IP Library Patent Application 15509997
Patent Application
App. No. 15/509,997

IMMUNOLOGICAL REAGENT

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Quick Facts
Patent No.
US None
App. No.
15/509,997
Abstract

The present invention provides an immunogenic composition comprising a charged antigen electrostatically associated with a Toll-Like Receptor (TLR) targeting moiety. The TLR targeting moiety comprises a TLR-2 agonist covalently attached to polyethylene glycol and to a hyper-branched charged peptide.

Claims (19)

1 . An immunogenic composition comprising a charged antigen electrostatically associated with a Toll-Like Receptor (TLR) targeting moiety, wherein the TLR targeting moiety comprises a TLR-2 agonist covalently attached to polyethylene glycol and to a hyper-branched charged peptide.

2 . The composition according to claim 1 , wherein the charged antigen comprises a cytotoxic T-cell (CTL) epitope.

3 . The composition according to claim 1 , wherein the charged antigen comprises a B-cell epitope and the antigen is present in the composition in a dose sparing amount.

4 . The composition according to claim 1 , wherein the TLR2 agonist is selected from the group consisting of Pam 2 Cys, Pam 3 Cys, Ste 2 Cys, Lau 2 Cys and Oct 2 Cys.

5 . The composition according to claim 4 , wherein the TLR2 agonist is Pam 2 Cys.

6 . The composition according to claim 1 , wherein the PEG (polyethyleneglycol) has 5 to 22 ethylene oxide subunits.

7 . The composition according to claim 6 , wherein the PEG (polyethyleneglycol) is (PEG) 1 .

8 . The composition according to claim 1 , wherein the hyper-branched charged peptide comprises R4, R8, K4, K8, E4, E8, D4, D8, H4, or H8.

9 . The composition according to claim 1 , wherein the TLR targeting moiety is of the formula:

10 . The composition according to claim 1 , wherein the TLR targeting moiety is of the formula:

11 . The composition according to claim 1 , wherein the TLR targeting moiety is of the formula:

12 . The composition according to claim 1 , wherein the TLR targeting moiety is of the formula:

13 . The composition according to claim 1 , wherein the TLR targeting moiety is of the formula:

14 . The composition according to claim 1 , wherein the TLR targeting moiety is of the formula:

15 . The composition according to claim 1 , wherein the TLR targeting moiety is of the formula:

16 . The composition according to claim 1 , wherein the TLR targeting moiety is of the formula:

17 . The composition according to claim 2 , wherein the CTL epitope is derived from a pathogen or a tumour antigen.

18 . A method of eliciting a CD8 − response in a subject, the method comprising administering to the subject the composition according to claim 1 .

19 . (canceled)

Assignments (5)
CHANGE OF NAME Recorded Aug 14, 2018
From: INNAVAC PTY LTD
To: ENA THERAPEUTICS PTY LTD
Reel/Frame 046804/0400 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 21, 2017
From: THE UNIVERSITY OF MELBOURNE
To: INNAVAC PTY LTD
Reel/Frame 043943/0693 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2017
From: JACKSON, DAVID CHARLES
To: THE UNIVERSITY OF MELBOURNE
Reel/Frame 043606/0362 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2017
From: CHUA, BRENDON YEW LOONG
To: THE UNIVERSITY OF MELBOURNE
Reel/Frame 043606/0404 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2017
From: SEKIYA, TOSHIKI
To: THE UNIVERSITY OF MELBOURNE
Reel/Frame 043606/0431 →