Dendritic cells modified to express CD40 ligand elicit therapeutic immunity against preexisting murine tumors Journal Article


Authors: Kikuchi, T.; Moore, M. A. S.; Crystal, R. G.
Article Title: Dendritic cells modified to express CD40 ligand elicit therapeutic immunity against preexisting murine tumors
Abstract: CD40 ligand (CD40L) is essential for the Initiation of antigen-specific T-cell responses. This study is based on the hypothesis that dendritic cells (DCs) genetically modified ex vivo to express CD40L will enhance in vivo presentation of tumor antigen to the cellular immune system with consequent induction of antitumor immunity to suppress tumor growth. To examine this concept, subcutaneous murine tumors were injected with bone marrow-derived DCs that had been modified in vitro with an adenovirus (Ad) vector expressing murine CD40L (AdmCD40L). In B16 (H-2(b), melanoma) and CT26 (H-2(d), colon cancer) murine models, intratumoral injection of 2 x 10(6) AdmCD40L-modified DCs (CD40L-DCs) to established (day 8) subcutaneous tumors resulted in sustained tumor regression and survival advantage. This antitumor effect was sustained when the number of CD40L-DCs were reduced 10-fold to 2 x 10(5). Analysis of spleens from CD40L-DC-treated animals demonstrated that CD40L-DCs injected into the subcutaneous CT26 flank tumors migrated to the spleen, resulting in activation of immune-relevant processes. Consistent with this concept, intratumoral administration of CD40L-DCs elicited tumor-specific cytotoxic T-lymphocyte responses, and the transfer of spleen cells from CD40L-DC-treated mice efficiently protected naive mice against a subsequent tumor challenge. In a distant 2-tumor model of metastatic disease, an untreated B16 tumor in the right flank regressed in parallel with a left B16 tumor treated with direct injection of CD40L-DCs, These results support the concept that genetic modification of DCs with a recombinant CD40L adenovirus vector may be a useful strategy for directly activating DCs for cancer immunotherapy. (Blood. 2000;95:91-99) (C) 2000 by The American Society of Hematology.
Keywords: adenovirus vector; colony-stimulating factor; cutting edge; antitumor immunity; gene-transfer; b-cells; antigen gene; cytotoxic t-lymphocytes; human blood; responses in-vitro
Journal Title: Blood
Volume: 96
Issue: 1
ISSN: 0006-4971
Publisher: American Society of Hematology  
Date Published: 2000-07-01
Start Page: 91
End Page: 99
Language: English
ACCESSION: WOS:000087813200015
PROVIDER: wos
PUBMED: 10891436
Notes: Article -- Source: Wos