Generation of a Novel Oncolytic Vaccinia Virus Using the IHD-W Strain

被引:7
作者
Shin, Jaeil [1 ]
Hong, Soon-Oh [1 ]
Kim, Minju [1 ]
Lee, Hyesun [1 ]
Choi, Hwanjun [1 ]
Kim, Joonsung [1 ]
Hong, Jieun [1 ]
Kang, Hyesoo [1 ]
Lee, Eunjin [1 ]
Lee, Soondong [1 ]
Kong, Byoungjae [1 ]
Kim, Minjung [1 ]
Choi, Heonsik [1 ]
Kim, Sujeong [1 ]
机构
[1] Kolon Life Sci, Inst BioInnovat Res, 110 Magokdong Ro, Seoul 07793, South Korea
基金
新加坡国家研究基金会;
关键词
oncolytic virus; vaccinia; IHD-W strain; THYMIDINE KINASE; CANCER; GENE; BIOGENESIS; EXPRESSION; PROTEINS; DELETION; VECTORS; THERAPY; FUSION;
D O I
10.1089/hum.2020.050
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Oncolytic viruses are promising cancer therapies due to their selective killing of tumor cells and ability to stimulate the host immune system. As an oncolytic virus platform, vaccinia virus has unique advantages, including rapid replication, a broad range of host targets, and a large capacity for transgene incorporation. In this study, we developed a novel oncolytic vaccinia virus with high potency and a favorable safety profile. We began with the International Health Department-White (IHD-W) strain, which had the strongest cytotoxicity against tumor cells among the four vaccinia virus strains tested. Next, several candidate viruses were constructed by deleting three viral genes (C11R,K3L, andJ2R) in various combinations, and their efficacy and safety were compared. The virus ultimately selected, named KLS-3010, exhibited strong antitumor activity against broad targetsin vitroandin vivo. Furthermore, KLS-3010 showed a favorable safety profile in mice, as determined by the biodistribution and body weight change. More promisingly, KLS-3010 was able to shift the tumor microenvironment to a proinflammatory state, as evidenced by an increase in activated lymphocytes after KLS-3010 administration, suggesting that this strain may elicit an oncolytic virus-mediated immune response. The KLS-3010 strain thus represents a promising platform for the further development of oncolytic virus-based cancer therapies.
引用
收藏
页码:517 / 527
页数:11
相关论文
共 35 条
[1]  
[Anonymous], 2018, [88] Grecco, Hernan E., "Pint," 2018. 3., P3
[2]   HIGH-FREQUENCY HOMOLOGOUS RECOMBINATION IN VACCINIA VIRUS-DNA [J].
BALL, LA .
JOURNAL OF VIROLOGY, 1987, 61 (06) :1788-1795
[3]   THE NATURE OF NATURALLY-OCCURRING MUTATIONS IN THE HEMAGGLUTININ GENE OF VACCINIA VIRUS AND THE SEQUENCE OF IMMEDIATELY ADJACENT GENES [J].
BROWN, CK ;
BLOOM, DC ;
MOYER, RW .
VIRUS GENES, 1991, 5 (03) :235-242
[4]   DELETION OF THE VACCINIA VIRUS GROWTH-FACTOR GENE REDUCES VIRUS VIRULENCE [J].
BULLER, RML ;
CHAKRABARTI, S ;
COOPER, JA ;
TWARDZIK, DR ;
MOSS, B .
JOURNAL OF VIROLOGY, 1988, 62 (03) :866-874
[5]   DECREASED VIRULENCE OF RECOMBINANT VACCINIA VIRUS EXPRESSION VECTORS IS ASSOCIATED WITH A THYMIDINE KINASE-NEGATIVE PHENOTYPE [J].
BULLER, RML ;
SMITH, GL ;
CREMER, K ;
NOTKINS, AL ;
MOSS, B .
NATURE, 1985, 317 (6040) :813-815
[6]   Syncytia Formation in Oncolytic Virotherapy [J].
Burton, Chase ;
Bartee, Eric .
MOLECULAR THERAPY-ONCOLYTICS, 2019, 15 :131-139
[7]  
Cotter CA, 2015, CURR PROTOC MICROBIO, V39
[8]   THE VACCINIA VIRUS K3L-GENE PRODUCT POTENTIATES TRANSLATION BY INHIBITING DOUBLE-STRANDED-RNA-ACTIVATED PROTEIN-KINASE AND PHOSPHORYLATION OF THE ALPHA SUBUNIT OF EUKARYOTIC INITIATION FACTOR-II [J].
DAVIES, MV ;
ELROYSTEIN, O ;
JAGUS, R ;
MOSS, B ;
KAUFMAN, RJ .
JOURNAL OF VIROLOGY, 1992, 66 (04) :1943-1950
[9]   Repulsion of Superinfecting Virions: A Mechanism for Rapid Virus Spread [J].
Doceul, Virginie ;
Hollinshead, Michael ;
van der Linden, Lonneke ;
Smith, Geoffrey L. .
SCIENCE, 2010, 327 (5967) :873-876
[10]   FUSION OF INTRACELLULAR AND EXTRACELLULAR FORMS OF VACCINIA VIRUS WITH THE CELL-MEMBRANE [J].
DOMS, RW ;
BLUMENTHAL, R ;
MOSS, B .
JOURNAL OF VIROLOGY, 1990, 64 (10) :4884-4892