
In controlling retrovirus infection and replication, cell-mediated immunity (CMI) is considered to be effective. To develop a synthetic peptide vaccine capable of inducing CMI, mannan-coated liposome encapsulating 20-mer synthetic peptide, spanning the 98-117 amino acids of bovine leukemia virus (BLV) envelope glycoprotein (Env) gp51 was constructed and inoculated to BALB/c mice. The liposome induced specific delayed-type hypersensitivity, lymphocyte proliferative responses, and a weak cytotoxic lymphocyte response. The spleen cells from the immunized mice produced a large amount of IFN-gamma and IL-2, whereas they released neither IL-4 or IL-10. Mannan-coated liposome containing two kinds of peptides (the 121-140 and 142-161 regions of BLV Env gp51) also induced peptide-specific lymphocyte proliferative response and IFN-g production in C57BL/6 mice. Thus, the synthetic T-cell epitope peptide-liposome system augmented a strong Th-1 type immunity in mice.
Drug Carriers, Immunity, Cellular, Mice, Inbred BALB C, Vaccines, Synthetic, Molecular Sequence Data, Gene Products, env, Viral Vaccines, Enzootic Bovine Leukosis, Th1 Cells, Cancer Vaccines, Peptide Fragments, Mice, Liposomes, Leukemia Virus, Bovine, Animals, Cattle, Hypersensitivity, Delayed, Amino Acid Sequence
Drug Carriers, Immunity, Cellular, Mice, Inbred BALB C, Vaccines, Synthetic, Molecular Sequence Data, Gene Products, env, Viral Vaccines, Enzootic Bovine Leukosis, Th1 Cells, Cancer Vaccines, Peptide Fragments, Mice, Liposomes, Leukemia Virus, Bovine, Animals, Cattle, Hypersensitivity, Delayed, Amino Acid Sequence
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