Anti-inflammatory peptides derived from C-reactive protein

Drug – bio-affecting and body treating compositions – Enzyme or coenzyme containing

Reexamination Certificate

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C435S212000, C435S218000, C435S219000, C514S002600, C514S015800, C530S300000, C530S326000, C530S328000

Reexamination Certificate

active

10373794

ABSTRACT:
A peptide corresponding to positions 62–71 of the sequence of human C-reactive protein (CRP) of the formula: Glu62-Ile-Leu-Ile-Phe-Trp-Ser-Lys-Asp-Ile71and modifications thereof obtained by substitution, deletion, or addition of amino acids, amidation of the C-terminal or acylation of the N-terminal, are capable of inhibiting in vitro the enzymatic activity of human Leukocyte Elastase (hLE) and/or of human Cathepsin G (hCG) and can be used for the treatment of chronic inflammation conditions such as rheumatoid arthritis, pulmonary emphysema, cystic fibrosis, bronchitis, asthma and some acute respiratory distress syndrome.

REFERENCES:
Wright et al. Am J Respir Med. 2003;2(3):211-9 (ABSTRACT).
van den Berg. Clin Exp Rheumatol. Sep.□Oct. 2002;20(5 Suppl 27):S21-5 (ABSTRACT).
Leff AR, “Future Directions in Asthma Therapy: Is a Cure Possible?”,Chest111(2Supp):61S-68S (1997).
Odeh M, “New insights into the pathogenesis and treatment of rheumatoid arthritis”,Clin Immunol Immunopathol83(2):103-116 (1997).
Stehbens et al, “Proteinase imbalance versus biomechanical stress in pulmonary emphysema”,Exp Mol Pathol69(1):46-62 (2000).
Shephard et al, “Peptides generated from C-reactive protein by a neutrophil membrane protease. Amino acid sequence and effects of peptides on neutrophil oxidative metabolsm and chemotaxis”,J Immunol145(5):1469-1476 (1990).
Shephard et al, “Characterization of neutrophil-mediated degradation of human C-reactive protein and identification of the protease”,Clin Exp Immunol87(3):509-513 (1992).
Shephard et al, “C-reactive protein (CRP) peptides inactivate enolase in human neutrophils leading to depletion of intracellular ATP and inhibition of superoxide generation”,Immunology;76(1):79-85 (1992).
West et al, “Gene therapy for pulmonary diseases”,Chest119(2):613-617 (2001).
Yavin et al, “Proteolysis of human C-reactive protein by neutrophil-derived lysosomal enzymes generated peptides which modulate neutrophil function: Implications to the anti-inflammatory mechanism”,Letters in Pept Sci2:7-16 (1995).
Yavin et al, “Synthetic peptides derived from the sequence of human C-reactive protein inhibit the enzymatic activities of human leukocyte elastase and human leukocyte cathespin G”,Int J Pept Protein Res48(5):465-76 (1996).
Yavin EA, “Binding pockets on the surface of human leukocyte elastase and human leukocyte cathepsin G. Implications to the design of inhibitors derived from human C-reactive protein”,Biomed Pept Proteins Nucleic Acids2(3):71-8 (1996-97).
Yavin EA, “Inhibition of the HLE and Cathespin G by Extended Peptides and Subunits Derived from Human C-reactive Protein”,Letters n Pept Sci4(3):157-166 (1997).
Yavin et al, “Peptides derived from human C-reactive protein inhibit the enzymatic activities of human leukocyte elastase and cathepsin G: use of overlapping peptide sequences to identify a unique inhibitor”,J Pept Res51(4):282-289 (1998).

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