Efficacy of dendritic cell-based immunotherapy produced from cord blood in vitro and in a humanized NSG mouse cancer model

Author:

Liu Gang12,Fan Xiaoyan3,Cai Ying4,Fu Zexian1,Gao Fei1,Dong Jiantao12,Li Kang1,Cai Jianhui123

Affiliation:

1. Department of Surgery, Hebei Medical University, 361 East Zhongshan Road,  Shijiazhuang 050017, China

2. Department of Surgery, Hebei General Hospital,  348 Heping West Road, Shijiazhuang 050051, China

3. Department of Oncology, Hebei General Hospital, 348 Heping West Road, Shijiazhuang 050051, China

4. Department of Research and Development, Hebei Engineering Technology Research Center for Cell Therapy, Hebei HOFOY Biotech Corporation Ltd, 238 Changjiang Aveneu, Shijiazhuang 500350, China

Abstract

Aim: To produce dendritic cells (DCs) from CD34+ stem cells from cord blood and explore their prophylactic and curative effect against tumors by vaccinating humanized NSG mice. Materials & methods: Separated CD34+ stem cells from cord blood were cultured for 30 days, and the resultant DCs (CD34-DCs) were collected. The basic function of the CD34-DCs and the cytotoxicity of CD34-cytotoxic-T lymphocytes (CTLs) were tested in vitro, and tumor inhibition in a humanized NSG mouse tumor model was observed. Results: The number of CD34-DCs reached approximately 9 log. These cells performed functions similar to those of DCs derived from monocytes from peripheral blood (PBMC-DCs). The CTLs of the CD34-DCs (CD34-CTLs) presented a better antitumor effect in vitro. The obvious prophylactic and therapeutic antitumor effects of the CD34-DC vaccine were observed in the humanized NSG mouse models. Conclusion: CD34-DCs from cord blood were sufficient in quantity and quality as a vaccine agent against tumors in vitro and in vivo.

Publisher

Future Medicine Ltd

Subject

Oncology,Immunology,Immunology and Allergy

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