US20020098199A1 - Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences - Google Patents

Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences Download PDF

Info

Publication number
US20020098199A1
US20020098199A1 US09/802,370 US80237001A US2002098199A1 US 20020098199 A1 US20020098199 A1 US 20020098199A1 US 80237001 A US80237001 A US 80237001A US 2002098199 A1 US2002098199 A1 US 2002098199A1
Authority
US
United States
Prior art keywords
iss
hepatitis
hbv
hcv
individual
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US09/802,370
Other languages
English (en)
Inventor
Gary Van Nest
Joseph Eiden
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dynavax Technologies Corp
Original Assignee
Dynavax Technologies Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dynavax Technologies Corp filed Critical Dynavax Technologies Corp
Priority to US09/802,370 priority Critical patent/US20020098199A1/en
Priority to PCT/US2001/007931 priority patent/WO2001068078A2/fr
Priority to AU4203201A priority patent/AU4203201A/xx
Priority to ES01913361T priority patent/ES2348877T3/es
Priority to AU2001242032A priority patent/AU2001242032B2/en
Priority to EP01913361A priority patent/EP1282427B1/fr
Priority to JP2001566642A priority patent/JP5128745B2/ja
Priority to AT01913361T priority patent/ATE473750T1/de
Priority to CA002402250A priority patent/CA2402250A1/fr
Priority to DE60142562T priority patent/DE60142562D1/de
Assigned to DYNAVAX TECHNOLOGIES CORPORATION reassignment DYNAVAX TECHNOLOGIES CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: EIDEN, JR, JOSEPH J., VAN NEST, GARY
Publication of US20020098199A1 publication Critical patent/US20020098199A1/en
Priority to US10/357,760 priority patent/US7727712B2/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7088—Compounds having three or more nucleosides or nucleotides
    • A61K31/713—Double-stranded nucleic acids or oligonucleotides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7088—Compounds having three or more nucleosides or nucleotides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/04—Immunostimulants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Definitions

  • This invention is in the field of immunomodulatory polynucleotides, more particularly their use in ameliorating or preventing hepatitis viral infection and/or symptoms of hepatitis virus infection.
  • Hepatitis is a generic term for disease involving inflammation of the liver.
  • agents can cause hepatitis, including viruses, drugs, toxins, and autoimmune disorders. Additionally, hepatitis can arise secondary to non liver-related disorders. Viral infection is the most common cause of hepatitis.
  • hepatitis viruses include the A, B, C, D, E, F, G and cryptogenic hepatitis viruses.
  • the hepatitis viruses are spread through a number of different virus families. Of these viruses, hepatitis B virus (HBV, a hepadnavirus) and hepatitis C virus (HCV, a flavivirus) pose the greatest public health problem in industrialized countries. Both hepatitis B and C are bloodborne diseases, although both viruses may also be transmitted perinatally and via sexual contact.
  • Hepatitis B and C can each give rise to acute and chronic infections. A relatively low level of mortality is due to acute B and C hepatitis (primarily due to fulminant hepatitis).
  • the chronic forms of each disease pose significant medical issues. HBV is the most prevalent chronic infectious disease in the world, and poses a substantially larger perinatal transmission risk than HCV, with 90% of children born to HBV-infected mothers becoming lifelong carriers. HCV is currently the leading cause of liver transplants in the United States.
  • HBV infections Only about half of HBV infections, and even fewer HCV infections, are symptomatic in the acute phase, which typically presents with symptoms such as jaundice, fatigue, abdominal pain and/or loss of appetite. Subclinical infections can be detected using diagnostic testing for viral antigens and/or DNA.
  • Chronic HBV infection is typically asymptomatic, although some symptoms of acute hepatitis B may be present.
  • the long term sequelae of chronic HBV infection include liver fibrosis/cirrhosis, liver cancer, liver failure and death.
  • HBV infection is a substantial public health issue in Asia, where comparatively large percentages of the population are chronically infected with HBV. Mirroring these high rates of chronic infection are rates of hepatocellular carcinoma (HCC), a liver cancer associated with chronic HBV infection.
  • HCC hepatocellular carcinoma
  • HBV and HCV are very different viruses, treatments for chronic infections with the two viruses are virtually identical.
  • Currently available treatments for chronic hepatitis B and C infection are limited to interferons.
  • Interferon ⁇ -2a, interferon ⁇ -2b and interferon alfacon-1 are currently used for the treatment of chronic hepatitis virus infection, although “combination” therapy with ribavirin (an anti-viral drug) and interferon ⁇ -2b has also been approved for the treatment of chronic hepatitis C.
  • ISS immunostimulatory sequences
  • the Th1 subset of helper cells is responsible for classical cell-mediated functions such as delayed-type hypersensitivity and activation of cytotoxic T lymphocytes (CTLs), whereas the Th2 subset functions more effectively as a helper for B-cell activation.
  • CTLs cytotoxic T lymphocytes
  • the type of immune response to an antigen is generally influenced by the cytokines produced by the cells responding to the antigen. Differences in the cytokines secreted by Th1 and Th2 cells are believed to reflect different biological functions of these two subsets. See, for example, Romagnani (2000) Ann. Allergy Asthma Immunol. 85:9-18.
  • mice injected intradermally with Escherichia coli (E. coli) ⁇ -galactosidase ( ⁇ -Gal) in saline or in the adjuvant alum responded by producing specific IgGI and IgE antibodies, and CD4 + cells that secreted IL-4 and IL-5 , but not IFN- ⁇ , demonstrating that the T cells were predominantly of the Th2 subset.
  • E. coli Escherichia coli
  • ⁇ -Gal ⁇ -galactosidase
  • mice injected intradernally (or with a tyne skin scratch applicator) with plasmid DNA (in saline) encoding ⁇ -Gal and containing an ISS responded by producing IgG2a antibodies and CD4 + cells that secreted IFN- ⁇ , but not IL-4 and IL-5, demonstrating that the T cells were predominantly of the Th1 subset.
  • specific IgE production by the plasmid DNA-injected mice was reduced 66-75%. Raz et al. (1996) Proc. Natl. Acad. Sci. USA 93:5141-5145.
  • the response to naked DNA immunization is characterized by production of IL-2, TNF ⁇ and IFN- ⁇ by antigen-stimulated CD4 + T cells, which is indicative of a Th1-type response.
  • This is particularly important in treatment of allergy and asthma as shown by the decreased IgE production.
  • the ability of immunostimulatory polynucleotides to stimulate a Th1-type immune response has been demonstrated with bacterial antigens, viral antigens and with allergens (see, for example, WO 98/55495).
  • the invention provides methods of suppressing and/or ameliorating hepatitis infection in an individual using immunostimulatory polynucleotide sequences. Accordingly, the invention provides methods for preventing, palliating, ameliorating, reducing, and/or eliminating one or more symptoms of HBV or HCV infection without administering HBV or HCV antigens.
  • a polynucleotide comprising an immunostimulatory sequence (an ISS) is administered to an individual who has been exposed to HBV and/or HCV or is infected with HBV and/or HCV.
  • the ISS-containing polynucleotide is administered without any HBV or HCV antigens (i.e., HBV or HCV antigen is not co-administered).
  • Administration of the ISS results in reduced incidence and/or severity of one or more symptoms of HBV and/or HCV infection.
  • the invention provides methods for preventing a symptom of acute hepatitis B virus (HBV) or hepatitis C virus (HCV) infection in an individual which entail administering an effective amount of a composition comprising a polynucleotide comprising an immunostimulatory sequence (ISS), (i.e., an amount of the composition sufficient to prevent a symptom of acute HBV or HCV infection) to the individual, wherein the ISS comprises the sequence 5′-C, G-3′ and wherein an HBV or HCV antigen is not administered in conjunction with administration of the composition (i.e., antigen is not administered with the ISS-containing polynucleotide), thereby preventing a symptom of acute HBV or HCV infection.
  • the individual may have been exposed to and/or infected by HBV or HCV.
  • Another embodiment of the invention provides methods of reducing severity of a symptom of acute HBV and/or HCV infection in an individual which entail administering an effective amount of a composition comprising a polynucleotide comprising an ISS to the individual, wherein the ISS comprises the sequence 5′-C, G-3′ and wherein an HBV or HCV antigen is not administered in conjunction with administration of the composition, thereby reducing severity of a symptom of acute HBV or HCV infection.
  • the individual may have been exposed to and/or infected by HBV or HCV.
  • Another embodiment of the invention provides methods of delaying development of a symptom of acute HBV or HCV infection in an individual which entail administering an effective amount of a composition comprising a polynucleotide comprising an ISS to the individual, wherein the ISS comprises the sequence 5′-C, G-3′ and wherein an HBV or HCV antigen is not administered in conjunction with administration of the composition, thereby delaying development of a symptom of acute HBV or HCV infection.
  • the individual may have been exposed to and/or infected by HBV and/or HCV.
  • Another embodiment of the invention provides methods of reducing duration of a symptom of acute HBV or HCV infection in an individual which entail administering an effective amount of a composition comprising a polynucleotide comprising an ISS to the individual, wherein the ISS comprises the sequence 5′-C, G-3′ and wherein an HBV or HCV antigen is not administered in conjunction with administration of the composition, thereby reducing duration of a symptom of acute HBV or HCV infection
  • the individual may have been exposed to and/or infected by HBV and/or HCV.
  • Another embodiment of the invention provides methods for preventing a symptom of chronic HBV or HCV infection in an individual which entail administering an effective amount of a composition comprising a polynucleotide comprising an ISS to the individual, wherein the ISS comprises the sequence 5′-C, G-3′ and wherein an HBV or HCV antigen is not administered in conjunction with administration of the composition, thereby preventing a symptom of chronic HBV or HCV infection.
  • the individual may have been exposed to and/or infected by HBV and/or HCV.
  • Another embodiment of the invention provides methods of reducing severity of a symptom of chronic HBV or HCV infection in an individual which entail administering an effective amount of a composition comprising a polynucleotide comprising an ISS to the individual, wherein the ISS comprises the sequence 5′-C, G-3′ and wherein an HBV or HCV antigen is not administered in conjunction with administration of the composition, thereby reducing severity of a symptom of chronic HBV or HCV infection.
  • the individual may have been exposed to and/or infected by HBV and/or HCV.
  • Another embodiment of the invention provides methods of delaying development of a symptom of chronic HBV or HCV infection in an individual which entail administering an effective amount of a composition comprising a polynucleotide comprising an ISS to the individual, wherein the ISS comprises the sequence 5′-C, G-3′ and wherein an HBV or HCV antigen is not administered in conjunction with administration of the composition, thereby delaying development of a symptom of chronic HBV or HCV infection.
  • the individual may have been exposed to and/or infected by HBV and/or HCV.
  • Another embodiment of the invention provides methods of reducing duration of a symptom of chronic HBV or HCV infection in an individual which entail administering an effective amount of a composition comprising a polynucleotide comprising an ISS to the individual, wherein the ISS comprises the sequence 5′-C, G-3′ and wherein an HBV or HCV antigen is not administered in conjunction with administration of the composition, thereby reducing duration of a symptom of chronic HBV or HCV infection.
  • the individual may have been exposed to and/or infected by HBVand/or HCV.
  • Another embodiment of the invention provides methods of suppressing an HBV or HCV infection in an individual infected with or at risk of being infected with HBV or HCV which entail administering an effective amount of a composition comprising a polynucleotide comprising an ISS to the individual, wherein the ISS comprises the sequence 5′-C, G-3′ and wherein an HBV or HCV antigen is not administered in conjunction with administration of the composition, thereby suppressing an HBV or HCV infection.
  • the invention provides methods for reducing viremia in an individual exposed to and/or infected with HBV and/or HCV which entail administering an effective amount of a composition comprising a polynucleotide comprising an ISS to the individual, wherein the ISS comprises the sequence 5′-C, G-3′ and wherein an HBV or HCV antigen is not administered in conjunction with administration of the composition, thereby reducing HBV or HCV viremia.
  • the invention provides methods for reducing blood levels of hepatitis virus antigens, preferably HBV or HCV antigens, in an individual which entail administering an effective amount of a composition comprising a polynucleotide comprising an ISS to the individual, wherein the ISS comprises the sequence 5′-C, G-3′ and wherein an HBV or HCV antigen is not administered in conjunction with administration of the composition, thereby reducing blood levels of hepatitis virus antigens.
  • the individual may have been exposed to and/or infected by HBV or HCV.
  • kits for use in ameliorating a symptom of acute or chronic HBV or HCV infection in an individual exposed to and/or infected with HBV or HCV comprise a composition comprising a polynucleotide comprising an ISS, wherein the ISS comprises the sequence 5′-C, G-3′, wherein the kit does not comprise an HBV or HCV antigen, and wherein the kits comprise instructions for administration of the composition to an individual infected with or exposed to HBV or HCV.
  • the ISS comprises the sequence 5′-purine, purine, C, G, pyrimidine, pyrimidine, C, G-3′ or 5′-purine, purine, C, G, pyrimidine, pyrimidine, C, C-3′.
  • the ISS comprises a sequence selected from the group consisting of AACGTTCC, AACGTTCG, GACGTTCC, and GACGTTCG.
  • the ISS comprises the sequence 5′-T, C, G-3′. In some embodiments of the methods and kits of the invention, the ISS comprises the sequence 5′-TGACTGTGAACGTTCGAGATGA-3′ (SEQ ID NO:1).
  • the individual is a mammal. In further embodiments, the mammal is human.
  • the virus is HBV.
  • the virus is HCV.
  • FIG. 1(A)-(D) are graphs depicting effects of administration of ISS and control reagents to STC mice on viral titer. Results shown are blood viral DNA titer (in copies per milliliter) over time (in days).
  • FIG. 1(A) depicts results for STC mice injected with ISS at day 0, 7, and 14 (week 0, 1 and 2);
  • FIG. 1(B) depicts results for STC mice injected with ISS at day 14 (week 2) only;
  • FIG. 1(C) depicts results for STC mice injected with 100 ng of murine IL-12 on days 12, 13 and 14;
  • FIG. 1(D) depicts results for STC mice injected with phosphate buffered saline (PBS) on days 0, 7 and 14. Error bars indicate ⁇ one standard deviation (SD).
  • SD phosphate buffered saline
  • FIG. 2 is a graph depicting effects of administration of ISS and control reagents to STC mice on hepatitis B surface antigen (HBsAg) levels. Results are shown as percent of value at day -1 over time (in days). Open squares indicate results for STC mice injected with ISS at day 0, 7, and 14 (week 0, 1 and 2); closed diamonds indicate results for STC mice injected with ISS at day 14 (week 2) only; closed square indicate results for STC mice injected with 100 ng of murine IL-12 on days 12, 13 and 14; and open diamonds indicate results for STC mice injected with phosphate buffered saline on days 0, 7 and 14.
  • HBsAg hepatitis B surface antigen
  • a polynucleotide comprising an immunostimulatory sequence is administered to an individual exposed to and/or infected with hepatitis B virus (HBV) or hepatitis C virus (HCV).
  • HBV hepatitis B virus
  • HCV hepatitis C virus
  • kits for treatment and/or prevention of hepatitis B and/or hepatitis C infection in exposed individuals comprise a polynucleotide comprising an ISS and instructions describing the administration of an ISS to an individual for the intended treatment.
  • Kits intended for use on individuals exposed to or infected with hepatitis B do not include hepatitis B viral antigens.
  • Kits intended for use on individuals exposed to or infected with hepatitis C do not include hepatitis C viral antigens.
  • Kits intended for use on individuals infected with both hepatitis B and hepatitis C contain neither hepatitis B nor hepatitis C viral antigens.
  • hepatitis B virus or “HBV” is a term well-understood in the art and refers to a virus which is a member of the family hepadnaviridae, which family consists of the genus Orthohepadnavirus (hepadnaviruses which infect mammals) and Avihepadnaviridae (hepadnaviruses which infect birds). HBV is a Orthohepadnavirus which infects humans.
  • Hepatitis B virus is a lipid-enveloped virus having a diameter of approximately 42 nm and comprises a circular, double stranded DNA genome.
  • the genome is contained in a capsid which is enclosed by a lipid envelope studded with the surface, or “s”, antigen (HBsAg).
  • s antigen
  • the 20 nm diameter particles are non-infectious.
  • the main structural component of the 25-27 nm diameter capsid is the core or “c” protein (HBcAg).
  • P protein polymerase
  • the HBV genome encodes a number of additional products, including the “e” protein or “HBeAg”, which is secreted by infected cells independently from the virion and other virion-related particles.
  • antigens and/or antibodies against such antigens are generally diagnostic for HBV.
  • hepatitis C virus or “HCV” is a term well-understood in the art and refers to a virus which is the sole member of an unnamed genus of the family flaviviridae. Unlike most flaviviridae, HCV does not utilize a vector such as an insect, and humans are the only known host (although chimpanzees may be infected experimentally). Hepatitis C virus is a lipid-enveloped virus having a diameter of approximately 30-80 nm in diameter. Unlike HBV, HCV has a positive strand RNA genome. However, HCV does not integrate like a retrovirus.
  • Serum titers of HCV tend to be relatively low, so most diagnostic assays rely on detecting patient antibodies to a viral protein such as the nucleocapsid protein or the NS3, NS4 and/or NS5 proteins. Additionally, diagnostic assays are available which detect genomic viral RNA.
  • acute hepatitis infection refers to acute hepatitis B and/or acute hepatitis C infection, although not all individuals infected with HBV and/or HCV will exhibit clinical symptoms of acute hepatitis.
  • Clinical symptoms of acute hepatitis include elevated bilirubin levels (up to an including frank jaundice), nausea, fatigue, elevated blood levels of liver enzymes (e.g., alanine aminotransferase or ALT and/or aspartate aminotransferase or AST), nausea, and joint and/or abdominal pain.
  • Acute hepatitis may be the result of an initial infection by HBV or HCV, or may be the result of a “flare up” or relapse in a chronically infected patient.
  • Acute hepatitis as a result of an initial infection by HBV or HCV may be distinguished from recurrent acute hepatitis by examination of anti-hepatitis virus immunoglobin. High levels of anti-virus IgM (and low levels of anti-virus IgG) are found in acute hepatitis due to an initial infection of HBV or HCV, while the reverse is found in relapsing or recurring acute hepatitis.
  • chronic hepatitis refers to a disorder in which liver inflammation due to chronic HBV or HCV infection is present for at least six continuous months.
  • Chronic hepatitis patients may suffer from fatigue, general malaise and/or abdominal pain.
  • Chronic hepatitis due to HBV or HCV may be diagnosed by the use of diagnostic testing for the presence of HBV or HCV.
  • Chronic hepatitis may be divided into two types (either or both of which are included in the invention), chronic active hepatitis and chronic persistent hepatitis.
  • Chronic active hepatitis is hepatitis which is causing active damage to the liver, such as ongoing hepatocellular necrosis.
  • Chronic persistent hepatitis is a hepatitis infection which is not currently causing damage, although pre-existing liver damage may be present. While the prognosis for patients with chronic persistent hepatitis is better than that for those with chronic active hepatitis, chronic persistent hepatitis may develop into chronic active hepatitis.
  • the sequelae of chronic hepatitis include portal hypertension, cirrhosis, and hepatocellular carcinoma (HCC).
  • “Exposure” to a virus denotes encounter with HBV or HCV which allows infection, such as, for example, upon transfer of blood or a blood product from an infected individual such as by transfusion of contaminated blood, or a “needle stick” accident or incident involving a needle used on an HBV or HCV positive individual.
  • An individual is “seronegative” for a virus if antibodies specific to the virus cannot be detected in blood or serum samples from the individual using methods standard in the art, such as ELISA. Conversely, an individual is “seropositive” for a virus if antibodies specific for the virus can be detected in blood or serum samples from the individual using methods standard in the art, such as ELISA. An individual is said to “seroconvert” for a virus when antibodies to the virus can be detected in blood or serum from an individual who was previously seronegative.
  • a “symptom of HBV or HCV” refers to a symptom HBV and/or HCV infection. Such symptoms are well known in the art and include symptoms of acute and chronic hepatitis B and C. Symptoms of HBV or HCV include physical symptoms such as jaundice, abdominal pain, fatigue, malaise, nausea, and vomiting, as well as clinical/laboratory findings associated with hepatitis, such as elevated liver enzyme levels (e.g., alanine aminotransferase, ALT, aspartate aminotransferase, AST, and/or lactate dehydrogenase, LDH), elevated bilirubin, HBV and/or HCV viremia or antigen levels, portal hypertension, cirrhosis, anorexia, and other symptoms recognized in the art.
  • liver enzyme levels e.g., alanine aminotransferase, ALT, aspartate aminotransferase, AST, and/or lactate dehydrogenase, LDH
  • “Suppressing” hepatitis virus infection refers to any aspect of hepatitis B or C virus infection, such as a physical symptom (e.g., jaundice, fatigue, abdominal pain), a hepatitis-associated laboratory finding (e.g., liver enzyme levels in blood or cirrhosis), viral replication, or amount (titer) of virus, which is curtailed, inhibited, or reduced (in terms of severity and/or duration) in an individual or a population of individuals treated with an ISS-containing polynucleotide in accordance with the invention as compared to an aspect of viral infection in an individual or a population of individuals not treated in accordance with the invention.
  • a physical symptom e.g., jaundice, fatigue, abdominal pain
  • a hepatitis-associated laboratory finding e.g., liver enzyme levels in blood or cirrhosis
  • viral replication e.g., a hepatitis-associated laboratory finding
  • amount (titer) of virus
  • Reduction in viral titer includes, but is not limited to, elimination of the virus from an infected site or individual.
  • Viral infection can be assessed by any means known in the art, including, but not limited to, detection of symptoms, measurement of liver function by laboratory testing, liver biopsy, direct or indirect measurement of liver portal vein pressure, and measurement of virus particles, viral nucleic acid or viral antigen titer and detection and/or measurement of anti-virus antibodies.
  • Anti-virus antibodies are widely used to detect and monitor viral infection and generally are commercially available.
  • “Palliating” a disease or one or more symptoms of a disease or infection means lessening the extent and/or time course of undesirable clinical manifestations of a disease state or infection in an individual or population of individuals treated with an ISS in accordance with the invention.
  • “delaying” development of viral infection or a symptom of hepatitis means to defer, hinder, slow, retard, stabilize, and/or postpone development of the disease or symptom when compared to not using the method(s) of the invention.
  • This delay can be of varying lengths of time, depending on the history of the disease and/or individual being treated. As is evident to one skilled in the art, a sufficient or significant delay can, in effect, encompass prevention, in that the individual does not develop the disease.
  • “Reducing severity of a symptom” or “ameliorating a symptom” of viral infection means a lessening or improvement of one or more symptoms of hepatitis as compared to not administering an ISS-containing polynucleotide. “Reducing severity” also includes shortening or reduction in duration of a symptom.
  • hepatitis B and hepatitis C these symptoms are well known in the art and include, but are not limited to, jaundice, abdominal pain, fatigue, malaise, nausea, and vomiting, as well as clinical/laboratory findings associated with hepatitis, such as elevated liver enzyme levels (e.g., ALT, AST, and/or LDH), elevated bilirubin, HBV and/or HCV viremia or antigen levels, portal hypertension, cirrhosis, anorexia, and other symptoms recognized in the art.
  • liver enzyme levels e.g., ALT, AST, and/or LDH
  • elevated bilirubin e.g., HBV and/or HCV viremia or antigen levels
  • portal hypertension cirrhosis, anorexia, and other symptoms recognized in the art.
  • “Reducing duration of viral infection” means the length of time of viral infection (usually indicated by symptoms) is reduced, or shortened, as compared to not administering an ISS-containing polynucleotide.
  • Preventing a symptom of infection” by a hepatitis virus means that the symptom does not appear after exposure to the virus.
  • infectious individual refers to an individual who has been infected by HBV and/or HCV.
  • Symptoms of HBV infection include seropositivity for anti-HBsAg, HBeAg, or HBcAg, presence of HBsAg, HBeAg, or HBcAg in samples from the individual, or presence of HBV DNA in samples from the individual, as well as other symptoms known in the art.
  • Symptoms of HCV infection include seropositivity for antibodies to nucleocapsid protein or the NS3, NS4 and/or NS5 proteins, presence of nucleocapsid protein or the NS3, NS4 and/or NS5 proteins in samples from the individual, or presence of HCV RNA or DNA in samples from the individual, as well as other symptoms known in the art.
  • a “biological sample” encompasses a variety of sample types obtained from an individual and can be used in a diagnostic or monitoring assay.
  • the definition encompasses blood and other liquid samples of biological origin, solid tissue samples such as a biopsy specimen or tissue cultures or cells derived therefrom, and the progeny thereof.
  • the definition also includes samples that have been manipulated in any way after their procurement, such as by treatment with reagents, solubilization, or enrichment for certain components, such as proteins or polynucleotides.
  • the term “biological sample” encompasses a clinical sample, and also includes cells in culture, cell supernatants, cell lysates, serum, plasma, biological fluid, and tissue samples.
  • “Viral titer” is a term well-known in the art and indicates the amount of virus in a given biological sample. “Viremia” is a term well-known in the art as the presence of virus in the bloodstream and/or viral titer in a blood or serum sample. Amount of virus are indicated by various measurements, including, but not limited to, amount of viral nucleic acid; presence of viral particles (such as HBsAg or hepatitis B surface antigen particles); replicating units (RU); plaque forming units (PFU). Generally, for fluid samples such as blood and urine, amount of virus is determined per unit fluid, such as milliliters. For solid samples such as tissue samples, amount of virus is determined per weight unit, such as grams. Methods for determining amount of virus are known in the art and described herein.
  • An “individual” is a vertebrate, preferably a mammal, more preferably a human. Mammals include, but are not limited to, humans, farm animals, sport animals, rodents, primates and certain pets. Vertebrates also include, but are not limited to, birds (i.e., avian individuals) and reptiles (i.e., reptilian individuals).
  • ISS refers to polynucleotide sequences that effect a measurable immune response as measured in vitro, in vivo and/or ex vivo.
  • measurable immune responses include, but are not limited to, antigen-specific antibody production, secretion of cytokines, activation or expansion of lymphocyte populations such as NK cells, CD4 + T lymphocytes, CD8 + T lymphocytes, B lymphocytes, and the like.
  • the ISS sequences preferentially activate a Th1-type response.
  • a polynucleotide for use in methods of the invention contains at least one ISS.
  • polynucleotide and “oligonucleotide” include single-stranded DNA (ssDNA), double-stranded DNA (dsDNA), single-stranded RNA (ssRNA) and double-stranded RNA (dsRNA), modified oligonucleotides and oligonucleosides or combinations thereof.
  • the oligonucleotide can be linearly or circularly configured, or the oligonucleotide can contain both linear and circular segments.
  • Adjuvant refers to a substance which, when added to an immunogenic agent such as antigen, nonspecifically enhances or potentiates an immune response to the agent in the recipient host upon exposure to the mixture.
  • an “effective amount” or a “sufficient amount” of a substance is an amount sufficient to effect beneficial or desired results, including clinical results.
  • An effective amount can be administered in one or more administrations.
  • a “therapeutically effective amount” is an amount to effect beneficial clinical results, including, but not limited to, alleviation of one or more symptoms associated with viral infection as well as prevention of disease (e.g., prevention of one or more symptoms of infection).
  • a microcarrier is considered “biodegradable” if it is degradable or erodable under normal mammalian physiological conditions. Generally, a microcarrier is considered biodegradable if it is degraded (i.e., loses at least 5% of its mass and/or average polymer length) after a 72 hour incubation at 37° C. in normal human serum. Conversely, a microcarrier is considered “nonbiodegradable” if it is not degraded or eroded under normal mammalian physiological conditions. Generally, a microcarrier is considered nonbiodegradable if it not degraded (i.e., loses less than 5% of its mass and/or average polymer length) after at 72 hour incubation at 37° C. in normal human serum.
  • ISS-MC complex refers to a complex of an ISS-containing polynucleotide and a microcarrier.
  • the components of the complex may be covalently or non-covalently linked.
  • Non-covalent linkages may be mediated by any non-covalent bonding force, including by hydrophobic interaction, ionic (electrostatic) bonding, hydrogen bonds and/or van der Waals attractions .
  • hydrophobic linkages the linkage is generally via a hydrophobic moiety (e.g., cholesterol) covalently linked to the ISS.
  • the invention provides methods of ameliorating (i.e., reducing severity) and/or preventing one or more symptoms of acute and/or chronic HBV and HCV virus infection which may include reducing incidence of or delaying of appearance of sequelae of HBV and/or HCV infection (i.e., cirrhosis or fulminant liver failure) by administering an ISS-containing polynucleotide (used interchangeably herein with “ISS”) to an individual without administering a HBV or HCV antigen.
  • ISS-containing polynucleotide used interchangeably herein with “ISS”
  • the invention also provides methods of reducing viremia as well as methods of reducing levels of hepatitis viral antigen(s) in blood.
  • hepatitis viruses not only cause acute disease but can also lead to chronic infection and other disease states.
  • transmission of hepatitis B and C can occur through blood and blood products, perinatally and via sexual contact.
  • the hepatitis virus may be HBV or HCV, although concurrent infections with both HBV and HCV may also be treated. It should be noted that hepatitis D virus infection may be present in individuals infected with HBV.
  • An ISS-containing composition which includes neither a HBV nor HCV antigen is administered to an individual exposed to, infected with, and/or exhibiting one or more symptoms of infection by HBV and/or HCV.
  • Individuals receiving ISS are preferably mammals, more preferably humans.
  • neither HBV or HCV antigen is administered to the individual in conjunction with administration of an ISS (i.e., is not administered in a separate administration at or about the time of administration of the ISS).
  • the individual has been exposed to HBV and/or HCV.
  • An exposed individual can be easily identified by a skilled clinician or epidemiologist.
  • an exposed individual is an individual that has been exposed to HBV and/or HCV by a route through which HBV and/or HCV can be transmitted.
  • an exposed individual may be a person who has been percutaneously exposed to blood or a blood product derived from an individual infected with HBV and/or HCV (e.g., by transfusion or by a “needle stick” accident).
  • the exposed individual may be a child born to an individual infected with HBV or HCV or the sexual partner of an HBV or HCV infected individual not practicing barrier methods of contraception.
  • the individual is infected with HBV and/or HCV.
  • Infection by HBV or HCV may be detected by diagnostic testing, or by clinical assessment of the infected individual. Because not all infected individuals exhibit overt symptoms of hepatitis, diagnostic assays which detect viral antigen(s), viral DNA or RNA, or host antibodies against viral antigen(s) are considered more reliable indicators of infection.
  • HBsAg is a diagnostic antigen for HBV and the nucleocapsid, NS3, NS4 and/or NS5 proteins are diagnostic antigens for HCV.
  • Infection is usually engendered by percutaneous exposure to blood or blood products from an infected individual, such as through transfusion, sharing of needles during intravenous drug use, or a “needle stick” incident, although sexual transmission and “vertical” transmission from mother to child during childbirth or the perinatal period are also routes for infection.
  • the individual may have chronic or acute hepatitis B and/or hepatitis C.
  • Acute hepatitis may be easily recognized by one of skill in the art, and is characterized by jaundice, fatigue, malaise, elevated blood levels of liver enzymes such as AST and/or ALT, dark urine and other symptoms known to those of skill in the art.
  • liver enzymes such as AST and/or ALT
  • dark urine and other symptoms known to those of skill in the art.
  • positive diagnostic test for HBV or HCV is required to identify hepatitis B or hepatitis C, respectively.
  • Chronic hepatitis B and hepatitis C are generally not characterized by any specific overt symptoms, although the sequelae of these disorders, such as hepatomegaly, disrupted clotting (due to reduced levels of clotting factors produced by the liver), ascites formation, cirrhosis, portal hypertension, and the like, are easily recognized by the clinician. However, altered liver fimction (as demonstrated by increased blood levels of liver enzymes) can be detected by laboratory testing. Additionally, chronic hepatitis B and hepatitis C sufferers may be subject to occasional “flare ups”, in which the symptoms of acute hepatitis return.
  • the methods of this invention entail administering a polynucleotide comprising an ISS (or a composition comprising such a polynucleotide).
  • the immunomodulatory polynucleotide contains at least one ISS, and can contain multiple ISSs.
  • the ISSs can be adjacent within the polynucleotide, or they can be separated by additional nucleotide bases within the polynucleotide. Alternately, multiple ISSs may be delivered as individual polynucleotides.
  • ISS have been described in the art and may be readily identified using standard assays which indicate various aspects of the immune response, such as cytokine secretion, antibody production, NK cell activation and T cell proliferation. See, e.g., WO 97/28259; WO 98/16247; WO 99/11275; Krieg et al. (1995); Yamamoto et al. (1992); Ballas et al. (1996); Klinman et al. (1997); Sato et al. (1996); Pisetsky (1996a); Shimada et al. (1986) Jpn. J. Cancer Res. 77:808-816; Cowdery et al. (1996) J. Immunol. 156:4570-4575; Roman et al. (1997); and Lipford et al. (1997a).
  • the ISS can be of any length greater than 6 bases or base pairs and generally comprises the sequence 5′-cytosine, guaineg-3′, preferably greater than 15 bases or base pairs, more preferably greater than 20 bases or base pairs in length.
  • the cytosine of the 5′-cytosine, guanine-3′ sequence is unmethylated.
  • An ISS may also comprise the sequence 5′-purine, purine, C, G. pyrimidine, pyrimidine, C, G-3′.
  • An ISS may also comprise the sequence 5′-purine, purine, C, G, pyrimidine, pyrimidine, C, C-3′.
  • an ISS may comprise (i.e., contain one or more of) the sequence 5′-T, C, G-3′.
  • an ISS may comprise the sequence 5′-C, G, pyrimidine, pyrimidine, C, G-3′ (such as 5′-CGTTCG-3′).
  • an ISS may comprise the sequence 5′-C, G, pyrimidine, pyrimidine, C, G, purine, purine-3′.
  • an ISS comprises the sequence 5′-purine, purine, C, G, pyrimidine, pyrimidine-3′ (such as 5′-AACGTT-3′).
  • an ISS may comprise the sequence 5′-purine, T, C, G, pyrimidine, pyrimidine-3′.
  • an ISS-containing polynucleotide is less than about any of the following lengths (in bases or base pairs): 10,000; 5,000; 2500; 2000; 1500; 1250; 1000; 750; 500; 300; 250; 200; 175; 150; 125; 100; 75; 50; 25; 10.
  • an ISS-containing polynucleotide is greater than about any of the following lengths (in bases or base pairs): 8; 10; 15; 20; 25; 30; 40; 50; 60; 75; 100; 125; 150; 175; 200; 250; 300; 350; 400; 500; 750; 1000; 2000; 5000; 7500; 10000; 20000; 50000.
  • the ISS can be any of a range of sizes having an upper limit of 10,000; 5,000; 2500; 2000; 1500; 1250; 1000; 750; 500; 300; 250; 200; 175; 150; 125; 100; 75; 50; 25; or 10 and an independently selected lower limit of 8; 10; 15; 20; 25; 30; 40; 50; 60; 75; 100; 125; 150; 175; 200; 250; 300; 350; 400; 500; 750; 1000; 2000; 5000; 7500, wherein the lower limit is less than the upper limit.
  • the ISS comprises any of the following sequences: In some embodiments, the ISS comprises any of the following sequences: GACGCTCC; GACGTCCC; GACGTTCC; GACGCCCC; AGCGTTCC; AGCGTCCC; AGCGCCCC; AACGTCCC; AACGCCCC; AACGTTCC; AACGCTCC; GGCGTTCC; GGCGTCCC; GGCGCCCC; GACGCTCG; GACGTCCG; GACGCCCG; GACGTTCG; AGCGCTCG; AGCGTTCG; AGCGTCCG; AGCGCCCG; AGCGTCCG; AGCGCCCG; AGCGTCCG; AGCGCCCG; AGCGTCCG; AGCGCCCG; AGCGTCCG; AGCGCCCG; AGCGTCCG; AGCGCCCG; AGCGTCCG; AGCGCCCG; AGCGTCCG; AGCGCCCG; AGCGTCCG; AGCGCCCG; AGCGTCCG; AGCGCCCG; AGCGTCCG; AGCGCCCG; AGCGTCCG; AGCGCCCG;
  • the immunomodulatory polynucleotide comprises the sequence 5′-TGACTGTGAACGTTCGAGATGA-3′ (SEQ ID NO:1).
  • the ISS comprises any of the following sequences: GACGCU; GACGUC; GACGUU; GACGUT; GACGTU; AGCGUU; AGCGCU; AGCGUC; AGCGUT; AGCGTU; AACGUC; AACGUU; AACGCU; AACGUT; AACGTU; GGCGUU; GGCGCU; GGCGUC; GGCGUT; GGCGTU.
  • the ISS comprises any of the following sequences: GABGCTCC; GABGTCCC; GABGTTCC; GABGCCCC; AGBGTTCC; AGBGTCCC; AGBGCCCC; AABGTCCC; AABGCCCC; AABGTTCC; AABGCTCC; GGBGTTCC; GGBGCTCC; GGBGTCCC; GGBGCCCC; GABGCTCC; GABGTCCC; GABGCCCC; GABGTTCC; AGBGCTCG; AGBGTTCG; AGBGTCCG; AGBGCCCG; AABGTCCG; AABGCCCG; AABGTTCG; AABGCTCG; GGBGTTCG; GGBGCTCG; GGBGTCCG; GGBGCCCG; GABGCTBG; AGBGCTBG; AGBGTCBG; AGBGCCBG; AGBGTCBG; AGBGTCBG; GABGCCBG; GABGTTBG; AGBGCTBG; AGBGTCBG; AGBGCCBG; AGBGTCBG; GABGTCBG; GABGCCBG; GABG
  • the ISS comprises any of the following sequences: GABGCUCC; GABGUCCC; GABGUTCC; GABGTUCC; GABGUUCC; AGBGUUCC; AGBGTUCC; AGBGUTCC; AGBGCUCC; AGBGUCCC; AABGUCCC; AABGUUCC; AABGUTCC; AABGTUCC; AABGCUCC; GGBGUUCC; GGBGUTCC; GGBGTUCC; GGBGCUCC; GGBGUCCC; GABGCUCG; GABGUCCG; GABGUUCG; GABGUTCG; GABGTUCG; AGBGCUCG; AGBGUUCG; AGBGUTCG; AGBGTUCG; AGBGUCCG; AGBGUCCG; AGBGUCCG; AGBGUCCG; AGBGUCCG; AGBGUCCG; AGBGUCCG; AGBGUCCG; AGBGUCCG; AGBGUCCG; AGBGUCCG; AGBGUCCG; AGBGUCCG; AGBGUCCG; AGBGUCCG; AGBGUCCG; AGBGUCCG
  • the ISS comprises any of the sequences: 5′-TGACCGTGAACGTTCGAGATGA-3′ (SEQ ID NO:2); 5′-TCATCTCGAACGTTCCACAGTCA-3′ (SEQ ID NO:3); 5′-TGACTGTGAACGTTCCAGATGA-3′ (SEQ ID NO:4); 5′-TCCATAACGTTCGCCTAACGTTCGTC-3′ (SEQ ID NO:5); 5′-TGACTGTGAABGTTCCAGATGA-3′ (SEQ ID NO:6), where B is 5-bromocytosine; 5′-TGACTGTGAABGTTCGAGATGA-3′ (SEQ ID NO:7), where B is 5-bromocytosine and 5′-TGACTGTGAABGTTBGAGATGA-3′ (SEQ ID NO:8), where B is 5-bromocytosine.
  • An ISS and/or ISS-containing polynucleotide may contain modifications.
  • Modifications of ISS include any known in the art, but are not limited to, modifications of the 3′-OH or 5′-OH group, modifications of the nucleotide base, modifications of the sugar component, and modifications of the phosphate group. Various such modifications are described below.
  • An ISS may be single stranded or double stranded DNA, as well as single or double-stranded RNA or other modified polynucleotides.
  • An ISS may or may not include one or more palindromic regions, which may be present in the motifs described above or may extend beyond the motif.
  • An ISS may comprise additional flanking sequences, some of which are described herein.
  • An ISS may contain naturally-occurring or modified, non-naturally occurring bases, and may contain modified sugar, phosphate, and/or termini.
  • phosphate modifications include, but are not limited to, methyl phosphonate, phosphorothioate, phosphoramidate (bridging or non-bridging), phosphotriester and phosphorodithioate and may be used in any combination. Other non-phosphate linkages may also be used.
  • oligonucleotides of the present invention comprise phosphorothioate backbones.
  • Sugar modifications known in the field, such as 2′-alkoxy-RNA analogs, 2′-amino-RNA analogs and 2′-alkoxy- or amino-RNA/DNA chimeras and others described herein, may also be made and combined with any phosphate modification.
  • base modifications include, but are not limited to, addition of an electron-withdrawing moiety to C-5 and/or C-6 of a cytosine of the ISS (e.g., 5-bromocytosine, 5-chlorocytosine, 5-fluorocytosine, 5-iodocytosine).
  • an electron-withdrawing moiety e.g., 5-bromocytosine, 5-chlorocytosine, 5-fluorocytosine, 5-iodocytosine.
  • the ISS can be synthesized using techniques and nucleic acid synthesis equipment which are well known in the art including, but not limited to, enzymatic methods, chemical methods, and the degradation of larger oligonucleotide sequences. See, for example, Ausubel et al. (1987); and Sambrook et al. (1989). When assembled enzymatically, the individual units can be ligated, for example, with a ligase such as T4 DNA or RNA ligase. U.S. Pat. No. 5,124,246. Oligonucleotide degradation can be accomplished through the exposure of an oligonucleotide to a nuclease, as exemplified in U.S. Pat. No. 4,650,675.
  • the ISS can also be isolated using conventional polynucleotide isolation procedures. Such procedures include, but are not limited to, hybridization of probes to genomic or cDNA libraries and synthesis of particular native sequences by the polymerase chain reaction.
  • Circular ISS can be isolated, synthesized through recombinant methods, or chemically synthesized. Where the circular ISS is obtained through isolation or through recombinant methods, the ISS will preferably be a plasmid.
  • the chemical synthesis of smaller circular oligonucleotides can be performed using any method described in the literature. See, for instance, Gao et al. (1995) Nucleic Acids Res. 23:2025-2029; and Wang et al. (1994) Nucleic Acids Res. 22:2326-2333.
  • oligonucleotides and modified oligonucleotides are known in the art.
  • Naturally occurring DNA or RNA, containing phosphodiester linkages is generally synthesized by sequentially coupling the appropriate nucleoside phosphoramidite to the 5′-hydroxy group of the growing oligonucleotide attached to a solid support at the 3′-end, followed by oxidation of the intermediate phosphite triester to a phosphate triester.
  • the oligonucleotide is removed from the support, the phosphate triester groups are deprotected to phosphate diesters and the nucleoside bases are deprotected using aqueous ammonia or other bases.
  • the ISS can also contain phosphate-modified oligonucleotides. Synthesis of polynucleotides containing modified phosphate linkages or non-phosphate linkages is also know in the art. For a review, see Matteucci (1997) “Oligonucleotide Analogs: an Overview” in Oligonucleotides as Therapeutic Agents, (D. J. Chadwick and G. Cardew, ed.) John Wiley and Sons, New York, N.Y.
  • the phosphorous derivative (or modified phosphate group) which can be attached to the sugar or sugar analog moiety in the oligonucleotides of the present invention can be a monophosphate, diphosphate, triphosphate, alkylphosphonate, phosphorothioate, phosphorodithioate or the like.
  • the preparation of the above-noted phosphate analogs, and their incorporation into nucleotides, modified nucleotides and oligonucleotides, per se, is also known and need not be described here in detail Peyrottes et al. (1996) Nucleic Acids Res. 24:1841-1848; Chaturvedi et al. (1996) Nucleic Acids Res.
  • Oligonucleotides with phosphorothioate backbones can be more immunogenic than those with phosphodiester backbones and appear to be more resistant to degradation after injection into the host.
  • ISS-containing polynucleotides used in the invention can comprise ribonucleotides (containing ribose as the only or principal sugar component), deoxyribonucleotides (containing deoxyribose as the principal sugar component), or, as is known in the art, modified sugars or sugar analogs can be incorporated in the ISS.
  • the sugar moiety can be pentose, deoxypentose, hexose, deoxyhexose, glucose, arabinose, xylose, lyxose, and a sugar “analog” cyclopentyl group.
  • the sugar can be in pyranosyl or in a furanosyl form.
  • the sugar moiety is preferably the furanoside of ribose, deoxyribose, arabinose or 2′-0-alkylribose, and the sugar can be attached to the respective heterocyclic bases either in ⁇ or ⁇ anomeric configuration.
  • Sugar modifications include, but are not limited to, 2′-alkoxy-RNA analogs, 2′-amino-RNA analogs and 2′-alkoxy- or amino-RNA/DNA chimeras.
  • the heterocyclic bases, or nucleic acid bases, which are incorporated in the ISS can be the naturally-occurring principal purine and pyrimidine bases, (namely uracil or thymine, cytosine, adenine and guanine, as mentioned above), as well as naturally-occurring and synthetic modifications of said principal bases.
  • the ISS can include one or several heterocyclic bases other than the principal five base components of naturally-occurring nucleic acids.
  • the heterocyclic base in the ISS includes, but is not limited to, uracil-5-yl, cytosin-5-yl, adenin-7-yl, adenin-8-yl, guanin-7-yl, guanin-8-yl, 4-aminopyrrolo [2.3-d] pyrimidin-5-yl, 2-amino-4-oxopyrolo [2,3-d] pyrimidin-5-yl, 2-amino-4-oxopyrrolo [2.3-d] pyrimidin-3-yl groups, where the purines are attached to the sugar moiety of the ISS via the 9-position, the pyrimidines via the 1-position, the pyrrolopyrimidines via the 7-position and the pyrazolopyrimidines via the 1-position.
  • the ISS may comprise at least one modified base as described, for example, in the commonly owned international application WO 99/62923.
  • modified base is synonymous with “base analog”, for example, “modified cytosine” is synonymous with “cytosine analog.”
  • modified nucleosides or nucleotides are herein defined as being synonymous with nucleoside or nucleotide “analogs.”
  • base modifications include, but are not limited to, addition of an electron-withdrawing moiety to C-5 and/or C-6 of a cytosine of the ISS.
  • the electron-withdrawing moiety is a halogen.
  • modified cytosines can include, but are not limited to, azacytosine, 5-bromocytosine, bromouracil, 5-chlorocytosine, chlorinated cytosine, cyclocytosine, cytosine arabinoside, 5-fluorocytosine, fluoropyrimidine, fluorouracil, 5,6-dihydrocytosine, 5-iodocytosine, hydroxyurea, iodouracil, 5-nitrocytosine, uracil, and any other pyrimidine analog or modified pyrimidine.
  • base-modified nucleosides and the synthesis of modified oligonucleotides using said base-modified nucleosides as precursors, has been described, for example, in U.S. Pat. Nos. 4,910,300, 4,948,882, and 5,093,232.
  • These base-modified nucleosides have been designed so that they can be incorporated by chemical synthesis into either terminal or internal positions of an oligonucleotide.
  • Such base-modified nucleosides present at either terminal or internal positions of an oligonucleotide, can serve as sites for attachment of a peptide or other antigen.
  • Nucleosides modified in their sugar moiety have also been described (including, but not limited to, e.g., U.S. Pat. Nos. 4,849,513, 5,015,733, 5,118,800, 5,118,802) and can be used similarly.
  • the ISS used in the methods of the invention may be produced as ISS microcarrier complexes.
  • ISS-microcarrier complexes comprise an ISS-containing polynucleotide bound to a microcarrier (MC).
  • ISS-MC complexes comprise an ISS bound to the surface of a microcarrier (i.e., the ISS is not encapsulated in the MC), adsorbed within a microcarrier (e.g., adsorbed to PLGA beads), or encapsulated within a MC (e.g., incorporated within liposomes).
  • ISS-containing oligonucleotides bound to microparticles have previously been shown to have immunostimulatory activity in vitro (Liang et al., (1996), J. Clin. Invest. 98:1119-1129).
  • ISS-containing oligonucleotides bound to gold, latex and magnetic particles are not active in stimulating proliferation of 7TD1 cells, which proliferate in response to ISS-containing oligonucleotides (Manzel et al., (1999), Antisense Nucl. Acid Drug Dev. 9:459-464).
  • Microcarriers are not soluble in pure water, and are less than about 50-60 ⁇ m in size, preferably less than about 10 ⁇ m in size, more preferably from about 10 nm to about 10 ⁇ m, 25 nm to about 5 ⁇ m, 50 nm to about 4.5 ⁇ m or 1.0 ⁇ m to about 2.0 ⁇ m in size.
  • Microcarrers may be any shape, such as spherical, ellipsoidal, rod-shaped, and the like, although spherical microcarriers are normally preferred.
  • Preferred microcarriers have sizes of or about 50 nm, 200 nm, 1 ⁇ m, 1.2 ⁇ m, 1.4 ⁇ m, 1.5 ⁇ m, 1.6 ⁇ m, 1.8 ⁇ m, 2.0 ⁇ m, 2.5 ⁇ m or 4.5 ⁇ m.
  • the “size” of a microcarier is generally the “design size” or intended size of the particles stated by the manufacturer. Size may be a directly measured dimension, such as average or maximum diameter, or may be determined by an indirect assay such as a filtration screening assay. Direct measurement of microcarrier size is typically carried out by microscopy, generally light microscopy or scanning electron microscopy (SEM), in comparison with particles of known size or by reference to a micrometer.
  • SEM scanning electron microscopy
  • microcarriers are considered to be of a stated size if measurements show the microcarriers are ⁇ about 5-10% of the stated measurement. Size characteristics may also be determined by dynamic light scattering. Alternately, microcarrier size may be determined by filtration screening assays. A microcarrier is less than a stated size if at least 97% of the particles pass through a “screen-type” filter (i.e., a filter in which retained particles are on the surface of the filter, such as polycarbonate or polyethersulfone filters, as opposed to a “depth filter” in which retained particles lodge within the filter) of the stated size.
  • a “screen-type” filter i.e., a filter in which retained particles are on the surface of the filter, such as polycarbonate or polyethersulfone filters, as opposed to a “depth filter” in which retained particles lodge within the filter
  • a microcarrier is larger than a stated size if at least about 97% of the microcarrier particles are retained by a screen-type filter of the stated size.
  • at least about 97% microcarriers of about 10 ⁇ m to about 10 nm in size pass through a 10 ⁇ m pore screen filter and are retained by a 10 nm screen filter.
  • Microcarriers may be solid phase (e.g., polystyrene beads) or liquid phase (e.g., liposomes, micelles, or oil droplets in an oil and water emulsion).
  • Liquid phase microcarriers include liposomes, micelles, oil droplets and other lipid or oil-based particles.
  • One preferred liquid phase microcarrier is oil droplets within an oil-in-water emulsion.
  • oil-in-water emulsions used as microcarriers comprise biocompatible substituents such as squalene.
  • Liquid phase microcarriers are normally considered nonbiodegradable, but may be biodegradable liquid phase microcarriers may be produced by incorporation of one or more biodegradable polymers in the liquid microcarrier formulation.
  • the microcarrier is oil droplets in an oil-in-water emulsion prepared by emulsification of squalene, sorbitan trioleate, TWEEN 80® in an aqueous pH buffer.
  • Solid phase microcarriers for use in ISS-microcarrier complexes may be made from biodegradable materials or nonbiodegradable materials, and may include or exclude agarose or modified agarose microcarriers.
  • Useful solid phase biodegradable microcarriers include, but are not limited to: biodegradable polyesters, such as poly(lactic acid), poly(glycolic acid), and copolymers (including block copolymers) thereof, as well as block copolymers of poly(lactic acid) and poly(ethylene glycol); polyorthoesters such as polymers based on3,9-diethylidene-2,4,8,10-tetraoxaspiro[5.5]undecane (DETOSU); polyanhydrides such as poly(anhydride) polymers based on sebacic acid, p-(carboxyphenoxy)propane, or p-(carboxyphenoxy)hexane; polyanhydride imides, such as polyanhydride polymers based on se
  • microcarriers may be covalently modified to incorporate one or more moieties for use in linking the ISS, for example by addition of amine groups for covalent linking using amine-reactive crosslinkers.
  • the ISS-microcarrier complexes may be covalently or non-covalently linked.
  • Covalently linked ISS-MC complexes may be directly linked or be linked by a crosslinking moiety of one or more atoms (typically the residue of a crosslinking agent).
  • the ISS may be modified to allow or augment binding to the MC (e.g., by incorporation of a free sulfhydryl for covalent crosslinking or addition of a hydrophobic moieties such as lipids, steroids, sterols such as cholesterol, and terpenes, for hydrophobic bonding), although unmodified ISS may be used for formation of non-covalent ISS-MC complex formation by electrostatic interaction or by base pairing (e.g., by base pairing at least one portion of the ISS with a complementary oligonucleotide bound to the microcarrier).
  • a free sulfhydryl for covalent crosslinking
  • a hydrophobic moieties such as lipids, steroids, sterols such as cholesterol, and terpenes, for hydrophobic bonding
  • unmodified ISS may be used for formation of non-covalent ISS-MC complex formation by electrostatic interaction or by base pairing (e.g., by base pairing at least one portion of the ISS with
  • ISS-containing polynucleotides may be linked to solid phase microcarriers or other chemical moieties to facilitate ISS-MC complex formation using conventional technology known in the art, such as use of available heterobifunctional crosslinkers (e.g., succinimidyl 4-(N-maleimidomethyl)cyclohexane-1-carboxylate or its sulfo-derivatives for covalently linking an amine-derivatized microcarrier and an ISS modified to contain a free sulfhydryl) or by addition of compounds such as cholesterol (e.g., by the method of Godard et al. (1995) Eur. J. Biochem.
  • heterobifunctional crosslinkers e.g., succinimidyl 4-(N-maleimidomethyl)cyclohexane-1-carboxylate or its sulfo-derivatives for covalently linking an amine-derivatized microcarrier and an ISS modified to contain a free sulf
  • modified nucleosides or nucleotides such as are known in the art, can be incorporated at either terminus, or at internal positions in the ISS. These can contain blocked functional groups which, when deblocked, are reactive with a variety of functional groups which can be present on, or attached to, the microcarrier or a moiety which would facilitate binding to a microcarrier.
  • noncovalently linked ISS-MC complexes utilize a binding pair (e.g., an antibody and its cognate antigen or biotin and streptavidin or avidin), where one member of the binding pair is bound to the ISS and the microcarrier is derivatized with the other member of the binding pair (e.g., a biotinylated ISS and a streptavidin-derivatized microcarrier may be combined to form a noncovalently linked ISS-MC complex).
  • a binding pair e.g., an antibody and its cognate antigen or biotin and streptavidin or avidin
  • Non-covalent ISS-MC complexes bound by electrostatic binding typically exploit the highly negative charge of the polynucleotide backbone.
  • microcarriers for use in non-covalently bound ISS-MC complexes are generally positively charged at physiological pH (e.g., about pH 6.8-7.4).
  • the microcarrier may intrinsically possess a positive charge, but microcarriers made from compounds not normally possessing a positive charge may be derivatized or otherwise modified to become positively charged.
  • the polymer used to make the microcarrier may be derivatized to add positively charged groups, such as primary amines.
  • positively charged compounds may be incorporated in the formulation of the microcarrier during manufacture (e.g., positively charged surfactants may be used during the manufacture of poly(lactic acid)/poly(glycolic acid) copolymers to confer a positive charge on the resulting microcarrier particles.
  • positively charged surfactants may be used during the manufacture of poly(lactic acid)/poly(glycolic acid) copolymers to confer a positive charge on the resulting microcarrier particles.
  • Solid phase microspheres are prepared using techniques known in the art. For example, they can be prepared by emulsion-solvent extraction/evaporation technique. Generally, in this technique, biodegradable polymers such as polyanhydrates, poly(alkyl- ⁇ -cyanoacrylates) and poly( ⁇ -hydroxy esters), for example, poly(lactic acid), poly(glycolic acid), poly(D,L-lactic-co-glycolic acid) and poly(caprolactone), are dissolved in a suitable organic solvent, such as methylene chloride, to constitute the dispersed phase (DP) of emulsion.
  • biodegradable polymers such as polyanhydrates, poly(alkyl- ⁇ -cyanoacrylates) and poly( ⁇ -hydroxy esters), for example, poly(lactic acid), poly(glycolic acid), poly(D,L-lactic-co-glycolic acid) and poly(caprolactone)
  • a suitable organic solvent such as methylene chloride
  • DP is emulsified by high-speed homogenization into excess volume of aqueous continuous phase (CP) that contains a dissolved surfactant, for example, polyvinylalcohol (PVA) or polyvinylpirrolidone (PVP).
  • CP aqueous continuous phase
  • surfactant in CP is to ensure the formation of discrete and suitably-sized emulsion droplet.
  • the organic solvent is then extracted into the CP and subsequently evaporated by raising the system temperature.
  • the solid microparticles are then separated by centrifugation or filtration, and dried, for example, by lyophilization or application of vaccum, before storing at 4° C.
  • cationic lipids or polymers for example, 1,2-dioleoyl- 1,2,3-trimethylammoniopropane (DOTAP), cetyltrimethylammonium bromide (CTAB) or polylysine, are added either to DP or CP, as per their solubility in these phases.
  • DOTAP 1,2-dioleoyl- 1,2,3-trimethylammoniopropane
  • CTAB cetyltrimethylammonium bromide
  • polylysine are added either to DP or CP, as per their solubility in these phases.
  • Physico-chemical characteristics such as mean size, size distribution and surface charge of dried microspheres may be determined. Size characteristics are determined, for example, by dynamic light scattering technique and the surface charge was determined by measuring the zeta potential.
  • ISS-containing polynucleotides can be adsorbed onto the cationic microspheres by overnight aqueous incubation of ISS and the particles at 4° C. Microspheres are characterized for size and surface charge before and after ISS association. Selected batches may then evaluated for activity as described herein.
  • An ISS-containing polynucleotide may be administered after exposure to HBV and/or HCV and/or after infection by HBV and/or HCV.
  • the ISS-containing polynucleotide may be administered to an infected individual in the absence of physical symptoms of viral infection (e.g., jaundice, fatigue, etc.). Accordingly, administration of ISS-containing polynucleotide may be at various times with respect to exposure to, infection by and/or onset of symptoms of infection by HBV and/or HCV.
  • treatments employing an ISS-containing polynucleotide may also be employed in conjunction with other treatments or as ‘second line’ treatments employed after failure of a ‘first line’ treatment (e.g., ISS-containing polynucleotide therapy may be employed after failure of interferon therapy). Further, an ISS-containing polynucleotide may be administered in a single dose or in multiple doses.
  • the ISS-containing polynucleotide may be administered on any schedule selected by the clinician, such as daily, every other day, every three days, every four days, every five days, every six days, weekly, biweekly, monthly or at ever longer intervals (which may or may not remain the same during the course of treatment) Where multiple administrations are given, the ISS-containing polynucleotide may be given in 2, 3, 4, 5, 6, 7, 8, 9, 10 or more separate administrations.
  • ISS-containing polynucleotide when IS S-containing polynucleotide is administered to an individual who has been exposed to HBV and/or HCV, ISS-containing polynucleotide may be administered prior to the appearance of physical symptom(s) of HBV and/or HCV.
  • ISS-containing polynucleotide is preferably administered to an individual exposed to HBV and/or HCV less than about 28, 21, or 14 days after exposure to HBV and/or HCV, preferably less than about 10 days after exposure to HBV and/ or HCV, more preferably less than about 7 days after exposure to HBV and/or HCV, even more preferably less than about 5 days after exposure to HBV and/or HCV.
  • ISS-containing polynucleotide is administered about 3 days after exposure to HBV and/or HCV. In other embodiments, the ISS-containing polynucleotide is administered as soon as possible following a known exposure (e.g., after a needle stick or other percutaneous exposure to a bodily fluid or other material known or thought to be contaminated with HBV and/or HCV). In such embodiments, the ISS-containing polynucleotide is preferably administered within 48, 36, 24, or 12 hours after exposure.
  • the ISS-containing polynucleotide is administered upon or after appearance of at least one symptom of HBV or HCV infection.
  • ISS-containing polynucleotide is administered within about 28, 21, 14, 7, 5 or 3 days following appearance of a symptom of HBV and/or HCV infection.
  • another therapy e.g., interferon-based therapy.
  • the ISS-containing polynucleotide may be administered at any point following infection.
  • the ISS-containing polynucleotide may be administered at any point following infection.
  • ISS polynucleotides may be formulated in any form known in the art, such as dry powder, semi-solid or liquid formulations.
  • ISS polynucleotides preferably administered in a liquid formulation, although solid or semi-solid formulations may also be acceptable, particularly where the ISS polynucleotide is formulated in a slow release depot form.
  • ISS polynucleotide formulations may contain additional components such as salts, buffers, bulking agents, osmolytes, antioxidants, detergents, surfactants and other pharmaceutically-acceptable excipients as are known in the art.
  • additional components such as salts, buffers, bulking agents, osmolytes, antioxidants, detergents, surfactants and other pharmaceutically-acceptable excipients as are known in the art.
  • liquid ISS polynucleotide formulations made in USP water for injection and are sterile, isotonic and pH buffered to a physiologically-acceptable pH, such as about pH 6.8 to 7.5.
  • ISS-containing polynucleotides may be formulated in delivery vehicles such as liposomes, oil/water emulsion or slow release depot formulations. Methods of formulating polynucleotides in such forms are well known in the art.
  • ISS-containing polynucleotide formulations may also include or exclude immunomodulatory agents such as adjuvants and immunostimulatory cytokines, which are well known in the art.
  • a suitable dosage range or effective amount is one that provides the desired reduction of symptom(s) and/or suppression of viral infection and depends on a number of factors, including the particular hepatitis virus, ISS sequence of the polynucleotide, molecular weight of the polynucleotide and route of administration. Dosages are generally selected by the physician or other health care professional in accordance with a variety of parameters known in the art, such as severity of symptoms, history of the patient and the like.
  • a dosage range may be selected from, for example, an independently selected lower limit such as about 0.1, 0.25, 0.5, 1, 2, 5, 10, 20, 30 40, 50 60, 80, 100, 200, 300, 400 or 500 ⁇ g/kg up to an independently selected upper limit, greater than the lower limit, of about 60, 80, 100, 200, 300, 400, 500, 750, 1000, 1500, 2000, 3000, 4000, 5000, 6000, 7000, 8000, 9000 or 10,000 ⁇ g/kg.
  • an independently selected lower limit such as about 0.1, 0.25, 0.5, 1, 2, 5, 10, 20, 30 40, 50 60, 80, 100, 200, 300, 400 or 500 ⁇ g/kg up to an independently selected upper limit, greater than the lower limit, of about 60, 80, 100, 200, 300, 400, 500, 750, 1000, 1500, 2000, 3000, 4000, 5000, 6000, 7000, 8000, 9000 or 10,000 ⁇ g/kg.
  • a dose may be about any of the following: 0.1 to 100 ⁇ g/kg, 0.1 to 50 ⁇ g/kg, 0.1 to 25 ⁇ g/kg, 0.1 to 10 ⁇ g/kg, 1 to 500 ⁇ g/kg, 100 to 400 ⁇ g/kg, 200 to 300 ⁇ g/kg, 1 to 100 ⁇ g/kg, 100 to 200 ⁇ g/kg, 300 to 400 ⁇ g/kg, 400 to 500 ⁇ g/kg, 500 to 1000 ⁇ g/kg, 500 to 5000 ⁇ g/kg, or 500 to 10,000 ⁇ g/kg.
  • parenteral routes of administration require higher doses of ISS compared to more direct application to infected tissue, as do ISS-containing polynucleotides of increasing length.
  • Polynucleotides comprising an ISS may be administered by systemic (e.g., parenteral) or local/regional administration, although systemic administration is preferred, due to the relative inaccessability of the site of infection.
  • systemic e.g., parenteral
  • local/regional administration polynucleotides comprising an ISS may be administered into the portal vein, but this route of administration is not preferred because of the invasiveness of the procedure.
  • the ISS-containing polynucleotide is administered parenterally.
  • Parenteral routes of administration include, but are not limited to, transdermal, transmucosal, nasopharyngeal, pulmonary and direct injection.
  • Parenteral administration by injection may be by any parenteral injection route, including, but not limited to, intravenous (IV), intraperitoneal (IP), intramuscular (IM), subcutaneous (SC) and intradermal (ID) routes.
  • Transdemnal and transmucosal administration may be accomplished by, for example, inclusion of a carrier (e.g., dimethylsulfoxide, DMSO), by application of electrical impulses (e.g., iontophoresis) or a combination thereof.
  • a carrier e.g., dimethylsulfoxide, DMSO
  • electrical impulses e.g., iontophoresis
  • a variety of devices are available for transdermal administration which may be used in accordance with the invention.
  • Nasopharyngeal and pulmonary routes of administration include, but are not limited to, intranasal, inhalation, transbronchial and transalveolar routes.
  • the ISS-containing polynucleotide may thus be administered by inhalation of aerosols, atomized liquids or powders.
  • Devices suitable for administration by inhalation of ISS-containing compositions include, but are not limited to, nebulizers, atomizers, vaporizers, and metered-dose inhalers.
  • Nebulizers, atomizers, vaporizers and metered-dose inhalers filled with or employing reservoirs containing formulations comprising the ISS-containing polynucleotide(s) are among a variety of devices suitable for use in inhalation delivery of the ISS-containing polynucleotide(s).
  • Other methods of delivering to respiratory mucosa include delivery of liquid formulations, such as by nose drops.
  • IV, IP, IM and ID administration may be by bolus or infusion administration.
  • administration may be by bolus, infusion or by implantable device, such as an implantable minipump (e.g., osmotic or mechanical minipump) or slow release implant.
  • implantable minipump e.g., osmotic or mechanical minipump
  • the ISS polynucleotide(s) may also be delivered in a slow release formulation adapted for IV, IP, IM, ID or SC administration.
  • Administration by inhalation is preferably accomplished in discrete doses (e.g., via a metered dose inhaler), although delivery similar to an infusion may be accomplished through use of a nebulizer.
  • Administration via the transdermal and transmucosal routes may be continuous or pulsatile.
  • administering results in prevention, palliation, and/or improvement in one or more symptoms of HBV or HCV.
  • the exact form of prevention, palliation or improvement will depend on the particular hepatitis virus, the symptoms experienced by the patient, and the stage of the hepatitis, but includes reduction or improvement in one or more physical symptoms such as jaundice, fatigue, abdominal pain and the like and/or clinical/laboratory findings associated with hepatitis such as viremia, blood levels of liver enzymes, portal hypertension, cirrhosis, and the like.
  • Symptoms of infection may be assessed before and/or after administration of ISS-containing polynucleotide.
  • the symptoms measured and the method of their measurement will vary depending on the particular hepatitis virus and the stage of infection.
  • Physical symptoms of acute HBV and/or HCV infection include jaundice, fatigue, abdominal pain, dark urine, and other symptoms known in the art.
  • Subjective physical symptoms such as abdominal pain and fatigue may be measured on a qualitative (e.g., presence/absence) basis or may be quantitated using a visual scale system. Jaundice may also be measured on a qualitative basis or may be quantitated by measurement of blood or serum levels of bilirubin.
  • Clinical/laboratory findings associated with hepatitis are normally measured through clinical assessment, diagnostic assays, and histologic testing.
  • blood/serum levels of liver enzymes may be quantitated by running a standard clinical laboratory liver function panel of tests which include quantitation of AST and ALT levels in the individual's blood or serum.
  • Viremia i.e., viral titer in a blood or serum sample
  • Viremia may be measured by any method known in the art, such as quantitation of viral particles (for example, by isolation and visualization or by assay of DNase resistant particles), detection of viral antigens in blood or serum samples, detection of antivirus antibodies in blood or serum samples and/or detection of viral nucleic acid (e.g., by PCR amplification using HBV or HCV specific primers or by in situ hybridization with virus-specific probes).
  • Viral titer may also be measured in liver tissue biopsies, generally by quantitation of viral nucleic acid, although viral antigens may also be used for calculation of viral titer. Viral titer from tissue samples is calculated in virus particles per unit weight of tissue.
  • kits for carrying out the methods of the invention i.e., treatment and/or prevention of HBV and/or HCV infection. Accordingly, a variety of kits are provided.
  • the kits may be used for any one or more of the following (and, accordingly, may contain instructions for any one or more of the following uses): reducing levels of a hepatitis B and/or hepatitis C antigen in blood in an individual who has been infected with hepatitis B and/or hepatitis C; reducing viremia in an individual infected with or exposed to hepatitis B and/or hepatitis C; preventing one or more symptoms of hepatitis B and/or hepatitis C infection in an individual exposed to hepatitis B, hepatitis C, or both hepatitis B and C; reducing severity of one or more symptoms of hepatitis B and/or hepatitis C infection in an individual who has been infected with hepatitis
  • kits of the invention comprise one or more containers comprising an ISS-containing polynucleotide and a set of instructions, generally written instructions although electronic storage media (e.g., magnetic diskette or optical disk) containing instructions are also acceptable, relating to the use and dosage of the ISS-containing polynucleotide for the intended treatment (e.g., reducing levels of a hepatitis B and/or hepatitis C antigen in blood in an individual who has been infected with hepatitis B and/or hepatitis C; reducing viremia in an individual infected with or exposed to hepatitis B and/or hepatitis C; preventing one or more symptoms of hepatitis B and/or hepatitis C infection in an individual exposed to hepatitis B, hepatitis C, or both hepatitis B and C; reducing severity of one or more symptoms of hepatitis B and/or hepatitis C infection in an individual
  • kits of the invention do not include any packages or containers which contain viral antigens from the hepatitis virus(es) the kit is intended to be used to treat. Accordingly, neither the container comprising the ISS-containing polynucleotide nor any other containers in the kit contain hepatitis B viral antigens in kits intended for use on individuals exposed to or infected with hepatitis B, neither the container comprising the ISS-containing polynucleotide nor any other containers in the kit contain hepatitis C viral antigens in kits intended for use on individuals exposed to or infected with hepatitis C, and neither the container comprising the ISS-containing polynucleotide nor any other containers in the kit contain hepatitis B or C viral antigens in kits intended for use on individuals infected with both hepatitis B and hepatitis C.
  • the ISS component of the kit may be packaged in any convenient, appropriate packaging.
  • the ISS is a freeze-dried formulation
  • an ampoule with a resilient stopper is normally used, so that the drug may be easily reconstituted by injecting fluid through the resilient stopper.
  • Ampoules with non-resilient, removable closures (e.g., sealed glass) or resilient stoppers are most conveniently used for injectable forms of ISS.
  • prefilled syringes may be used when the kit is supplied with a liquid formulation of the ISS-containing polynucleotide.
  • packages for use in combination with a specific device such as an inhaler, nasal administration device (e.g., an atomizer) or an infusion device such as a minipump.
  • any ISS-containing polynucleotide described herein may be used, such as, for example, any polynucleotide comprising any of the following ISS: the sequence 5′-cytosine, guanine-3′, the sequence 5′-T, C, G-3′, the sequence 5′-C, G, pyrimidine, pyrimidine, C, G-3′, the sequence 5′-purine, purine, C, G, pyrimidine, pyrimidine, C, G-3′, the sequence 5′-purine, purine, C, G, pyrimidine, pyrimidine, C, C-3′; the sequence SEQ ID NO: 1018; the sequence 5′-purine, purine, B, G, pyrimidine, pyrimidine-3′ wherein B is 5-bromocytosine or the sequence 5′-purine, purine, B, G, pyrimidine, pyrimidine, C, G-3′ wherein B is 5-bromocytosine
  • ISS activity was tested in an animal model of chronic hepatitis.
  • An ISS-containing phosphorothioate oligonucleotide (5′-TGACTGTGAACGTTCGAGATGA-3′) (SEQ ID NO:1), was delivered to STC strain transgenic mice, followed by measurement of HBV DNA and HBsAg production.
  • STC line mice were developed at Stanford University by Patricia Marion. The majority of these mice secrete HBV of the Ayw genotype (Galibert et al. (1979) Nature 281:646) to titers of 10 6-8 viral genome equivalents per ml of serum STC mice were derived from the FVB strain, and were constructed by microinjection of HBV genomic DNA. STC mice have been shown to be responsive to drugs which inhibit HBV replication, and so are considered a good model of chronic HBV.
  • mice Approximately one month old mice were bled and tested for serum levels of HBsAg, which is predictive of viral DNA titer. A pool of 40 STC mice with approximately equal levels of HBsAg were selected and randomly assigned to four treatment groups of 10 animals each. The groups were treated as follows:
  • FIG. 1 The results of the quantitative PCR assays for serum HBV DNA levels in HBV-producing mice treated with ISS, murine IL-12 or PBS, are summarized in FIG. 1. The results are plotted as means of the HBV DNA levels of each of the 4 groups in each of the serial samples. Samples were blinded to the person conducting the assays. Both ISS and murine IL-12 were effective in reducing viral titer in STC mice. The most dramatic titer drop was seen in Group 2 (single subcutaneous injection of ISS at day 14), where the mean viral DNA titer was reduced by 90 fold three days after injection.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Immunology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Virology (AREA)
  • Biochemistry (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
US09/802,370 2000-03-10 2001-03-09 Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences Abandoned US20020098199A1 (en)

Priority Applications (11)

Application Number Priority Date Filing Date Title
US09/802,370 US20020098199A1 (en) 2000-03-10 2001-03-09 Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences
EP01913361A EP1282427B1 (fr) 2000-03-10 2001-03-12 Procedes de suppression de l'infection par un virus de l'hepatite mettant en jeu des sequences polynucleotidiques immunomodulatrices
AU4203201A AU4203201A (en) 2000-03-10 2001-03-12 Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences
ES01913361T ES2348877T3 (es) 2000-03-10 2001-03-12 Secuencias de polinucleotidos inmunoestimuladores para uso en la supresion de infeccion por el virus de la hepatitis.
AU2001242032A AU2001242032B2 (en) 2000-03-10 2001-03-12 Immunostimulatory polynucleotide sequences for use in suppressing hepatitis virus infection
PCT/US2001/007931 WO2001068078A2 (fr) 2000-03-10 2001-03-12 Procedes de suppression de l"infection par un virus de l"hepatite mettant en jeu des sequences polynucleotidiques immunomodulatrices
JP2001566642A JP5128745B2 (ja) 2000-03-10 2001-03-12 免疫調節性ポリヌクレオチド配列を用いた肝炎ウイルス感染症の抑制方法
AT01913361T ATE473750T1 (de) 2000-03-10 2001-03-12 Immunostimulierende polynukleotide sequenzen zur verwendung bei der unterdrückung von hepatitis virus infektion
CA002402250A CA2402250A1 (fr) 2000-03-10 2001-03-12 Procedes de suppression de l'infection par un virus de l'hepatite mettant en jeu des sequences polynucleotidiques immunomodulatrices
DE60142562T DE60142562D1 (de) 2000-03-10 2001-03-12 Immunostimulierende polynukleotide sequenzen zur verwendung bei der unterdrückung von hepatitis virus infektion
US10/357,760 US7727712B2 (en) 2000-03-10 2003-02-03 Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US18830100P 2000-03-10 2000-03-10
US09/802,370 US20020098199A1 (en) 2000-03-10 2001-03-09 Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US10/357,760 Continuation US7727712B2 (en) 2000-03-10 2003-02-03 Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences

Publications (1)

Publication Number Publication Date
US20020098199A1 true US20020098199A1 (en) 2002-07-25

Family

ID=26883932

Family Applications (2)

Application Number Title Priority Date Filing Date
US09/802,370 Abandoned US20020098199A1 (en) 2000-03-10 2001-03-09 Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences
US10/357,760 Expired - Fee Related US7727712B2 (en) 2000-03-10 2003-02-03 Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences

Family Applications After (1)

Application Number Title Priority Date Filing Date
US10/357,760 Expired - Fee Related US7727712B2 (en) 2000-03-10 2003-02-03 Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences

Country Status (9)

Country Link
US (2) US20020098199A1 (fr)
EP (1) EP1282427B1 (fr)
JP (1) JP5128745B2 (fr)
AT (1) ATE473750T1 (fr)
AU (2) AU2001242032B2 (fr)
CA (1) CA2402250A1 (fr)
DE (1) DE60142562D1 (fr)
ES (1) ES2348877T3 (fr)
WO (1) WO2001068078A2 (fr)

Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20010044416A1 (en) * 2000-01-20 2001-11-22 Mccluskie Michael J. Immunostimulatory nucleic acids for inducing a Th2 immune response
US20010046967A1 (en) * 2000-03-10 2001-11-29 Gary Van Nest Methods of preventing and treating respiratory viral infection using immunomodulatory polynucleotide
US20020107212A1 (en) * 2000-03-10 2002-08-08 Nest Gary Van Methods of reducing papillomavirus infection using immunomodulatory polynucleotide sequences
US20030133988A1 (en) * 2001-08-07 2003-07-17 Fearon Karen L. Immunomodulatory compositions, formulations, and methods for use thereof
US20030148316A1 (en) * 2001-08-01 2003-08-07 Lipford Grayson B. Methods and compositions relating to plasmacytoid dendritic cells
US20030191079A1 (en) * 1994-07-15 2003-10-09 University Of Iowa Research Foundation Methods for treating and preventing infectious disease
US20030216340A1 (en) * 2000-03-10 2003-11-20 Gary Van Nest Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences
US20040105872A1 (en) * 2002-09-18 2004-06-03 The Government Of The Usa As Represented By The Secretary Of The Dept. Of Health & Human Services Method of treating and preventing infections in immunocompromised subjects with immunostimulatory CpG oligonucleotides
US20040131628A1 (en) * 2000-03-08 2004-07-08 Bratzler Robert L. Nucleic acids for the treatment of disorders associated with microorganisms
US20040143112A1 (en) * 1994-07-15 2004-07-22 Krieg Arthur M. Immunomodulatory oligonucleotides
US20040241841A1 (en) * 2001-08-14 2004-12-02 Klinman Dennis M Method for rapid generation of mature dendritic cells
US20050026245A1 (en) * 2001-12-20 2005-02-03 Klinman Dennis M. Use of cpg oligodeoxynucleotides to induce angiogenesis
US20050059626A1 (en) * 2000-03-10 2005-03-17 Gary Van Nest Methods of preventing and treating viral infections using immunomodulatory polynucleotide sequences
US20050218499A1 (en) * 2004-03-31 2005-10-06 Advanced Semiconductor Engineering, Inc. Method for manufacturing leadless semiconductor packages
US20050277604A1 (en) * 1994-07-15 2005-12-15 University Of Iowa Research Foundation Immunostimulatory nucleic acid molecules
US6977245B2 (en) 1999-04-12 2005-12-20 The United States Of America As Represented By The Department Of Health And Human Services Oligodeoxynucleotide and its use to induce an immune response
US20060264391A1 (en) * 2000-03-10 2006-11-23 Gary Van Nest Methods of ameliorating symptoms of herpes infection using immunomodulatory polynucleotide sequences
US20070190073A1 (en) * 1999-11-15 2007-08-16 Stephen Tuck Immunomodulatory compositions containing an immunostimulatory sequence linked to antigen and methods of use thereof
US7488490B2 (en) 1997-03-10 2009-02-10 University Of Iowa Research Foundation Method of inducing an antigen-specific immune response by administering a synergistic combination of adjuvants comprising unmethylated CpG-containing nucleic acids and a non-nucleic acid adjuvant
US7521063B2 (en) 2000-01-14 2009-04-21 The United States Of America As Represented By The Department Of Health And Human Services Multiple CPG oligodeoxynucleotides and their use to induce an immune response
US20090263413A1 (en) * 2006-05-31 2009-10-22 Tomokatsu Iwamura Immunostimulatory oligonucleotides and use thereof in pharmaceuticals
US7666674B2 (en) 2001-07-27 2010-02-23 The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Use of sterically stabilized cationic liposomes to efficiently deliver CPG oligonucleotides in vivo
US7935675B1 (en) 1994-07-15 2011-05-03 University Of Iowa Research Foundation Immunostimulatory nucleic acid molecules
US7956043B2 (en) 2002-12-11 2011-06-07 Coley Pharmaceutical Group, Inc. 5′ CpG nucleic acids and methods of use
US7998492B2 (en) 2002-10-29 2011-08-16 Coley Pharmaceutical Group, Inc. Methods and products related to treatment and prevention of hepatitis C virus infection
US8466116B2 (en) 2001-12-20 2013-06-18 The Unites States Of America As Represented By The Secretary Of The Department Of Health And Human Services Use of CpG oligodeoxynucleotides to induce epithelial cell growth
US8574599B1 (en) 1998-05-22 2013-11-05 Ottawa Hospital Research Institute Methods and products for inducing mucosal immunity

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7129222B2 (en) 2000-03-10 2006-10-31 Dynavax Technologies Corporation Immunomodulatory formulations and methods for use thereof
US20030129251A1 (en) 2000-03-10 2003-07-10 Gary Van Nest Biodegradable immunomodulatory formulations and methods for use thereof
ES2487645T3 (es) 2001-06-21 2014-08-22 Dynavax Technologies Corporation Compuestos inmunomoduladores quiméricos y métodos de uso de los mismos
NZ538628A (en) * 2002-08-12 2008-06-30 Dynavax Tech Corp Immunomodulatory compositions, methods of making, and methods of use thereof
SI1575977T1 (sl) 2002-12-23 2010-01-29 Dynavax Tech Corp Imunostimulirni sekvenčni polinukleotidi in postopki za njihovo uporabo
US8158768B2 (en) 2002-12-23 2012-04-17 Dynavax Technologies Corporation Immunostimulatory sequence oligonucleotides and methods of using the same
CA2600036A1 (fr) * 2005-03-04 2006-09-14 Dynavax Technologies Corporation Compositions contenant des molecules conjuguees structurellement stables
US9452212B2 (en) 2011-04-14 2016-09-27 Dynavax Technologies Corporation Methods and compositions for eliciting an immune response against hepatitis B virus
KR101475630B1 (ko) * 2013-05-31 2014-12-22 동국대학교 산학협력단 포도근 추출물 또는 이의 분획물을 유효성분으로 포함하는 c형 간염의 예방 또는 치료용 조성물

Family Cites Families (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4458066A (en) 1980-02-29 1984-07-03 University Patents, Inc. Process for preparing polynucleotides
US4948882A (en) 1983-02-22 1990-08-14 Syngene, Inc. Single-stranded labelled oligonucleotides, reactive monomers and methods of synthesis
US4650675A (en) 1983-08-18 1987-03-17 The Children's Medical Center Corporation Oligonucleotide conjugates
US4849513A (en) 1983-12-20 1989-07-18 California Institute Of Technology Deoxyribonucleoside phosphoramidites in which an aliphatic amino group is attached to the sugar ring and their use for the preparation of oligonucleotides containing aliphatic amino groups
US5118802A (en) 1983-12-20 1992-06-02 California Institute Of Technology DNA-reporter conjugates linked via the 2' or 5'-primary amino group of the 5'-terminal nucleoside
US5015733A (en) 1983-12-20 1991-05-14 California Institute Of Technology Nucleosides possessing blocked aliphatic amino groups
US5118800A (en) 1983-12-20 1992-06-02 California Institute Of Technology Oligonucleotides possessing a primary amino group in the terminal nucleotide
US5093232A (en) 1985-12-11 1992-03-03 Chiron Corporation Nucleic acid probes
US4910300A (en) 1985-12-11 1990-03-20 Chiron Corporation Method for making nucleic acid probes
US5124246A (en) 1987-10-15 1992-06-23 Chiron Corporation Nucleic acid multimers and amplified nucleic acid hybridization assays using same
US5278302A (en) 1988-05-26 1994-01-11 University Patents, Inc. Polynucleotide phosphorodithioates
EP0468520A3 (en) 1990-07-27 1992-07-01 Mitsui Toatsu Chemicals, Inc. Immunostimulatory remedies containing palindromic dna sequences
US5616461A (en) 1992-05-14 1997-04-01 Dana-Farber Cancer Institute Assay for antiviral activity using complex of herpesvirus origin of replication and cellular protein
US5849719A (en) 1993-08-26 1998-12-15 The Regents Of The University Of California Method for treating allergic lung disease
WO1995026204A1 (fr) 1994-03-25 1995-10-05 Isis Pharmaceuticals, Inc. Stimulation immunitaire par des analogues d'oligonucleotides de phosphorothioate
US6239116B1 (en) 1994-07-15 2001-05-29 University Of Iowa Research Foundation Immunostimulatory nucleic acid molecules
US6207646B1 (en) 1994-07-15 2001-03-27 University Of Iowa Research Foundation Immunostimulatory nucleic acid molecules
US20030050263A1 (en) 1994-07-15 2003-03-13 The University Of Iowa Research Foundation Methods and products for treating HIV infection
WO1996002555A1 (fr) 1994-07-15 1996-02-01 The University Of Iowa Research Foundation Oligonucleotides immunomodulateurs
US5874089A (en) 1995-10-02 1999-02-23 Georgetown University School Of Medicine Protecting against canine oral papillomavirus (copy)
ATE437943T1 (de) 1996-01-30 2009-08-15 Univ California Expressionsvektoren, die eine antigen-spezifische immunantwort induzieren, und methoden für ihre verwendung.
ATE292980T1 (de) 1996-10-11 2005-04-15 Univ California Immunostimulierende oligonucleotidekonjugate
JP2001513776A (ja) 1997-02-28 2001-09-04 ユニバーシティ オブ アイオワ リサーチ ファウンデーション ＬＰＳ関連障害の処置における非メチル化ＣｐＧジヌクレオチドを含む核酸の使用
US6406705B1 (en) 1997-03-10 2002-06-18 University Of Iowa Research Foundation Use of nucleic acids containing unmethylated CpG dinucleotide as an adjuvant
DK1005368T3 (da) 1997-03-10 2010-01-04 Ottawa Hospital Res Inst Anvendelse af nukleinsyrer, der indeholder ikke-metyleret CpG dinukleotid i kombination med alun som hjælpestoffer
JP2001526688A (ja) 1997-05-19 2001-12-18 メルク エンド カンパニー インコーポレーテッド オリゴヌクレオチドアジュバント
ATE370740T1 (de) 1997-05-20 2007-09-15 Ottawa Health Research Inst Verfahren zur herstellung von nukleinsäurekonstrukten
CA2291483C (fr) * 1997-06-06 2012-09-18 Dynavax Technologies Corporation Oligonucleotides immunostimulateurs, compositions correspondantes et leurs procedes d'utilisation
DK1009413T3 (da) 1997-09-05 2007-06-11 Univ California Anvendelse af immunstimulerende oligonukleotider til forebyggelse eller behandling af astma
GB9727262D0 (en) 1997-12-24 1998-02-25 Smithkline Beecham Biolog Vaccine
ES2284247T3 (es) 1998-04-03 2007-11-01 University Of Iowa Research Foundation Metodos y productos para estimular el sistema inmunitario usando oligonucleotidos y citoquinas inmunoterapeuticos.
AU3884199A (en) 1998-05-06 1999-11-23 Ottawa Health Research Institute Methods for the prevention and treatment of parasitic infections and related diseases using cpg oligonucleotides
JP2002514397A (ja) 1998-05-14 2002-05-21 コーリー ファーマシューティカル ゲーエムベーハー ＣｐＧオリゴヌクレオチドを用いる造血調節の方法
US6562798B1 (en) 1998-06-05 2003-05-13 Dynavax Technologies Corp. Immunostimulatory oligonucleotides with modified bases and methods of use thereof
AU764532B2 (en) 1998-07-27 2003-08-21 University Of Iowa Research Foundation, The Stereoisomers of CpG oligonucleotides and related methods
EP1113818B1 (fr) 1998-09-18 2006-05-17 Dynavax Technologies Corporation PROCEDES DE TRAITEMENT DE TROUBLES ASSOCIES A IgE ET COMPOSITIONS POUVANT ETRE UTILISEES A CET EFFET
WO2000021556A1 (fr) 1998-10-09 2000-04-20 Dynavax Technologies Corporation Compositions anti-hiv comprenant des polynucleotides immunostimulants et des antigenes hiv
CA2370708A1 (fr) 1999-04-20 2000-10-26 Smithkline Beecham Biologicals S.A. Vaccin
WO2000067023A1 (fr) 1999-04-29 2000-11-09 Coley Pharmaceutical Gmbh Criblage de modificateurs fonctionnels de l'adn immunostimulant
US6514948B1 (en) 1999-07-02 2003-02-04 The Regents Of The University Of California Method for enhancing an immune response
US7479285B1 (en) 1999-08-19 2009-01-20 Dynavax Technologies Corporation Methods of modulating an immune response using immunostimulatory sequences and compositions for use therein
JP2003527352A (ja) * 2000-01-13 2003-09-16 アンティジェニクス インコーポレーテッド Ｃｐｇおよびサポニンの自然免疫刺激化合物、ならびにそれらの方法
EP1253947A4 (fr) 2000-01-31 2005-01-05 Univ California Polynucleotides immunomodulateurs dans le traitement d'une infection par un pathogene intracellulaire
IL151345A0 (en) 2000-02-23 2003-04-10 Univ California Method for treating inflammatory bowel disease and other forms of gastrointestinal inflammation
US20030129251A1 (en) 2000-03-10 2003-07-10 Gary Van Nest Biodegradable immunomodulatory formulations and methods for use thereof
US7129222B2 (en) 2000-03-10 2006-10-31 Dynavax Technologies Corporation Immunomodulatory formulations and methods for use thereof
US20020028784A1 (en) 2000-03-10 2002-03-07 Nest Gary Van Methods of preventing and treating viral infections using immunomodulatory polynucleotide sequences
US20020107212A1 (en) 2000-03-10 2002-08-08 Nest Gary Van Methods of reducing papillomavirus infection using immunomodulatory polynucleotide sequences
US7157437B2 (en) 2000-03-10 2007-01-02 Dynavax Technologies Corporation Methods of ameliorating symptoms of herpes infection using immunomodulatory polynucleotide sequences
US20020098199A1 (en) 2000-03-10 2002-07-25 Gary Van Nest Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences
US20010046967A1 (en) 2000-03-10 2001-11-29 Gary Van Nest Methods of preventing and treating respiratory viral infection using immunomodulatory polynucleotide
US6534062B2 (en) 2000-03-28 2003-03-18 The Regents Of The University Of California Methods for increasing a cytotoxic T lymphocyte response in vivo
CA2405424A1 (fr) 2000-04-07 2001-10-18 The Regents Of The University Of California Ameliorations synergiques apportees a des vaccins polynucleotidiques

Cited By (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8309527B2 (en) 1994-07-15 2012-11-13 University Of Iowa Research Foundation Immunomodulatory oligonucleotides
US7879810B2 (en) 1994-07-15 2011-02-01 University Of Iowa Research Foundation Immunostimulatory nucleic acid molecules
US7713529B2 (en) 1994-07-15 2010-05-11 University Of Iowa Research Foundation Methods for treating and preventing infectious disease
US8008266B2 (en) 1994-07-15 2011-08-30 University Of Iowa Foundation Methods of treating cancer using immunostimulatory oligonucleotides
US7935675B1 (en) 1994-07-15 2011-05-03 University Of Iowa Research Foundation Immunostimulatory nucleic acid molecules
US20030191079A1 (en) * 1994-07-15 2003-10-09 University Of Iowa Research Foundation Methods for treating and preventing infectious disease
US7402572B2 (en) 1994-07-15 2008-07-22 University Of Iowa Research Foundation Immunostimulatory nucleic acid molecules
US7223741B2 (en) 1994-07-15 2007-05-29 University Of Iowa Research Foundation Immunostimulatory nucleic acid molecules
US20060058251A1 (en) * 1994-07-15 2006-03-16 University Of Iowa Research Foundation Methods for treating and preventing infectious disease
US20040106568A1 (en) * 1994-07-15 2004-06-03 University Of Iowa Research Foundation Methods for treating and preventing infectious disease
US20050277604A1 (en) * 1994-07-15 2005-12-15 University Of Iowa Research Foundation Immunostimulatory nucleic acid molecules
US20040143112A1 (en) * 1994-07-15 2004-07-22 Krieg Arthur M. Immunomodulatory oligonucleotides
US20040152656A1 (en) * 1994-07-15 2004-08-05 University Of Iowa Research Foundation Immunomodulatory oligonucleotides
US20050101554A1 (en) * 1994-07-15 2005-05-12 University Of Iowa Research Foundation Methods for treating and preventing infectious disease
US7488490B2 (en) 1997-03-10 2009-02-10 University Of Iowa Research Foundation Method of inducing an antigen-specific immune response by administering a synergistic combination of adjuvants comprising unmethylated CpG-containing nucleic acids and a non-nucleic acid adjuvant
US8202688B2 (en) 1997-03-10 2012-06-19 University Of Iowa Research Foundation Use of nucleic acids containing unmethylated CpG dinucleotide as an adjuvant
US8574599B1 (en) 1998-05-22 2013-11-05 Ottawa Hospital Research Institute Methods and products for inducing mucosal immunity
US8227446B2 (en) 1999-04-12 2012-07-24 The United States Of America, As Represented By The Secretary Of The Department Of Health And Human Services Oligodeoxynucleotide and its use to induce an immune response
US6977245B2 (en) 1999-04-12 2005-12-20 The United States Of America As Represented By The Department Of Health And Human Services Oligodeoxynucleotide and its use to induce an immune response
US7960356B2 (en) 1999-04-12 2011-06-14 The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Oligodeoxynucleotide and its use to induce an immune response
US20070190073A1 (en) * 1999-11-15 2007-08-16 Stephen Tuck Immunomodulatory compositions containing an immunostimulatory sequence linked to antigen and methods of use thereof
US7628990B2 (en) 1999-11-15 2009-12-08 Dynavax Technologies Corporation Immunomodulatory compositions containing an immunostimulatory sequence linked to antigen and methods of use thereof
US7521063B2 (en) 2000-01-14 2009-04-21 The United States Of America As Represented By The Department Of Health And Human Services Multiple CPG oligodeoxynucleotides and their use to induce an immune response
US20010044416A1 (en) * 2000-01-20 2001-11-22 Mccluskie Michael J. Immunostimulatory nucleic acids for inducing a Th2 immune response
US20040131628A1 (en) * 2000-03-08 2004-07-08 Bratzler Robert L. Nucleic acids for the treatment of disorders associated with microorganisms
US20060264391A1 (en) * 2000-03-10 2006-11-23 Gary Van Nest Methods of ameliorating symptoms of herpes infection using immunomodulatory polynucleotide sequences
US7727712B2 (en) 2000-03-10 2010-06-01 Dynavax Technologies Corporation Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences
US20040009942A1 (en) * 2000-03-10 2004-01-15 Gary Van Nest Methods of preventing and treating respiratory viral infection using immunomodulatory polynucleotide sequences
US20030216340A1 (en) * 2000-03-10 2003-11-20 Gary Van Nest Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences
US8226957B2 (en) 2000-03-10 2012-07-24 Dynavax Technologies Corporation Methods of preventing and treating respiratory viral infection using immunomodulatory polynucleotide sequences
US20010046967A1 (en) * 2000-03-10 2001-11-29 Gary Van Nest Methods of preventing and treating respiratory viral infection using immunomodulatory polynucleotide
US20070060540A1 (en) * 2000-03-10 2007-03-15 Gary Van Nest Methods of ameliorating symptoms of herpes infection using immunomodulatory polynucleotide sequences
US7157437B2 (en) 2000-03-10 2007-01-02 Dynavax Technologies Corporation Methods of ameliorating symptoms of herpes infection using immunomodulatory polynucleotide sequences
US20080009459A1 (en) * 2000-03-10 2008-01-10 Gary Van Nest Methods of reducing papillomavirus infection using immunomodulatory polynucleotide sequences
US20050059626A1 (en) * 2000-03-10 2005-03-17 Gary Van Nest Methods of preventing and treating viral infections using immunomodulatory polynucleotide sequences
US20100035975A1 (en) * 2000-03-10 2010-02-11 Gary Van Nest Methods of preventing and treating respiratory viral infection using immunomodulatory polynucleotide sequences
US20020107212A1 (en) * 2000-03-10 2002-08-08 Nest Gary Van Methods of reducing papillomavirus infection using immunomodulatory polynucleotide sequences
US7666674B2 (en) 2001-07-27 2010-02-23 The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Use of sterically stabilized cationic liposomes to efficiently deliver CPG oligonucleotides in vivo
US20030148316A1 (en) * 2001-08-01 2003-08-07 Lipford Grayson B. Methods and compositions relating to plasmacytoid dendritic cells
US20030133988A1 (en) * 2001-08-07 2003-07-17 Fearon Karen L. Immunomodulatory compositions, formulations, and methods for use thereof
US20100291218A1 (en) * 2001-08-07 2010-11-18 Fearon Karen L Immunomodulatory compositions, formulations, and methods for use thereof
US8586555B2 (en) 2001-08-07 2013-11-19 Dynavax Technologies Corporation Immunomodulatory compositions, formulations, and methods for use thereof
US7354909B2 (en) 2001-08-14 2008-04-08 The United States Of America As Represented By Secretary Of The Department Of Health And Human Services Method for rapid generation of mature dendritic cells
US20080241176A1 (en) * 2001-08-14 2008-10-02 The Gov. Of The U.S.A As Represented By The Secretary Of The Dept. Of Health & Human Services Method for rapid generation of mature dendritic cells
US20040241841A1 (en) * 2001-08-14 2004-12-02 Klinman Dennis M Method for rapid generation of mature dendritic cells
US7959934B2 (en) 2001-08-14 2011-06-14 The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Method for rapid generation of mature dendritic cells
US20050026245A1 (en) * 2001-12-20 2005-02-03 Klinman Dennis M. Use of cpg oligodeoxynucleotides to induce angiogenesis
US7615227B2 (en) 2001-12-20 2009-11-10 The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Use of CpG oligodeoxynucleotides to induce angiogenesis
US8466116B2 (en) 2001-12-20 2013-06-18 The Unites States Of America As Represented By The Secretary Of The Department Of Health And Human Services Use of CpG oligodeoxynucleotides to induce epithelial cell growth
US7935351B2 (en) 2001-12-20 2011-05-03 The United States Of America As Represented By The Department Of Health And Human Services Use of CPG oligodeoxynucleotides to induce angiogenesis
US8263091B2 (en) 2002-09-18 2012-09-11 The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Method of treating and preventing infections in immunocompromised subjects with immunostimulatory CpG oligonucleotides
US20040105872A1 (en) * 2002-09-18 2004-06-03 The Government Of The Usa As Represented By The Secretary Of The Dept. Of Health & Human Services Method of treating and preventing infections in immunocompromised subjects with immunostimulatory CpG oligonucleotides
US7998492B2 (en) 2002-10-29 2011-08-16 Coley Pharmaceutical Group, Inc. Methods and products related to treatment and prevention of hepatitis C virus infection
US7956043B2 (en) 2002-12-11 2011-06-07 Coley Pharmaceutical Group, Inc. 5′ CpG nucleic acids and methods of use
US20050218499A1 (en) * 2004-03-31 2005-10-06 Advanced Semiconductor Engineering, Inc. Method for manufacturing leadless semiconductor packages
US20090263413A1 (en) * 2006-05-31 2009-10-22 Tomokatsu Iwamura Immunostimulatory oligonucleotides and use thereof in pharmaceuticals
US8592566B2 (en) 2006-05-31 2013-11-26 Toray Industries, Inc. Immunostimulatory oligonucleotides and use thereof in pharmaceuticals

Also Published As

Publication number Publication date
CA2402250A1 (fr) 2001-09-20
ATE473750T1 (de) 2010-07-15
US7727712B2 (en) 2010-06-01
WO2001068078A2 (fr) 2001-09-20
AU2001242032B2 (en) 2005-09-15
AU4203201A (en) 2001-09-24
JP2003526662A (ja) 2003-09-09
WO2001068078A3 (fr) 2002-09-12
US20030216340A1 (en) 2003-11-20
EP1282427B1 (fr) 2010-07-14
DE60142562D1 (de) 2010-08-26
ES2348877T3 (es) 2010-12-16
EP1282427A2 (fr) 2003-02-12
JP5128745B2 (ja) 2013-01-23

Similar Documents

Publication Publication Date Title
US7727712B2 (en) Methods of suppressing hepatitis virus infection using immunomodulatory polynucleotide sequences
AU2001242032A1 (en) Immunostimulatory polynucleotide sequences for use in suppressing hepatitis virus infection
US8226957B2 (en) Methods of preventing and treating respiratory viral infection using immunomodulatory polynucleotide sequences
AU2001245627B2 (en) Immunostimulatory polynucleotide sequences for use in preventing and treating viral infections
AU2001243587A1 (en) Methods of preventing and treating respiratory viral infection using immunomodulatory polynucleotide sequences.
EP1261353B1 (fr) Methodes permettant de reduire l'infection par papillomavirus au moyen de sequences polynucleotidiques immunomodulatoires
EP1265622B1 (fr) Traitement d'une infection herpetique au moyen de sequences polynucleotidiques immunomodulatrices
AU2001245627A1 (en) Immunostimulatory polynucleotide sequences for use in preventing and treating viral infections
KR20030064882A (ko) 면역조절 폴리뉴클레오티드 및 그것의 사용 방법
AU2001243588A1 (en) Immunostimulatory polynucleotide sequences for use in preventing and treating viral infections
AU2001281459A1 (en) Treatment of herpes infection using immunomodulatory polynucleotide sequences

Legal Events

Date Code Title Description
AS Assignment

Owner name: DYNAVAX TECHNOLOGIES CORPORATION, CALIFORNIA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:VAN NEST, GARY;EIDEN, JR, JOSEPH J.;REEL/FRAME:012215/0334

Effective date: 20010920

STCB Information on status: application discontinuation

Free format text: EXPRESSLY ABANDONED -- DURING EXAMINATION