US2003212028A1PendingUtilityA1

Immunomodulatory polynucleotides in treatment of an infection by an intracellular pathogen

Priority: Jan 31, 2000Filed: Jan 28, 2003Published: Nov 13, 2003
Est. expiryJan 31, 2020(expired)· nominal 20-yr term from priority
A61K 31/711A61P 37/06A61K 45/06A61K 31/7024A61K 31/00
51
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Claims

Abstract

The present invention features methods for treatment or prevention of infection by intracellular pathogens (e.g., Mycobacterium species) by administration of an immunomodulatory nucleic acid molecule. In one embodiment, immunomodulatory nucleic acid molecule are administered in combination with another anti-pathogenic agent to provide a synergistic anti-pathogenic effect.

Claims

exact text as granted — not AI-modified
That which is claimed is:  
     
         1 . A method for treating an intracellular pathogen infection in a subject, the method comprising: 
 administering to a subject an immunomodulatory nucleic acid molecule in an amount effective to inhibit intracellular replication of the intracellular pathogen; and    administering to the subject an anti-pathogenic agent in an amount effective to decrease or inhibit growth of the intracellular pathogen,    thereby treating the pathogen.    
     
     
         2 . The method of  claim 1 , wherein the immunomodulatory nucleic acid molecule is selected from the group consisting of an immunostimulatory oligodeoxyribonucleotide (ISS-ODN); an isolated, detoxified bacterial polynucleotide; and an ISS-enriched plasmid DNA.  
     
     
         3 . The method of  claim 1 , wherein the immunomodulatory nucleic acid molecule comprises a CpG motif selected from the group consisting of: 
 a) 5′-Purine-Purine-[C]-[G]-Pyrimidine-Pyrimidine-3′;    b) 5′-Purine-TCG-Pyrimidine-Pyrimidine-3′;    c) 5′-[TCG] n -3′, where n is any integer that is 1 or greater; and    d) 5′-Purine-Purine-CG-Pyrimidine-Pyrimidine-CG-3′.    e) 5′-Purine-TCG-Pyrimidine-Pyrimidine-CG-3′   
     
     
         4 . The method of  claim 1 , wherein the immunomodulatory nucleic acid molecule comprises a sequence selected from the group consisting of: AACGCC, AACGCT, AACGTC, AACGTT, AGCGCC, AGCGCT, AGCGTC, AGCGTT, GACGCC, GACGCT, GACGTC, GACGTT, GGCGCC, GGCGCT, GGCGTC, GGCGTT, ATCGCC, ATCGCT, ATCGTC, ATCGTT,GTCGCC,GTCGCT,GTCGTC,GTCGTT,TCGTCG,TCGTCGTCG, AACGCCCG,AACGCTCG,AACGTCCG,AACGTTCG,AGC.GCCCG,AGCGCTCG, AGCGTCCG,AGCGTTCG,GACGCCCG,GACGCTCG,GACGTCCG,GACGTTCG, GGCGCCCG,GGCGCTCG,GGCGTCCG,GGCGTTCG, ATCGCCCG,ATCGCTCG, ATCGTCCG,ATCGTTCG, GTCGCCCG, GTCGCTCG, GTCGTCCG, and GTCGTTCG.  
     
     
         5 . The method of  claim 4 , wherein the immunomodulatory nucleic acid molecule comprises the sequence AACGTTCG.  
     
     
         6 . The method of  claim 1 , wherein the immunomodulatory nucleic acid molecule is administered in an amount effective to provide synergistic anti-pathogenic activity with the anti-pathogenic agent.  
     
     
         7 . The method of  claim 1 , wherein the immunomodulatory nucleic acid molecule and the anti-pathogenic agent are administered concurrently.  
     
     
         8 . The method of  claim 1 , wherein the intracellular pathogen is a bacterium.  
     
     
         9 . The method of  claim 8 , wherein the bacterium is a Mycobacterium bacterium.  
     
     
         10 . The method of  claim 9 , wherein the bacterium is selected from the group consisting of  Mycobacterium tuberculosis  and  Mycobacterium avium.    
     
     
         11 . The method of  claim 1 , wherein said administering enhances indoleamine 2,3-dioxygenase activity in the subject.  
     
     
         12 . The method of  claim 1 , wherein the subject is immunocompromised.  
     
     
         13 . The method of  claim 12 , wherein the immunocompromised subject has a reduced number of CD4+ T cells relative to an immunocompetent subject.  
     
     
         14 . A method for treating a mycobacterial infection in a subject, the method comprising: 
 administering to a subject an immunomodulatory nucleic acid molecule in an amount effective to inhibit replication of a Mycobacterium bacterium, thereby treating mycobacterial indection in the subject.    
     
     
         15 . The method of  claim 14 , wherein the immunomodulatory nucleic acid molecule is selected from the group consisting of an immunostimulatory oligodeoxyribonucleotide (ISS-ODN); an isolated, detoxified bacterial polynucleotide; and an ISS-enriched plasmid DNA.  
     
     
         16 . The method of  claim 14 , wherein the immunomodulatory nucleic acid molecule comprises a CpG motif selected from the group consisting of: 
 a) 5′-Purine-Purine-[C]-[G]-Pyrimidine-Pyrimidine-3′;    b) 5′-Purine-TCG-Pyrimidine-Pyrimidine-3′;    c) 5′-[TCG] n -3′, where n is any integer that is 1 or greater; and    d) 5′-Purine-Purine-CG-Pyrimidine-Pyrimidine-CG-3′.    e) 5′-Purine-TCG-Pyrimidine-Pyrimidine-CG-3′   
     
     
         17 . The method of  claim 14 , wherein the immunomodulatory nucleic acid molecule comprises a sequence selected from the group consisting of: AACGCC, AACGCT, AACGTC, AACGTT, AGCGCC, AGCGCT, AGCGTC, AGCGTT, GACGCC, GACGCT, GACGTC, GACGTT, GGCGCC, GGCGCT, GGCGTC, GGCGTT, ATCGCC, ATCGCT, ATCGTC, ATCGTT, GTCGCC, GTCGCT, GTCGTC, GTCGTT, TCGTCG, TCGTCGTCG, AACGCCCG, AACGCTCG, AACGTCCG, AACGTTCG, AGCGCCCG, AGCGCTCG, AGCGTCCG, AGCGTTCG, GACGCCCG, GACGCTCG, GACGTCCG, GACGTTCG, GGCGCCCG, GGCGCTCG, GGCGTCCG, GGCGTTCG, ATCGCCCG, ATCGCTCG, ATCGTCCG, ATCGTTCG, GTCGCCCG, GTCGCTCG, GTCGTCCG, and GTCGTTCG.  
     
     
         18 . The method of  claim 17 , wherein the immunomodulatory nucleic acid molecule comprises the sequence AACGTTCG.  
     
     
         19 . The method of  claim 14 , wherein said administering results in induction of an immune response effective against infection by a mycobacterial pathogen.  
     
     
         20 . The method of  claim 14 , wherein the immunomodulatory nucleic acid molecule is administered with an anti-pathogenic agent.  
     
     
         21 . The method of  claim 20 , wherein the immunomodulatory nucleic acid molecule is administered in an amount effective to provide synergistic anti-pathogenic activity with the anti-pathogenic agent.  
     
     
         22 . The method of  claim 20 , wherein the immunomodulatory nucleic acid molecule and the anti-pathogenic agent are administered concurrently.  
     
     
         23 . The method of  claim 14 , wherein the bacterium is  Mycobacterium tuberculosis.    
     
     
         24 . The method of  claim 14 , wherein the bacterium is  Mycobacterim avium.    
     
     
         25 . The method of  claim 14 , wherein the subject is immunocompromised.  
     
     
         26 . The method of  claim 25 , wherein the immunocompromised subject has a reduced number of CD4+ T cells relative to a immunocompetent subject.  
     
     
         27 . A method for inducing in a subject an immune response against a Mycobacteriurn bacterium, the method comprising: 
 administering to a subject an amount of an immunomodulatory nucleic acid molecule in an amount effective to elicit an immune response against a Mycobacterium bacterium;    wherein said administering results in induction of an immune response effective to protect the subject against onset of disease or to decrease severity of symptoms of disease caused by infection by the Mycobacterium bacterium.    
     
     
         28 . The method of  claim 27 , wherein the immunomodulatory nucleic acid molecule comprises a CpG motif selected from the group consisting of: 
 a) 5′-Purine-Purine-[C]-[G]-Pyrimidine-Pyrimidine-3′;    b) 5′-Purine-TCG-Pyrimidine-Pyrimidine-3′;    c) 5′-[TCG]α-3′, where n is any integer that is 1 or greater; and    d) 5′-Purine-Purine-CG-Pyrimidine-Pyrimidine-CG-3′.    e) 5′-Purine-TCG-Pyrimidine-Pyrimidine-CG-3′   
     
     
         29 . The method of  claim 27 , wherein the immunomodulatory nucleic acid molecule comprises a sequence selected from the group consisting of: AACGCC, AACGCT, AACGTC, AACGTT, AGCGCC, AGCGCT, AGCGTC, AGCGTT, GACGCC, GACGCT, GACGTC, GACGTT, GGCGCC, GGCGCT, GGCGTC, GGCGTT, ATCGCC, ATCGCT, ATCGTC, ATCGTT, GTCGCC, GTCGCT, GTCGTC, GTCGTT, TCGTCG, TCGTCGTCG, AACGCCCG, AACGCTCG, AACGTCCG, AACGTTCG, AGCGCCCG, AGCGCTCG, AGCGTCCG, AGCGTTCG, GACGCCCG, GACGCTCG, GACGTCCG, GACGTTCG, GGCGCCCG, GGCGCTCG, GGCGTCCG, GGCGTTCG, ATCGCCCG, ATCGCTCG, ATCGTCCG, ATCGTTCG, GTCGCCCG, GTCGCTCG, GTCGTCCG, and GTCGTTCG.  
     
     
         30 . The method of  claim 29 , wherein the immunomodulatory nucleic acid molecule comprises the sequence AACGTTCG.  
     
     
         31 . The method of  claim 27 , wherein the bacterium is  Mycobacterium tuberculosis.    
     
     
         32 . The method of  claim 27 , wherein the bacterium is  Mycobacterium avium.    
     
     
         33 . The method of  claim 27 , wherein the subject is immunocompromised.  
     
     
         34 . The method of  claim 33 , wherein the immunocompromised subject has a reduced number of CD4+ T cells relative to an immunocompetent subject.  
     
     
         35 . A method treating a mycobacterial infection, the method comprising: 
 administering to a subject an amount of an immunomodulatory nucleic acid molecule in an amount effective to inhibit intracellular replication of a Mycobacterium bacterium in the subject; and    administering to the subject an antimicrobial agent in an amount effective to decrease or inhibit growth of the Mycobacterium bacterium;    wherein said administering is effective to decrease severity of symptoms of disease caused by the Mycobacterium bacterium.    
     
     
         36 . The method of  claim 35 , wherein the immunomodulatory nucleic acid molecule is administered in an amount effective to provide a synergistic, antimicrobial effect with the antimicrobial agent.  
     
     
         37 . The method of  claim 35 , wherein the immunomodulatory nucleic acid comprises a sequence selected from the group consisting of: AACGCC, AACGCT, AACGTC, AACGTT, AGCGCC, AGCGCT, AGCGTC, AGCGTT, GACGCC, GACGCT, GACGTC, GACGTT, GGCGCC, GGCGCT, GGCGTC, GGCGTT, ATCGCC, ATCGCT, ATCGTC, ATCGTT, GTCGCC, GTCGCT, GTCGTC, GTCGTT, TCGTCG, TCGTCGTCG, AACGCCCG, AACGCTCG, AACGTCCG, AACGTTCG, AGCGCCCG, AGCGCTCG, AGCGTCCG, AGCGTTCG, GACGCCCG, GACGCTCG, GACGTCCG, GACGTTCG, GGCGCCCG, GGCGCTCG, GGCGTCCG, GGCGTTCG, ATCGCCCG, ATCGCTCG, ATCGTCCG, ATCGTTCG, GTCGCCCG, GTCGCTCG, GTCGTCCG, and GTCGTTCG.  
     
     
         38 . The method of  claim 37 , wherein the immunomodulatory nucleic acid comprises the sequence AACGTTCG.  
     
     
         39 . The method of  claim 35 , wherein said administering of the immunomodulatory nucleic acid enhances indoleamine 2,3-dioxygenase activity in the subject.  
     
     
         40 . A method for treating an intracellular pathogen infection in a subject, the method comprising: 
 administering to a subject an immunomodulatory nucleic acid molecule in an amount effective to enhance indoleamine 2,3-dioxygenase activity in the subject, thereby inhibiting intracellular replication by an intracellular pathogen and treating infection in the subject.    
     
     
         41 . The method of  claim 40 , wherein the immunomodulatory nucleic acid molecule is selected from the group consisting of an immunostimulatory oligodeoxyribonucleotide (ISS-ODN); an isolated, detoxified bacterial polynucleotide; and an ISS-enriched plasmid DNA.  
     
     
         42 . The method of  claim 40 , wherein the immunomodulatory nucleic acid molecule comprises a CpG motif selected from the group consisting of: 
 a) 5′-Purine-Purine-[C]-[G]-Pyrimidine-Pyrimidine-3′;    b) 5′-Purine-TCG-Pyrimidine-Pyrimidine-3′;    c) 5′-[TCG] n ,-3′, where n is any integer that is 1 or greater; and    d) 5′-Purine-Purine-CG-Pyrimidine-Pyrimidine-CG-3′.    e) 5′-Purine-TCG-Pyrimidine-Pyrimidine-CG-3′   
     
     
         43 . The method of  claim 40 , wherein the immunomodulatory nucleic acid molecule comprises a sequence selected from the group consisting of: AACGCC, AACGCT, AACGTC, AACGTT, AGCGCC, AGCGCT, AGCGTC, AGCGTT, GACGCC, GACGCT, GACGTC, GACGTT, GGCGCC, GGCGCT, GGCGTC, GGCGTT, ATCGCC, ATCGCT, ATCGTC, ATCGTT, GTCGCC, GTCGCT, GTCGTC, GTCGTT, TCGTCG, TCGTCGTCG, AACGCCCG, AACGCTCG, AACGTCCG, AACGTTCG, AGCGCCCG, AGCGCTCG, AGCGTCCG, AGCGTTCG, GACGCCCG, GACGCTCG, GACGTCCG, GACGTTCG, GGCGCCCG, GGCGCTCG, GGCGTCCG, GGCGTTCG, ATCGCCCG, ATCGCTCG, ATCGTCCG, ATCGTTCG, GTCGCCCG, GTCGCTCG, GTCGTCCG, and GTCGTTCG.  
     
     
         44 . The method of  claim 43 , wherein the immunomodulatory nucleic acid molecule comprises the sequence AACGTTCG.  
     
     
         45 . The method of  claim 40 , wherein the immunomodulatory nucleic acid molecule is administered with an anti-pathogenic agent.  
     
     
         46 . The method of  claim 45 , wherein the immunomodulatory nucleic acid molecule is administered in an amount effective to provide synergistic anti-pathogenic activity with the anti-pathogenic agent.  
     
     
         47 . The method of  claim 45 , wherein the immunomodulatory nucleic acid molecule and the anti-pathogenic agent are administered concurrently.  
     
     
         48 . The method of  claim 40 , wherein the intracellular pathogen is a Mycobacterium bacterium.  
     
     
         49 . The method of  claim 48 , wherein the bacterium is selected from the group consisting of  Mycobacterium tuberculosis  and  Mycobacterium avium.    
     
     
         50 . The method of  claim 40 , wherein the subject is immunocompromised.  
     
     
         51 . The method of  claim 50 , wherein the immunocompromised subject has a reduced number of CD4+ T cells relative to an immunocompetent subject.

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