Ka. Sheikh et al., CAMPYLOBACTER-JEJUNI LIPOPOLYSACCHARIDES IN GUILLAIN-BARRE-SYNDROME -MOLECULAR MIMICRY AND HOST SUSCEPTIBILITY, Neurology, 51(2), 1998, pp. 371-378
Objective: This study was designed to determine if the presence of spe
cific ganglioside-like moieties in Campylobacter lipopolysaccharides (
LPSs) is related to the development of Guillain-Barre syndrome (GBS),
and to discover how frequently such moieties, including GM1, are prese
nt in these LPSs. Methods: We studied Campylobacter isolates and sera
from seven patients with GBS (five acute motor axonal neuropathy, one
acute inflammatory demyelinating polyneuropathy, and one Fisher's synd
rome), and compared them with similar specimens from patients with Cam
pylobacter enteritis alone. Results: All GBS patients had antiganglios
ide antibodies. Anti-GM1 and anti-GD1a titers were significantly eleva
ted in post-Campylobacter GBS, both axonal and demyelinating, compared
with normal control subjects or those with uncomplicated Campylobacte
r diarrhea. Campylobacter isolated from patients with GBS and with ent
eritis alone had similar ganglioside-like moieties. Conclusions: These
results indicate that patients who develop GBS respond differently to
the ganglioside-like epitopes on Campylobacter than do non-GBS diarrh
ea patients. Our findings support a role for host susceptibility as a
determinant for the outcome following Campylobacter infection. These f
indings have important implications for the development of vaccines ag
ainst Campylobacter jejuni.