Gn. Verne et al., ANTI-MYENTERIC NEURONAL ANTIBODIES IN PATIENTS WITH ACHALASIA - A PROSPECTIVE-STUDY, Digestive diseases and sciences, 42(2), 1997, pp. 307-313
Achalasia is a motility disorder of the esophagus characterized by the
loss of inhibitory neurons in the distal esophagus. Although idiopath
ic in nature, autoimmune mechanisms have been proposed, and we set out
to determine the presence of myenteric neuronal antibodies. We prospe
ctively studied 18 patients with well-characterized achalasia (by clin
ical, x-ray, and manometric evidence), nine with gastroesophageal refl
ux disease, and analyzed the sera from 22 disease-free controls. Using
double-label, indirect immunofluorescence techniques, rat esophageal
and intestinal sections were double-labeled with sera (dilutions of 1:
50 to 1:400) from the three groups and with neurofilament antibody to
localize neurons. Seven of 18 achalasia patients had sera that stained
the majority of neurons within plexi in the esophageal and intestinal
sections, including both NADPH diaphorase (nitric oxide synthase) -po
sitive and -negative neurons. None of the gastroesophageal reflux pati
ents or the controls showed staining. Neuronal antibodies in achalasia
provide an attractive hypothesis to explain this diffuse; possibly im
mune-based disorder.