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Several vaccine strategies aim to generate cell-mediated immunity (CMI) against microorganisms or tumors. While epitope-based vaccines offer advantages, knowledge of specific epitopes and frequency of major histocompatibility complex (MHC) alleles is required. Here we show that using promiscuous overlapping synthetic peptides (OSP) as immunogens generated peptide-specific CMI in all vaccinated outbred mice and in different strains of inbred mice; CMI responses also recognized viral proteins. OSP immunogens also induced CMI ex vivo in dendritic cell/T-cell cocultures involving cells from individuals with different HLA haplotypes. Thus, broad CMI was induced by OSP in different experimental settings, using different immunogens, without identifying either epitopes or MHC backgrounds of the vaccinees.

Original publication

DOI

10.1016/j.vaccine.2006.04.070

Type

Journal article

Journal

Vaccine

Publication Date

11/09/2006

Volume

24

Pages

6356 - 6365

Keywords

Amino Acid Sequence, Animals, Dendritic Cells, HIV Envelope Protein gp120, HLA Antigens, Immunity, Cellular, Lymphocyte Activation, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL, T-Lymphocytes, Cytotoxic, Vaccines, Subunit