We have demonstrated that ingested murine interferon alpha (IFN-alpha) supp
ressed clinical relapse in chronic relapsing experimental autoimmune enceph
alomyelitis (CR-EAE), decreased inflammation and suppressed the adoptive tr
ansfer of EAE, and is a biological response modifier in patients with multi
ple sclerosis. We examined the relative levels of the Ms mRNA signal using
semiquantitative reverse transcription-polymerase chain reaction analysis o
n splenocytes from mice and peripheral blood mononuclear cells from man aft
er IFN-alpha ingestion. Both mice and man demonstrated inducible levels of
Mx mRNA after ingesting IFN-alpha, Murine spleen T cells and CD8(+) T cells
also demonstrated upregulation of Mx mRNA., Murine whole splenocytes demon
strated upregulation of Mx mRNA after IFN-alpha ingestion of 10 and 100 U,
but not after 0, 1000, 5000 U. Ingested IFN-alpha acts via established path
ways of type 1 IFN signalling. (C) 1999 Academic Press.