TY - JOUR
T1 - Delayed type hypersensitivity to gangliosides in the Lewis rat
AU - Offner, Halina
AU - Standage, Blayne A.
AU - Burger, Denis R.
AU - Vandenbark, Arthur A.
N1 - Funding Information:
This work was supported by the Veterans Administration and the Medical Research Foundation of Oregon. Address for correspondence: Halina Offner, Ph.D., Surgical Research Laboratory 151S, V.A. Medical Center, 3711 S.W.U.S. Veterans Hospital Road, Portland, OR 97207, U.S.A.
PY - 1985
Y1 - 1985
N2 - Systematic study of the immunologic properties of gangliosides has been hampered by the lack of a suitable assay. In this study, significant delayed type hypersensitivity reactions to gangliosides were observed in Lewis rats immunized with whole guinea pig spinal cord (GP-SC) in complete Freund's adjuvant (CFA). The reaction was manifested by an increase in ear thickness after intradermal injection of a mixture of gangliosides and methylated bovine serum albumin (mBSA). No responses were observed to either gangliosides or mBSA alone. The reaction to gangliosides increased after immunization, persisted for 48 h, and was characterized by perivascular infiltration of mononuclear cells. Further evidence for a cellular response was demonstrated by the transfer of ganglioside-specific ear swelling by cultured spleen cells. The response to gangliosides was not due to contamination with myelin basic protein (BP) since no reaction to gangliosides was observed in GP-BP/CFA-immunized rats, and no reaction to BP was observed in ganglioside/CFA-immunized rats. In BP-immunized rats, responsiveness to BP persisted after recovery from clinical EAE for at least 60 days. However, no response to gangliosides was observed in BP-immunized animals after recovery from clinical EAE, suggesting the lack of autosensitization to gangliosides due to the disease process itself.
AB - Systematic study of the immunologic properties of gangliosides has been hampered by the lack of a suitable assay. In this study, significant delayed type hypersensitivity reactions to gangliosides were observed in Lewis rats immunized with whole guinea pig spinal cord (GP-SC) in complete Freund's adjuvant (CFA). The reaction was manifested by an increase in ear thickness after intradermal injection of a mixture of gangliosides and methylated bovine serum albumin (mBSA). No responses were observed to either gangliosides or mBSA alone. The reaction to gangliosides increased after immunization, persisted for 48 h, and was characterized by perivascular infiltration of mononuclear cells. Further evidence for a cellular response was demonstrated by the transfer of ganglioside-specific ear swelling by cultured spleen cells. The response to gangliosides was not due to contamination with myelin basic protein (BP) since no reaction to gangliosides was observed in GP-BP/CFA-immunized rats, and no reaction to BP was observed in ganglioside/CFA-immunized rats. In BP-immunized rats, responsiveness to BP persisted after recovery from clinical EAE for at least 60 days. However, no response to gangliosides was observed in BP-immunized animals after recovery from clinical EAE, suggesting the lack of autosensitization to gangliosides due to the disease process itself.
KW - Experimental allergic encephalomyelitis
KW - Freund's adjuvant
KW - Gangliosides
KW - Guinea pig spinal cord
KW - Lewis rat
KW - Methylated bovine serum albumin
KW - Myelin basic protein
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U2 - 10.1016/S0165-5728(85)80015-1
DO - 10.1016/S0165-5728(85)80015-1
M3 - Article
C2 - 2410448
AN - SCOPUS:0021880519
SN - 0165-5728
VL - 9
SP - 147
EP - 157
JO - Advances in Neuroimmunology
JF - Advances in Neuroimmunology
IS - C
ER -