Cargando…

Construction of doxycyline-dependent mini-HIV-1 variants for the development of a virotherapy against leukemias

T-cell acute lymphoblastic leukemia (T-ALL) is a high-risk type of blood-cell cancer. We describe the improvement of a candidate therapeutic virus for virotherapy of leukemic cells. Virotherapy is based on the exclusive replication of a virus in leukemic cells, leading to the selective removal of th...

Descripción completa

Detalles Bibliográficos
Autores principales: Jeeninga, Rienk E, Jan, Barbara, van den Berg, Henk, Berkhout, Ben
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1592508/
https://www.ncbi.nlm.nih.gov/pubmed/17005036
http://dx.doi.org/10.1186/1742-4690-3-64
_version_ 1782130410379018240
author Jeeninga, Rienk E
Jan, Barbara
van den Berg, Henk
Berkhout, Ben
author_facet Jeeninga, Rienk E
Jan, Barbara
van den Berg, Henk
Berkhout, Ben
author_sort Jeeninga, Rienk E
collection PubMed
description T-cell acute lymphoblastic leukemia (T-ALL) is a high-risk type of blood-cell cancer. We describe the improvement of a candidate therapeutic virus for virotherapy of leukemic cells. Virotherapy is based on the exclusive replication of a virus in leukemic cells, leading to the selective removal of these malignant cells. To improve the safety of such a virus, we constructed an HIV-1 variant that replicates exclusively in the presence of the nontoxic effector doxycycline (dox). This was achieved by replacement of the viral TAR-Tat system for transcriptional activation by the Escherichia coli-derived Tet system for inducible gene expression. This HIV-rtTA virus replicates in a strictly dox-dependent manner. In this virus, additional deletions and/or inactivating mutations were introduced in the genes for accessory proteins. These proteins are essential for virus replication in untransformed cells, but dispensable in leukemic T cells. These minimized HIV-rtTA variants contain up to 7 deletions/inactivating mutations (TAR, Tat, vif, vpR, vpU, nef and U3) and replicate efficiently in the leukemic SupT1 T cell line, but do not replicate in normal peripheral blood mononuclear cells. These virus variants are also able to efficiently remove leukemic cells from a mixed culture with untransformed cells. The therapeutic viruses use CD4 and CXCR4 for cell entry and could potentially be used against CXCR4 expressing malignancies such as T-lymphoblastic leukemia/lymphoma, NK leukemia and some myeloid leukemias.
format Text
id pubmed-1592508
institution National Center for Biotechnology Information
language English
publishDate 2006
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-15925082006-10-07 Construction of doxycyline-dependent mini-HIV-1 variants for the development of a virotherapy against leukemias Jeeninga, Rienk E Jan, Barbara van den Berg, Henk Berkhout, Ben Retrovirology Research T-cell acute lymphoblastic leukemia (T-ALL) is a high-risk type of blood-cell cancer. We describe the improvement of a candidate therapeutic virus for virotherapy of leukemic cells. Virotherapy is based on the exclusive replication of a virus in leukemic cells, leading to the selective removal of these malignant cells. To improve the safety of such a virus, we constructed an HIV-1 variant that replicates exclusively in the presence of the nontoxic effector doxycycline (dox). This was achieved by replacement of the viral TAR-Tat system for transcriptional activation by the Escherichia coli-derived Tet system for inducible gene expression. This HIV-rtTA virus replicates in a strictly dox-dependent manner. In this virus, additional deletions and/or inactivating mutations were introduced in the genes for accessory proteins. These proteins are essential for virus replication in untransformed cells, but dispensable in leukemic T cells. These minimized HIV-rtTA variants contain up to 7 deletions/inactivating mutations (TAR, Tat, vif, vpR, vpU, nef and U3) and replicate efficiently in the leukemic SupT1 T cell line, but do not replicate in normal peripheral blood mononuclear cells. These virus variants are also able to efficiently remove leukemic cells from a mixed culture with untransformed cells. The therapeutic viruses use CD4 and CXCR4 for cell entry and could potentially be used against CXCR4 expressing malignancies such as T-lymphoblastic leukemia/lymphoma, NK leukemia and some myeloid leukemias. BioMed Central 2006-09-27 /pmc/articles/PMC1592508/ /pubmed/17005036 http://dx.doi.org/10.1186/1742-4690-3-64 Text en Copyright © 2006 Jeeninga et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Jeeninga, Rienk E
Jan, Barbara
van den Berg, Henk
Berkhout, Ben
Construction of doxycyline-dependent mini-HIV-1 variants for the development of a virotherapy against leukemias
title Construction of doxycyline-dependent mini-HIV-1 variants for the development of a virotherapy against leukemias
title_full Construction of doxycyline-dependent mini-HIV-1 variants for the development of a virotherapy against leukemias
title_fullStr Construction of doxycyline-dependent mini-HIV-1 variants for the development of a virotherapy against leukemias
title_full_unstemmed Construction of doxycyline-dependent mini-HIV-1 variants for the development of a virotherapy against leukemias
title_short Construction of doxycyline-dependent mini-HIV-1 variants for the development of a virotherapy against leukemias
title_sort construction of doxycyline-dependent mini-hiv-1 variants for the development of a virotherapy against leukemias
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1592508/
https://www.ncbi.nlm.nih.gov/pubmed/17005036
http://dx.doi.org/10.1186/1742-4690-3-64
work_keys_str_mv AT jeeningarienke constructionofdoxycylinedependentminihiv1variantsforthedevelopmentofavirotherapyagainstleukemias
AT janbarbara constructionofdoxycylinedependentminihiv1variantsforthedevelopmentofavirotherapyagainstleukemias
AT vandenberghenk constructionofdoxycylinedependentminihiv1variantsforthedevelopmentofavirotherapyagainstleukemias
AT berkhoutben constructionofdoxycylinedependentminihiv1variantsforthedevelopmentofavirotherapyagainstleukemias