U. Enders et al., THE SPECTRUM OF IMMUNE-RESPONSES TO CAMPYLOBACTER-JEJUNI AND GLYCOCONJUGATES IN GUILLAIN-BARRE-SYNDROME AND IN OTHER NEUROIMMUNOLOGICAL DISORDERS, Annals of neurology, 34(2), 1993, pp. 136-144
An acute infectious illness frequently precedes the Guillain-Barre syn
drome. Recently, Campylobacter jejuni was claimed to be a predominant
precipitating agent that may also trigger a humoral immune response to
glycoconjugates of peripheral myelin in Guillain-Barre syndrome. Beca
use of conflicting reports, we determined the frequency of a recent in
fection with C. jejuni in 38 patients with Guillain-Barre syndrome usi
ng a highly sensitive and specific immunoblot technique, and of the pr
esence of circulating antibodies to gangliosides. We detected IgM and/
or IgG C. jejuni directed antibodies in 15 of 38 patients with Guillai
n-Barre syndrome. In contrast, only 7 of 39 healthy control subjects,
3 of 20 patients with multiple sclerosis, and 2 of 72 patients with ne
uroborreliosis showed IgA or IgM antibody responses to C. jejuni. In G
uillain-Barre syndrome, C. jejuni-specific antibodies were predominant
ly directed to outer membrane proteins of one specific serotype, Lior
11, whereas the most common serotype associated with enteritis in Germ
any is Lior 4. Two of 27 patients with Guillain-Barre syndrome had gan
glioside-specific IgA antibodies; 1 of 32 patients, antibodies of IgM;
and 4 of 31 patients, antibodies of IgG class. There was no correlati
on between severity, type (axonal versus demyelinating), and outcome o
f the disease and the presence or absence of a humoral immune response
to C. jejuni or to glycoconjugates. Our findings do not support previ
ous suggestions that a preceding C. jejuni infection heralds a poorer
outcome or that antibodies to gangliosides carry prognostic significan
ce. The predilective humoral immune response to outer membrane protein
s of one specific C. jejuni serotype raises new important questions co
ncerning the immunopathogenic link between an acute C. jejuni infectio
n and subsequent Guillain-Barre syndrome.