RNA molecules encoding cytokine fusion proteins and methods of use thereof
The present invention relates to cytokine fusion proteins and to nucleic acid molecules encoding such cytokine fusion proteins. The present invention further relates to cells, non-human organisms, pharmaceutical compositions and kits comprising the cytokine fusion proteins or the nucleic acid molecules encoding them, as well as to their use as medicaments.
1. An RNA molecule encoding a fusion protein, wherein the fusion protein comprises a molecule/structure having the general formula
N′-A-L A -A-L A -A-L-B—C′ (Formula I) or
N′—B-L-A-L A -A-L A -A-C′ (Formula II),
wherein A comprises an extracellular domain of a ligand of the tumor necrosis factor (TNF) superfamily or a functional variant thereof, said extracellular domain comprises at least a functional TNF homology domain (THD), and said variant of the extracellular domain has at least 95% sequence identity to the extracellular domain and is able to bind to a member of the TNF superfamily upon trimerization,
B comprises an interleukin, or a functional fragment or a functional variant of the functional fragment, said variant has at least 95% sequence identity to the functional fragment of the interleukin and is able to bind to a receptor of the interleukin, and
L comprises a peptide linker, and
L A is, at each occurrence, independently a covalent bond or a peptide linker.
2. The RNA molecule according to claim 1 , wherein L further comprises a multimerization domain allowing the multimerization of the fusion protein.
3. The RNA molecule according to claim 2 , wherein the multimerization domain is a dimerization domain and is selected from the group consisting of an IgE heavy-chain domain 2 (EHD2), an IgM heavy-chain domain 2 (MHD2), an IgG heavy-chain domain 3 (GHD3), an IgA heavy-chain domain 3 (AHD2), an IgD heavy-chain domain 3 (DHD3), an IgE heavy-chain domain 4 (EHD4), an IgM heavy-chain domain 4 (MHD4), an Fc domain, and an uteroglobin dimerization domain.
4. The RNA molecule according to claim 2 , wherein, upon expression of the fusion protein, the fusion protein is present as a multimeric complex.
5. The RNA molecule according to claim 1 , wherein the ligand is selected from the group consisting of CD40 ligand (CD40L), CD27 ligand (CD27L), 4-1BB ligand (4-1BBL), OX40 ligand (OX40L), A proliferation-inducing ligand (APRIL), CD30 ligand (CD30L), Ectodysplasin-A1 (EDA-A1), Ectodysplasin-A2 (EDA-A2), fas ligand (FasL), GITR ligand (GITRL), LIGHT, Lymphotoxin-alpha (LT-alpha), TL1A, tumor necrosis factor alpha (TNF-alpha), TNF-related apoptosis-inducing ligand (TRAIL), receptor activator of NF-kB ligant (RANKL), and TWEAK.
6. The RNA molecule according to claim 5 , wherein the extracellular domain of CD40L comprises or consists of amino acid residues 51 to 261 or 116 to 261 of SEQ ID NO: 1, the extracellular domain of CD27L comprises or consists of amino acid residues 52 to 193 of SEQ ID NO: 2, the extracellular domain of 4-1BBL comprises or consists of amino acid residues 71 to 254 of SEQ ID NO: 3, and/or the extracellular domain of OX40L comprises or consists of amino acid residues 51 to 183 of SEQ ID NO: 4.
7. The RNA molecule according to claim 1 , wherein the interleukin is selected from the group consisting of IL2, IL12, IL21, IL27, IL1-alpha, IL1-beta, IL7, IL15, IL18, IL9, IL23, IL4, IL6, IL10, IL31 and IL33.
8. The RNA molecule according to claim 7 , wherein the interleukin is a heterodimeric interleukin being present as a single polypeptide.
9. The RNA molecule according to claim 1 , wherein the fusion protein further comprises at least one label or tag allowing the detection and/or isolation of the fusion protein.
10. The RNA molecule according to claim 1 , wherein the fusion protein enhances proliferation of natural killer (NK) cells and/or T cells.
11. The RNA molecule according to claim 1 , which is an in vitro-transcribed (IVT) RNA molecule.
12. The RNA molecule according to claim 1 , wherein L further comprises a dimerization domain allowing the dimerization of the fusion protein.
13. The RNA molecule according to claim 2 , wherein, upon expression of the fusion protein, the fusion protein is present as a dimeric complex.
14. The RNA molecule according to claim 5 , wherein the ligand is selected from the group consisting of CD40L, CD27L, 4-1BBL, and OX40L.
15. The RNA molecule according to claim 10 , wherein the fusion protein enhances proliferation of CD8 + T cells.
16. The RNA molecule according to claim 1 , wherein, upon expression of the fusion protein, the three extracellular domains or functional variants thereof, form a homotrimer capable of binding to a receptor of the ligand.
17. A cell transformed or transfected with an RNA molecule according to claim 1 .
18. A non-human organism transformed or transfected with an RNA molecule according to claim 1 .
19. A pharmaceutical composition comprising (i) as an active agent, an RNA molecule according to claim 1 and (ii) a pharmaceutically acceptable carrier and/or excipient.
20. A pharmaceutical composition comprising (i) as an active agent, a cell according to claim 17 and (ii) a pharmaceutically acceptable carrier and/or excipient.
21. A kit comprising an RNA molecule according to claim 1 .
22. A kit comprising a cell according to claim 17 .
23. A kit comprising a pharmaceutical composition of claim 19 .
24. A kit comprising a pharmaceutical composition of claim 20 .
25. A method comprising administering an effective amount of an RNA molecule according to claim 1 to a subject in need thereof.
26. A method comprising administering an effective amount of a cell according to claim 17 to a subject in need thereof.
27. A method comprising administering an effective amount of a pharmaceutical composition according to claim 19 to a subject in need thereof.
28. A method comprising administering an effective amount of a pharmaceutical composition according to claim 20 to a subject in need thereof.