Title: Method of treating sepsis and ARDS with chemokine .beta.-4
United States Patent: 6,406,688
Inventors: White; John Richard (Coatesville, PA); Pelus; Louis Martin (Richboro, PA)Assignee: Human Genome Sciences, Inc. (Rockville, MD)
Appl. No.: 496273Filed: February 1, 2000
The invention relates to the method of preventing and treating sepsis and ARDS using chemokine .beta.-4 or a biologically active fragment thereof, alone or in conjunction with an anti-infective agent.
DETAILED DESCRIPTION OF THE INVENTION
It is the object of this invention to provide a new method
of treatment of sepsis and ARDS comprising administering to an animal in
need thereof, including humans, an effective amount of chemokine protein
or biologically active fragments thereof, alone or in combination with
other anti-infective agents. As used herein the term "chemokine"
means Chemokine Beta-4 (SEQ ID NOs: 1 and 2). The initial 24 amino acids
represent the deduced leader sequence of Chemokine Beta-4 such that the
putative mature polypeptide comprises 72 amino acids.
TABLE 1
Chemokine Patent Applications
Application
Gene Name Date Filed Number
Macrophage Inflammatory Dec-22-93 08/173,209
Protein-Gamma
Macrophage Inflammatory Protein-3 Mar-8-84 WO95/17092
and -4
Macrophage Migration Inhibitory May-16-94 WO95/31468
Factor-3
Human Chemokine Beta-9 Jun-6-95 WO96/06169
Human Chemokine Polypeptides Aug-23-94 WO96/05856
Human Chemokine Beta-11 and Human Feb-8-95 US95/01780
Chemokine Alpha 1
Human Chemokine Beta-13 Jun-5-95 08/464,594
Human Chemokine Beta-12 Jun-6-95 08/468,541
Chemokine Alpha-2 Mar-19-96 60/013,653
Chemokine Alpha-3 Mar-18-96 US96/03686
Novel Chemokine for Mobilizing Sep-29-95 60/006,051
Stem Cells
Short Form Chemokine Beta-8 Oct-24-95 60/004,517
This invention further relates to a method of preventing sepsis and ARDS
comprising administering to an animal in need thereof an effective amount
of modified chemokine protein or biologically active fragments thereof
alone or in combination with other anti-infective agents.Known anti-infective agents include, without limitation, anti-microbial agents routinely used for the treatment of sepsis such as amino-glycosides (such as amikacin, tobramycin, netilmicin, and gentamicin), cephalosporins such as ceftazidime, related beta-lactam agents such as maxalactam, carbopenems such as imipenem, monobactam agents such as aztreonam; ampicillin and broad-spectrum penicillins, (e.g., penicillinase-resistant penicillins, ureidopenicillins or antipseudomonal penicillin or Augmentin) that are active against P. aeruginosa, Enterobacter species, indole-positive Proteus species, and Serratia. Also included within the definition of anti-infective agents are antifungal agents, amphotericin and the like as well as anti-viral agents such as famvir and acyclovir.
The compound is useful in the treatment and prevention of sepsis and ARDS in humans and other animals such as dairy cattle, horses, calves or poultry.
Chemokine protein or biologically active fragments of Chemokine Beta-4 have been described. The use of chemokine protein or biologically active fragments thereof for the prevention and treatment of sepsis has not been reported. It has now been discovered that chemokine protein or biologically active fragments thereof significantly increases the survival of animals challenged with lethal sepsis causing organisms. Treatment with the compound of this invention, alone or in combination with an anti-infective agent prior to contemplated thoracic or abdominal surgery would be useful in reducing the likelihood of post-operative sepsis. It may also be used post-operatively for the treatment of sepsis and ARDS caused by a variety of reasons as outlined previously.
To effectively treat a human or other animal chemokine protein or biologically active fragments thereof may be amstered by injection in the dose range of about 10 fg/kg to about 100 mg/kg/dose, preferably between about 1 and 50 mg/kg/dose, or orally in the dose range of about 10 fg/kg to about 100 mg/kg body weight per dose, preferably between about 1 and 50 mg/kg body weight; if administered by infusion or similar techniques, the dose may be in the range of about 10 fg/kgto about 100 mg/kg/dose, preferably between about 1 and 50 mg/kg/dose; if administered subcutaneously the dose may be in the range of about 10 fg/kg to about 100 mg/kg/dose, preferably between about 1 and 50 mg/kg/dose.
Depending on the patient's condition, the compounds of this invention can be administered for prophylactic and/or therapeutic treatments. In therapeutic application, the compound is administered to a patient already suffering from a disease in an amount sufficient to cure or at least partially arrest the disease and its complications. It may be given at any time after surgery, preferably prior to 24 hours after surgery. In prophylactic applications, a composition containing chemokine protein or biologically active fragments thereof, is administered to a patient not already in a disease state to enhance the patient's resistance. It may be given one day or one week prior to surgery, preferably one to two days prior to surgery. It may be administered parenterally or orally.
Single or multiple administrations of the compounds can be carried out with dose levels and pattern being selected by the treating physician. In any event, a quantity of the compounds of the invention sufficient to effectively treat the patient should be administered.
The compounds of this invention, may also be administered in conjunction with a conventional anti-infective as disclosed herein above, such as gentamicin, augmentin or ceftazidime. The particular anti-infective chosen should be one to which the infective organism is susceptible and is selected or modified during therapy as the infecting microorganism is more particularly identified.
Additionally, various adjunctive agents in the treatment of septic shock also may be useful in combination with the components of this invention. They include sympathomimetic amines (vasopressors) such as norepinephrine, epinephrine, isoproterenol, dopamine, and dobutamine; anti-inflammatory agents such as methylprednisolone anti-inflammatory agents such as indomethacin and phenylbutazone; and corticosteroids such as betamethasone, hydrocortisone, methylprednisolone, or dexamethasone; anti-coagulants such as heparin, anti-thrombin III or coumarin type drugs for certain conditions and schedules; diuretics such as furosemide or ethacrynic acid; and antagonist of opiates and beta-endorphins such as naloxone; an antagonist of tumor necrosis factor or of interleukin-1; phenothiazines; anti-histamines; glucagon; .alpha.-adrenergic blocking agents, vasodilators; plasma expanders; packed red blood cells; platelets; cryoprecipitates; fresh frozen plasma; bacterial permeability protein; clindamycin; and antibodies to (lipid A), the J5 mutant of E. coli or to endotoxin core glycolipids. Methods for preparing such antibodies are described widely in the literature.
One of the most important aspects in the treatment of the clinical septic shock syndrome is its apparently intractable resistance to the effects of a variety of highly potent antimicrobial agents. Despite the development of newer antimicrobial agents, the overall incidence of clinical sepsis has increased, and mortality remains unacceptably high, often approaching 60% of diagnosed patients. The discovery of the increased survival with the treatment of chemokine protein or biologically active fragments thereof both prophylactically and after infection provides a new and useful therapy of sepsis and ARDS.
The compounds of this invention, may also be administered in conjunction with hematopoietic maturation agents, such as G-CSF, F1t3, M-CSF or GM-CSF. These compounds affect the mobilization of the chemokines of the invention and are believed to enhance the anti-sepsis and anti-ARDS efficacy of chemokines.
The biological activity of chemokine protein or biologically active fragments thereof are demonstrated by the following assays:
Rats. Male Fischer 344 rats obtained from Taconic farms weighing 200 to 250 g. are utilized. The rats are housed 2 per cage in standard plastic caging and fed lab chow and water ad libitum.
Chemokine protein or biologically active fragments thereof, is prepared in E. coli by the method given in Example 5. The compound is dissolved in DPBS containing 0.5% heat inactivated autologous normal rat serum. The animals are dosed intraperitoneally with chemokine 24 hours and 2 hours before infection. Control animals are dosed with dilution buffer on the same schedule. Starting two hours after infection the rats are treated twice daily with subcutaneous gentamicin.
E coli. A clinical isolate of E. coli isolated from sputum is utilized. The organisms are tested for antibiotic sensitivity by the disc-agar diffusion technique and found to be sensitive to gentamicin, ampicillin, cephalothin, chloramphenicol, kanamycin, tetracycline, trimethoprin/sulfamethoxazole and resistant to penicillin G, erythromycin, and vancomycin. The organism is animal passed in mice and subsequently recovered and plated onto MacConkey's agar. The reisolated organisms are grown overnight in brain-heart infusion broth, and then stored frozen at -70oC. To inoculate the fibrin clot, organisms from thawed stocks are inoculated into brainheart infusion broth and incubated overnight on a rotary shaker (120 rpm) at 37oC. The E. coli is harvested by centrifugation, washed 3x and finally resuspended in normal saline. The number of organisms is quantified by turbidimentry, and the concentration adjusted with normal saline. All inoculum sizes are based on viable counts determined by scoring colony forming units on MacConkeys agar.
Fibrin Clot. The E. coli infected fibrin clots are made from a 1% solution of bovine fibrinogen (Type 1-S, Sigma) in sterile saline. The clot is formed by adding sequentially human thrombin (Hanna Pharma.) bacteria, and fibrinogen solution to 24 well plastic plates. Bacterial numbers of 2.0 to 3.0x109 are used in inoculate the fibrin clots. The resulting mixture is then incubated at room temperature for 30 minutes before implantation.
Animal Model. The rats are anethetized with ketamine/xylazine (40 mg/kg/5 mg/kg) then the abdominal surfaced is shaved and a midline laporatomy performed. Bacterial peritonitis is induced by implanting a fibrin-thrombin clot containing E. coli into the abdominal cavity. After implantation the muscle layers are closed with 4-0 silk suture, and the wound closed with surgical staples. The animals are closely observed, any animals obviously moribound are euthanized.
Gentamicin. Rats are treated subcutaneously with gentamicin sulfate (Elkins-Sinn, N.J.) 5 mg/kg twice a day for five days.
Statistics. All continuously variable data are expressed as the percent survival from several pooled studies. The Fisher's Exact test is used to determine the statistical significance of the differences between the survival rates at 14 days. The differences between the groups are considered statistically significant at p<0.05.
Claim 1 of 10 Claims
What is claimed is:
1. A method of treating sepsis and adult respiratory distress syndrome (ARDS)
comprising administering to an animal in need thereof an effective amount
of a polypeptide selected from the group consisting of:
(a) a polypeptide comprising the amino acid sequence in SEQ ID NO:2;
(b) a polypeptide comprising amino acids 25 to 96 in SEQ ID NO:2;
(c) a polypeptide comprising a portion of the amino acid sequence in SEQ
ID NO:2, wherein said portion is chemotactic for leukocytes.
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