IP Library Patent Application 17703111
Patent Application
App. No. 17/703,111

METHOD OF TREATMENT

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Patent No.
US None
App. No.
17/703,111
Abstract

The present invention relates generally to the field of immunomodulation. Taught herein is an agent for inhibiting immunostimulation mediated by a Toll-like receptor useful in the treatment of viral and microbial pathogenesis, diseases involving elements of autoimmunity and inflammation as well as cancer. The agent antagonizes disulfide bond formation between C98 and C475 of Toll-like receptor 7 (TLR7) thereby preventing TLR7 activation. Pharmaceutical compositions are also enabled herein.

Claims (21)

1 . A peptide of up to 190 amino acids in length, comprising the amino acid sequence DX 1 RCNCX 2 PX 3 X 4 (SEQ ID NO: 27) wherein:

X 1 is L, F or M;

X 2 is V or I;

X 3 is V or I or A or P; and

X 4 is P or L or K or R.

2 . The peptide of claim 1 , wherein the peptide comprises the amino acid sequence DFRCNCVPIP (SEQ ID NO: 26).

3 . The peptide of claim 1 , wherein the peptide comprises the amino acid sequence DLRCNCVPVL (SEQ ID NO: 1).

4 . The peptide of claim 1 , wherein the peptide further comprises a moiety attached to the N-terminal or C-terminal end of the peptide which enables uptake of the peptide into the cell.

5 . The peptide of claim 4 , wherein the moiety is a hydrophilic peptide, an amphiphilic peptide, a peptide with a periodic amino acid sequence or a conjugate with cholestanol.

6 . The peptide of claim 4 , wherein the moiety is a hydrophilic peptide selected from the group consisting of TAT (SEQ ID NO: 2), SynB1 (SEQ ID NO: 3), SynB3 (SEQ ID NO: 4), PTD-4 (SEQ ID NO: 5), PTD-5 (SEQ ID NO: 6), FHV coat (SEQ ID NO: 7), BMV Gag-(7-25) (SEQ ID NO: 8), HTLV-II Rex-(4-16) (SEQ ID NO: 9), D-Tat (SEQ ID NO: 10) and R9-Tat (SEQ ID NO: 11).

7 . The peptide of claim 4 , wherein the moiety is an amphiphilic peptide selected from the group consisting of Transportan chimera (SEQ ID NO: 12), MAP (SEQ ID NO: 13), SBP (SEQ ID NO: 14), FBP (SEQ ID NO: 15), MPG [MPGac] (SEQ ID NO: 16), MPG (ΔNLS) (SEQ ID NO: 17), Pep-1 (SEQ ID NO: 18) and Pep-2 (SEQ ID NO: 19).

8 . The peptide of claim 4 , wherein the moiety is a periodic amino acid sequence comprising a polyarginine or a polylysine sequence.

9 . The peptide of claim 1 , wherein the peptide is up to 100 amino acids in length.

10 . The peptide of claim 1 , wherein the peptide is up to 40 amino acids in length.

11 . A pharmaceutical composition comprising the peptide of claim 1 and one or more pharmaceutical carriers, excipients and/or diluents.

12 . A method for inhibiting TLR7-mediated immunostimulatory activity in a TLR7-expressing cell, the method comprising contacting the cell with the peptide of claim 1 .

13 . The method of claim 12 , wherein the cell is of a subject with an autoimmune disease, a viral pathogenesis, a microbial pathogenesis, an inflammation or a cancer.

14 . The method of claim 13 , wherein the cell is of a subject with a viral pathogenesis.

15 . A method for inhibiting TLR7-mediated immunostimulatory activity in a TLR7-expressing cell in a subject, the method comprising administering to the subject an effective amount of the peptide of claim 1 .

16 . The method of claim 15 , wherein the subject has an autoimmune disease, a viral pathogenesis, a microbial pathogenesis, an inflammation or a cancer.

17 . The method of claim 16 , wherein the subject has a viral pathogenesis.

Assignments (2)
NUNC PRO TUNC ASSIGNMENT Recorded Jun 2, 2026
From: UNIVERSITY OF SOUTH AUSTRALIA
To: ADELAIDE UNIVERSITY
Reel/Frame 075695/0898 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 24, 2022
From: SELEMIDIS, STAVROS; BROOKS, DOUG A.; O'LEARY, JOHN
To: ROYAL MELBOURNE INSTITUTE OF TECHNOLOGY; UNIVERSITY OF SOUTH AUSTRALIA; THE PROVOST, FELLOWS, FOUNDATION SCHOLARS, AND THE OTHER MEMBERS OF BOARD, OF THE COLLEGE OF THE HOLY AND UNDIVIDED TRINITY OF QUEEN ELIZABETH, NEAR DUBLIN; MONASH UNIVERSITY
Reel/Frame 059389/0920 →