Use of attenuated paramyxoviruses for cancer therapy

被引:37
作者
Lech, Patrycja J. [1 ]
Russell, Stephen J. [1 ]
机构
[1] Mayo Clin, Dept Mol Med, Rochester, MN 55905 USA
关键词
antitumor immunity; cancer; CEA; cell carriers; clinical trials; immune response; measles virus; mumps virus; Newcastle disease virus; NIS; noninvasive imaging; oncolytic; radiovirotherapy; NEWCASTLE-DISEASE-VIRUS; ONCOLYTIC MEASLES-VIRUS; PHASE-I TRIAL; COMPLEMENT-REGULATORY PROTEINS; ACTIVE SPECIFIC IMMUNOTHERAPY; SUICIDE GENE-THERAPY; TUMOR-CELL VACCINE; REPLICATION-SELECTIVE ADENOVIRUS; APOPTOSIS-INDUCING LIGAND; PROSTATE-SPECIFIC ANTIGEN;
D O I
10.1586/ERV.10.124
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Paramyxoviruses, measles virus (MV), mumps virus (MuV) and Newcastle disease virus (NDV), are well known for causing measles and mumps in humans and Newcastle disease in birds. These viruses have been tamed (attenuated) and successfully used as vaccines to immunize their hosts. Remarkably, pathogenic MuV and vaccine strains of MuV, MV and NDV efficiently infect and kill cancer cells and are consequently being investigated as novel cancer therapies (oncolytic virotherapy). Phase I/II clinical trials have shown promise but treatment efficacy needs to be enhanced. Technologies being developed to increase treatment efficacy include: virotherapy in combination with immunosuppressive drugs (cyclophosphamide); retargeting of viruses to specific tumor types or tumor vasculature; using infected cell carriers to protect and deliver the virus to tumors; and genetic manipulation of the virus to increase viral spread and/or express transgenes during viral replication. Transgenes have enabled noninvasive imaging or tracking of viral gene expression and enhancement of tumor destruction.
引用
收藏
页码:1275 / 1302
页数:28
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