Use of inactivated nonreplicating modified vaccinia virus Ankara (MVA) as monoimmunotherapy or in combination with immune checkpoint blocking agents for solid tumors

Patent metadata

Field	Value
Publication number	US-11426460-B2
Application number	US-202016779174-A
Country	US
Kind code	B2
Filing date	Jan 31, 2020
Priority date	Feb 25, 2015
Publication date	Aug 30, 2022
Grant date	Aug 30, 2022

Abstract

The present disclosure relates to infection-competent, but nonreplicative inactivated modified vaccinia Ankara (MVA) and its use as immunotherapy, alone, or in combination with immune checkpoint blocking agents for the treatment of malignant solid tumors. Particular embodiments relate to inducing an immune response in a subject diagnosed with a solid malignant tumor.

First claim

The invention claimed is:

1. A method for treating a solid malignant tumor in a subject in need thereof, the method comprising delivering to tumor cells of the subject a therapeutically effective amount of inactivated modified vaccinia Ankara (inactivated MVA) virus, thereby resulting in treatment of the tumor, wherein the tumor is a carcinoma.

2. The method of claim 1 , wherein the treatment comprises one or more of the following:
inducing the immune system of the subject to mount an immune response against the tumor;
reducing the size of the tumor;
eradicating the tumor;
inhibiting growth of the tumor;
inhibiting metastasis of the tumor;
reducing or eradicating metastatic tumor;
inducing apoptosis of the tumor cells; and
prolonging survival of the subject as compared to an untreated control subject.

3. The method of claim 1 , wherein the tumor includes tumor located at the site of inactivated MVA delivery, or tumor located both at the site and elsewhere in the body of the subject.

4. The method of claim 1 , wherein the inactivated MVA does not comprise a heterologous nucleic acid encoding or expressing a tumor antigen.

5. The method of claim 1 , further comprising conjointly administering to the subject a therapeutically effective amount of an immune checkpoint blocking agent.

6. The method of claim 5 , wherein the inactivated MVA is delivered parenterally, intratumorally, intravenously, and/or intraperitoneally to the subject, and wherein the immune checkpoint blocking agent is administered parenterally, intratumorally, intravenously, and/or intraperitoneally to the subject.

7. The method of claim 5 , wherein the immune checkpoint blocking agent modulates the activity of one or more checkpoint proteins selected from the group consisting of: CTLA-4, CD80, CD86, PD-1, PD-L1, PD-L2, TIGIT, LAG3, B7-H3, B7-H4, TIM3, ICOS, BTLA, and CD28.

8. The method of claim 5 , wherein the inactivated MVA is delivered to the subject separately, sequentially, or simultaneously with the immune checkpoint blocking agent.

9. The method of claim 5 , wherein one or both of the inactivated MVA and the immune checkpoint blocking agent are respectively delivered and administered during a period of time of several weeks, months, or years, or indefinitely as long as benefits persist or a maximum tolerated dose is reached.

10. The method of claim 5 , wherein the inactivated MVA is delivered at a dosage per administration of about 105 to about 1010 plaque-forming units (pfu).

11. The method of claim 5 , wherein the combination of the inactivated MVA and the immune checkpoint blocking agent has a synergistic effect in the treatment of the tumor, wherein the immune checkpoint blocking agent is selected from an anti-CTLA-4 antibody, an anti-PD-1 antibody, or an anti-PD-L1 antibody.

12. The method of claim 1 , wherein the inactivated MVA is heat-inactivated MVA or UV-inactivated MVA.

13. A method of eliciting an immune response in a subject in need thereof, the method comprising delivering to the subject a therapeutically effective amount of an inactivated modified vaccinia Ankara (inactivated MVA) virus, thereby inducing at least one or more of the following:
increasing at least one of cytotoxic CD8+ T cells and effector CD4+ T cells;
inducing maturation of dendritic cells through induction of type I IFN;
reducing immune suppressive (regulatory) CD4+ T cells; and
inducing type I IFN, inflammatory cytokine and chemokine production in immune cells and stromal fibroblasts as compared to untreated control cells.

14. The method of claim 13 , wherein the inactivated MVA delivered to the subject is effective to recruit and activate CD4+ effector T cells accompanied by a reduction of regulatory CD4+ T cells.

15. The method of claim 13 , wherein the inactivated MVA is delivered parenterally, intratumorally, intravenously, or intraperitoneally.

16. The method of claim 13 , wherein the inactivated MVA is delivered at a dosage per administration of about 105 to about 1010 plaque-forming units (pfu).

17. The method of claim 13 , wherein the delivery is repeated with a frequency within the range from once per month to once per week or more, and continues for several weeks, months, years, or indefinitely until a maximum tolerated dose is reached.

18. The method of claim 13 , wherein the inactivated MVA induces type I interferon (type I IFN) in infected cells and/or activates type I IFN gene expression by inducing higher levels of IFNA4 and IFNB mRNA and/or increasing phospho-IRF3 compared to MVA.

19. The method of claim 13 , wherein delivery of inactivated MVA induces higher levels of production of at least one of IFN-β, IL-6, CCL4, and CCL5, and/or higher levels of gene expression of IFN-β, IL6, CCL4, and CCL5 than MVA.

20. The method of claim 13 , wherein the inactivated MVA is heat-inactivated MVA or UV-inactivated MVA.

Assignees

• Memorial Sloan Kettering Cancer Center

Inventors

• Deng Liang
• Shuman Stewart
• Wolchok Jedd D
• Merghoub Taha
• Dai Peihong
• Wang Weiyi

Classifications

• A61P35/00

  Antineoplastic agents · CPC title

• A61K2039/585

  wherein the target is cancer · CPC title

• C07K16/2827

  against B7 molecules, e.g. CD80, CD86 · CPC title

• C12N2710/24132

  Use of virus as therapeutic agent, other than vaccine, e.g. as cytolytic agent · CPC title

• A61K2039/5252

  inactivated (killed) · CPC title