“…when compared with their non-Down's institutionalised peers (Blumberg & Alter 1965, Blumberg et al 1967, Sutnick et al 1968). These findings have been confirmed by a number of studies (Krugman & Giles 1970, Skinhoj et al 1971, Chance 1972, Hollinger et al 1972, Boughton & Hawkes 1973, Rundle et al 1975). Blumberg et al (1970) have suggested that the Down's patients were either uniquely susceptible to the virus or retained the agent chronically due to an inherited immunologic defect possibly involving impaired lymphocyte function.…”