We recently demonstrated that autoimmune T cells protect neurons from secon
dary degeneration after central nervous system (CNS) axotomy in rats. Here
we show, using both morphological and electrophysiological analyses, that t
he neuroprotection is long-lasting and is manifested functionally. After pa
rtial crush injury of the rat optic nerve, systemic injection of autoimmune
T cells specific to myelin basic protein significantly diminished the loss
of retinal ganglion cells and conducting axons, and significantly retarded
the loss of the visual response evoked by light stimulation. These results
support our challenge to the traditional concept of autoimmunity as always
harmful, and suggest that in certain situations T cell autoimmunity may ac
tually be beneficial. It might be possible to employ T cell intervention to
slow down functional loss in the injured CNS. (C) 2000 Published by Elsevi
er Science B.V. All rights reserved.