“…The approaches have included killed virus (Fink & Rauscher, 1964), subunit vaccines (Fischinger et al, 1976;Hunsmann et al, 1975;Hunsmann et al, 1981;Hunsmann, 1985), recombinant vaccinia viruses expressing viral gene products (Earl et al, 1986;Morrison et al 1987), peptide vaccines (Bayer & Hunsman, 1987), and live attenuated viruses. Attenuation was achieved by prolonged passage through tissue culture (Mayyasi & Moloney, 1967;Ruan & Lilly, 1992), or by the use of live pathogenic virus blocked by antiretroviral drugs such as azidothymidin (AZT) and interferon alpha from replicating (Ruprecht et al, 1990(Ruprecht et al, , 1996. When mice were immunized with the SU (gp70, molecular weight 70,000 Dalton) and TM (p15E, molecular weight 15,000 Dalton, E stands for envelope) antigens of the murine leukemia virus (MuLV) substrain Friend leukemia virus (FLV) neutralizing antibodies were induced and protection from disease was reported (Fischinger et al, 1976;Hunsmann et al, 1975;Hunsmann, 1985;Schäfer et al, 1977;Thiel et al, 1987).…”