TY - JOUR
T1 - Adoptive transfer of experimental allergic encephalomyelitis and localization of the encephalitogenic epitope in the SWR mouse
AU - Cross, Anne H.
AU - Hashim, George A.
AU - Raine, Cedric S.
N1 - Funding Information:
A.H.C. was supported by a fellowship from the National Multiple Sclerosis Society, NMSS FG 749-A-1. Supported in part by NS 08952 and NS 11920; and NMSS RG 1001-G-7.
PY - 1991/1
Y1 - 1991/1
N2 - Adoptively-transferred experimental allergic encephalomyelitis (EAE) was induced in the SWR (H-2q) strain of mouse using lymph node cells, spleen cells, or cell lines sensitized to whole myelin basic protein (MBP). With the aid of synthetic peptides, the minimal encephalitogenic epitope of MBP for the SWR strain was localized to amino acids 87-99 of the MBP molecule. The 87-99 sequence is also encephalitogenic for the SJL strain of mouse and the Lewis rat. EAE was induced with a protocol similar to that for the induction of EAE in the SJL strain with the exception that sublethal irradiation of recipients was necessary. Mice developed typical clinical and pathological EAE 6-14 days post-transfer of cells sensitized to either whole MBP or peptide 87-99, after which they remitted. No relapses were observed. Thus, adoptively transferred EAE can be induced in irradiated H-2q mice for which the encephalitogenic epitope is one of the nested encephalitogenic epitopes for SJL (H-2s) mice, namely residues 87-99.
AB - Adoptively-transferred experimental allergic encephalomyelitis (EAE) was induced in the SWR (H-2q) strain of mouse using lymph node cells, spleen cells, or cell lines sensitized to whole myelin basic protein (MBP). With the aid of synthetic peptides, the minimal encephalitogenic epitope of MBP for the SWR strain was localized to amino acids 87-99 of the MBP molecule. The 87-99 sequence is also encephalitogenic for the SJL strain of mouse and the Lewis rat. EAE was induced with a protocol similar to that for the induction of EAE in the SJL strain with the exception that sublethal irradiation of recipients was necessary. Mice developed typical clinical and pathological EAE 6-14 days post-transfer of cells sensitized to either whole MBP or peptide 87-99, after which they remitted. No relapses were observed. Thus, adoptively transferred EAE can be induced in irradiated H-2q mice for which the encephalitogenic epitope is one of the nested encephalitogenic epitopes for SJL (H-2s) mice, namely residues 87-99.
KW - Autoimmunity
KW - Encephalitogenic epitope
KW - Experimental allergic encephalomyelitis
KW - Multiple sclerosis
KW - Myelin basic protein
UR - http://www.scopus.com/inward/record.url?scp=0026078703&partnerID=8YFLogxK
U2 - 10.1016/0165-5728(91)90087-N
DO - 10.1016/0165-5728(91)90087-N
M3 - Article
C2 - 1701448
AN - SCOPUS:0026078703
SN - 0165-5728
VL - 31
SP - 59
EP - 66
JO - Journal of Neuroimmunology
JF - Journal of Neuroimmunology
IS - 1
ER -