With the aim to improve the efficacy of therapeutic vaccines that target self-antigens， we have developed a novel fusion protein vaccine on the basis of the C-terminal multimerizing end of the variable lymphocyte receptor B (VLRB)， the Ig equivalent in jawless fishes. Recombinant vaccines were produced in by fusing the VLRB sequence to 4 different cancer-associated target molecules. The anti-self-immune response generated in mice that were vaccinated with VLRB vaccines was compared with the response in mice that received vaccines that contained bacterial thioredoxin (TRX)， previously identified as an efficient carrier. The anti-self-Abs were analyzed with respect to titers， binding properties， and du... More
With the aim to improve the efficacy of therapeutic vaccines that target self-antigens， we have developed a novel fusion protein vaccine on the basis of the C-terminal multimerizing end of the variable lymphocyte receptor B (VLRB)， the Ig equivalent in jawless fishes. Recombinant vaccines were produced in by fusing the VLRB sequence to 4 different cancer-associated target molecules. The anti-self-immune response generated in mice that were vaccinated with VLRB vaccines was compared with the response in mice that received vaccines that contained bacterial thioredoxin (TRX)， previously identified as an efficient carrier. The anti-self-Abs were analyzed with respect to titers， binding properties， and duration of response. VLRB-vaccinated mice displayed a 2- to 10-fold increase in anti-self-Ab titers and a substantial decrease in Abs against the foreign part of the fusion protein compared with the response in TRX-vaccinated mice ( < 0.01). VLRB-generated Ab response had duration similar to the corresponding TRX-generated Abs， but displayed a higher diversity in binding characteristics. Of importance， VLRB vaccines could sustain an immune response against several targets simultaneously. VLRB vaccines fulfill several key criteria for an efficient therapeutic vaccine that targets self-antigens as a result of its small size， its multimerizing capacity， and nonexposed foreign sequences in the fusion protein.-Saupe， F.， Reichel， M.， Huijbers， E. J. M.， Femel， J.， Markgren， P.-O.， Andersson， C. E.， Deindl， S.， Danielson， U. H.， Hellman， L. T.， Olsson， A.-K. Development of a novel therapeutic vaccine carrier that sustains high antibody titers against several targets simultaneously.
