ISOLATION AND CHARACTERIZATION OF T-LYMPHOCYTES FROM SURAL NERVE BIOPSIES IN PATIENTS WITH GUILLAIN-BARRE-SYNDROME AND CHRONIC INFLAMMATORYDEMYELINATING POLYNEUROPATHY
A. Bensmith et al., ISOLATION AND CHARACTERIZATION OF T-LYMPHOCYTES FROM SURAL NERVE BIOPSIES IN PATIENTS WITH GUILLAIN-BARRE-SYNDROME AND CHRONIC INFLAMMATORYDEMYELINATING POLYNEUROPATHY, Journal of Neurology, Neurosurgery and Psychiatry, 61(4), 1996, pp. 362-368
Objectives-To characterise cultured T lymphocytes from nerve biopsies
in patients with Guillain-Barre syndrome and chronic inflammatory demy
elinating polyneuropathy (CIDP). Methods-Sural nerve biopsies, obtaine
d from six patients with Guillain-Barre syndrome, four with CIDP, and
six controls with other neuropathies, were cultured with 20 U/ml recom
binant interleukin-2 (IL-2) for eight weeks. Flow cytometry was used t
o determine the phenotype of cultured T lymphocytes. Their proliferati
ve responses to a range of bacterial antigens were also examined. Resu
lts-T cell lines were established from four of six patients with Guill
ain-Barre syndrome, one of four with CIDP, one patient with peripheral
nerve vasculitis, and none of five controls with noninflammatory neur
opathies. One of these T cell lines from a patient with Guillain-Barre
syndrome, preceded by Campylobacter jejuni infection, consisted entir
ely of gamma delta TCR(+) T lymphocytes. The peripheral blood of this
patient also contained an increased frequency of gamma delta T cells w
hen stimulated with C jejuni. The nerve derived T cell lines failed to
show a proliferative response to bacterial antigens or to a preparati
on of myelin proteins. Conclusions-A new technique to isolate T cells
from nerve biopsies in patients with Guillain-Barre syndrome and CIDP
is reported. This technique may prove to be a useful tool in the inves
tigation of the pathogenesis of other inflammatory neuropathies such a
s peripheral nerve vasculitis. The isolation of a gamma delta TCR(+) n
erve T Pathology cell line is of interest because of the possibility t
hat these cells might respond to glycolipid epitopes common to C jejun
i and peripheral nerve gangliosides.