RRC ID 36822
Author Imamura Y, Haruta M, Tomita Y, Matsumura K, Ikeda T, Yuno A, Hirayama M, Nakayama H, Mizuta H, Nishimura Y, Senju S.
Title Generation of Large Numbers of Antigen-Expressing Human Dendritic Cells Using CD14-ML Technology.
Journal PLoS ONE
Abstract We previously reported a method to expand human monocytes through lentivirus-mediated introduction of cMYC and BMI1, and we named the monocyte-derived proliferating cells, CD14-ML. CD14-ML differentiated into functional DC (CD14-ML-DC) upon addition of IL-4, resulting in the generation of a large number of DC. One drawback of this method was the extensive donor-dependent variation in proliferation efficiency. In the current study, we found that introduction of BCL2 or LYL1 along with cMYC and BMI1 was beneficial. Using the improved method, we obtained CD14-ML from all samples, regardless of whether the donors were healthy individuals or cancer patients. In vitro stimulation of peripheral blood T cells with CD14-ML-DC that were loaded with cancer antigen-derived peptides led to the establishment of CD4+ and CD8+ T cell lines that recognized the peptides. Since CD14-ML was propagated for more than 1 month, we could readily conduct genetic modification experiments. To generate CD14-ML-DC that expressed antigenic proteins, we introduced lentiviral antigen-expression vectors and subjected the cells to 2 weeks of culture for drug-selection and expansion. The resulting antigen-expressing CD14-ML-DC successfully induced CD8+ T cell lines that were reactive to CMVpp65 or MART1/MelanA, suggesting an application in vaccination therapy. Thus, this improved method enables the generation of a sufficient number of DC for vaccination therapy from a small amount of peripheral blood from cancer patients. Information on T cell epitopes is not necessary in vaccination with cancer antigen-expressing CD14-ML-DC; therefore, all patients, irrespective of HLA type, will benefit from anti-cancer therapy based on this technology.
Volume 11(4)
Pages e0152384
Published 2016
DOI 10.1371/journal.pone.0152384
PII PONE-D-15-44069
PMID 27050553
PMC PMC4822879
MeSH Adult Antigens / biosynthesis* Cell Differentiation Cell Proliferation Dendritic Cells / cytology* Dendritic Cells / immunology Female Humans Lipopolysaccharide Receptors / immunology* Lymphocyte Activation Male Middle Aged Young Adult
IF 2.766
Times Cited 0
WOS Category ONCOLOGY
Resource
DNA material Genome Network Project W01A023B19 (HGE009243) pCMV-VSV-G-RSV-Rev (RDB04393) pCAG-HIVgp (RDB04394) CSII-EF-RfA (RDB04387).