Method of reducing tissue damage at an inflammatory site using a monoclonal antibody

Bibliographic Details
Title: Method of reducing tissue damage at an inflammatory site using a monoclonal antibody
Patent Number: 4,935,234
Publication Date: June 19, 1990
Appl. No: 07/165,025
Application Filed: March 07, 1988
Abstract: A method of reducing tissue injury in humans or other animal species using a monoclonal antibody to inhibit specific phagocyte functions. The monoclonal antibody is selected to bind to phagocytic leukocytes for the purpose of inhibiting migration to an inflammatory site in the body and to inhibit the adhesion and spreading of activated leukocytes reaching such an area and then, block release of toxic substances by these cells. The monoclonal antibody is administered in vivo prior or early in the course of an experience leading to an injurious inflammatory response such as can result from restoration of myocardial blood flow interrupted by an acute coronary thrombosis.
Inventors: Todd, III, Robert F. (Ann Arbor, MI); Simpson, Paul J. (Ann Arbor, MI); Lucchesi, Benedict R. (Ann Arbor, MI); Scholossman, Stuart F. (Newton Centre, MA); Griffin, James D. (Sherborn, MA)
Assignees: Dana-Farber Cancer Institute (Boston, MA)
Claim: We claim
Claim: 1. A method of treating a human or animal host with the intent of reducing tissue damage occurring at an inflammatory site in any part of the body of a host experiencing a phagocyte-mediated inflammatory condition, said method comprising
Claim: administering in vivo a monoclonal antibody which will bind specifically only to the CD11b part of the CD11/CD18 glycoprotein of the Mo1 antigen expressed on the surface of granulocytes and other phagocytic cells and will inhibit the CD11/CD18 adhesion dependent cellular interactions of such cells reflecting their immonoloical inflammatory response function which contributes to such damage.
Claim: 2. The method of claim 1 in which said monoclonal antibody binds to an epitope on the CD11b, 155,000 dalton molecular weight peptide molecule of the Mo1 glycoprotein expressed on the surface of such cells.
Claim: 3. The method of claim 1 in which said inflammatory site is located at the vascular endothelial cell interface or subcellular matrix of a body part.
Claim: 4. The method of claim 1 in which said inflammatory site is in endothelial tissue of a body part.
Claim: 5. The method of claim 1 in which said inflammatory site is in a joint of the body part.
Claim: 6. The method of claim 1 in which said inflammatory site is developed from a myocardial infarct condition.
Claim: 7. The method of claim 1 in which the monocolonal antibody is administered intravenously at a selected time period prior to or during said inflammatory condition.
Claim: 8. The method of claim 1 in which said monoclonal antibody binds the Mo1 glycoprotein of neturophils.
Claim: 9. A method of reducing myocardial inflammation damage in a human patient experiencing acute coronary thrombosis, said patient having been treated initially either medically or surgically to renew myocardial blood flow at the inflammatory site, said method comprising supplying intravenously at least prior to such blood flow renewal a quantity of a murine monoclonal antibody which binds specifically only an epitope expressed on CD11b part of CD11/CD18 glycoprotein of the Mo1 surface antigen of neutrophils whereby to inhibit the adhesive-dependent cellular interactions of the neturophils at said site reflecting their immunological response function whereby to decrease the deleterious action of neturophils at said site.
Claim: 10. A method of treating a human host with the intent of reducing tissue damage occurring at an inflammatory site in the body of the human experiencing an inflammatory condition, said method comprising
Claim: infusing into the body prior to or during said inflammatory condition a quantity of murine monoclonal antibody which will bind specifically only to an epitope expressed on the CD11b, 155,000 dalton molecular weight peptide of the Mo1 antigen expressed on the surface of neutorphils and will inhibit the CD11/CD18 adhesion dependent intercellular reactions of neturophils reflecting their immunological response function which contributes to such damage.
Current U.S. Class: 424/858; 530/387; 530/388; 530/806; 530/808; 43524/027
Current International Class: A61K 39395; C07K 1528; C12P 2108
Patent References Cited: 4840793 June 1989 Todd et al.
Other References: Arnout et al., J. Clin. Invest., 72, 171-9, 1983.
Todd et al., J. Immunol. 126(4), 1935-42, 1981.
Todd et al., Hybridoma, 1(3), 329-37, 1982.
Todd et al., J. Clin. Invest., 74, 1280-90, 1984.
Primary Examiner: Draper, Garnette
Assistant Examiner: Kushan, Jeff
Attorney, Agent or Firm: Cass, Myron C.
Accession Number: edspgr.04935234
Database: USPTO Patent Grants
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Language:English