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35 results about "Monospecific antibody" patented technology

Monospecific antibodies are antibodies whose specificity to antigens is singular (mono- + specific) in any of several ways: antibodies that all have affinity for the same antigen; antibodies that are specific to one antigen or one epitope; or antibodies specific to one type of cell or tissue. Monoclonal antibodies are monospecific, but monospecific antibodies may also be produced by other means than producing them from a common germ cell. Regarding antibodies, monospecific and monovalent overlap in meaning; both can indicate specificity to one antigen, one epitope, or one cell type (including one microorganism species). However, antibodies that are monospecific to a certain tissue, or all monospecific to the same tissue because clones, can be polyvalent in their epitope binding.

Monoclonal antibody hPAM4

This invention relates to monovalent and multivalent, monospecific antibodies and to multivalent, multispecific antibodies. One embodiment of these antibodies has one or more identical binding sites where each binding site binds with a target antigen or an epitope on a target antigen. Another embodiment of these antibodies has two or more binding sites where these binding sites have affinity towards different epitopes on a target antigen or different target antigens, or have affinity towards a target antigen and a hapten. The present invention further relates to recombinant vectors useful for the expression of these functional antibodies in a host. More specifically, the present invention relates to the tumor-associated antibody designated PAM4. The invention further relates to humanized and human PAM4 antibodies, and the use of such antibodies in diagnosis and therapy.
Owner:IMMUNOMEDICS INC

Monoclonal antibody cPAM4

This invention relates to monovalent and multivalent, monospecific antibodies and to monovalent and multivalent, multispecific antibodies. One embodiment of these antibodies has one or more identical binding sites where each binding site binds with a target antigen or an epitope on a target antigen. Another embodiment of these antibodies has two or more binding sites where these binding sites have affinity towards different epitopes on a target antigen or different target antigens, or have affinity towards a target antigen and a hapten. The present invention further relates to recombinant vectors useful for the expression of these functional antibodies in a host. More specifically, the present invention relates to the tumor-associated antibody designated PAM4. The invention further relates to chimeric PAM4 antibodies, and the use of such antibodies in diagnosis and therapy.
Owner:IMMUNOMEDICS INC

Fusion proteins for HIV therapy

Disclosed herein are fusion antibodies created to provide both an antigen-binding site that targets the CD4 receptor and an antigen-binding site that targets the HIV envelope. The fusion antibodies disclosed herein provide improved potency and breadth against HIV as compared to monospecific antibodies, and additionally provide high barrier against viral resistance. Also disclosed are pharmaceutical formulations and therapeutic methods utilizing such fusion proteins.
Owner:THE ROCKEFELLER UNIV

Synergistic Anti-CD47 Therapy for Hematologic Cancers

Methods are provided for treatment of hematologic cancers, particularly lymphomas and leukemias, including without limitation myelogenous and lymphocytic leukemias. A combination of antibodies specific for CD47; and specific for a cancer associated cell surface marker are administered to the patient, and provide for a synergistic decrease in cancer cell burden. The combination of antibodies may comprise a plurality of monospecific antibodies, or a bispecific or multispecific antibody. Markers of interest include without limitation, CD20, CD22, CD52, CD33; CD96; CD44; CD123; CD97; CD99; PTHR2; and HAVCR2.
Owner:THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIV

Synergistic anti-CD47 therapy for hematologic cancers

Methods are provided for treatment of hematologic cancers, particularly lymphomas and leukemias, including without limitation myelogenous and lymphocytic leukemias. A combination of antibodies specific for CD47; and specific for a cancer associated cell surface marker are administered to the patient, and provide for a synergistic decrease in cancer cell burden. The combination of antibodies may comprise a plurality of monospecific antibodies, or a bispecific or multispecific antibody. Markers of interest include without limitation, CD20, CD22, CD52, CD33; CD96; CD44; CD123; CD97; CD99; PTHR2; and HAVCR2.
Owner:THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIV

Methods of purifying bispecific antibodies

The invention relates to the purification of bispecific antibodies carrying a different specificity for each binding site of the immunoglobulin molecule from a mixture of monospecific antibodies. The bispecific antibodies are composed of a single heavy chain and two different light chains, one containing a Kappa constant domain and the other a Lambda constant domain. This invention in particular relates to the isolation of these bispecific antibodies from mixtures that contain monospecific antibodies having two Kappa light chains or portions thereof and monospecific antibodies having two Lambda light chains or portions thereof. The invention also provides the methods of efficiently purifying these bispecific antibodies.
Owner:NOVIMMUNE

Separation and extraction method for cytomembrane microvesicles (MVs) and exosomes (EXs)

The invention relates to a separation and extraction method for cytomembrane microvesicles (MVs) and exosomes (EXs). The method is characterized by comprising the following steps that a, 3-10 ml of a peripheral blood sample is drawn and placed in an anticoagulation tube to be stored, the sample is diluted with phosphate buffer normal saline (PBS) by 2-4 times, and then centrifugation is carried out to obtain supernate plasma; b, the supernate plasma is subjected to centrifugal separation again, and sediment is MVs; c, ultra-centrifugation is carried out on the supernate plasma in the step b, and sediment is EXs. According to the method, a previous method adopting mono-specificity antibodies is broken through, and the specificity and sensibility of the extracted cell MVs and EXs are higher than those in the prior art. A specificity and sensibility direction is provided for a further study of the MVs and the EXs as biomarkers of diseases.
Owner:WUHAN DAFU BIOTECH CO LTD

Monoclonal Antibody hPAM4

This invention relates to monovalent and multivalent, monospecific antibodies and to multivalent, multispecific antibodies. One embodiment of these antibodies has one or more identical binding sites where each binding site binds with a target antigen or an epitope on a target antigen. Another embodiment of these antibodies has two or more binding sites where these binding sites have affinity towards different epitopes on a target antigen or different target antigens, or have affinity towards a target antigen and a hapten. The present invention further relates to recombinant vectors useful for the expression of these functional antibodies in a host. More specifically, the present invention relates to the tumor-associated antibody designated PAM4. The invention further relates to humanized and human PAM4 antibodies, and the use of such antibodies in diagnosis and therapy.
Owner:IMMUNOMEDICS INC

Method for detecting EVs (extracellular vesicles) released by ECs (endothelial cells) and EPCs (endothelial progenitor cells) in blood

The invention relates to a method for detecting EVs (extracellular vesicles) released by ECs (endothelial cells) and EPCs (endothelial progenitor cells) in blood. EC-MVs (microvesicles), EPC-MVs, EC-EXs (exosomes) and EPC-EXs are separated from a circulatory system with two specific antibody linked immunomagnetic sand methods. The method breaks through a single specific antibody method, and the specificity and the sensitivity of extracted cells MVs and EXs are higher than those in the prior art. Besides, the cells MVs and EXs are detected with an NTS (nanoparticle tracing analysis) technique in combination of a specific antibody micro-beads method and a Q-dots method. The method can quickly, accurately and objectively analyze the levels of EC-MVs, EPC-MVs, EC-EXs and EPC-EXs in complicated samples such as blood and has advantages which a traditional analysis method does not possess. Besides, the specific and sensitive method is provided for further research of MVs and EXs serving as biomarkers of diseases.
Owner:WUHAN DAFU BIOTECH CO LTD

Antibodies capable of specifically binding two epitopes on tissue factor pathway inhibitor

The application discloses a combination of two monospecific TFPI antibodies, wherein one antibody is capable of specifically binding TFPI (1-181) and the other antibody is capable of specifically binding TFPI (182-276), as well as bispecific anti-TFPI antibodies derived from two such monospecific antibodies. Both the combination of the two monospecific antibodies and the bispecific antibody strongly enhance thrombin generation by neutralising full length TFPIα, even where the concentration of TFPI is abnormally elevated.
Owner:NOVO NORDISK AS

Antibodies capable of specifically binding two epitopes on tissue factor pathway inhibitor

The application discloses a combination of two monospecific TFPI antibodies, wherein one antibody is capable of specifically binding TFPI (1-181) and the other antibody is capable of specifically binding TFPI (182-276), as well as bispecific anti-TFPI antibodies derived from two such monospecific antibodies. Both the combination of the two monospecific antibodies and the bispecific antibody strongly enhance thrombin generation by neutralising full length TFPI[alpha], even where the concentration of TFPI is abnormally elevated.
Owner:NOVO NORDISK AS

Method for generating multispecific antibodies from monospecific antibodies

Herein is reported a method for the generation of multispecific antibodies by a half- antibody exchange reaction between two 2 / 3-IgGs destabilized in one half by asymmetric perturbing mutations fostering the generation of correctly assemble full length bispecific antibodies. The method can be performed in the absence of reducing agents and does not require hinge region disulfide bonds in the starting 2 / 3-IgGs.
Owner:F HOFFMANN LA ROCHE & CO AG

Generating multispecific antibody mixtures and methods of uses thereof

The invention relates to the generation of multispecific antibody mixtures include a subset of antibodies isolated from a mixture of two or more monospecific antibodies and one or more bispecific antibodies, wherein all antibodies in the subset have the same common heavy chain. The invention also relates to methods of isolating, purifying, or otherwise producing such a subset of antibodies by using at least one affinity chromatography step. The invention also relates to methods of using such a subset of antibodies in a variety of therapeutic indications.
Owner:NOVIMMUNE

Methods of purifying bispecific antibodies

The invention relates to the purification of bispecific antibodies carrying a different specificity for each binding site of the immunoglobulin molecule from a mixture of monospecific antibodies. The bispecific antibodies are composed of a single heavy chain and two different light chains, one containing a Kappa constant domain and the other a Lambda constant domain. This invention in particular relates to the isolation of these bispecific antibodies from mixtures that contain monospecific antibodies having two Kappa light chains or portions thereof and monospecific antibodies having two Lambda light chains or portions thereof. The invention also provides the methods of efficiently purifying these bispecific antibodies.
Owner:NOVIMMUNE

Method for in vivo generation of multispecific antibodies from monospecific antibodies

Herein is reported a method for the generation of multispecific antibodies directly on the cell-surface at the site of action by a half-antibody exchange reaction between two 2 / 3-IgGs or two 2 / 3-BiFabs destabilized in one half by asymmetric perturbing mutations fostering the generation of correctly assembled full length bi-or multi-specific antibodies. The method is performed in the absence hingeregion disulfide bonds in the starting 2 / 3-IgGs or 2 / 3-BiFabs.
Owner:F HOFFMANN LA ROCHE & CO AG

Method for in vivo generation of multispecific antibodies from monospecific antibodies

Herein is reported a method for the generation of multispecific antibodies directly on the cell-surface at the site of action by a half-antibody exchange reaction between two 2 / 3-IgGs or two 2 / 3-BiFabs destabilized in one half by asymmetric perturbing mutations fostering the generation of correctly assembled full length bi- or multi-specific antibodies. The method is performed in the absence hinge region disulfide bonds in the starting 2 / 3-IgGs or 2 / 3-BiFabs.
Owner:F HOFFMANN LA ROCHE INC

Methods and systems for generating, validating and using monoclonal antibodies

Provided herein is an antibody library, wherein the antibody library may comprise a plurality of monoclonal antibodies, monospecific antibodies or immunoprecipitated antibodies. Also provided herein are methods of generating and using such antibody libraries.
Owner:CDI LAB +1

Dual specific antibodies

The invention provides dual specific antibodies and methods of making and using such antibodies. In general, the dual specific antibodies are generated by identification of a monospecific antibody having light chain variable region VL residues that are electrostatic or hydrophobic and altering the nucleic acid sequence encoding one or more solvent accessible residues in the VH of the antibody either alone or in combination with alteration of the nucleic acid sequence encoding the VL of the antibody. The altered VH and the VL are expressed and dual specific antibodies, or antigen-binding fragments thereof, are selected. Exemplary dual specific antibodies are also provided as well as methods of using the antibodies.
Owner:GENENTECH INC

Application of reagents for detecting cd105, cd144, cd34, kdr, annexin V and CD63 in preparation of reagents for detecting extracellular vesicles released by endothelial and endothelial progenitor cells in blood

The invention relates to a method for detecting EVs (extracellular vesicles) released by ECs (endothelial cells) and EPCs (endothelial progenitor cells) in blood. EC-MVs (microvesicles), EPC-MVs, EC-EXs (exosomes) and EPC-EXs are separated from a circulatory system with two specific antibody linked immunomagnetic sand methods. The method breaks through a single specific antibody method, and the specificity and the sensitivity of extracted cells MVs and EXs are higher than those in the prior art. Besides, the cells MVs and EXs are detected with an NTS (nanoparticle tracing analysis) technique in combination of a specific antibody micro-beads method and a Q-dots method. The method can quickly, accurately and objectively analyze the levels of EC-MVs, EPC-MVs, EC-EXs and EPC-EXs in complicated samples such as blood and has advantages which a traditional analysis method does not possess. Besides, the specific and sensitive method is provided for further research of MVs and EXs serving as biomarkers of diseases.
Owner:WUHAN DAFU BIOTECH CO LTD

Anti-cxcr4 antibodies

The present invention relates to monospecific antibodies against CXCR4 or binding fragments thereof, to the use of such anti-CXCR4 antibodies or binding fragments in treating diseases whose pathogenesis is related to activation of CXCR4, as well as to pharmaceutical compositions comprising such anti-CXCR4 antibodies or binding fragments.
Owner:エムエスエムプロテインテクノロジーズインコーポレイテッド
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