IP Library Granted Patent US 9,724,422
Granted Patent B2
US 9,724,422 · App. 13/988,829 · Granted Aug 8, 2017

Human lactoferrin derived peptide for use as an antigen masking agent

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Quick Facts
Patent No.
US 9,724,422
App. No.
13/988,829
Granted
Aug 8, 2017
Kind
B2
Abstract

The invention refers to a human lactoferrin derived peptide for use as an antigen masking agent in the production of a pharmaceutical composition for delivery of a biological active substance in a mammalian organism, where the biological active substance is able to induce an undesired immune response by the mammalian organism, where the pharmaceutical composition comprises a supramolecular aggregate of the biological active substance and the human lactoferrin derived peptide, with the effect that after delivery of pharmaceutical composition to the mammalian organism, there is no or only a diminished induction of the undesired immune response against the biological active substance.

Claims (23)

1. A pharmaceutical composition, comprising:

a supramolecular aggregate of a biological active substance and a human lactoferrin derived peptide,

wherein the human lactoferrin derived peptide consists of the amino acid sequence of KCFQWQRNMRKVRGPPVSCIKR (SEQ ID NO: 1) or a sequence which is at least 90% homologous to SEQ ID NO: 1,

wherein the biological active substance induces an undesired immune response by a mammalian organism, with an effect that after delivery of the pharmaceutical composition to the mammalian organism, there is no or only a diminished induction of the undesired immune response against the biological active substance, and

wherein the biological active substance is in a sample of blood which is transfused to the mammalian organism.

2. The composition according to claim 1 , wherein the human lactoferrin derived peptide consists of a sequence that is at least 90% homologous to SEQ ID NO: 1, and cysteine residues in positions 2 and 19 are present.

3. The composition according to claim 2 , wherein the undesired immune response is an IgG immune response.

4. The composition according to claim 2 , wherein the undesired immune response is an IgE immune response.

5. The composition according to claim 2 , wherein the biological active substance is selected from the group consisting of a biological active protein, a biological active peptide, an antisera antibody, a polyclonal antibody, and a monoclonal antibody.

6. The composition according to claim 1 , wherein the undesired immune response is an IgG immune response.

7. The composition according to claim 6 , wherein the biological active substance is selected from the group consisting of a biological active protein, a biological active peptide, an antisera antibody, a polyclonal antibody, and a monoclonal antibody.

8. The composition according to claim 1 , wherein the undesired immune response is an IgE immune response.

9. The composition according to claim 1 , wherein the biological active substance is selected from the group consisting of a biological active protein, a biological active peptide, an antisera antibody, a polyclonal antibody, and a monoclonal antibody.

10. The composition according to claim 1 , wherein the biological active substance is in or on a surface of an organ which is transplanted to the mammalian organism.

11. The composition according to claim 1 , wherein the biological active substance and the human lactoferrin derived peptide are not covalently bound to each other in the supramolecular aggregate.

12. The composition according to claim 1 , wherein the biological active substance and the human lactoferrin derived peptide are covalently bound to each other in the supramolecular aggregate.

13. The composition according to claim 1 , wherein the human lactoferrin derived peptide consists of the amino acid sequence of SEQ ID NO: 1 or a sequence which is at least 95% homologous to SEQ ID NO: 1.

14. A pharmaceutical composition, comprising:

a supramolecular aggregate of a biological active substance and a human lactoferrin derived peptide,

wherein the human lactoferrin derived peptide consists of the amino acid sequence of KCFQWQRNMRKVRGPPVSCIKR (SEQ ID NO: 1) or a sequence which is at least 90% homologous to SEQ ID NO: 1,

wherein the biological active substance induces an undesired immune response by a mammalian organism, with an effect that after delivery of the pharmaceutical composition to the mammalian organism, there is no or only a diminished induction of the undesired immune response against the biological active substance, and

wherein the biological active substance is in or on a surface of an organ which is transplanted to the mammalian organism.

15. The composition according to claim 14 , wherein the human lactoferrin derived peptide consists of the amino acid sequence of SEQ ID NO: 1 or a sequence which is at least 95% homologous to SEQ ID NO: 1.

Assignments (4)
CHANGE OF NAME Recorded Feb 11, 2020
From: EVONIK ROEHM GMBH
To: ROEHM GMBH
Reel/Frame 051893/0671 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 11, 2020
From: ROEHM GMBH
To: EVONIK DEGUSSA GMBH
Reel/Frame 051893/0727 →
CHANGE OF NAME Recorded Feb 11, 2020
From: EVONIK DEGUSSA GMBH
To: EVONIK OPERATIONS GMBH
Reel/Frame 051894/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 29, 2013
From: HARTWIG, BENEDIKT; TOME ALCALDE, JUAN; WINDHAB, NORBERT; ANSUATEGUI PANZANO, MARIA DEL PILAR; VARA CARRERA, MATIAS JAVIER
To: EVONIK ROEHM GMBH
Reel/Frame 030891/0828 →