Method of ex vivo enhancement of immune cell activity for cancer immunotherapy with a small molecule ablative compound
View Patent ↗A cancer immunotherapy method is disclosed in which “induced immune anticancer agents” are isolated after being induced in an animal host by intralesional (IL) administration of a halogenated xanthene tumor-ablative compound into a solid cancerous tumor of that host animal. A sample of the induced immune anticancer agents is removed (collected) from the tumor-bearing host, banked if desired, cultured and preferentially expanded to form an immunologically-effective enriched tumor-specific immune anticancer agent composition. That composition is reintroduced in to the host from which the predecessor induced immune anticancer agents were taken, or into another immunologically suitable host in need.
1. A method of forming a composition of enriched tumor-specific immune anticancer agents from a host mammal comprising the steps of:
(A) intralesionally contacting cancerous tumor tissue in a mammalian host with a tumor-ablating amount of a halogenated xanthene;
(B) maintaining said mammalian host for a period of time sufficient to induce the mammal's immune system to produce, relative to the amount prior to treatment, a statistically significantly enhanced concentration of halogenated xanthene-induced immune anticancer components comprising one or more of a) a lymph-soluble cytokine selected from the group consisting of IL-2, TNF-α, LT, GM-CSF, IFN-γ, and HMGB1, b) immune cells that are peripheral blood mononuclear cells and c) antibodies that bind to an antigen displayed on a whole tumor cell or chemoablated cell debris;
(C) collecting from said mammalian host a sample comprising one or more of an aliquot of peripheral blood, tumor tissue or lymphoid or lymph node tissue that contains said halogenated xanthene-induced immune anticancer components of step (B); and
(D) culturing and preferentially expanding in vitro said halogenated xanthene-induced immune anticancer components present in said sample to form an enriched tumor-specific immune anticancer agent composition.
2. The method of claim 1 , wherein said immune cells are NK cells.
3. The method of claim 1 , wherein said immune cells are T cells.
4. The method of claim 1 , wherein said immune cells are dendritic cells.
5. The method of claim 1 , wherein said immune cells are B cells.
6. The method of claim 1 , wherein said induced immune anticancer components collected in step (C) include anti-tumor antibodies and cytokines.
7. The method of claim 6 , wherein said cytokines include HMGB1.
8. The method of claim 6 , wherein said cytokines include IFN-γ.
9. The method of claim 1 , wherein said composition of enriched tumor-specific immune anticancer agents of step (D) is further adjusted to form an immunologically-effective enriched tumor-specific immune anticancer agent preparation that contains an immunologically-effective concentration of enriched tumor-specific immune anticancer agents dissolved or dispersed in a pharmaceutically acceptable diluent, said composition also containing a parenteral injection-appropriate salt content, osmolality and pH value.
10. The method of claim 9 , including the further step of collecting the immunologically-effective enriched tumor-specific immune anticancer agent preparation.
11. The method of claim 1 , wherein said lymphoid tissue of step (C) includes draining lymph nodes, thymus cells and splenic cells.
12. The method of claim 1 , wherein T cells are separated from said sample and are preferentially expanded in step (D).
13. The method of claim 1 including the further step of banking said sample prior to step (D).
14. The method of claim 1 including the further step of banking said sample after step (D).
15. The method of claim 1 , wherein said halogenated xanthene is a compound of Formula 1 or Formula 2, below, in which R 1 is independently F, Cl, Br, I, H or C 1 -C 4 alkyl; R 2 , R 3 , R 4 , and R 5 are independently Cl, H or I wherein at least one substituent of R 2 , R 3 , R 4 , and R 5 is I and at least one is Cl or H; R 6 independently H or C 1 -C 4 alkyl; R 11 is H or C 1 -C 4 alkyl; R 12 is H or C 1 -C 7 acyl
16. The method of claim 1 , wherein the contacted cancerous tumor tissue is selected from one or more of the group consisting of melanoma, prostate, breast, bladder, renal, pancreatic, colon, colorectal, gall bladder, primary or metastatic liver cancer, and small cell and non-small cell lung cancer.
17. The method of claim 1 , wherein the contacted cancerous tumor tissue is melanoma.
18. A method of treating an mammalian host with a cancerous tumor that comprises the step of administering an effective amount of an immunologically-effective enriched tumor-specific immune anticancer agent preparation of claim 10 to said animal host.
19. The method according to claim 18 , wherein said immunologically-effective enriched tumor-specific immune anticancer agent preparation includes one or more of NK cells, T cells, B cells and dendritic cells.
20. The method according to claim 18 , wherein said immunologically-effective enriched tumor-specific immune anticancer agent preparation includes one or both of HMGB1 and IFN-γ.
21. The method according to claim 18 , wherein the enriched tumor-specific immune anticancer agents of said immunologically-effective enriched tumor-specific immune anticancer agent preparation are autologous to said host mammal.
22. The method according to claim 18 further including the step of administering one or more systemic inhibitors of immune system down regulation to said host mammal.
23. The method according to claim 22 , wherein said systemic inhibitor of immune system down regulation is a monoclonal antibody that immunoreacts with one or more of CTLA-4, PD-1, PD-L1 and PD-L2.
24. The method according to claim 22 , wherein said systemic inhibitor of immune system down regulation is administered to said host mammal after administration of said tumor-ablating amount of a halogenated xanthene and before collecting said sample that contains said induced immune anticancer components from said host mammal.
25. A method of treating an mammalian host with a plurality of cancerous tumors that comprises the steps of:
(A) contacting tissue of a first cancerous tumor in said mammalian host with a tumor-ablating amount of a halogenated xanthene;
(B) maintaining said mammalian host for a period of time sufficient to induce the mammal's immune system to produce relative to the amount prior to treatment, a statistically significant enhanced concentration of halogenated xanthene-induced immune anticancer components comprising one or more of a) a lymph-soluble cytokine selected from the group consisting of Il-2, TNF-α, LT, GM-CSF, IFN-γ, and HMGB1, b) immune cells that are peripheral blood mononuclear cells and c) antibodies that bind to an antigen displayed on a whole tumor cell or chemoablated cell debris;
(C) collecting a sample from said mammalian host comprising one or more of an aliquot of peripheral blood, tumor tissue or lymphoid or lymph node tissue that contains said halogenated xanthene-induced immune anticancer components of step (B);
(D) contacting tissue of a second cancerous tumor in said mammalian host with said induced immune anticancer components of step (C) from said mammalian host; and
(E) maintaining said mammalian host for a second period of time sufficient to induce the mammal's immune system to produce, relative to the amount prior to treatment, second induced immune anticancer components comprising one or more of a) a lymph-soluble cytokine selected from the group consisting of IL-2, TNF-α, LT, GM-CSF, IFN-γ, and HMGB1, b) immune cells that are peripheral blood mononuclear cells and c) antibodies that bind to an antigen displayed on a whole tumor cell or chemoablated cell debris.
26. The method according to claim 25 including the additional steps of:
(F) collecting a second sample comprising one or more of an aliquot of second induced immune anticancer components of step (E) from said mammalian host; and
(G) culturing and preferentially expanding in vitro said second induced immune anticancer components of step (F) present in said sample to form an enriched tumor-specific immune anticancer agent composition.