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Pro-angiogenic peptides and uses thereof

a technology of peptides and peptides, applied in the field of therapeutic peptides and endogenous cytokine modulation, can solve the problems of affecting the healing process, affecting the quality of life, and causing deleterious inflammation, so as to reduce the expression of at least one harmful cytokine, and modulate the expression of cytokin

Active Publication Date: 2019-02-19
SUSAVION BIOSCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Chronic wounds affect more than 6.5 million patients each year and cause significant impairment of quality of life.
The consequence is a vicious cycle of recruitment of neutrophils in response to IL-8, damage to tissues, and more production of IL-8 leading to deleterious inflammation as a side effect.
Increased levels of certain types of clinically deleterious cytokines, such as IL-8 and ICAM-1, at a site of infection or injury can therefore cause deleterious side effects which can hinder the process of healing.
The use of such peptides for clinical applications has, however, been hampered by several problematic issues including deleterious side effects.
However, Substance P has also been shown to stimulate neurons to release factors that recruit inflammatory cytokines and neutrophils to the site of a wound, thereby causing pain and inflammation.
Therefore, the use of peptides or growth factors and their analogs as therapeutic agents for wound healing can be problematic for a number of reasons, including efficacy, cost, and deleterious side effects such as inflammation.
1. the requirement for expression of a polynucleotide containing the nucleotide sequence encoding the protein, which can complicate production and significantly increase costs;
2. the requirement for purification of expressed proteins from the other proteins of the host cell, which can complicate production and significantly increase costs;
3. administration of angiogenic growth factors without the further ability to activate phagocytes and thereby enhance efficacy or ameliorate infection or other concomitant disorders;
4. administration of angiogenic growth factors without the further ability to reduce inflammation, thereby reducing deleterious side effects; and
5. administration of a peptide which can stimulate the release of factors that recruit inflammatory cytokines and neutrophils to the site of a wound, causing pain and inflammation.

Method used

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  • Pro-angiogenic peptides and uses thereof
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Examples

Experimental program
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Effect test

example 1

Peptide Design and Synthesis

[0103]A screen of peptide sequences identified one set of sequences of interest. The corresponding peptides were synthesized by solid-phase methods using standard Fmoc side chain protection. Branched peptides were constructed on a central tri-lysine framework, which allows four identical sequences within the same structure. A (Gly)3-Ser (GGGS, SEQ ID NO:3) linker sequence was included to distance the active sequence from the central framework. Distances between the active sequences can be adjusted by decreasing or increasing the length of the linker, including without limitation the use of two linkers in tandem (GGGSGGGS, SEQ ID NO:4) or by inserting any inert linker such as polyethylene glycol (PEG) of a variable length. The branched structure was designed to have enhanced activity by causing receptor clustering (cross-linking) on the surface of responsive cells.

[0104]The peptides were synthesized on PAL-PEG-polystyrene resin (Applied Biosystems, Foster ...

example 2

Core Peptide Sequences: WNSTL (SEQ ID NO:1) and NQHTPR (SEQ ID NO:2)

[0110]The peptides (WNSTL, SEQ ID NO:1) and (NQHTPR, SEQ ID NO:2) were identified through a screen of peptide sequences as potentially of interest. The sequences were synthesized on a tri-lysine core according to Posnett et al., J. Biol. Chem., 263: 1719-25, 1988, with a linker (GGGS, SEQ ID NO:3) included with the sequence to extend the active peptide away from the core.

[0111]FIGS. 2A-B illustrate the chemical structure of these two embodiments of the invention. In these embodiments, R═H or can be an adduct containing a fluorescent tag such as the dansyl group shown in FIG. 3. The peptide constructs illustrated contain four identical sequences, each of which is connected to a branched central tri-lysine framework via a (Gly)3Ser (GGGS, SEQ ID NO:3) linker. FIG. 2A is a branched peptide construct according to one embodiment of the invention, a peptide construct which contains four copies of the core sequence WNSTL (...

example 4

Pro-Angiogenic Activity of Peptides

[0147]Tumors require vascularization to obtain nutrients to support growth. Therefore, stimulation of growth of a tumor in response to administration of a construct of this invention is an indication of angiogenesis. For this example, a xenograph model system with the nude mouse (nu / nu) was used to determine the effect of peptide on growth of 786-0 human renal cell adenocarcinoma cell line injected into the flank of a mouse so as to induce a tumor. After the tumor was established, peptide was injected subcutaneously on alternate days. The weight of the tumor was estimated by calculation of the volume.

[0148]FIG. 4 illustrates data resulting from assays for pro-angiogenic activity for one embodiment of the invention. The bar graph in FIG. 4 shows the average weight of the tumor in mice treated with the peptide construct containing four copies of the core sequence WNSTL (SEQ ID NO:1) at a dose of 0.05 nmole / gm as compared with a control group. The pep...

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Abstract

This present invention is directed to peptides, compositions, and methods for modulating endogenous cytokine expression in a subject. More specifically, the invention provides peptides useful in regulating the release of a specific pattern of cytokines that promote angiogenesis and / or can be used to modulate the immune system of a subject.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]More than one reissue application has been filed for the reissue of U.S. Pat. No. 8,460,697 B2. The reissue applications are application Ser. No. 14 / 734,785 (issued as U.S. Pat. No. RE46,425) and Ser. No. 15 / 278,016 (the present application), all of which are reissue divisional applications of U.S. Pat. No. 8,460,697 B2. The present application is a reissue divisional of application Ser. No. 14 / 734,785 (issued as U.S. Pat. No. RE46,425), which is an application for reissue of U.S. Pat. No. 8,460,697 B2, which is related to and claims the benefit of U.S. Provisional Application No. 61 / 221,021 filed Jun. 26, 2009, and; U.S. Pat. No. 8,460,697 B2 is also a continuation-in-part of U.S. patent application Ser. No. 11 / 955,143 filed Dec. 12, 2007, which in turn claims the benefit of U.S. Provisional Application No. 60 / 869,862 filed Dec. 13, 2006, the contents of each of which are incorporated herein by reference thereto.INCORPORATION-BY-REFERENC...

Claims

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Application Information

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Patent Type & Authority Patents(United States)
IPC IPC(8): C07K7/06C07K14/00
CPCC07K7/06A61K38/00C07K14/49C07K14/001
Inventor EGGINK, LAURA L.HOOBER, J. KENNETH
Owner SUSAVION BIOSCI
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