Dendritic cells (DC) are potent antigen-presenting cells (APC) capable
of inducing strong T-cell-mediated immunity, Infusion of lymphoma-spe
cific antigen-loaded autologous DC has been demonstrated to result in
the generation of antigen-specific immunity and reduction in tumor bur
den in B-cell lymphoma patients. Cellular immunotherapy employing anti
gen-loaded DC could have a potential therapeutic impact in tumors and
viral infections, including HIV infection, However, DC in HIV-infected
individuals and breast cancer patients are believed to be functionall
y defective. Therefore, the potential of using allogeneic DC offers si
gnificant implications for DC immunotherapy in AIDS and immunocompromi
sed cancer patients. To explore the potential of allogeneic DC therapy
in vivo, we tested the ability of allogeneic DC to generate primary p
eptide-specific CD8(+) cytotoxic T-lymphocyte (CTL) responses in vitro
., Our results indicate that DC from HLA class I-matched individuals e
licit primary immune responses in vitro using viral peptides as naive
antigens, A primary peptide-specific immune response could also be det
ected even when only one HLA allele (HLA-A0201) was matched between t
he allogeneic DC and T-lymphocytes, The ability to generate primary pe
ptide-specific responses in vitro is strongly indicative of the in viv
o therapeutic potential of allogeneic DC, (C) 1998 Elsevier Science In
c.