INDUCTION OF ANTIGEN-SPECIFIC CYTOLYTIC T-CELLS IN-SITU IN HUMAN-MELANOMA BY IMMUNIZATION WITH SYNTHETIC PEPTIDE-PULSED AUTOLOGOUS ANTIGEN-PRESENTING CELLS
B. Mukherji et al., INDUCTION OF ANTIGEN-SPECIFIC CYTOLYTIC T-CELLS IN-SITU IN HUMAN-MELANOMA BY IMMUNIZATION WITH SYNTHETIC PEPTIDE-PULSED AUTOLOGOUS ANTIGEN-PRESENTING CELLS, Proceedings of the National Academy of Sciences of the United Statesof America, 92(17), 1995, pp. 8078-8082
Human melanoma cells can process the MAGE-1 gene product and present t
he processed nonapeptide EADPTGHSY on their major histocompatibility c
omplex class I molecules, HLA-A1, as a determinant for cytolytic T lym
phocytes (CTLs), Considering that autologous antigen presenting cells
(APCs) pulsed with the synthetic nonapeptide might, therefore, be immu
nogenic, melanoma patients whose tumor cells express the MAGE-1 gene a
nd who are HLA-A1(+) were immunized with a vaccine made of cultured au
tologous APCs pulsed with the synthetic nonapeptide. Analyses of the n
ature of the in vivo host immune response to the vaccine revealed that
the peptide-pulsed APCs are capable of inducing autologous melanoma-r
eactive and the nonapeptide-specific CTLs in situ at the immunization
site and at distant metastatic disease sites.