TY - JOUR
T1 - Generation of autologous peptide- and protein-pulsed dendritic cells for patient-specific immunotherapy.
AU - O'Neill, David
AU - Bhardwaj, Nina
PY - 2005
Y1 - 2005
N2 - This chapter presents a detailed protocol for the generation of mature, monocyte-derived dendritic cells (DC) that are loaded or "pulsed" with tumor-associated peptide antigens for use as patient-specific immunotherapy. The protocol can easily be adapted for the treatment of patients with a variety of tumors or chronic viral infections by simply changing the peptide antigens used. The vaccine may use major histocompatibility complex (MHC) class I- or class II-restricted peptides to elicit stimulation of CD8+ cytotoxic T-lymphocytes (CTL) or CD4+ T-helper cells, respectively. It also provides an example of loading DC with a purified protein antigen-in this instance, keyhole limpet hemocyanin (KLH). KLH may be used to boost the immunogenicity of the vaccine and as a control to test for the induction of CD4+ T-helper-cell responses. Other antigenic proteins may be added or substituted. Once prepared, the DC are frozen in aliquots and samples are tested for identity, purity, viability, and sterility. After these "release" criteria are met, vaccine aliquots can be thawed, drawn up into syringes, and injected back into the patient.
AB - This chapter presents a detailed protocol for the generation of mature, monocyte-derived dendritic cells (DC) that are loaded or "pulsed" with tumor-associated peptide antigens for use as patient-specific immunotherapy. The protocol can easily be adapted for the treatment of patients with a variety of tumors or chronic viral infections by simply changing the peptide antigens used. The vaccine may use major histocompatibility complex (MHC) class I- or class II-restricted peptides to elicit stimulation of CD8+ cytotoxic T-lymphocytes (CTL) or CD4+ T-helper cells, respectively. It also provides an example of loading DC with a purified protein antigen-in this instance, keyhole limpet hemocyanin (KLH). KLH may be used to boost the immunogenicity of the vaccine and as a control to test for the induction of CD4+ T-helper-cell responses. Other antigenic proteins may be added or substituted. Once prepared, the DC are frozen in aliquots and samples are tested for identity, purity, viability, and sterility. After these "release" criteria are met, vaccine aliquots can be thawed, drawn up into syringes, and injected back into the patient.
UR - http://www.scopus.com/inward/record.url?scp=16644372532&partnerID=8YFLogxK
M3 - Article
C2 - 15585916
AN - SCOPUS:16644372532
SN - 1543-1894
VL - 109
SP - 97
EP - 112
JO - Methods in molecular medicine
JF - Methods in molecular medicine
ER -