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Combined Cytolytic Effects of a Vaccinia Virus Encoding a Single Chain Trimer of MHC-I with a Tax-Epitope and Tax-Specific CTLs on HTLV-I-Infected Cells in a Rat Model
Title: | Combined Cytolytic Effects of a Vaccinia Virus Encoding a Single Chain Trimer of MHC-I with a Tax-Epitope and Tax-Specific CTLs on HTLV-I-Infected Cells in a Rat Model |
Authors: | Ohashi, Takashi Browse this author →KAKEN DB | Nakamura, Takafumi Browse this author | Kidokoro, Minoru Browse this author | Zhang, Xianfeng Browse this author →KAKEN DB | Shida, Hisatoshi Browse this author →KAKEN DB |
Issue Date: | 2014 |
Publisher: | Hindawi Publishing Corporation |
Journal Title: | Biomed Research International |
Volume: | 2014 |
Start Page: | 902478 |
Publisher DOI: | 10.1155/2014/902478 |
PMID: | 24791004 |
Abstract: | Adult T cell leukemia (ATL) is a malignant lymphoproliferative disease caused by human T cell leukemia virus type I (HTLV-I). To develop an effective therapy against the disease, we have examined the oncolytic ability of an attenuated vaccinia virus (VV), LC16m8 Delta(m8 Delta), and an HTLV-I Tax-specific cytotoxic T lymphocyte (CTL) line, 4O1/C8, against an HTLV-I-infected rat T cell line, FPM1. Our results demonstrated that m8 Delta was able to replicate in and lyse tumorigenic FPM1 cells but was incompetent to injure 4O1/C8 cells, suggesting the preferential cytolytic activity toward tumor cells. To further enhance the cytolysis of HTLV-Iinfected cells, we modified m8 Delta and obtained m8 Delta/RT1AlSCTax180L, which can express a single chain trimer (SCT) of rat major histocompatibility complex class I with a Tax-epitope. Combined treatment withm8 Delta/RT1AlSCTax180L and 4O1/C8 increased the cytolysis of FPM1V.EFGFP/8R cells, a CTL-resistant subclone of FPM1, compared with that using 4O1/C8 and m8. presenting an unrelated peptide, suggesting that the activation of 4O1/C8 by m8 Delta/RT1AlSCTax180L further enhanced the killing of the tumorigenic HTLV-I-infected cells. Our results indicate that combined therapy of oncolytic VVs with SCTs and HTLV-I-specific CTLs may be effective for eradication of HTLV-I-infected cells, which evade from CTL lysis and potentially develop ATL. |
Rights: | Copyright © 2014 Takashi Ohashi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
Type: | article |
URI: | http://hdl.handle.net/2115/55821 |
Appears in Collections: | 遺伝子病制御研究所 (Institute for Genetic Medicine) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)
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Submitter: 大橋 貴
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