Nucleic acid comprising or coding for a histone stem-loop and a poly(a) sequence or a polyadenylation signal for increasing the expression of an encoded allergenic antigen or an autoimmune self-antigen

Abstract

The present invention relates to a nucleic acid sequence, comprising or coding for a coding region, encoding at least one peptide or protein comprising an allergenic antigen or an autoimmune self-antigen or a fragment, variant or derivative thereof, at least one histone stem-loop and a poly(A) sequence or a polyadenylation signal. Furthermore the present invention provides the use of the nucleic acid for increasing the expression of said encoded peptide or protein. It also discloses its use for the preparation of a pharmaceutical composition, especially a vaccine, e.g. for use in the treatment of allergies or autoimmune diseases. The present invention further describes a method for increasing the expression of a peptide or protein comprising an allergenic antigen or an autoimmune self-antigen or a fragment, variant or derivative thereof, using the nucleic acid comprising or coding for a histone stem-loop and a poly(A) sequence or a polyadenylation signal.

1 - 21 . (canceled) 
     
     
         22 . A method for increasing the expression of an encoded polypeptide comprising the steps:
 a) providing the nucleic acid sequence comprising:
 i) a polypeptide coding region, encoding an autoimmune self-antigen, wherein the autoimmune self-antigen is a polypeptide capable of inducing an immune response in a subject; 
 ii) at least one histone stem-loop, and 
 iii) a poly(A) sequence or a polyadenylation signal, 
   b) administering the nucleic acid sequence to an organism.   
     
     
         23 . The method of  claim 22 , wherein the autoimmune self-antigen is selected from the group consisting of myelin basic protein (MBP), proteolipid protein (PLP), myelin oligodendrocyte glycoprotein (MOG), CD44, preproinsulin, proinsulin, insulin, glutamic acid decaroxylase (GAD65), tyrosine phosphatase-like insulinoma antigen 2 (IA2), zinc transporter (ZnT8), heat shock protein 60 (HSP60), interphotoreceptor retinoid-binding protein (IRBP), acetylcholine receptor AchR, insulin-like growth factor-1 receptor (IGF-1R), m-protein from beta-hemolytic streptocci (pseudo-autoantigen), macrophage migration inhibitory factor, Ro/La RNP complex, alpha-fodrin, islet cell autoantigen, beta-fodrin, islet cell autoantigen, poly(ADP)ribose polymerase (PARP), NuMA, NOR-90, Ro60 autoantigen, p27 antigen, Ro60 autoantigen, a low-density lipoprotein, a Sm antigens of the U-1 small nuclear ribonucleoprotein complex, a RNP ribonucleoproteins, oxLDL, beta(2)GPI, HSP60/65, oxLDL/beta(2)GPI, cardiac beta(1)-adrenergic receptor, histidyl-tRNA synthetase (HisRS), and topoisomerase I. 
     
     
         24 . The method of  claim 22 , wherein the nucleic acid molecule does not comprise a sequence encoding a reporter protein, a marker or selection protein. 
     
     
         25 . The method of  claim 22 , wherein the nucleic molecule does not comprise sequence encoding a reporter protein, a marker or selection protein. 
     
     
         26 . The method of  claim 22 , wherein the nucleic acid molecule is a RNA. 
     
     
         27 . The method of  claim 22 , wherein the poly(A) sequence comprises a sequence of about 25 to about 400 adenosine nucleotides. 
     
     
         28 . The method of  claim 22 , wherein the polyadenylation signal comprises the consensus sequence NN(U/T)ANA. 
     
     
         29 . The method of  claim 22 , wherein at least one guanosine, uridine, adenosine, thymidine, or cytidine position of the nucleic acid molecule is substituted with an analogue of these nucleotides selected from 2-amino-6-chloropurineriboside-5′-triphosphate, 2-aminoadenosine-5′-triphosphate, 2-thiocytidine-5′-triphosphate, 2-thiouridine-5′-triphosphate, 4-thiouridine-5′-triphosphate, 5-aminoallylcytidine-5′-triphosphate, 5-aminoallyluridine-5′-triphosphate, 5-bromocytidine-5′-triphosphate, 5-bromouridine-5′-triphosphate, 5-iodocytidine-5′-triphosphate, 5-iodouridine-5 triphosphate, 5-methylcytidine-5′-triphosphate, 5-methyluridine-5′-triphosphate, 6-azacytidine-5′-triphosphate, 6-azauridine-5′-triphosphate, 6-chloropurineriboside-5′-triphosphate, 7-deazaadenosine-5′-triphosphate, 7-deazaguanosine-5′-triphosphate, 8-azaadenosine-5′-triphosphate, 8-azidoadenosine-5′-triphosphate, benzimidazole-riboside-5′-triphosphate, N1-methyladenosine-5′-triphosphate, N1-methylguanosine-5′-triphosphate, N6-methyladenosine-5′-triphosphate, 06-methylguanosine-5′-triphosphate, pseudouridine-5′-triphosphate, or puromycin-5′-triphosphate, and xanthosine-5 triphosphate. 
     
     
         30 . The method of  claim 22 , wherein the G/C content of the polypeptide coding region is increased compared with the G/C content of the coding region of a wild-type nucleic acid encoding the autoimmune disease antigen or the allergenic antigen. 
     
     
         31 . The method of  claim 26 , wherein the RNA comprises a 5′ cap structure and a poly(A) sequence of about 25 to about 400 adenosine nucleotides. 
     
     
         32 . The method of  claim 22 , wherein the nucleic acid molecule comprises a sequence of at least 10 consecutive cytidines. 
     
     
         33 . The method of  claim 22 , wherein the nucleic acid molecule further comprises a stabilizing sequence from the alpha globin 3′ UTR, positioned 3′ relative to the polypeptide coding region of the nucleic acid molecule. 
     
     
         34 . The method of  claim 22 , wherein the nucleic acid molecule is formulated in a pharmaceutically acceptable carrier. 
     
     
         35 . The method of  claim 22 , further comprising an adjuvant in conjunction with the nucleic acid molecule. 
     
     
         36 . The method of  claim 22 , wherein the nucleic acid molecule is provide in complex with a cationic or polycationic compound. 
     
     
         37 . The method of  claim 22 , wherein the polycationic polypeptide in complex with the nucleic acid molecule comprise protamine.