Nano-vehicle derived from tumor tissue, and cancer vaccine using same
The present invention relates to a cancer vaccine, and specifically, to a pharmaceutical composition for treating cancer containing a nano-vehicle derived from tumor tissue, and a method for treating cancer using the nano-vehicle derived from tumor tissue, and the like. According to the present invention, a nano-vehicle antigen derived from tumor tissue indicates a high yield while having properties similar to those of an exocellular vehicle, and can be variously modified, and is thus expected to be very useful for developing the cancer vaccine.
1. A pharmaceutical composition for treatment of cancer, comprising nanovesicles derived from a tumor tissue,
wherein
the nanovesicles are prepared by a method comprising:
(a) separating cells from a tumor tissue;
(b) constructing nanovesicles from a suspension of the cells by a process selected from the group consisting of extrusion, sonication, cell lysis, homogenation, freeze-thawing, electroporation, mechanical degradation, and chemical treatment;
(c) isolating the constructed nanovesicles from the suspension; and
(d) incubating a suspension of the nanovesicles in presence of an adjuvant,
or by a method comprising:
(e) separating cells from a tumor tissue;
(f) adding an adjuvant to a suspension of the cells to load the adjuvant into the cells; and
(g) constructing nanovesicles from the cell suspension by a process selected from the group consisting of extrusion, sonication, cell lysis, homogenation, freeze-thawing, electroporation, mechanical degradation, and chemical treatment.
2. The pharmaceutical composition of claim 1 , wherein the tumor tissue is transformed to express a heat-shock protein.
3. The pharmaceutical composition of claim 1 , further comprising an immune adjuvant.
4. The pharmaceutical composition of claim 3 , wherein the immune adjuvant is polyI:C.
5. The pharmaceutical composition of claim 1 , wherein the nanovesicles comprise a component other than that sourced from a plasma membrane of the tumor tissue.
6. The pharmaceutical composition of claim 5 , wherein the component is cyclodextrin or polyethylene glycol.
7. The pharmaceutical composition of claim 1 , wherein the nanovesicles have a chemically modified membrane.
8. The pharmaceutical composition of claim 7 , wherein the nanovesicles are chemically modified with a thiol group or an amine group.
9. A method for treating cancer, comprising administering a pharmaceutical composition comprising tumor tissue-derived nanovesicles of claim 1 to a subject in need thereof.
10. The method of claim 9 , wherein the tumor tissue is transformed to express a heat shock protein.
11. The method of claim 9 , wherein the pharmaceutical composition further comprises an immune adjuvant.
12. The method of claim 11 , wherein the immune adjuvant is polyI:C.
13. The method of claim 9 , wherein the nanovesicles comprise a component other than that sourced from a plasma membrane of the tumor tissue.
14. The method of claim 13 , wherein the component is cyclodextrin or polyethylene glycol.
15. The method of claim 9 , wherein the nanovesicles have a chemically modified membrane.
16. The method of claim 15 , wherein the nanovesicles are chemically modified with a thiol group or an amine group.
17. A method for preparing tumor tissue-derived nanovesicles, comprising:
(a) separating cells from a tumor tissue;
(b) constructing nanovesicles from a suspension of the cells by a process selected from the group consisting of extrusion, sonication, cell lysis, homogenation, freeze-thawing, electroporation, mechanical degradation, and chemical treatment;
(c) isolating the constructed nanovesicles from the suspension; and
(d) incubating a suspension of the nanovesicles in presence of an adjuvant.
18. A method for preparing tumor tissue-derived nanovesicles, comprising:
(a) separating cells from a tumor tissue;
(b) adding an adjuvant to a suspension of the cells to load the adjuvant into the cells; and
(c) constructing nanovesicles from the cell suspension by a process selected from the group consisting of extrusion, sonication, cell lysis, homogenation, freeze-thawing, electroporation, mechanical degradation, and chemical treatment.
19. A cancer vaccine, comprising tumor tissue-derived nanovesicles of claim 1 as an antigen.