An effective cancer-cell vaccine is created by expressing major-histocompat
ibility-complex (MHC) class II molecules without the invariant chain protei
n (li) that normally blocks the antigenic-peptide-binding site of MHC class
II molecules at their synthesis in the endoplasmic reticulum. Such tumor-c
ell constructs are created either by the transfer of genes for MHC class II
alpha and beta chains, or by the induction of MHC class II molecules and I
i protein with a transacting factor, followed by Ii suppression using antis
ense methods. Preclinical validation of this approach is reviewed with the
goal of using this immunotherapy for metastatic human cancers.