NOVEL IMMUNOSTIMULATING VECTOR SYSTEM
Provided is a novel vector for immunostimulation and methods of using same in immunotherapy, in particular cancer immunotherapy. The novel vector comprises nucleic acid sequences encoding 4-1BB ligand (4-1BBL, CD137 ligand), single chain IL-12 (sc IL-12) and IL-2, wherein the vector provides for an increased expression of 4-1BBL as compared to the expression levels of sc IL-12 and IL-2. Specifically, the nucleic acid sequences encoding 4-1BBL, sc IL-12 and IL-2 are organized in the vector in 5′ to 3′ orientation in a sequential order 1, 2, 3, with the proviso that the gene encoding sc IL-12 is not at position 1. Embodiments of the present disclosure include virus particles comprising the novel vector as well as cancer or immune cells transduced or transfected with the novel vector.
1 - 19 . (canceled)
20 . A vector comprising
(a) human cDNA sequences encoding 4-1BB ligand (4-1BBL), single chain IL-12 (scIL-12) and IL-2, and
(b) at least one regulatory nucleic acid sequence providing for an increased expression level of 4-1BBL as compared to the expression levels of scIL-12 and IL-2,
wherein the nucleic acid sequences encoding scIL-12 and IL-2 are located downstream of the nucleic acid sequence encoding 4-1BBL;
and wherein
(i) the human cDNA sequence encoding 4-1BBL has at least 90% sequence identity to the nucleic acid sequence of SEQ ID NO: 1 and encodes a 4-1BBL protein specifically binding to activated T cells;
(ii) the human cDNA sequence encoding IL-2 has at least 90% sequence identity to the nucleic acid sequence of SEQ ID NO: 3 and encodes an IL-2 protein having immune stimulating activity; and
(iii) the human cDNA sequence encoding scIL-12 shows at least 90% sequence identity to the nucleic acid sequence of SEQ ID NO: 5 and encodes a scIL-12 protein having immune stimulating activity.
21 . The vector of claim 20 , wherein the expression level of 4-1BBL is increased as compared to the expression level of 4-1BBL obtained by the expression construct of vector Im01 depicted in FIG. 20 .
22 . The vector of claim 20 , wherein the expression level of scIL-12 is decreased and/or the expression level of IL-2 is increased as compared to the expression levels of scIL-12 and/or IL-2 obtained by the expression construct of vector Im01 depicted in FIG. 20 .
23 . The vector of claim 20 , wherein the vector is any one of an adenoviral vector, an adeno-associated virus vector, a lentiviral vector, a herpes simplex virus vector, a pox virus vector, an RNA vector, a plasmid vector, a nanoparticle vector, and naked DNA.
24 . The vector of claim 20 , wherein
(i) the human cDNA sequence encoding 4-1BBL has at least 95% sequence identity to the nucleic acid sequence of SEQ ID NO: 1 and encodes a 4-1BBL protein specifically binding to activated T cells;
(ii) the human cDNA sequence encoding IL-2 has at least 95% sequence identity to the nucleic acid sequence of SEQ ID NO: 3 and encodes an IL-2 protein having immune stimulating activity; and
(iii) the human cDNA sequence encoding scIL-12 shows at least 95% sequence identity to the nucleic acid sequence of SEQ ID NO: 5 and encodes a scIL-12 protein having immune stimulating activity.
25 . The vector of claim 20 , wherein the nucleic acid sequence encoding scIL-12 is located downstream of the nucleic acid sequence encoding IL-2.
26 . The vector of claim 20 , wherein the at least one regulatory nucleic acid sequence is at least one promoter sequence.
27 . The vector of claim 26 , wherein a promoter is located upstream of the nucleic acid sequence encoding 4-1BBL, but not upstream of the nucleic acid sequences encoding scIL-12 and/or IL-2.
28 . The vector of claim 20 , wherein the nucleic acid sequences encoding 4-1BBL, scIL-12 and IL-2 are linked by internal ribosomal entry sites (IRES).
29 . A composition, in particular a pharmaceutical composition, or a medicament, comprising the vector of claim 20 .
30 . A method of treating a viral infection, a viral infectious disease, and/or an immune system disorder, comprising administering to a subject in need thereof a therapeutically effective amount of the vector of claim 20 or a therapeutically effective amount of a pharmaceutical composition comprising the vector of claim 20 .
31 . The method of claim 30 , wherein the expression level of 4-1BBL is increased as compared to the expression level of 4-1BBL obtained by the expression construct of vector Im01 depicted in FIG. 20 .
32 . The method of claim 30 , wherein the expression level of scIL-12 is decreased and/or the expression level of IL-2 is increased as compared to the expression levels of scIL-12 and/or IL-2 obtained by the expression construct of vector Im01 depicted in FIG. 20 .
33 . The method of claim 30 , wherein the vector is any one of an adenoviral vector, an adeno-associated virus vector, a lentiviral vector, a herpes simplex virus vector, a pox virus vector, an RNA vector, a plasmid vector, a nanoparticle vector, and naked DNA.
34 . The method of claim 30 , wherein
(i) the human cDNA sequence encoding 4-1BBL has at least 95% sequence identity to the nucleic acid sequence of SEQ ID NO: 1 and encodes a 4-1BBL protein specifically binding to activated T cells;
(ii) the human cDNA sequence encoding IL-2 has at least 95% sequence identity to the nucleic acid sequence of SEQ ID NO: 3 and encodes an IL-2 protein having immune stimulating activity; and
(iii) the human cDNA sequence encoding scIL-12 shows at least 95% sequence identity to the nucleic acid sequence of SEQ ID NO: 5 and encodes a scIL-12 protein having immune stimulating activity.
35 . The method of claim 30 , wherein the nucleic acid sequence encoding scIL-12 is located downstream of the nucleic acid sequence encoding IL-2.
36 . The method of claim 30 , wherein the at least one regulatory nucleic acid sequence is at least one promoter sequence.
37 . The method of claim 30 , wherein a promoter is located upstream of the nucleic acid sequence encoding 4-1BBL, but not upstream of the nucleic acid sequences encoding scIL-12 and/or IL-2.
38 . The method of claim 30 , wherein the nucleic acid sequences encoding 4-1BBL, scIL-12 and IL-2 are linked by internal ribosomal entry sites (IRES).