IP Library Granted Patent US 7,626,007
Granted Patent B2
US 7,626,007 · App. 10/405,738 · Granted Dec 1, 2009

Transcription factor regulating TNF-α

Assignee: Trustees of Boston University
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Quick Facts
Patent No.
US 7,626,007
App. No.
10/405,738
Granted
Dec 1, 2009
Kind
B2
Abstract

Disclosed herein is an isolated polypeptide comprising the amino acid sequence set forth in SEQ ID NO: 1. The isolated polypeptide binds to the DNA binding domain located from −550 to −487 in the promoter of the human TNF-α gene. Additionally, the level of the mRNA transcript encoding the isolated polypeptide is substantially increased in response to LPS stimulation in cultured THP-1 cells.

Claims (11)

1. A method for inhibiting lipopolysaccharide-induced tumor necrosis factor-alpha factor (LITAF)-dependent induction of tumor necrosis factor-alpha (TNF-α) gene expression in a human cell comprising the steps:

a) providing an antisense oligonucleotide that reduces or inhibits expression of the LITAF gene, wherein said antisense oligonucleotide comprises a sequence that is complementary to at least 150 contiguous nucleotides set forth within nucleotides 1-320 of SEQ ID NO: 2 including the start site of translation beginning at nucleotide 234 of SEQ ID NO: 2; and

b) delivering the antisense oligonucleotide into said cell; wherein said antisense oligonucleotide reduces or inhibits LITAF-dependent TNF-α gene expression in said cell.

2. The method of claim 1 , wherein said antisense oligonucleotide comprises a sequence that is complementary to at least 200 contiguous nucleotides.

3. The method of claim 1 , wherein the antisense oligonucleotide further comprises a sequence that is complementary to the downstream adjacent 3′ coding sequence set forth in SEQ ID NO: 2.

4. The method of claim 1 , wherein said antisense oligonucleotide comprises a sequence that is complementary to at least 320 contiguous.

5. The method of claim 4 , wherein the antisense oligonucleotide comprises a sequence that is complementary to nucleotides 1-320 of SEQ ID NO: 2.

6. The method of claim 1 , wherein said antisense oligonucleotide is encoded within a viral vector.

7. The method of claim 6 , wherein said viral vector is an adenoviral vector.

8. The method of claim 1 , wherein said antisense oligonucleotide is formulated in a liposome carrier.

9. The method of claim 1 , wherein said antisense oligonucleotide is a ribonucleic acid (RNA) molecule.

Assignments (1)
CONFIRMATORY LICENSE Recorded Sep 4, 2019
From: BOSTON UNIVERSITY MEDICAL CAMPUS
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 050257/0015 →
Continuity (3)
Division 0954746100 · Apr 12, 2000
Provisional Application 6012887500 · Apr 12, 1999
Related Publication 20030166159A1 · Sep 4, 2003