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Modulation of immunostimulatory properties by small oligonucleotide-based compounds

a technology of immunostimulatory properties and oligonucleotides, which is applied in the direction of immunological disorders, antibody medical ingredients, peptide/protein ingredients, etc., can solve the problems of not cure the disease, achieve the effect of enhancing the immunostimulatory capacity, enhancing the immune response, and modifying the immune respons

Inactive Publication Date: 2010-07-01
IDERA PHARMA INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The immunomers significantly enhance immunostimulatory capabilities, inducing stronger cytokine responses and immune modulation, effectively treating airway inflammation and asthma by converting Th2 responses to Th1 responses, reducing IL-4, IL-5, and IgE production, and increasing IFN-γ and IgG2a levels, thereby providing a potential cure for allergic asthma.

Problems solved by technology

Steroid treatment is effective only in minimizing the manifestations of inflammation, however, and does not cure the disease.

Method used

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  • Modulation of immunostimulatory properties by small oligonucleotide-based compounds
  • Modulation of immunostimulatory properties by small oligonucleotide-based compounds
  • Modulation of immunostimulatory properties by small oligonucleotide-based compounds

Examples

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example 1

Synthesis of Oligonucleotides Containing Immunomodulatory Moieties

[0173]Oligonucleotides were synthesized on a 1 μmol scale using an automated DNA synthesizer (Expedite 8909; PerSeptive Biosystems, Framingham, Mass.), following the linear synthesis or parallel synthesis procedures outlined in FIGS. 5 and 6.

[0174]Deoxyribonucleoside phosphoramidites were obtained from Applied Biosystems (Foster City, Calif.). 1′,2′-dideoxyribose phosphoramidite, propyl-1-phosphoramidite, 2-deoxyuridine phosphoramidite, 1,3-bis-[5-(4,4′-dimethoxytrityl)pentylamidyl]-2-propanol phosphoramidite and methyl phosphonamidite were obtained from Glen Research (Sterling, Va.). β-L-2′-deoxyribonucleoside phosphoramidite, α-2′-deoxyribonucleoside phosphoramidite, mono-DMT-glycerol phosphoramidite and di-DMT-glycerol phosphoramidite were obtained from ChemGenes (Ashland, Mass.). (4-Aminobutyl)-1,3-propanediol phosphoramidite was obtained from Clontech (Palo Alto, Calif.). Arabinocytidine phosphoramidite, arabinog...

example 2

Analysis of Spleen Cell Proliferation

[0176]In vitro analysis of splenocyte proliferation was carried out using standard procedures as described previously (see, e.g., Zhao et al., Biochem Pharma 51:173-182 (1996)). The results are shown in FIG. 8A. These results demonstrate that at the higher concentrations, Immunomer 6, having two accessible 5′ ends results in greater splenocyte proliferation than does Immunomer 5, having no accessible 5′ end or Oligonucleotide 4, with a single accessible 5′ end. Immunomer 6 also causes greater splenocyte proliferation than the LPS positive control.

example 3

In Vivo Splenomegaly Assays

[0177]To test the applicability of the in vitro results to an in vivo model, selected oligonucleotides were administered to mice and the degree of splenomegaly was measured as an indicator of the level of immunostimulatory activity. A single dose of 5 mg / kg was administered to BALB / c mice (female, 4-6 weeks old, Harlan Sprague Dawley Inc, Baltic, Conn.) intraperitoneally. The mice were sacrificed 72 hours after oligonucleotide administration, and spleens were harvested and weighed. The results are shown in FIG. 8B. These results demonstrate that Immunomer 6, having two accessible 5′ ends, has a far greater immunostimulatory effect than do Oligonucleotide 4 or Immunomer 5.

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Abstract

The invention relates to the therapeutic use of oligonucleotides as immunostimulatory agents in immunotherapy applications. More particularly, the invention provides immunomers for use in methods for generating an immune response or for treating a patient in need of immunostimulation. The immunomers of the invention comprise at least two oligonucleotides linked at their 3′ ends, internucleoside linkages or functionalized nucleobase or sugar to a non-nucleotidic linker, at least one of the oligonucleotides being an immunostimulatory oligonucleotide and having an accessible 5′ end.

Description

RELATED APPLICATION[0001]This application is a Divisional Application of U.S. patent application Ser. No. 10 / 852,598 filed May 24, 2004, which claims the benefit of U.S. Provisional Application No. 60 / 528,277, filed Dec. 5, 2003, which is incorporated by reference in its entirety.BACKGROUND OF THE INVENTION[0002]1. Field of the Invention[0003]The invention relates to immunology and immunotherapy applications using oligonucleotides as immunostimulatory agents.[0004]2. Summary of the Related Art[0005]Oligonucleotides have become indispensable tools in modern molecular biology, being used in a wide variety of techniques, ranging from diagnostic probing methods to PCR to antisense inhibition of gene expression and immunotherapy applications. This widespread use of oligonucleotides has led to an increasing demand for rapid, inexpensive and efficient methods for synthesizing oligonucleotides.[0006]The synthesis of oligonucleotides for antisense and diagnostic applications can now be routi...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K39/00A61K31/7088A61K38/02A61K38/16A61P11/00A61K39/39
CPCA61K39/39A61K2039/55561C12N15/117C12N2310/17C12N2310/315C12N2310/318C12N2310/3183C12N2310/32C12N2310/33C12N2310/336C12N2310/52A61P1/04A61P11/00A61P11/02A61P11/06A61P17/02A61P17/04A61P31/00A61P31/10A61P31/12A61P33/00A61P35/00A61P37/00A61P37/04A61P37/08A61P43/00C07H21/00
Inventor AGRAWAL, SUDHIRZHU, FU-GANGKANDIMALLA, EKAMBAR
Owner IDERA PHARMA INC