IP Library Granted Patent US 12,397,055
Granted Patent B2
US 12,397,055 · App. 17/580,919 · Granted Aug 26, 2025

Methods of tumor vaccination

Inventors: Erik Hans Manting (Leiden, NL); Satwinder Kaur Singh (Leiden, NL); Jeroen Rovers (Leiden, NL)
Assignee: MENDUS B.V.
A61K40/42A61K40/19A61K40/24A61P35/00A61K2039/545A61K2039/55A61K2039/585A61K2039/892
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Quick Facts
Patent No.
US 12,397,055
App. No.
17/580,919
Granted
Aug 26, 2025
Kind
B2
Abstract

Provided herein are methods for treating a tumor or generating an immune response against a tumor in a subject in need, including one or more intratumoral administration steps each comprising administering to the subject at a tumor site, an effective amount of a first composition, and one or more vaccination steps each comprising administering to the subject at a site distal to the tumor site, an effective amount of a second composition. The first and second composition may each comprise an allogeneic leukemia-derived cell that is useful in eliciting an immune response against the tumor.

Claims (38)

1. A method for treating a tumor in a subject in need thereof, comprising:

one or more intratumoral administration steps each comprising administering to the subject at a tumor site, an effective amount of an allogeneic leukemia-derived cell, wherein the allogeneic leukemia-derived cell has a mature dendritic cell phenotype and is inactivated; and

one or more vaccination steps each comprising administering to the subject at a site distal to the tumor site, an effective amount of the allogeneic leukemia-derived cell;

wherein the allogeneic leukemia-derived cell comprises one or more exogenous tumor associated antigens or one or more nucleic acid molecules encoding the one or more exogenous tumor associated antigens.

2. The method of claim 1 , wherein the one or more intratumoral administration steps each comprises administering the first composition into the tumor or at a site proximal to the tumor, optionally wherein the site proximal to the tumor is peritumoral.

3. The method of claim 1 , wherein the first composition is prepared for intratumoral administration, optionally wherein the first composition comprises a diluent or solvent acceptable for intratumoral administration.

4. The method of claim 1 , wherein the one or more vaccination steps each comprise administering the second composition via a route selected from the group consisting of intramuscular, subcutaneous, intravenous, intraarterial, intraperitoneal, intrasternal, intradermal, transcutaneous, transdermal, delivery to the interstitial space of a tissue, and delivery to a non-tumor tissue.

5. The method of claim 1 , wherein the one or more vaccination steps each comprises intravenously administering the second composition.

6. The method of claim 1 , wherein the one or more intratumoral administration steps are performed before the one or more vaccination steps.

7. The method of claim 6 ,

wherein

the one or more vaccination steps following the one or more intratumoral administration steps each comprise administering to the subject an effective amount of a third composition comprising an allogeneic leukemia-derived cell via a route selected from the group consisting of intramuscular, subcutaneous, intravenous, intraarterial, intraperitoneal, intrasternal, intradermal, transcutaneous, transdermal, delivery to the interstitial space of a tissue, and delivery to a non-tumor tissue.

8. The method of claim 1 , wherein the time between the one or more intratumoral administration steps and the one or more vaccination steps is sufficient for an immune response to be mounted as a result of the one or more vaccination steps.

9. The method of claim 1 , wherein the one or more intratumoral administration steps are performed at the same time as the one or more vaccination steps.

10. The method of claim 7 , wherein the time between the one or more vaccination steps following the one or more intratumoral administration steps, and the one or more intratumoral administration steps is sufficient for an immune response to be mounted as a result of the first vaccination step of the one or more vaccination steps.

11. The method of claim 1 ,

wherein the exogenous tumor associated antigen is selected from the group consisting of WT-1, MUC-1, RHAMM, PRAME, p53, and Survivin, or

wherein the allogeneic leukemia-derived cell comprises WT-1, MUC-1, PRAME, and Survivin.

12. The method of claim 1 , wherein the allogeneic leukemia-derived cell is derived from the DCOne cell line.

13. The method of claim 1 , wherein the allogeneic leukemia-derived cell comprises a genetic aberration between chromosome 11p15.5 to 11p12, optionally wherein the genetic aberration encompasses about 16 Mb of genomic regions.

14. The method of claim 1 , wherein the allogeneic leukemia-derived cell is CD34-positive, CD1a-positive, CD83-positive, CD80-positive, CD86-positive, and CD40-positive.

15. The method of claim 1 , wherein the allogeneic leukemia-derived cell has been inactivated via irradiation.

16. The method of claim 7 , wherein the first composition further comprises one or more pharmaceutically-acceptable carriers, adjuvants, excipients and/or diluents,

the second composition further comprises one or more pharmaceutically-acceptable carriers, adjuvants, excipients and/or diluents, and/or

the third composition further comprises one or more pharmaceutically-acceptable carriers, adjuvants, excipients and/or diluents.

17. The method of claim 1 , wherein the subject has previously suffered from the tumor.

18. The method of claim 1 , wherein the tumor is a solid tumor.

19. A method for treating a tumor in a subject in need thereof, comprising:

one or more intratumoral administration steps each comprising administering to the subject an effective amount of an allogeneic leukemia-derived cell into the tumor or at a site proximal to the tumor, wherein the allogeneic leukemia-derived cell comprises a mature dendritic cell phenotype and is inactivated; and

one or more vaccination steps each comprising administering to the subject at a site distal to the tumor site, an effective amount of the allogeneic leukemia-derived cell via a route selected from the group consisting of intramuscular, subcutaneous, intravenous, intraarterial, intraperitoneal, intrasternal, intradermal, transcutaneous, transdermal, delivery to the interstitial space of a tissue, and delivery to a non-tumor tissue;

wherein the allogeneic leukemia-derived cell comprises one or more exogenous tumor associated antigens or one or more nucleic acid molecules encoding the one or more exogenous tumor associated antigens.

20. The method of claim 6 , wherein the one or more vaccination steps following the one or more intratumoral administration steps are administered via the same route as the one or more vaccination steps.

21. The method of claim 6 , wherein the one or more vaccination steps following the one or more intratumoral administration steps are administered via a different route as the one or more vaccination steps.

22. The method of claim 1 , wherein the time between the one or more intratumoral administration steps and the one or more vaccination steps is sufficient for an immune response to be mounted as a result of the first vaccination step of the one or more vaccination steps.

23. The method of claim 1 , wherein-the time between the one or more intratumoral administration steps and the one or more vaccination steps is about 2 days to about 21 days.

24. The method of claim 1 , wherein the one or more intratumoral administration steps are performed at the same time as the first vaccination step of the one or more vaccination steps.

25. The method of claim 7 , wherein the time between the one or more vaccination steps following the one or more intratumoral administration steps, and the one or more intratumoral administration steps is about 2 days to about 21 days.

26. The method of claim 7 , wherein the one or more vaccination steps following the one or more intratumoral administration steps, and the one or more intratumoral administration steps are performed at the same time.

Assignments (2)
CHANGE OF NAME Recorded May 16, 2023
From: DCPRIME B.V.
To: MENDUS B.V.
Reel/Frame 063663/0906 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2022
From: MANTING, ERIK HANS; SINGH, SATWINDER KAUR; ROVERS, JEROEN
To: DCPRIME B.V.
Reel/Frame 059772/0436 →
Continuity (2)
Provisional Application 63140617 · Jan 22, 2021
Related Publication 20220249639A1 · Aug 11, 2022
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