There has been a regain of interest in the immunological applications
of peptides assembled partly or totally from D-amino acids. Such pepti
des are much more stable to proteolysis than natural L-peptides and th
ey have considerable potential as synthetic vaccines and as immunomodu
lators in T-cell responses. Retro-inverso, also called retro-all-D or
retroenantio, peptide analogues that closely mimic the structure of pr
otein antigens are obtained by assembling amino acid residues in the r
everse order from that in the parent peptides and replacing L- by D-am
ino acids. Retro-all-D peptides corresponding to an immunodominant epi
tope oi foot-and-mouth disease virus have been shown to elicit high le
vels of neutralizing antibodies in experimental animals. Certain retro
-all-D peptide analogues of T-cell epitopes are able to bind to MHC cl
ass II molecules and may either lead to T-cell activation or inhibit d
eleterious T-cell responses.