Abstract
We have previously shown that adoptive transfer of experimental allergic encephalomyelitis can be greatly enhanced by culturing sensitized lymph node cells (LNC) with specific antigen, myelin basic protein (BP). In the present study, successful transfer was accomplished with 5×106 Lewis rat LNC after 48 h culture with BP. Disease transfer was inhibited by the addition to culture of dibutyryl adenosine 3’,5’-cyclic monophosphate (Bt2 cAMP) or the phosphodiesterase inhibitor, isobutyl methylxanthine (MIX), but not by Bt2cGMP. BP-induced lymphoproliferation was also inhibited, but with a slightly different dose-response relationship. An early step in the lymphocyte activation process appears to be most sensitive to the inhibitory effects of Bt2cAMP.
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Abbreviations
- BP:
-
myelin basic protein
- Bt2cAMP:
-
dibutyryl cyclic AMP
- LNC:
-
lymph node cells
- EAE:
-
experimental allergic encephalomyelitis
- MIX:
-
isobutyl methylxanthine
- CFA:
-
complete Freund’s adjuvant
- H-T dR:
-
tritiated thymidine
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An erratum to this article is available at http://dx.doi.org/10.1007/BF02834197.
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Richert, J.R., Kies, M.W. & Alvord, E.C. Adoptive transfer of experimental allergic encephalomyelitis. Neurochemical Pathology 1, 81–90 (1983). https://doi.org/10.1007/BF02834133
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DOI: https://doi.org/10.1007/BF02834133