Experimental allergic neuritis (EAN) was induced in normal and irradia
ted Lewis rats by passively transferring T cells sensitized to SP-26,
a peptide fragment of P-2 myelin protein. The recipients became sick 4
-8 days post transfer and the degree of disability correlated directly
with the dose of T cells. Smaller doses caused demyelination of nerve
roots and sciatic nerves and larger doses produced more severe demyel
ination and significant axonal degeneration. Irradiated recipients dev
eloped similar clinical EAN and showed macrophage-mediated demyelinati
on despite severe suppression of the host inflammatory response.