New applications of gene therapy technology
OwnerMichael Z. Gilmaninventor
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Abstract
This invention provides new applications of regulated gene therapy relating to treatment of cancer and other disorders.
Claims23
A cell containing
- (a) a first DNA construct or pair of first DNA constructs encoding chimeric proteins comprising (i) at least one receptor domain capable of binding to a selected ligand and (ii) another protein domain, heterologous with respect to the receptor domain, and
- (b) a target gene encoding an angiogenesis inhibitor under the expression control of a transcriptional control element responsive to binding of ligand to the ligand binding domain.
A cell containing
- (a) a first DNA construct or pair of first DNA constructs encoding chimeric proteins comprising (i) at least one receptor domain capable of binding to a selected ligand and (ii) another protein domain, heterologous with respect to the receptor domain, and
- (b) a target gene encoding a tumor specific antigen under the expression control of a transcriptional control element responsive to binding of ligand to the ligand binding domain.
A cell containing
- (a) a DNA construct encoding a chimeric protein consisting essentially of (i) a receptor domain capable of binding to a selected ligand, (ii) a transcription activation domain, heterologous with respect to the receptor domain, (iii) and a DNA binding domain;
- and
- (b) a target gene encoding beta-interferon or a cytokine under the expression control of a transcriptional control element responsive to binding of ligand to the ligand binding domain.
A recombinant virus containing
- (a) a first DNA construct or pair of first DNA constructs encoding chimeric proteins comprising (i) at least one receptor domain capable of binding to a selected ligand and (ii) another protein domain, heterologous with respect to the receptor domain, and
- (b) a target gene encoding an angiogenesis inhibitor, a tumor specific antigen, a cytokine or beta-interferon under the expression control of a transcriptional control element responsive to binding of ligand to the ligand binding domain.
A method for rendering cells capable of regulatable expression of a target gene following exposure of the cells to a selected ligand, which method comprises introducing into the cells:
- (a) a first DNA construct or pair of first DNA constructs encoding chimeric proteins comprising (i) at least one receptor domain capable of binding to a selected ligand and (ii) another protein domain, heterologous with respect to the receptor domain, and
- (b) a target gene under the expression control of a transcriptional control element responsive to binding of ligand to the ligand binding domain,
- wherein the target gene encodes an angiogenesis inhibitor or a tumor specific antigen.
A method for rendering cells capable of regulatable expression of a target gene following exposure of the cells to a selected ligand, which method comprises introducing into the cells:
- (a) a DNA construct encoding a chimeric protein consisting essentially of (i) a receptor domain capable of binding to a selected ligand, (ii) a transcription activation domain, heterologous with respect to the receptor domain, (iii) and a DNA binding domain;
- and
- (b) a target gene encoding beta-interferon or a cytokine under the expression control of a transcriptional control element responsive to binding of ligand to the ligand binding domain.
A method for treating cancer in a mammalian host organism containing cells which:
- contain (a) a first DNA construct or pair of first DNA constructs encoding chimeric proteins comprising (i) at least one receptor domain capable of binding to a selected ligand and (ii) another protein domain, heterologous with respect to the receptor domain, and
- (b) a target gene under the expression control of a transcriptional control element responsive to binding of ligand to the ligand binding domain;
- and
- which express the target gene, following exposure to the selected ligand;
- wherein the target gene encodes an angiogenesis inhibitor, a tumor-specific antigen or a cytokine;
- which method comprises administering to said mammalian host an effective amount of a selected ligand capable of binding to the chimeric protein to effect observable expression of the target gene.
A method for treating MS episodes in a mammalian host organism containing cells which:
- contain (a) a first DNA construct or pair of first DNA constructs encoding chimeric proteins comprising (i) at least one receptor domain capable of binding to a selected ligand and (ii) another protein domain, heterologous with respect to the receptor domain, and
- (b) a target gene encoding beta-interferon under the expression control of a transcriptional control element responsive to binding of ligand to the ligand binding domain;
- and
- which express the target gene, following exposure to the selected ligand;
- which method comprises administering to said mammalian host an effective amount of a selected ligand capable of binding to the chimeric protein to effect observable expression of the target beta-interferon gene.
A method for treating HIV infection in a mammalian host organism containing cells which:
- contain (a) a first DNA construct or pair of first DNA constructs encoding chimeric proteins comprising (i) at least one receptor domain capable of binding to a selected ligand and (ii) another protein domain, heterologous with respect to the receptor domain, and
- (b) a target gene under the expression control of a transcriptional control element responsive to binding of ligand to the ligand binding domain;
- and
- which express the target gene, following exposure to the selected ligand;
- wherein the target gene encodes a ribozyme or antisense message directed against an HIV nucleotide sequence;
- which method comprises administering to said mammalian host an effective amount of a selected ligand capable of binding to the chimeric protein to effect observable expression of the target gene.
Dependencies are inferred from the claim text.