Receptor Binding by Cholera Toxin B-Subunit and Amino Acid Modification Improves Minimal Peptide Immunogenicity

Abstract EN

We increase our understanding of augmenting a cellular immune response, by using an HIV-1 protease-derived epitope (PR75–84), and variants thereof, coupled to the C-terminal, of the B subunit of cholera toxin (CTB).

Fusion proteins were used for immunizations of HLA-A0201 transgenic C57BL/6 mice.

We observed different capacities to elicit a cellular immune response by peptides with additions of five to ten amino acids to the PR epitope.

There was a positive correlation between the magnitude of the elicited cellular immune response and the capacity of the fusion protein to bind GM-1.

This binding capacity is affected by its ability to form natural pentamers of CTB.

Our results suggest that functional CTB pentamers containing a foreign amino acid-modified epitope is a novel way to overcome the limited cellular immunogenicity of minimal peptide antigens.

This way of using a functional assay as readout for improved cellular immunogenicity might become highly valuable for difficult immunogens such as short peptides (epitopes).