The amino acid sequence of HIV reverse transcriptase (RT) from residue 245
to residue 262 was expressed on the surface of filamentous phage fd, fused
to the major coat protein gVIIIp. The chimeric phage was used to assess the
ability of anti-RT (248-262) human T cell lines and clones to become activ
ated by the phage-displayed peptide. The RT peptide displayed on phage was
recognized by the T-cells and induced production of Abs. However, not all T
cells raised against the synthetic RT (248-262) peptide could respond. Lac
k of recognition did not depend on differences in the ability of different
APCs to present the phage, but was apparently determined by the TCR specifi
city. The results presented here may be relevant to the design of recombina
nt protein-based subunit vaccines. (C) 1999 Elsevier Science Ltd. All right
s reserved.