J. Honnorat et al., ANTIBODIES TO A SUBPOPULATION OF GLIAL-CELLS AND A 66 KDA DEVELOPMENTAL PROTEIN IN PATIENTS WITH PARANEOPLASTIC NEUROLOGICAL SYNDROMES, Journal of Neurology, Neurosurgery and Psychiatry, 61(3), 1996, pp. 270-278
Background-Paraneoplastic neurological syndromes (PNS) are inflammator
y disorders that probably depend on autoimmune processes. Several auto
antibodies (anti-Hu, anti-Ri, and anti-Yo) have been characterised in
PNS and proved to be helpful in the diagnosis. However, these do not a
ccount for all the cases and the possibility that other types of antib
odies could be detected was investigated. Methods and results-Of 45 pa
tients with PNS whose serum was probed on paraformaldehyde fixed rat b
rain sections, 11 patients were identified whose serum samples recogni
sed a cytoplasmic antigen in a subpopulation of glial cells in the whi
te matter of adult rat brainstem, cerebellum, and spinal cord that wer
e double labelled with a monoclonal antibody specific for oligodendroc
ytes. All serum samples reacted with a 66 kDa protein of newborn rat b
rain on western blot analysis. These antibodies were designated as ant
i-CV2 antibodies. Only one of the 11 patients had one of the well char
acterised autoantibodies (anti-Hu). Five patients had cerebellar degen
eration, three had Limbic encephalitis, two had encephalomyelitis, and
one had Lambert-Eaton myasthenic syndrome. The tumours were small cel
l lung cancer or undifferentiated mediastinal cancer in seven patients
, uterine sarcoma in two, and malignant thymoma in two. Among 1061 con
trol serum samples, only two patients had anti-CV2 antibodies. One had
small cell lung cancer and the other malignant thymoma. Conclusions-T
he detection of anti-CV2 antibodies in patients with neurological diso
rders should be considered as an indication of the presence of an occu
lt cancer.