Targeted delivery of therapeutic agents and imaging reagents to pancreatic cancer cells
US-2020179530-A1 · Jun 11, 2020 · US
US10357577B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10357577-B2 |
| Application number | US-201113810434-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 18, 2011 |
| Priority date | Jul 16, 2010 |
| Publication date | Jul 23, 2019 |
| Grant date | Jul 23, 2019 |
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The invention relates generally to bacterial nitroreductase enzymes and methods of use thereof: more particularly, although not exclusively, the enzymes have use in non-invasive imaging techniques, monitoring of therapeutic cell populations and gene-directed enzyme prodrug therapy. The invention also relates to the use of bacterial nitroreductase enzymes in radioimaging and/or ablation of biological agents and to compositions of use in such methods.
Opening claim text (preview).
What we claim is: 1. A method of radioimaging of at least one of a cell and a biological agent in a subject, the method comprising the steps of: a) introduction of a bacterial NfsA family nitroreductase to a subject; and b) introduction of a radiolabeled imaging probe to the subject; wherein the method further comprises radioimaging at least one of the cell and biological agent; wherein the NfsA family nitroreductase is capable of activating the imaging probe; and wherein steps a) and b) may be carried out concurrently or sequentially in any order; wherein the radiolabeled imaging probe comprises a radiolabeled 2-nitroimidazole compound. 2. The method of claim 1 , further comprising a step of: c) introduction of a prodrug to the subject; wherein the NfsA family nitroreductase is capable of activating the prodrug and wherein steps a) to c) may be carried out concurrently or sequentially in any order. 3. The method of claim 1 wherein the NfsA family nitroreductase is introduced using gene-directed enzyme prodrug therapy (GDEPT), virus-directed enzyme prodrug therapy (VDEPT), bacterial-directed enzyme prodrug therapy (BDEPT), Clostridia -directed enzyme prodrug therapy (CDEPT) or antibody-directed enzyme prodrug therapy (ADEPT). 4. The method of claim 2 wherein the NfsA family nitroreductase is introduced via a transformed cell and/or biological agent that expresses the NfsA family nitroreductase and the sensitivity of the transformed cell and/or biological agent to the prodrug is improved relative to a cell or biological agent that does not express the NfsA family nitroreductase. 5. The method of claim 2 wherein the prodrug comprises a nitroheterocyclic, nitrocarbocyclic, nitroaromatic, mononitrobenzamide, dinitrobenzamide or quinone-derived compound. 6. The method of claim 2 wherein the prodrug is selected from the group consisting of NLCQ-1, RSU-1069, RB6145, CI-1010, Misonidazole, Etanidazole, Nimorazole, Metronidazole, Tinidazole, Ornidazole, Nitrofurantoin, Nitrofurazone, Nifuratel, Nifurtimox, Furazolidinone, SN26634, SN27857, KSI 19, LH7, EF5 (pentafluoroetanidazole), EF3 (trifluoroetanidazole), CB 1954, TH-302, PR-104A, SN27686, SN31609, SN32102, SN28065, SN28099, mitomycin C, porfiromycin, E09 and RHI. 7. The method of claim 2 wherein the prodrug and the radiolabeled imaging probe are the same compound. 8. The method of claim 2 , wherein introducing said prodrug is used to diagnose and/or treat a disease selected from the group consisting of cancer, Parkinson's disease, Alzheimer's disease, stroke, heart disease, rheumatological diseases and a disease treated by stem-cell transplantation. 9. The method of claim 1 wherein the NfsA nitroreductase is an NfsA family nitroreductase according to SEQ ID NO 1 to 20. 10. The method of claim 1 wherein the NfsA nitroreductase has an S41Y mutation that confers an increased sensitivity to one or more bioreductive substrates.
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