There are disclosed compound of formula I, in which R.sub.1 represents a
hydrophobic moiety adapted to occupy the C' channel of human CDId,
R.sub.2 represents a hydrophobic moiety adapted to occupy the A' channel
of human CDId, such that R.sub.1 fills at least at least 30% of the
occupied volume of the C' channel compared to the volume occupied by the
terminal nC.sub.14H.sub.29 of the sphingosine chain of
.alpha.-galactosylceramide when bound to human CDId and R.sub.2 fills at
least 30% of the occupied volume of the A' channel compared to the volume
occupied by the terminal nC.sub.25H.sub.51 of the acyl chain of
.alpha.-galactosylceramide when bound to human CDId R.sub.3 represents
hydrogen or OH, R.sup.a and R.sup.b each represent hydrogen and in
addition, when R.sup.3 represents hydrogen, R.sup.a and R.sup.b together
may form a single bond, X represents or --CHA(CHOH).sub.nY or
--P(.dbd.0)(0.sup.-)0CH.sub.2(CH0H).sub.mY, in which Y represents
CHB.sub.1B.sub.2, n represents an integer from 1 to 4, m represents 0 or
1, A arepresents hydrogen, one of B.sub.1 and B.sub.2 represents H, OH or
phenyl, and the other represents hydrogen or one of B.sub.1 and B.sub.2
represents hydroxyl and the other represents phenyl, in addition, when n
represents 4, then A together with one of B.sub.1 and B.sub.2 together
forms a single bond and the other of B.sub.1 and B.sub.2 represents H, OH
or OSO.sub.3H and pharmaceutically acceptable salts thereof; the
compounds of formula I are indicted for use in the treatment of a virus,
microbial infection, parasite, an autoimmune disease, cancer, allergy or
asthma
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