COMBINATION OF VACCINATION AND INHIBITION OF THE PD-1 PATHWAY

Abstract

The present invention relates to a vaccine/inhibitor combination comprising an RNA vaccine comprising at least one RNA comprising at least one open reading frame (ORF) coding for at least one antigen and a composition comprising at least one PD-1 pathway inhibitor, preferably directed against PD-1 receptor or its ligands PD-L1 and PD-L2. The present invention furthermore relates to a pharmaceutical composition and a kit of parts comprising the components of such a vaccine/inhibitor combination. Additionally the present invention relates to medical use of such a vaccine/inhibitor combination, the pharmaceutical composition and the kit of parts comprising such a vaccine/inhibitor combination, particularly for the prevention or treatment of tumor or cancer diseases or infectious diseases. Furthermore, the present invention relates to the use of an RNA vaccine in therapy in combination with a PD-1 pathway inhibitor and to the use of a PD-1 pathway inhibitor in therapy in combination with an RNA vaccine.

Claims

1-28. (canceled)

29. A method of treating a subject having a cancer comprising administering to the subject: (i) an immunogenic composition comprising mRNA encoding at least one epitope of a tumour-specific antigen (TSA), wherein said mRNA comprises a 5′ Cap and a Poly-A sequence of about 25 to about 400 adenosine nucleotides, wherein said mRNA is provided in complex with a cationic or polycationic carrier; and (ii) a PD-1 pathway inhibitor, said PD-1 pathway inhibitor comprising an antagonistic antibody that binds to PD-1.

30. The method of claim 29, wherein the subject has previously been administered a PD-1 pathway inhibitor.

31. The method of claim 29, wherein the PD-1 pathway inhibitor is administered before said immunogenic composition.

32. The method of claim 29, wherein the immunogenic composition and the PD-1 pathway inhibitor are administered sequentially.

33. The method of claim 29, wherein the immunogenic composition and the PD-1 pathway inhibitor are administered concurrently.

34. The method of claim 29, wherein the subject has a melanoma.

35. The method of claim 29, wherein the subject has a metastatic solid tumor.

36. The method of claim 29, wherein the PD-1 pathway inhibitor is administered intravenously.

37. The method of claim 36, wherein the immunogenic composition is administered subcutaneously, intravenously, intradermally or intramuscularly.

38. The method of claim 37, wherein the immunogenic composition is administered intramuscularly.

39. The method of claim 36, wherein at least one epitope of the TSA comprises a tumour specific mutation.

40. The method of claim 36, wherein the immunogenic composition comprises mRNA at least two epitopes of the TSA.

41. The method of claim 36, wherein the immunogenic composition comprises mRNA encoding at least two epitopes from different TSAs.

42. The method of claim 41, wherein at least two epitopes of the different TSAs comprise tumour specific mutations.

43. The method of claim 41, wherein at least two epitopes of the different TSAs are encoded on the same mRNA molecule.

44. The method of claim 41, wherein the immunogenic composition comprises mRNA encoding at least three, four, five or more epitopes from different TSAs.

45. The method of claim 44, wherein the epitopes of the different TSAs are encoded on the same mRNA molecule.

46. The method of claim 44, wherein the epitopes of the different TSAs are from 5T4, 707-AP, 9D7, AFP, AlbZIP HPG1, alpha-5-beta-1-integrin, alpha-5-beta-6-integrin, alpha-actinin-4, alpha-methylacyl-coenzyme A racemase, ART-4, ARTC1, B7H4, BAGE-1, BCL-2, bcr/abl, beta-catenin, BING-4, BRCA1, BRCA2, CA 15-3/CA 27-29, CA 19-9, CA72-4, CA125, calreticulin, CAMEL, CASP-8, cathepsin B, cathepsin L, CD19, CD20, CD22, CD25, CDE30, CD33, CD4, CD52, CD55, CD56, CD80, CDC27, CDK4, CDKN2A, CEA, CLCA2, CML28, CML66, COA-1, coactosin-like protein, collage XXIII, COX-2, CT-9/BRD6, Cten, cyclin B1, cyclin D1, cyp-B, CYPB1, DAM-10, DAM-6, DEK-CAN, EFTUD2, EGFR, ELF2, EMMPRIN, EpCam, EphA2, EphA3, ErbB3, ETV6-AML1, EZH2, FGF-5, FN, Frau-1, G250, GAGE-1, GAGE-2, GAGE-3, GAGE-4, GAGE-5, GAGE-6, GAGE7b, GAGE-8, GDEP, GnT-V, gp100, GPC3, GPNMB, HAGE, HAST-2, hepsin, Her2/neu, HERV-K-MEL, HLA-A*0201-R17I, HLA-A11, HLA-A2, HNE, homeobox NKX3.1, HOM-TES-14/SCP-1, HOM-TES-85, HPV-E6, HPV-E7, HSP70-2M, HST-2, hTERT, iCE, IGF-1R, IL-13Ra2, IL-2R, IL-5, immature laminin receptor, kallikrein-2, kallikrein-4, Ki67, KIAA0205, KIAA0205/m, KK-LC-1, K-Ras, LAGE-A1, LDLR-FUT, MAGE-A1, MAGE-A2, MAGE-A3, MAGE-A4, MAGE-A6, MAGE-A9, MAGE-A10, MAGE-A12, MAGE-B1, MAGE-B2, MAGE-B3, MAGE-B4, MAGE-B5, MAGE-B6, MAGE-B10, MAGE-B16, MAGE-B17, MAGE-C1, MAGE-C2, MAGE-C3, MAGE-D1, MAGE-D2, MAGE-D4, MAGE-E1, MAGE-E2, MAGE-F1, MAGE-H1, MAGEL2, mammaglobin A, MART-1/melan-A, MART-2, MART-2, matrix protein 22, MC1R, M-CSF, ME1, mesothelin, MG50/PXDN, MMP11, MN/CA IX-antigen, MRP-3, MUC-1, MUC-2, MUM-1, MUM-2, MUM-3, myosin class I, NA88-A, N-acetylglucosaminyltransferase-V, Neo-PAP, Neo-PAP, NFYC, NGEP, NMP22, NPM/ALK, N-Ras, NSE, NY-ESO-B, NY-ESO-1, OA1, OFA-iLRP, OGT, OGT, OS-9, OS-9, osteocalcin, osteopontin, p15, p190 minor bcr-abl, p53, p53, PAGE-4, PAI-1, PAI-2, PAP, PART-1, PATE, PDEF, Pim-1-Kinase, Pin-1, Pml/PARalpha, POTE, PRAME, PRDX5, prostein, proteinase-3, PSA, PSCA, PSGR, PSM, PSMA, PTPRK, RAGE-1, RBAF600, RHAMM/CD168, RU1, RU2, S-100, SAGE, SART-1, SART-2, SART-3, SCC, SIRT2, Sp17, SSX-1, SSX-2/HOM-MEL-40, SSX-4, STAMP-1, STEAP-1, survivin, survivin-2B, SYT-SSX-1, SYT-SSX-2, TA-90, TAG-72, TARP, TEL-AML1, TGFbeta, TGFbetaRII, TGM-4, TPI, TRAG-3, TRG, TRP-1, TRP-2/6b, TRP/INT2, TRP-p8, tyrosinase, UPA, VEGFR1, VEGFR-2/FLK-1 or WT1.

47. The method of claim 46, wherein the epitopes of the different TSAs are from NY-ESO-1 and/or MAGE-A3.

48. The method of claim 44, wherein the immunogenic composition is administered intramuscularly.

49. The method of claim 48, wherein the mRNA comprises a modification of a nucleobase.

50. The method of claim 48, wherein the carrier comprises a cationic or polycationic lipid.

Description

BRIEF DESCRIPTION OF THE FIGURES

[0356] The figures shown in the following are merely illustrative and shall describe the present invention in a further way. These figures shall not be construed to limit the present invention thereto.

[0357] FIG. 1: The RNA vaccine (OVA-RNActive R1710) acts synergistically with anti-PD-1 antibody. C57 BL/6 mice were challenged subcutaneously with 3×10.sup.5 syngenic E.G7-OVA tumor cells on day 0 and then treated with either OVA RNActive vaccine (32 μg) alone or in combination with anti-PD-1 antibody or control IgG (100 μg i.p.) in accordance with the indicated schedule.

[0358] FIG. 2: Survival proportions of mice bearing E.G7-OVA tumors treated with different therapies. According to Example 2, mice were treated with either OVA-RNActive vaccine or anti-PD-1 antibody alone or in combination.

[0359] FIG. 3: G/C optimized mRNA sequence of R1710 coding for Gallus gallus ovalbumin as comprised in the OVA-RNActive vaccine.

EXAMPLES

[0360] The examples shown in the following are merely illustrative and shall describe the present invention in a further way. These examples shall not be construed to limit the present invention thereto.

Example 1: Preparation of the mRNA Vaccine

[0361] 1. Preparation of DNA and mRNA constructs [0362] For the present examples a DNA sequence, encoding Gallus gallus ovalbumin mRNA (R1710) was prepared and used for subsequent in vitro transcription reactions. [0363] According to a first preparation, the DNA sequence coding for the above mentioned mRNA was prepared. The construct was prepared by modifying the wild type coding sequence by introducing a GC-optimized sequence for stabilization, followed by a stabilizing sequence derived from the alpha-globin-3′-UTR (muag (mutated alpha-globin-3′-UTR)), a stretch of 64 adenosines (poly-A-sequence), a stretch of 30 cytosines (poly-C-sequence), and a histone stem loop. In SEQ ID NO: 2 (see FIG. 3) the sequence of the corresponding mRNA is shown.

2. In Vitro Transcription

[0364] The respective DNA plasmid prepared according to Example 1 was transcribed in vitro using T7 polymerase. Subsequently the mRNA was purified using PureMessenger® (CureVac, Tubingen, Germany).

3. Reagents

[0365] Complexation Reagent: protamine

4. Preparation of the Vaccine

[0366] The mRNA R1710 was complexed with protamine by addition of protamine to the mRNA in the ratio (1:2) (w/w) (adjuvant component). After incubation for 10 min, the same amount of free mRNA R1710 used as antigen-providing RNA was added. [0367] OVA-RNActive vaccine (R1710): comprising an adjuvant component consisting of mRNA coding for Gallus gallus ovalbumin (R1710) according to SEQ ID NO. 2 complexed with protamine in a ratio of 2:1 (w/w) and the antigen-providing free mRNA coding for Gallus gallus ovalbumin (R1710) according to SEQ ID NO. (ratio 1:1; complexed RNA:free RNA).

Example 2: Combination of an Anti-PD1 Antibody and an RNA Vaccine

[0368] On day zero, C57BL/6 mice were implanted subcutaneously (right flank) with 3×10.sup.5 E.G7-OVA cells per mouse (volume 100 μl in PBS). E.G7-OVA is a mouse T cell lymphoma cell line stably expressing Gallus gallus ovalbumin (OVA). Intradermal vaccination with the RNA vaccine comprising OVA mRNA R1720 (32 μg/mouse/vaccination day) (according to Example 1) or Ringer-lactate (RiLa) as buffer control and treatment with the anti-PD-1/CD279 monoclonal antibody (100 μg i.p.) or an isotype control according to Table 1 started on day 4 and was repeated on days 7, 11, 14, 18 and 21. Animals received the antibody injection in the morning and were vaccinated in the afternoon with a minimum of four hours between the treatments.

TABLE-US-00001 TABLE 1 Animal groups Number Injected RNA per Injected antibody per Group of mice vaccination day and mouse treatment day and mouse A 10 100% Ringer Lactate — (RiLa) buffer B 10 32 μg — C 6 — 100 μg anti-PD-1 D 6 32 μg 100 μg anti-PD-1 E 6 32 μg 100 μg control-IgG2a

[0369] The anti-PD-1/CD279 antibody (clone RMP1-14, rat IgG2a) and the isotype control antibody (clone 2A3, rat IgG2a) were purchased from BioXCell (West Lebanon, N.H., USA).

[0370] Tumour growth was monitored by measuring the tumour size in 2 dimensions (length and width) using a calliper (starting on day 4). Tumour volume was calculated according to the following formula:

[00001]$\mathrm{volume}\left({\mathrm{mm}}^3\right)=\frac{\mathrm{length}\left(\mathrm{mm}\right)\times \pi \times {\mathrm{width}}^2\left({\mathrm{mm}}^2\right)}{6}$

[0371] The results are shown in FIGS. 1 and 2.

[0372] As can be seen in FIG. 1, the OVA mRNA vaccine (OVA-RNActive R1710) alone or in combination with control-IgG delayed tumor growth by approximately 5 days compared to the buffer-treated control group. Treatment with anti-PD-1 antibody alone was comparable to vaccination alone, whereas simultaneous application of the RNA vaccine/anti-PD-1 combination led to significant inhibition of tumor growth, indicating a synergistic effect. Lines represent the development of mean tumor volume and error bars the SEM. Statistical analysis was based on the 2way Anova with Bonferroni posttest.

[0373] As can be seen in FIG. 2, the administration of the OVA mRNA vaccine (OVA-RNActive R1710) or anti-PD-1 antibody alone had already a significant effect on survival, whereas simultaneous application of the RNA vaccine/anti-PD-1 combination led to 50% survival (3 of 6 animals), indicating a synergistic effect.