IP Library › Granted Patent US 11,813,485
Granted Patent B2
US 11,813,485 · App. 17/161,498 · Granted Nov 14, 2023

Systems and methods for histotripsy immunosensitization

Inventors: Zhen Xu (Ann Arbor, MI); Clifford Suhyun Cho (Ann Arbor, MI)
Assignees: The Regents of the University of Michigan; The United States Government as represented by the Department of Veterans Affairs
A61N7/00A61K39/0011A61B10/0045
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Quick Facts
Patent No.
US 11,813,485
App. No.
17/161,498
Granted
Nov 14, 2023
Kind
B2
Abstract

Systems and methods for histotripsy and immunotherapy are provided. In some embodiments, histotripsy can be applied to a target tissue volume to lyse and solubilize the target tissue volume to release tumor antigens. In some embodiments, an immune response of the treatment can be evaluated. In other embodiments, an immune therapy can be applied after applying the histotripsy. In one embodiment, the lysed and solubilized cells can be extracted from the tissue. The extracted cells can be used to create immune therapies, including vaccines.

Claims (36)

1. A method of treating tissue, comprising:

identifying at least one target tumor;

determining a treatment volume and a treatment location of the at least one target tumor that will increase a cell response of releasing tumor antigens; and

applying histotripsy treatment based on the treatment volume and the treatment location to the at least one target tumor to mechanically lyse and solubilize tumor cells to release the tumor antigens.

2. The method of claim 1 , wherein the cell response includes immunogenic cell death, infiltration of inflammatory and antigen presenting cells, infiltration and activation of T cells, increased tumor-specific T cells, infiltration of natural killer cells, B cells and CD4+ T cells, and/or depletion of immunosuppressive regulatory T cells and myeloid-derived suppressor cells.

3. The method of claim 1 , wherein the treatment volume of the at least one target tumor ranges from 25% to 90% of a volume of the at least one target tumor.

4. The method of claim 3 , wherein the treatment volume of the at least one target tumor is at least 1 cm 3 in volume.

5. The method of claim 1 , further comprising evaluating an immune response of the lysed and solubilized tumor cells.

6. The method of claim 5 , wherein evaluating the immune response includes assessment of immunological cell death and/or immune activation.

7. The method of claim 5 , wherein evaluating the immune response comprises imaging the at least one target tumor and/or performing a tissue biopsy on the at least one target tumor.

8. The method of claim 7 , wherein the imaging comprises CT, MRI, and/or PET imaging.

9. The method of claim 7 , wherein performing the tissue biopsy comprises performing a liquid biopsy.

10. The method of claim 1 , further comprising applying immune therapy after applying the histotripsy treatment.

11. The method of claim 10 , wherein the immune therapy is selected from the group consisting of checkpoint inhibitors, immunostimulatory therapies, cancer vaccines, oncolytic viruses, neutralizing immune inhibitors, and activating cytokines.

12. The method of claim 11 , wherein the checkpoint inhibitors include CTLA-4, LAG3, TIM3, and combinations thereof.

13. The method of claim 11 , wherein the checkpoint inhibitors include PD-1 blockade, PD-L1 blockade, and combinations thereof.

14. The method of claim 1 , further comprising harvesting the lysed and solubilized tumor cells.

15. The method of claim 14 , further comprising:

preparing an immune directed therapy using the lysed and solubilized tumor cells; and

administering the immune directed therapy into a patient.

16. The method of claim 15 , wherein administering the immune directed therapy is selected from the group consisting of oral administration, systemic infusion, loco-regional catheter-based infusion, intratumoral injection, loco-regional injection, subcutaneous injection, and combinations thereof.

17. The method of claim 15 , wherein the immune directed therapy is a cell therapy.

18. The method of claim 1 , wherein applying the histotripsy treatment is configured to elicit an immune response in at least one distant tumor of the same phenotype as the at least one target tumor.

19. The method of claim 18 , wherein the at least one distant tumor is located in a different organ or anatomical location than the at least one target tumor.

20. The method of claim 1 , wherein the at least one target tumor is located in the group consisting of a liver, a kidney, a spleen, a pancreas, a colorectal, a bowel, a stomach, an esophagus, a breast, a lung, a head, a neck, a thyroid, skin, nervous tissue, hematological malignancies, a sarcoma, primary and metastatic lesions, and brain tissue.

21. The method of claim 1 , wherein the treatment location comprises only a central portion of the at least one target tumor.

22. The method of claim 1 , wherein the treatment location comprises only a periphery of the at least one target tumor.

23. The method of claim 1 , wherein the treatment location comprises a plurality of programmed treatment locations distributed spatially through the at least one target tumor.

24. A method of treating tissue previously treated with radiation therapy and/or resistant to the radiation therapy, comprising:

identifying at least one target tumor;

determining a treatment volume and a treatment location of the at least one target tumor that will increase cell response of releasing tumor antigens; and

applying histotripsy treatment to the at least one target tumor to mechanically lyse and solubilize tumor cells to release the tumor antigens.

25. A method of treating tissue previously treated with immunotherapy and non-responsive or resistant to immunotherapy, comprising:

identifying at least one target tumor;

determining a treatment volume and a treatment location of the at least one target tumor that will increase cell response of releasing tumor antigens; and

applying histotripsy treatment to the at least one target tumor to mechanically lyse and solubilize tumor cells to release the tumor antigens.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2023
From: XU, ZHEN
To: THE REGENTS OF THE UNIVERSITY OF MICHIGAN
Reel/Frame 064750/0337 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2023
From: CHO, CLIFFORD SUHYUN
To: THE REGENTS OF THE UNIVERSITY OF MICHIGAN; THE UNITED STATES GOVERNMENT AS REPRESENTED BY THE DEPARTMENT OF VETERANS AFFAIRS
Reel/Frame 064750/0501 →
Continuity (2)
Provisional Application 62966960 · Jan 28, 2020
Related Publication 20210252313A1 · Aug 19, 2021
Cited By (15)
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