Methods for identifying agents and their use for the prevention of restenosis
View Patent ↗Agents that inhibit or prevent restenosis are identified by assaying test agents in a battery of assays to measure the effect of the test agent on cell proliferation, thrombosis, tissue modeling, and inflammation. Treatment for restenosis is provided using compositions of the invention.
1. A method for identifying an agent useful in reducing the incidence of restenosis, said method comprising testing said agent in a plurality of in vitro assays that assess the ability of the agent to inhibit smooth muscle proliferation in an assay as recited in step (h) or (i); to not inhibit endothelial cell proliferation in an assay as recited in step (a), (b), (e), or (f); to inhibit matrix remodeling in an assay as recited in step (a), (c), (e), (g), (k), (1) or (m); to not act as a pro-thrombotic in an assay as recited in step (a), (e), (g), or (k); and to act as an anti-inflammatory in an assay as recited in step (a), (d), (e), (g), (i), (k), (1); wherein the assays are selected from:
(a) culturing umbilical vein endothelial cells in the presence of added IL-1β+TNF-α+IFN-γ, and recording changes in at least one cellular parameter readout as a result of introduction of the agent, said parameters being selected from: MCP-1, uPAR, tissue factor, thrombomodulin, SRB, and proliferation;
(b) culturing umbilical vein endothelial cells; and recording changes in proliferation as a result of introduction of the agent;
(c) culturing umbilical vein endothelial cells in the presence of added IL-4+histamine, and recording changes in at least one cellular parameter readout as a result of introduction of the agent, said parameters being selected from: VEGFRII, uPAR, and SRB;
(d) culturing peripheral blood mononuclear cells and umbilical vein endothelial cells in the presence of added TLR4, and recording changes in at least one cellular parameter readout as a result of introduction of the agent, said parameters being selected from: CD40, M-CSF, PGE2, TNF-α, and SRB;
(e) culturing coronary artery endothelial cells in the presence of added IL-1β+TNF-α+IFN-γ, and recording changes in at least one cellular parameter readout as a result of introduction of the agent, said parameters being selected from: MCP-1, CD 141, CD 142, IP-10, IL-8, tissue factor, thrombomodulin, SRB, and proliferation;
(f) culturing coronary artery endothelial cells and recording changes in proliferation as a result of introduction of the agent;
(g) culturing coronary artery smooth muscle cells cultured in the presence of added IL-1β+TNF-α+IFN-γ, and recording changes in at least one cellular parameter readout as a result of introduction of the agent, said parameters being selected from: MCP-1, uPAR, tissue factor, thrombomodulin, SRB and proliferation;
(h) culturing coronary artery smooth muscle cells and recording changes in proliferation as a result of introduction of the agent;
(i) culturing umbilical artery smooth muscle cells in the presence of added IL-1β+TNF-α+IFN-γ, and recording changes in at least one cellular parameter readout as a result of introduction of the agent, said parameters being selected from: MCP-1, CD141, CD142, IP-10, IL-8, SRB, and proliferation;
(j) culturing umbilical artery smooth muscle cells and recording changes in proliferation as a result of introduction of the agent;
(k) culturing umbilical vein endothelial cells and umbilical artery smooth muscle cells in the presence of added IL-1β+TNF-α+IFN-γ, and recording changes in at least one cellular parameter readout as a result of introduction of the agent, said parameters being selected from: CD40, uPAR, IP-10, tissue factor, thrombomodulin, M-CSF, and SRB;
(l) culturing fibroblasts cultured in the presence of added IL-1β+TNF-α+IFN-γ, and recording changes in at least one cellular parameter readout as a result of introduction of the agent, said parameters being selected from: Collagen I and IP-10;
(m) culturing fibroblasts in the presence of added TGF-β, and recording changes in at least one cellular parameter readout as a result of introduction of the agent, said parameters being selected from: Collagen I, SRB and PAI-1;
and wherein said agent is tested in at least one assay that assesses the ability of the agent to inhibit smooth muscle proliferation as recited in steps (g), (h), (i) and (j) and at least one assay that assesses the ability of the agent to not inhibit endothelial cell proliferation as recited in steps (a), (b), (c) (d), (e), and (f), wherein an agent that inhibits smooth muscle proliferation and does not inhibit endothelial cell proliferation is selected as being useful in reducing the incidence of restenosis.
2. The method of claim 1 , wherein the cellular parameter readout is selected from uPAR expression of endothelial cells or smooth muscle cells; PGE 2 expression in endothelial cells or monocytes; thrombomodulin expression in endothelial cells and smooth muscle cells, tissue factor expression in endothelial cells and smooth muscle cells, CD40 expression in monocytes or endothelial cells; IP-10 expression in endothelial cells or human dermal fibroblasts; MCP-1 expression in vascular endothelial cells or smooth muscle cells, collagen I expression in human dermal fibroblasts; VEGFR2 expression in endothelial cells; PAI-1 expression in human dermal fibroblasts or smooth muscle cells; IL-8 expression in smooth muscle cells; M-CSF expression in endothelial cells or smooth muscle cells, TNF-α expression in monocytes.
3. The method of claim 1 , wherein each assay is scored according to modulation of the selected readout parameters, and wherein an agent that scores higher than a control compound that is an approved therapeutic agent for inhibition of restenosis.
4. The method of claim 1 , further comprising determining a log ratio of smooth muscle cell to endothelial cell proliferation for the compounds, where an agent having a ratio of greater than 1 preferentially inhibit smooth muscle cell proliferation relative to endothelial cell proliferation and is selected as a candidate drug.
5. A method for identifying an agent useful in reducing the incidence of restenosis, said method comprising testing said agent in a plurality of in vitro assays that assess the ability of the agent to inhibit smooth muscle proliferation in an assay as recited in step (d) or (e); to not inhibit endothelial cell proliferation in an assay as recited in step (a), (b); to inhibit matrix remodeling in an assay as recited in step (a) or (d); to not act as a pro-thrombotic in an assay as recited in step (a) or (d); and to act as an anti-inflammatory in an assay as recited in step (a), (c), or (d); wherein the assays comprise each of:
(a) culturing umbilical vein endothelial cells in the presence of added IL-1β+TNF-α+IFN-γ, and recording changes in at least one cellular parameter readout as a result of introduction of the agent, said parameters being selected from: MCP-1, uPAR, tissue factor, thrombomodulin, SRB, and proliferation;
(b) culturing umbilical vein endothelial cells; and recording changes in proliferation as a result of introduction of the agent;
(c) culturing peripheral blood mononuclear cells and umbilical vein endothelial cells cultured in the presence of added TLR4, and recording changes in at least one cellular parameter readout as a result of introduction of the agent, said parameters being CD40, M-CSF, PGE2, TNF-α, and SRB;
(d) culturing coronary artery smooth muscle cells cultured in the presence of added IL-1β+TNF-α+IFN-γ, and recording changes in at least one cellular parameter readout as a result of introduction of the agent, said parameters being: MCP-1, uPAR, tissue factor, thrombomodulin, SRB and proliferation;
(e) culturing coronary artery smooth muscle cells and recording changes in proliferation as a result of introduction of the agent;
and wherein an agent that inhibits smooth muscle proliferation in one of the foregoing assays and does not inhibit endothelial cell proliferation in one of the foregoing assays is selected as being useful in reducing the incidence of restenosis.