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US 2021/0230596 A1Published application
RIG-I Agonists and Methods of Using Same
AssigneeYale University
InventorsAnna Marie Pyle, Olga Fedorova
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Abstract
The present invention provides RIG-I agonists. In certain embodiments, the agonists of the invention can be used to induce a type I interferon response in a cell.
Claims31
A polyribonucleic acid (RNA) molecule capable of inducing an interferon response,
- wherein at least one of the following applies:
- (a)
- wherein the RNA molecule is single stranded and comprises a first nucleotide sequence, which 5′-end is conjugated to one end of a linker,
- wherein the other end of the linker is conjugated to the 3′-end of a second nucleotide sequence,
- wherein the linker is free of a nucleoside, nucleotide, deoxynucleoside, or deoxynucleotide, or any surrogates or modifications thereof,
- wherein the first nucleotide sequence is substantially complementary to the second nucleotide sequence,
- wherein the first nucleotide sequence and the second nucleotide sequence can hybridize to form a double-stranded section,
- wherein the number of base pairs in the double stranded section is an integer ranging from 8 to 20,
- whereby the RNA molecule forms a hairpin structure,
- (b)
- wherein the RNA molecule is single stranded and comprises a first nucleotide sequence, which 5′-end is conjugated to one end of an element selected from the group consisting of a loop and a linker,
- wherein the other end of the element is conjugated to the 3′-end of a second nucleotide sequence,
- wherein the first nucleotide sequence is substantially complementary to the second nucleotide sequence,
- wherein the first nucleotide sequence and the second nucleotide sequence can hybridize to form a double-stranded section,
- wherein the number of base pairs in the double stranded section is an integer ranging from 8 to 20,
- whereby the RNA molecule forms a hairpin structure with a 3′-overhang.
13 more elements
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20-28. (canceled)
Dependencies are inferred from the claim text.