TY - JOUR
T1 - Efficient generation of antigen-specific cytotoxic T cells using retrovirally transduced CD40-activated B cells
AU - Kondo, Eisei
AU - Topp, Max S.
AU - Kiem, Hans Peter
AU - Obata, Yuichi
AU - Morishima, Yasuo
AU - Kuzushima, Kiyotaka
AU - Tanimoto, Mitsune
AU - Harada, Mine
AU - Takahashi, Toshitada
AU - Akatsuka, Yoshiki
PY - 2002/8/15
Y1 - 2002/8/15
N2 - The development of rapid, efficient, and safe methods for generating Ag-specific T cells is necessary for the clinical application of adoptive immunotherapy. We show that B cells stimulated with CD40 ligand and IL-4 (CD40-B cells) can be efficiently transduced with retroviral vectors encoding a model Ag, CMV tegument protein pp65 gene, and maintain high levels of costimulatory molecules after gene transfer. CTL lines specific for pp65 were readily generated in all four healthy CMV-seropositive donors by stimulating autologous CD8+ T cells with these transduced CD40-B cells, both of which were derived from 10 mi peripheral blood. ELISPOT assays revealed that the CTL lines used multiple HLA alleles as restricting elements. Thus, CD40-B cells transduced retrovirally with Ag-encoding cDNA can be potent APC and facilitate to generate Ag-specific CTL in vitro.
AB - The development of rapid, efficient, and safe methods for generating Ag-specific T cells is necessary for the clinical application of adoptive immunotherapy. We show that B cells stimulated with CD40 ligand and IL-4 (CD40-B cells) can be efficiently transduced with retroviral vectors encoding a model Ag, CMV tegument protein pp65 gene, and maintain high levels of costimulatory molecules after gene transfer. CTL lines specific for pp65 were readily generated in all four healthy CMV-seropositive donors by stimulating autologous CD8+ T cells with these transduced CD40-B cells, both of which were derived from 10 mi peripheral blood. ELISPOT assays revealed that the CTL lines used multiple HLA alleles as restricting elements. Thus, CD40-B cells transduced retrovirally with Ag-encoding cDNA can be potent APC and facilitate to generate Ag-specific CTL in vitro.
UR - http://www.scopus.com/inward/record.url?scp=0037103241&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0037103241&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.169.4.2164
DO - 10.4049/jimmunol.169.4.2164
M3 - Article
C2 - 12165546
AN - SCOPUS:0037103241
SN - 0022-1767
VL - 169
SP - 2164
EP - 2171
JO - Journal of Immunology
JF - Journal of Immunology
IS - 4
ER -