WO2000006194A3 - Depletion of cells responsible for antibody-mediated graft rejection - Google Patents

Depletion of cells responsible for antibody-mediated graft rejection Download PDF

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Publication number
WO2000006194A3
WO2000006194A3 PCT/US1999/017190 US9917190W WO0006194A3 WO 2000006194 A3 WO2000006194 A3 WO 2000006194A3 US 9917190 W US9917190 W US 9917190W WO 0006194 A3 WO0006194 A3 WO 0006194A3
Authority
WO
WIPO (PCT)
Prior art keywords
methods
compositions
graft rejection
cause
xenograft
Prior art date
Application number
PCT/US1999/017190
Other languages
French (fr)
Other versions
WO2000006194A2 (en
WO2000006194A9 (en
Inventor
Arou Thall
Original Assignee
Biotransplant Inc
Arou Thall
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 Biotransplant Inc, Arou Thall filed Critical Biotransplant Inc
Priority to AU56688/99A priority Critical patent/AU5668899A/en
Publication of WO2000006194A2 publication Critical patent/WO2000006194A2/en
Publication of WO2000006194A3 publication Critical patent/WO2000006194A3/en
Publication of WO2000006194A9 publication Critical patent/WO2000006194A9/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/10Dispersions; Emulsions
    • A61K9/127Liposomes
    • A61K9/1271Non-conventional liposomes, e.g. PEGylated liposomes, liposomes coated with polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6801Drug-antibody or immunoglobulin conjugates defined by the pharmacologically or therapeutically active agent
    • A61K47/6803Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates
    • A61K47/6811Drugs conjugated to an antibody or immunoglobulin, e.g. cisplatin-antibody conjugates the drug being a protein or peptide, e.g. transferrin or bleomycin
    • A61K47/6817Toxins
    • A61K47/6819Plant toxins
    • A61K47/6825Ribosomal inhibitory proteins, i.e. RIP-I or RIP-II, e.g. Pap, gelonin or dianthin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/68Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6835Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
    • A61K47/6849Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a receptor, a cell surface antigen or a cell surface determinant
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Toxicology (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • Transplantation (AREA)
  • Botany (AREA)
  • Molecular Biology (AREA)
  • Cell Biology (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
  • Peptides Or Proteins (AREA)

Abstract

The present invention provides compositions, and methods of using said compositions, which are useful to reduce allogeneic or xenogeneic graft rejection. The invention provides methods and compositions for promoting in an animal of a first species a state of tolerance against Galα1,3Gal epitopes present on a xenograft from an animal of a second species, thereby preventing hyperacute rejection (HAR) of the xenograft. The methods and compositions according to the invention cause the elimination or anergy of specific lymphoid cells which are responsible for the production of xenoreactive natural antibodies (XNAs) which cause HAR of the xenograft. The invention also provides immunotoxin compositions and methods of using the same which are useful to reduce allogeneic or xenogeneic antibody-mediated graft rejection. The methods and compositions according to the invention cause the reduction or elimination of specific cells responsible for the production of antibodies that cause graft rejection.
PCT/US1999/017190 1997-02-05 1999-07-29 Depletion of cells responsible for antibody-mediated graft rejection WO2000006194A2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU56688/99A AU5668899A (en) 1998-07-29 1999-07-29 Depletion of cells responsible for antibody-mediated graft rejection

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US79592597A 1997-02-05 1997-02-05
US13795698A 1998-02-05 1998-02-05
US12474498A 1998-07-29 1998-07-29
US09/124,744 1998-07-29

Publications (3)

Publication Number Publication Date
WO2000006194A2 WO2000006194A2 (en) 2000-02-10
WO2000006194A3 true WO2000006194A3 (en) 2000-08-24
WO2000006194A9 WO2000006194A9 (en) 2001-12-13

Family

ID=27383151

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1999/017190 WO2000006194A2 (en) 1997-02-05 1999-07-29 Depletion of cells responsible for antibody-mediated graft rejection

Country Status (1)

Country Link
WO (1) WO2000006194A2 (en)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8106251B2 (en) 2002-08-21 2012-01-31 Revivicor, Inc. Tissue products derived from porcine animals lacking any expression of functional alpha 1,3 galactosyltransferase
DE60330468D1 (en) 2002-08-21 2010-01-21 Revivicor Inc PIGS WITHOUT ANY EXPRESSION OF FUNCTIONAL ALPHA-1,3-GALACTOSYLTRANSFERASE
CA2548080A1 (en) 2003-11-05 2005-05-26 University Of Pittsburgh Porcine isogloboside 3 synthase protein, cdna, genomic organization, and regulatory region
CN112480257A (en) 2005-03-23 2021-03-12 根马布股份公司 CD38 antibodies for the treatment of multiple myeloma
EP1748050A1 (en) * 2005-07-28 2007-01-31 Rijksuniversiteit Groningen Targeting-enhanced activation of galectins
GB0605395D0 (en) * 2006-03-16 2006-04-26 Norwegian Radium Hospital Res Anti-cancer therapy
DK2081595T3 (en) 2006-09-26 2019-07-15 Genmab As ANTI-CD38 PLUS CORTICOSTEROID PLUS A NON-CORTICOSTEROID KEMOTERAPEUTIKA FOR TUMOR TREATMENT
WO2011154453A1 (en) 2010-06-09 2011-12-15 Genmab A/S Antibodies against human cd38
US9603927B2 (en) 2014-02-28 2017-03-28 Janssen Biotech, Inc. Combination therapies with anti-CD38 antibodies
US9732154B2 (en) 2014-02-28 2017-08-15 Janssen Biotech, Inc. Anti-CD38 antibodies for treatment of acute lymphoblastic leukemia
US20160376328A1 (en) * 2014-03-11 2016-12-29 Molecular Templates, Inc. Proteins comprising amino-terminal proximal shiga toxin a subunit effector regions and cell-targeting immunoglobulin-type binding regions
MA40608A (en) 2014-09-09 2016-03-17 Janssen Biotech Inc Combination therapies with anti-cd38 antibodies
IL307913A (en) 2014-12-04 2023-12-01 Janssen Biotech Inc Anti-cd38 antibodies for treatment of acute myeloid leukemiaanti-cd38 antibodies for treatment of acute myeloid leukemiaanti-cd38 antibodies for treatment of acute myeloid leukemiaanti-cd38 antibodies for treatment of acute myeloid leukemiaanti-cd38 antibodies for treatment of acute myeloid leukemiaanti-cd38 antibodies for treatment of acute myeloid leukemiaanti-cd38 antibodies for treatment of ac
CN108136218B (en) 2015-05-20 2022-12-13 詹森生物科技公司 anti-CD 38 antibodies for the treatment of light chain amyloidosis and other CD 38-positive hematologic malignancies
AU2016282674B2 (en) 2015-06-22 2022-01-13 Janssen Biotech, Inc. Combination therapies for heme malignancies with anti-CD38 antibodies and survivin inhibitors
US20170044265A1 (en) 2015-06-24 2017-02-16 Janssen Biotech, Inc. Immune Modulation and Treatment of Solid Tumors with Antibodies that Specifically Bind CD38
AU2016350717B2 (en) 2015-11-03 2023-08-10 Janssen Biotech, Inc. Subcutaneous formulations of anti-CD38 antibodies and their uses
US10781261B2 (en) 2015-11-03 2020-09-22 Janssen Biotech, Inc. Subcutaneous formulations of anti-CD38 antibodies and their uses
MA50514A (en) 2017-10-31 2020-09-09 Janssen Biotech Inc HIGH-RISK MULTIPLE MYELOMA TREATMENT METHODS

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994021799A1 (en) * 1993-03-16 1994-09-29 Austin Research Institute USE OF PORCINE GAL α(1,3) GALACTOSYL TRANSFERASE IN XENOGRAFT THERAPIES
WO1997011963A1 (en) * 1995-09-27 1997-04-03 The Austin Research Institute ANTI-GALα(1,3)GAL ANTIBODY BINDING PEPTIDES

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994021799A1 (en) * 1993-03-16 1994-09-29 Austin Research Institute USE OF PORCINE GAL α(1,3) GALACTOSYL TRANSFERASE IN XENOGRAFT THERAPIES
WO1997011963A1 (en) * 1995-09-27 1997-04-03 The Austin Research Institute ANTI-GALα(1,3)GAL ANTIBODY BINDING PEPTIDES

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
ALEXEEV L.P. ET AL: "Pretreatment of kidney allografts with anti-CD5 immunotoxin: A new chance for high responder recipients.", TRANSPLANTATION PROCEEDINGS, (1997) 29/8 A (3605-3606)., XP000770271 *
GALILI U: "Interaction of the natural anti-gal antibody with alpha- galactosyl epitopes: a major obstacle for xenotransplantation in humans", IMMUNOLOGY TODAY,GB,ELSEVIER PUBLICATIONS, CAMBRIDGE, vol. 14, no. 10, 1 January 1993 (1993-01-01), pages 480 - 482, XP000672917, ISSN: 0167-5699 *
UCKUN F M ET AL: "Developmental hierarchy during early human B-cell ontogeny after autologous bone marrow transplantation using autografts deplete of CD19 + B-cell precursors by an anti- CD19 pan-B-cell immunotoxin containing pokeweed antiviral protein.", BLOOD, (1992 JUN 15) 79 (12) 3369-79., XP000611308 *
VAN OOSTERHOUT, Y. V. J. M. ET AL: "Suitability of a cocktail of CD34 and CD7 ricin A - immunotoxins for in vivo treatment of acute graft -versus-host-disease.", BLOOD, (NOV. 15, 1997) VOL. 90, NO. 10 SUPPL. 1 PART 2, PP. 376B. MEETING INFO.: THIRTY-NINTH ANNUAL MEETING OF THE AMERICAN SOCIETY OF HEMATOLOGY SAN DIEGO, CALIFORNIA, USA DECEMBER 5-9, 1997 THE AMERICAN SOCIETY OF HEMATOLOGY., XP000872341 *

Also Published As

Publication number Publication date
WO2000006194A2 (en) 2000-02-10
WO2000006194A9 (en) 2001-12-13

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