Publication: Dendritic cells pulsed with total tumor RNA for activation NK-like T cells against glioblastoma multiforme
Issued Date
2005-11-01
Resource Type
ISSN
15737373
0167594X
0167594X
Other identifier(s)
2-s2.0-29244463830
Rights
Mahidol University
Rights Holder(s)
SCOPUS
Bibliographic Citation
Journal of Neuro-Oncology. Vol.75, No.2 (2005), 111-118
Suggested Citation
Prachya Vichchatorn, Adisak Wongkajornsilp, Sawang Petvises, Sumalee Tangpradabkul, Samart Pakakasama, Suradej Hongeng Dendritic cells pulsed with total tumor RNA for activation NK-like T cells against glioblastoma multiforme. Journal of Neuro-Oncology. Vol.75, No.2 (2005), 111-118. doi:10.1007/s11060-005-2317-2 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/16280
Research Projects
Organizational Units
Authors
Journal Issue
Thesis
Title
Dendritic cells pulsed with total tumor RNA for activation NK-like T cells against glioblastoma multiforme
Abstract
Dendritic cells (DCs) are potent antigen presenting cells and play critical role in T cell-mediated immunity. DCs have been shown to induce strong anti-tumor responses both in vitro and in vivo. Their efficacies in tumor therapy are being investigated in clinical trials. Previous evidence has shown that these DCs enhance the cytotoxicity of NK cells. We generated NK-like T cells (CD3+CD56+), a novel type of effector cells differentiated from normal lymphocyte, which is now being used for adoptive immunotherapy in clinical trials. This study aimed to elucidate the effects of NK-like T cells after co-culturing with DCs against tumor cells. The result revealed that tumor-derived RNA-pulsed DCs can enhance the immune responses of NK-like T cells against glioblastoma multiforme cell line but these effector cells did not appear to have the cytotoxic effect against normal cells (human umbilical vein endothelial cells (HUVEC) and fibroblasts) in vitro. This study may be beneficial for the development of new immunologic effector cells for using in adoptive immunotherapy for glioblastoma multiforme in the future. © Springer 2005.
