Production and characterization of a monoclonal antibody (A1-3) that binds selectively to activated monocytes and inhibits monocyte procoagulant activity. 1986

V A Ewan, and W Cieplinski, and W W Hancock, and I Goldschneider, and A W Boyd, and F R Rickles

We describe the generation and characterization of a new monoclonal antibody, A1-3, which possesses two unique properties. First, A1-3 binds selectively to stimulated human monocytes. Secondly, A1-3 inhibits the procoagulant activity expressed by stimulated monocytes and by human brain tissue factor. Unstimulated human peripheral blood cells (granulocytes, lymphocytes, monocytes, red blood cells, and platelets), prepared in the absence of detectable endotoxin, express no procoagulant activity and fail to bind A1-3. Stimulation of peripheral blood monocytes. alveolar macrophages, or the monocyte-like cell line U937, however, results in the expression of procoagulant activity and the binding of A1-3. The surface antigen recognized by A1-3 was recovered from endotoxin-stimulated human monocyte vesicles by immune precipitation and demonstrated an apparent m.w. of approximately 52,000. It is proposed that the monoclonal antibody A1-3 detects a differentiation antigen on human monocytes that is expressed in response to stimuli for monocyte activation.

UI MeSH Term Description Entries
D008070 Lipopolysaccharides Lipid-containing polysaccharides which are endotoxins and important group-specific antigens. They are often derived from the cell wall of gram-negative bacteria and induce immunoglobulin secretion. The lipopolysaccharide molecule consists of three parts: LIPID A, core polysaccharide, and O-specific chains (O ANTIGENS). When derived from Escherichia coli, lipopolysaccharides serve as polyclonal B-cell mitogens commonly used in laboratory immunology. (From Dorland, 28th ed) Lipopolysaccharide,Lipoglycans
D008262 Macrophage Activation The process of altering the morphology and functional activity of macrophages so that they become avidly phagocytic. It is initiated by lymphokines, such as the macrophage activation factor (MAF) and the macrophage migration-inhibitory factor (MMIF), immune complexes, C3b, and various peptides, polysaccharides, and immunologic adjuvants. Activation, Macrophage,Activations, Macrophage,Macrophage Activations
D008807 Mice, Inbred BALB C An inbred strain of mouse that is widely used in IMMUNOLOGY studies and cancer research. BALB C Mice, Inbred,BALB C Mouse, Inbred,Inbred BALB C Mice,Inbred BALB C Mouse,Mice, BALB C,Mouse, BALB C,Mouse, Inbred BALB C,BALB C Mice,BALB C Mouse
D009000 Monocytes Large, phagocytic mononuclear leukocytes produced in the vertebrate BONE MARROW and released into the BLOOD; contain a large, oval or somewhat indented nucleus surrounded by voluminous cytoplasm and numerous organelles. Monocyte
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D000911 Antibodies, Monoclonal Antibodies produced by a single clone of cells. Monoclonal Antibodies,Monoclonal Antibody,Antibody, Monoclonal
D000918 Antibody Specificity The property of antibodies which enables them to react with some ANTIGENIC DETERMINANTS and not with others. Specificity is dependent on chemical composition, physical forces, and molecular structure at the binding site. Antibody Specificities,Specificities, Antibody,Specificity, Antibody
D000954 Antigens, Surface Antigens on surfaces of cells, including infectious or foreign cells or viruses. They are usually protein-containing groups on cell membranes or walls and may be isolated. Cell Surface Antigens,Surface Antigens,Surface Markers, Immunological,Cell Surface Antigen,Immunologic Surface Markers,Markers, Immunological Surface,Surface Antigen,Surface Markers, Immunologic,Antigen, Cell Surface,Antigen, Surface,Antigens, Cell Surface,Immunological Surface Markers,Markers, Immunologic Surface,Surface Antigen, Cell,Surface Antigens, Cell

Related Publications

V A Ewan, and W Cieplinski, and W W Hancock, and I Goldschneider, and A W Boyd, and F R Rickles
April 1981, Journal of immunology (Baltimore, Md. : 1950),
V A Ewan, and W Cieplinski, and W W Hancock, and I Goldschneider, and A W Boyd, and F R Rickles
April 1986, Journal of immunology (Baltimore, Md. : 1950),
V A Ewan, and W Cieplinski, and W W Hancock, and I Goldschneider, and A W Boyd, and F R Rickles
June 1985, Journal of immunology (Baltimore, Md. : 1950),
V A Ewan, and W Cieplinski, and W W Hancock, and I Goldschneider, and A W Boyd, and F R Rickles
January 1977, Haemostasis,
V A Ewan, and W Cieplinski, and W W Hancock, and I Goldschneider, and A W Boyd, and F R Rickles
April 1998, Cancer,
V A Ewan, and W Cieplinski, and W W Hancock, and I Goldschneider, and A W Boyd, and F R Rickles
October 2023, Protein expression and purification,
V A Ewan, and W Cieplinski, and W W Hancock, and I Goldschneider, and A W Boyd, and F R Rickles
May 1986, Investigative ophthalmology & visual science,
V A Ewan, and W Cieplinski, and W W Hancock, and I Goldschneider, and A W Boyd, and F R Rickles
June 2013, Journal of thrombosis and haemostasis : JTH,
V A Ewan, and W Cieplinski, and W W Hancock, and I Goldschneider, and A W Boyd, and F R Rickles
September 1988, Journal of leukocyte biology,
V A Ewan, and W Cieplinski, and W W Hancock, and I Goldschneider, and A W Boyd, and F R Rickles
August 2022, HLA,
Copied contents to your clipboard!