TY - JOUR
T1 - Autoimmune T cells retard the loss of function in injured rat optic nerves
AU - Moalem, Gila
AU - Yoles, Eti
AU - Leibowitz-Amit, Raya
AU - Muller-Gilor, Shir
AU - Mor, Felix
AU - Cohen, Irun R.
AU - Schwartz, Michal
N1 - Funding Information:
We thank Shirley Smith for editorial assistance, Phil Taylor for statistical assistance, and Igor Friedmann for help with graphics. Dr. Dvora Teitelbaum generously donated guinea pig MBP. I.R.C. is the incumbent of the Mauerberger Chair in Immunology. M.S. holds the Maurice and Ilse Katz Professorial Chair in Neuroimmunology. The work is supported by a grant from the US army awarded to M.S., and a grant from the Alan Brown Foundation for Spinal Cord Injury awarded to M.S.
PY - 2000/7/1
Y1 - 2000/7/1
N2 - We recently demonstrated that autoimmune T cells protect neurons from secondary degeneration after central nervous system (CNS) axotomy in rats. Here we show, using both morphological and electrophysiological analyses, that the neuroprotection is long-lasting and is manifested functionally. After partial 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 actually be beneficial. It might be possible to employ T cell intervention to slow down functional loss in the injured CNS. (C) 2000 Published by Elsevier Science B.V.
AB - We recently demonstrated that autoimmune T cells protect neurons from secondary degeneration after central nervous system (CNS) axotomy in rats. Here we show, using both morphological and electrophysiological analyses, that the neuroprotection is long-lasting and is manifested functionally. After partial 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 actually be beneficial. It might be possible to employ T cell intervention to slow down functional loss in the injured CNS. (C) 2000 Published by Elsevier Science B.V.
KW - Autoimmunity
KW - CNS
KW - Injury
UR - http://www.scopus.com/inward/record.url?scp=0034237630&partnerID=8YFLogxK
U2 - 10.1016/S0165-5728(00)00240-X
DO - 10.1016/S0165-5728(00)00240-X
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C2 - 10814797
AN - SCOPUS:0034237630
SN - 0165-5728
VL - 106
SP - 189
EP - 197
JO - Journal of Neuroimmunology
JF - Journal of Neuroimmunology
IS - 1-2
ER -