Anticancer combinations
Abstract
Provided herein, inter alia, are compositions and kits comprising a bacterial cell and a tumor penetrating agent. Also provided are methods of treating cancer in a subject including the step of administering to the subject an effective amount of a bacterial cell and a tumor penetrating agent. Provided are methods of stimulating an immune system in a subject. The methods include administering to the subject an effective amount of a bacterial cell and a tumor penetrating agent. Also provided are methods of enhancing delivery of an anti-cancer agent to a tumor cell including the step of contacting the tumor cell with a bacterial cell, a tumor penetrating agent and an anti-cancer agent.
Claims
exact text as granted — not AI-modified1 . A method of treating cancer in a subject comprising administering to the subject a combined effective amount of a bacterial cell and a tumor penetrating agent, wherein administration treats the cancer in the subject.
2 . The method of claim 1 , wherein the combined effective amount is a combined synergistic amount.
3 . A method of stimulating an immune system in a subject comprising administering to the subject a combined effective amount of a bacterial cell and a tumor penetrating agent, wherein administration of the bacterial cell and the tumor penetrating agent stimulates the immune system of the subject.
4 . The method of claim 3 , wherein the immune response is an anti-cancer immune response.
5 . The method of claim 1 , further comprising administering to the subject an anti-cancer agent.
6 . (canceled)
7 . A method of enhancing delivery of an anti-cancer agent to a tumor cell comprising contacting the tumor cell with a bacterial cell, a tumor penetrating agent and an anti-cancer agent, wherein contacting the tumor cell with the bacterial cell and cell penetrating agent enhances delivery of the anti-cancer agent.
8 . The method of claim 7 , wherein the anti-cancer agent is selected from the group consisting of a small molecule, a nucleic acid, a polypeptide, and an antibody.
9 . The method of claim 1 , wherein the bacterial cell is a Salmonella bacterial cell.
10 . (canceled)
11 . The method of claim 9 , wherein the Salmonella bacterial cell is selected from the group consisting of YS1646 (ATCC #202165), RE88, LH430, SL7207, χ8429, χ8431 an χ8468.
12 . The method of claim 1 , wherein the bacterial cell comprises an antisense nucleic acid.
13 . (canceled)
14 . The method of claim 12 , wherein the antisense nucleic acid targets an immunosuppressive target.
15 . The method of claim 14 , wherein the immunosuppressive target is STAT3, IDO1, IDO2, Arginase 1, iNOS, CTLA-4, TGF-β, IL-10, pGE2 or VEGF.
16 . (canceled)
17 . (canceled)
18 . The method of claim 12 , wherein the antisense nucleic acid is selected from the group consisting of SEQ ID NO:3-31.
19 . The method of claim 1 , wherein the tumor penetrating agent is a hyaluronidase polypeptide.
20 . (canceled)
21 . (canceled)
22 . (canceled)
23 . (canceled)
24 . A composition comprising a Salmonella bacterial cell and a hyaluronidase polypeptide.
25 . (canceled)
26 . The composition of claim 24 , wherein the Salmonella bacterial cell is selected from the group consisting of YS1646 (ATCC #202165), RE88, LH430, SL7207, χ8429, χ8431 an χ8468.
27 . The composition of claim 24 , wherein the bacterial cell comprises an antisense nucleic acid.
28 . (canceled)
29 . The composition of claim 27 , wherein the antisense nucleic acid targets an immunosuppressive target selected from STATS, IDO1, IDO2, Arginase 1, iNOS, CTLA-4, TGF-β, IL-10, PGE2 and VEGF.
30 . (canceled)
31 . (canceled)
32 . (canceled)
33 . The composition of claim 27 , wherein the antisense nucleic acid is selected from the group consisting of SEQ ID NO:3-31.
34 . (canceled)
35 . (canceled)
36 . (canceled)
37 . The composition of claim 24 , further comprising an anti-cancer agent.
38 . (canceled)
39 . (canceled)
40 . (canceled)
41 . (canceled)Join the waitlist — get patent alerts
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