Abstract
Summary
Passive transfer of allergic encephalomyelitis by injection of living, immunized lymph node cells into normal recipients constitutes a graft of lymphoid cells. It has been accomplished previously when histocompatibility barriers were absent, minor, or undefined. Treatment with an immunosuppressive drug and cells bearing donor-type antigens has now made passive transfer possible despite differences in major transplantation antigens between Lewis donor and BN recipient rats.
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