Branched oligonucleotides as pathogen-inhibitory agents
AssigneeHybridon, Inc.
InventorsSudhir Agrawal, Susan Meschwitz
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Abstract
Novel antisense oligonucleotides are disclosed. The present oligonucleotides have increased resistance to nuclease attack and manifest increased efficacy in combating pathogenic infections. The present oligonucleotides comprise two or more identical or different sequences, each complementary to a nucleic acid sequence of a pathogen that is essential to the pathogen's metabolism and/or reproduction. The sequences may be complementary to the same or different target nucleic acid sequence within a single pathogen, to target sequences on different strains of the same pathogen, or to target sequences on different pathogens. In the preferred embodiment, the sequences are coupled via a 3′-3′ linkage, which greatly reduces 3′ nucleolytic degradation.
Claims8
An oligonucleotide of 16 to 100 nucleotides in length, comprising from two to six identical sequences of at least 8 nucleotides in length linked together, wherein each of said two to six identical sequences is complementary to the gag or tat nucleic acid sequence of human immunodeficiency virus (HIV), and wherein said oligonucleotide inhibits HIV replication.
An oligonucleotide of 16 to 100 nucleotides in length, comprising from two to six different oligonucleotide sequences of at least 8 nucleotides in length linked together, wherein each of said two to six different oligonucleotide sequences is complementary to a different target nucleic acid sequence of human immunodeficiency virus (HIV) gag or tat, none of said target sequences or their complementary sequences being contiguous, and wherein said oligonucleotide inhibits HIV replication.
Dependencies are inferred from the claim text.