity in reports on cellular immunity (14). Some studies indicate a reduced cellular response (8,11,12,17,21); others indicate a normal response (13,16,19,20). We (9), among others (6, 7), have attempted to develop an animal model to permit study of the immunological factors operative in the disease and in the viral infection. Antithymocyte serum (ATS) treatment of newborn hamsters rendered them susceptible to intraperitoneal (i.p.) injection of an SSPE strain of measles virus (Lec), a route of injection to which the untreated hamster is resistant. Such ATS-treated animals developed delayed overt signs of CNS involvement 3 weeks after virus inoculation. Only a small number ofthe treated hamsters survived, and with time these developed high titers of circulating antibody to measles virus, suggesting development ofa chronic, latent viral infection. Virus was isolated from the ATS-treated hamsters with CNS disease, but not from the survivors tested.