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Abstract
Encephalitogenic activity of myelin basic protein (MBP) isolated in a form retaining
binding to all myelin lipids was tested in Lewis rats. Immunization with this new
stable lipid-bound and native-like preparation (LB-MBP), induced experimental autoimmune
encephalomyelitis (EAE) as intensively as the classical lipid free MBP (LF-MBP). During
the course of the disease, high affinity specific response to LB-MBP and high frequency
of LB-MBP specific precursors was observed in peripheral lymphoid organs, indicating
that the disease occurred in presence of anti LB-MBP specific T-cell responsivity.
Short term lines, generated from lymphocytes collected at the onset of the disease
from LB-MBP immunized rats, showed a strong dose-dependent response to LB-MBP, but
not to LF-MBP. The present data indicate that in rat, LB-MBP maintains encephalitogenic
activity and induces expansion of a specific T-cell population. These data suggest
also that LB-MBP is a new autoantigen that may be relevant in human diseases.
Keywords
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Article info
Publication history
Accepted:
April 12,
1993
Received in revised form:
March 8,
1993
Received:
October 12,
1992
Identification
Copyright
© 1993 Published by Elsevier Inc.