J. Hayrinen et al., ANTIBODIES TO POLYSIALIC ACID AND ITS N-PROPYL DERIVATIVE - FINDING PROPERTIES AND INTERACTION WITH HUMAN EMBRYONAL BRAIN GLYCOPEPTIDES, The Journal of infectious diseases, 171(6), 1995, pp. 1481-1490
There is no efficient vaccine against group B meningococcal meningitis
because of tolerance induced by host tissue polysialic acid cross-rea
cting with the capsular polysaccharide. The specificities of polysiali
c acid-antibody interactions were studied using a ligand binding assay
. Antibodies 735, 20-1, 2-1B, 2-2B, 5E1, and t5E1 and antibodies again
st N-propionylated group B meningococcal polysaccharide-tetanus toroid
conjugate (NP-4, 106-6) bound polysialylated human embryonal brain gl
ycopeptides but not control glycopeptides or disialosyllactose, wherea
s antibodies 109-3 and I-627 were more specific for the N-propionylate
d polysaccharide. Antiganglioside antibodies (KM538, KM641) did not cr
oss-react with polysialic acid. Human class-switched antibodies 5E1 (I
gM) and t5E1 (IgG) reacted identically with all compounds tested and n
o temperature-dependent differences were observed. All anti-polysialos
yl antibodies required a polysaccharide chain of 8-10 residues for bin
ding independent of the immunizing antigen, animal species, or immunog
lobulin class. The results suggest careful evaluation of polysialic ac
id cross-reactivity in vaccine development.