Abstract:
:C57BL/6 (B6) mice were immunized with a highly antigenic 10-mer peptide (P12-10), which is encoded by the murine AIDS (MAIDS) defective virus gag p12 gene, emulsified in incomplete Freund's adjuvant (ICFA). One week later, the mice were inoculated with the MAIDS virus to see if the immunization affects progression of MAIDS. It was demonstrated that the immunization significantly delayed progression of MAIDS, although it failed to induce appreciable cytotoxic T lymphocyte (CTL) responses against the P12-10 antigen. In contrast, immunization of B6 mice with the P12-10 coupled with liposome induced substantial CTL responses but failed to protect the mice against MAIDS development. This segregation between CTL activity and in vivo protection efficacy might be worth considering when we exploit vaccines for augmenting cellular immunity mediated by CD8+ T cells.
journal_name
Vaccinejournal_title
Vaccineauthors
Mizuochi T,Horino A,Uchida Tdoi
10.1016/s0264-410x(98)00082-6subject
Has Abstractpub_date
1998-12-01 00:00:00pages
2026-30issue
20eissn
0264-410Xissn
1873-2518pii
S0264410X98000826journal_volume
16pub_type
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