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WO1997000956A1 - Molecules d'adherence reagissant a l'hypoxemie, anticorps specifiques et leurs utilisations - Google Patents

Molecules d'adherence reagissant a l'hypoxemie, anticorps specifiques et leurs utilisations Download PDF

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Publication number
WO1997000956A1
WO1997000956A1 PCT/US1996/010701 US9610701W WO9700956A1 WO 1997000956 A1 WO1997000956 A1 WO 1997000956A1 US 9610701 W US9610701 W US 9610701W WO 9700956 A1 WO9700956 A1 WO 9700956A1
Authority
WO
WIPO (PCT)
Prior art keywords
antibody
cells
cell
human
cell adhesion
Prior art date
Application number
PCT/US1996/010701
Other languages
English (en)
Inventor
Douglas V. Faller
Steven J. Mentzer
Irene Ginis
Original Assignee
Trustees Of Boston University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Trustees Of Boston University filed Critical Trustees Of Boston University
Priority to AU63906/96A priority Critical patent/AU6390696A/en
Publication of WO1997000956A1 publication Critical patent/WO1997000956A1/fr

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K16/00Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K14/00Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705Receptors; Cell surface antigens; Cell surface determinants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00Medicinal preparations containing antigens or antibodies

Definitions

  • Antibodies can be generated by injecting purified or semi-purified cell adhesion molecules into mammals and harvesting the resulting antisera, or by creating hybridoma cell lines of mammalian origin, such as murine or human, that express anti-cell adhesion molecule antibodies.
  • Adhesion molecules are derived from and can be purified from human cells such as endothelial cells, muscle cells, neural cells, hematopoietic cells and neoplastic cells. In mature forms, they exist as cell surface receptors and may be complexed with lipids, saccharides and polysaccharides (e.g. glycosylation), fatty acids (e.g. acylation), other cell surface molecules (factors and co-factors) and additional proteins. Antibodies that bind to these cell surface ligands can prevent their association with other cells and cell surface molecules and, thus, prevent or at least substantially reduce adhesion.
  • Reduction of hypoxia- or ischemia-induced adhesion can ameliorate the symptoms associated with oxygen depravation (ischemia) and prevent the tissue damage sometimes associated with, for example, coronary thrombosis, cerebral vascular disease, arteriosclerosis, fibrosis, angiogenesis and tumor formation, plaque formation in arteries or veins, and inflammation as may occur in response to infections of viral, bacterial or parasitic origin.
  • ischemia oxygen depravation
  • Antibodies to inhibit cell adhesion are also useful to prevent pathological consequences associated with anaphylaxis and other allergic responses compounded by adhesion of cells to damaged tissues. Antibodies may also be useful to treat or prevent the pathological consequences associated with inflammation and the inflammatory process. Many of the steps involve adhesion to cells or other substances. Interference with adhesion can ameliorate or prevent some of the pathological effects associated with inflammation. Antibodies can be administered parenterally or non-parenterally provided they can pass through the gut wall barrier. Preferably methods of parenteral administration include intravenous, subcutaneous, intramuscular or intra-arterial injection of an effective amount.
  • Monoclonal antibody HAL 1/13 a murine immunoglobulin (IgC 2a ) was generated by immunizing BALB/c mice with 5 x IO 7 RD cells injected intraperitoneally at least once in one ml serum-free medium.
  • IL per ml.
  • the cells were washed 5 times with PBS and incubated for 10 minutes at 4°C with a solution containing 2 mM cysteine/5 mM cold Nal, washed one more time and then lysed with ice-cold lysis buffer (1 % triton

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Immunology (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Biochemistry (AREA)
  • Cell Biology (AREA)
  • Toxicology (AREA)
  • Zoology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

L'invention concerne de nouvelles molécules d'adhérence cellulaire et leurs ligands, des gènes codant les molécules d'adhérence cellulaire ou les ligands, ainsi que des anticorps se fixant spécifiquement à ces molécules. On peut utiliser des anticorps afin d'inhiber le processus de l'adhérence cellulaire et de traiter des maladies associées à l'adhérence, telles que l'athérosclérose, l'infarctus du myocarde et la néoplasie métastatique. Ces anticorps peuvent être monoclonaux ou polyclonaux et peuvent être dirigés vers un déterminant antigénique, ou vers un groupe de déterminants antigéniques, de la molécule d'adhérence cellulaire. L'invention concerne également des procédés de traitement ou de prévention de maladies associées à l'adhérence cellulaire, telles que des attaques, l'infarctus du myocarde et les conséquences pathologiques associées à l'anaphylaxie et à l'inflammation.
PCT/US1996/010701 1995-06-20 1996-06-20 Molecules d'adherence reagissant a l'hypoxemie, anticorps specifiques et leurs utilisations WO1997000956A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU63906/96A AU6390696A (en) 1995-06-20 1996-06-20 Hypoxia-responsive adhesion molecules, specific antibodies, nd their uses

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US49305395A 1995-06-20 1995-06-20
US08/493,053 1995-06-20

Publications (1)

Publication Number Publication Date
WO1997000956A1 true WO1997000956A1 (fr) 1997-01-09

Family

ID=23958712

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1996/010701 WO1997000956A1 (fr) 1995-06-20 1996-06-20 Molecules d'adherence reagissant a l'hypoxemie, anticorps specifiques et leurs utilisations

Country Status (2)

Country Link
AU (1) AU6390696A (fr)
WO (1) WO1997000956A1 (fr)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0887076A3 (fr) * 1997-05-07 1999-03-31 Saturnus A.G. Prévention d'ahérences et un systeme d'insufflation endoscopique
WO1999048916A3 (fr) * 1998-03-27 2000-01-20 Univ Leland Stanford Junior Genes et proteines d'origine humaine exprimes dans des conditions d'hypoxie, et utilisations de ceux-ci
WO2001023426A3 (fr) * 1999-09-30 2001-11-01 Varian Associates Genes humains et proteines relatifs a l'hypoxie et leurs utilisations
US8008312B2 (en) 2005-01-07 2011-08-30 Emory University CXCR4 antagonists for the treatment of HIV infection
US8080659B2 (en) 2006-07-11 2011-12-20 Emory University CXCR4 antagonists including diazine and triazine structures for the treatment of medical disorders
US8338448B2 (en) 2008-03-28 2012-12-25 Altiris Therapeutics, Inc. Chemokine receptor modulators

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1990003400A1 (fr) * 1988-09-28 1990-04-05 Dana-Farber Cancer Institute Molecules d'adhesion intercellulaire et leurs ligands de liaison
WO1991016928A1 (fr) * 1990-04-27 1991-11-14 Celltech Limited ANTICORPS ANTI-MOLECULE 1 d'ADHERENCE INTERCELLULAIRE CHIMERIQUE ADAPTES AU MODELE HUMAIN, PROCEDE DE PREPARATION ET D'UTILISATION
WO1993019784A1 (fr) * 1992-04-07 1993-10-14 The Board Of Trustees Of The Leland Stanford Junior University Nouvelle molecule d'adherence endotheliale pour monocytes
WO1994025067A1 (fr) * 1993-05-04 1994-11-10 Cytel Corporation Anticorps diriges contre la selectine p et leurs utilisations

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1990003400A1 (fr) * 1988-09-28 1990-04-05 Dana-Farber Cancer Institute Molecules d'adhesion intercellulaire et leurs ligands de liaison
WO1991016928A1 (fr) * 1990-04-27 1991-11-14 Celltech Limited ANTICORPS ANTI-MOLECULE 1 d'ADHERENCE INTERCELLULAIRE CHIMERIQUE ADAPTES AU MODELE HUMAIN, PROCEDE DE PREPARATION ET D'UTILISATION
WO1993019784A1 (fr) * 1992-04-07 1993-10-14 The Board Of Trustees Of The Leland Stanford Junior University Nouvelle molecule d'adherence endotheliale pour monocytes
WO1994025067A1 (fr) * 1993-05-04 1994-11-10 Cytel Corporation Anticorps diriges contre la selectine p et leurs utilisations

Non-Patent Citations (8)

* Cited by examiner, † Cited by third party
Title
G. HOWARD ET AL.: "Altered cardiac tissue gene expression during acute hypoxic exposure.", MOLECULAR AND CELLULAR BIOCHEMISTRY, vol. 69, no. 2, February 1986 (1986-02-01), BOSTON, MA, USA, pages 155 - 160, XP000608995 *
I. GINIS ET AL.: "Characterization of a hypoxia-responsive adhesion molecule for leukocytes on human endothelial cells.", THE JOURNAL OF IMMUNOLOGY, vol. 155, no. 2, 15 July 1995 (1995-07-15), BALTIMORE, MD, USA, pages 802 - 810, XP002018002 *
I. GINIS ET AL.: "Hypoxia induces lymphocyte adhesion to human mesenchymal cells via an LFA-1-dependent mechanism.", AMERICAN JOURNAL OF PHYSIOLOGY, vol. 264, no. 3 part 1, March 1993 (1993-03-01), BETHESDA, MD, USA, pages C617 - C624, XP000608994 *
M. ALESSIO ET AL.: "Analysis of the human CD36 leucocyte differentiation antigen by means of the monoclonal antibody NL07.", CELLULAR IMMUNOLOGY, vol. 137, no. 2, 15 October 1991 (1991-10-15), NEW YORK, NY, USA, pages 487 - 500, XP000608990 *
M. DE LA TORRE ET AL.: "Expression of the 85-kd membrane protein in primary human breast cancer.", HUMAN PATHOLOGY, vol. 26, no. 2, February 1995 (1995-02-01), PHILADELPHIA, PA, USA, pages 180 - 185, XP000608991 *
P. BELITSOS ET AL.: "Homotypic cell aggregation induced by anti-CD44 (pgp-1) monoclonal antibodies and related to CD44 (pgp-1) expression.", THE JOURNAL OF IMMUNOLOGY, vol. 144, no. 5, 1 March 1990 (1990-03-01), BALTIMORE, MD, USA, pages 1661 - 1670, XP002018000 *
S. SEITER ET AL.: "Prevention of tumor metastasis formation by anti-variant CD44.", THE JOURNAL OF EXPERIMENTAL MEDICINE, vol. 177, February 1993 (1993-02-01), NEW YORK, NY, USA, pages 443 - 455, XP002018001 *
Y. SUGIMOTO ET AL.: "Molecular cloning and characterization of the complementary DNA for the Mr 85,000 protein overexpressed in adriamycin-resistant human tumor cells.", CANCER RESEARCH, vol. 53, no. 11, 1 June 1993 (1993-06-01), BALTIMORE, MD, USA, pages 2538 - 2543, XP002017999 *

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0887076A3 (fr) * 1997-05-07 1999-03-31 Saturnus A.G. Prévention d'ahérences et un systeme d'insufflation endoscopique
WO1999048916A3 (fr) * 1998-03-27 2000-01-20 Univ Leland Stanford Junior Genes et proteines d'origine humaine exprimes dans des conditions d'hypoxie, et utilisations de ceux-ci
WO2001023426A3 (fr) * 1999-09-30 2001-11-01 Varian Associates Genes humains et proteines relatifs a l'hypoxie et leurs utilisations
US8008312B2 (en) 2005-01-07 2011-08-30 Emory University CXCR4 antagonists for the treatment of HIV infection
US8114884B2 (en) 2005-01-07 2012-02-14 Emory University CXCR4 antagonists for the treatment of medical disorders
US8080659B2 (en) 2006-07-11 2011-12-20 Emory University CXCR4 antagonists including diazine and triazine structures for the treatment of medical disorders
US8338448B2 (en) 2008-03-28 2012-12-25 Altiris Therapeutics, Inc. Chemokine receptor modulators
EP2664618A2 (fr) 2008-03-28 2013-11-20 Altiris Therapeutics Modulateurs du récepteur de chimiokine
US9314468B2 (en) 2008-03-28 2016-04-19 Altiris Therapeutics, Inc. Chemokine receptor modulators

Also Published As

Publication number Publication date
AU6390696A (en) 1997-01-22

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