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Untitled - D Ank Unlimited

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anti-endothelial cell autoantibody 51 antigen-binding cell (ABC) assays<br />

disease. A rim or peripheral pattern of nuclear staining of<br />

cells interacting with antinuclear antibody represents morphologic<br />

expression of anti-double-stranded DNA antibody.<br />

anti-endothelial cell autoantibody<br />

An antibody that may cause vasculitis as part of an autoimmune<br />

response.<br />

anti-epithelial membrane antigen (EMA) antibody<br />

A mouse monoclonal antibody directed against a mucin<br />

epitope present on most human epithelial cells. This antibody<br />

reacts with epithelial mucin, a heavily glycosylated molecule<br />

with a molecular weight of about 400 kDa. Epithelial membrane<br />

antigen is widely distributed in epithelial tissues and<br />

tumors arising from them. Normal glandular epithelium and<br />

tissue from non-neoplastic diseases stain in lumen membranes<br />

and cytoplasm. Malignant neoplasms of glandular epithelium<br />

frequently show a change in pattern with the appearance of<br />

adjacent cell membrane staining. EMA is of value in distinguishing<br />

both large cell anaplastic carcinoma from diffuse<br />

histiocytic lymphoma and small cell anaplastic carcinoma<br />

from well and poorly differentiated lymphocytic lymphomas.<br />

anti-estrogen receptor antibodies<br />

A mouse monoclonal antibody specific for estrogen receptors<br />

(ERs). The ER content of breast cancer tissue is an<br />

important parameter in the prediction of prognosis and<br />

response to endocrine therapy. Monoclonal antibodies to<br />

ER allow determination of the receptor status of breast<br />

tumors in routine histopathology laboratories. Although<br />

monoclonal antibodies that recognize ER were effective<br />

initially only on frozen sections, currently available<br />

monoclonal antibodies are effective on formalin-fixed,<br />

paraffin-embedded tissues for determining ER in routinely<br />

processed and archival material.<br />

anti-Ewing’s sarcoma marker<br />

A mouse monoclonal anti-human MIC2 gene product<br />

(Ewing’s sarcoma marker) antibody reacts only with glioblastoma<br />

and ependymoma of the central nervous system<br />

and certain islet cell tumors of the pancreas. Because the<br />

MIC2 gene products are most strongly expressed on the cell<br />

membranes of Ewing’s sarcoma (ES) and primitive peripheral<br />

neuroectodermal tumors (pPNET), demonstration of the<br />

gene products allows for the differentiation of these tumors<br />

from other round cell tumors of childhood and adolescence.<br />

anti-factor VIII antibody<br />

A mouse monoclonal antibody that gives positive staining in<br />

the cytoplasm of normal vascular endothelial cells of arteries,<br />

veins, capillaries, and endocardial cells. Factor-VIII-related<br />

antigen is also present in megakaryocytes and platelets.<br />

Antifibrillarin antibodies.<br />

antifibrillarin antibodies<br />

Antibodies to this 34-kDa protein constituent of U3 ribonucleoproteins<br />

(RNPs) are detectable in the sera of about<br />

8% of patients with diffuse and limited scleroderma. Also<br />

called anti-U3-RNP antibodies.<br />

antigen<br />

A substance that reacts with the products of an immune<br />

response stimulated by a specific immunogen, including<br />

both antibodies and/or T lymphocyte receptors. Currently<br />

considered to be one of many kinds of substances with<br />

which an antibody molecule or T cell receptor may bind.<br />

These include sugars, lipids, intermediary metabolites,<br />

autocoids, hormones, complex carbohydrates, phospholipids,<br />

nucleic acids, and proteins. By contrast, the “traditional”<br />

definition of antigen is a substance that may<br />

stimulate B and/or T cell limbs of the immune response and<br />

react with the products of that response, including immunoglobulin<br />

antibodies and/or specific receptors on T cells.<br />

See immunogen definition. The “traditional” definition of<br />

antigen more correctly refers to an immunogen. A complete<br />

antigen is one that induces an immune response and<br />

also reacts with the products of the response, whereas an<br />

incomplete antigen or hapten is unable to induce an immune<br />

response alone but is able to react with the products (e.g.,<br />

antibodies). Haptens may be rendered immunogenic by<br />

covalently linking them to a carrier molecule. Following<br />

the administration of an antigen (immunogen) to a host<br />

animal, antibody synthesis and/or cell-mediated immunity<br />

or immunologic tolerance may result. To be immunogenic,<br />

a substance usually needs to be foreign, although some<br />

autoantigens represent exceptions. An immunogen should<br />

usually have a molecular weight of at least 1000 and should<br />

be either a protein or a polysaccharide. Nevertheless, immunogenicity<br />

depends also upon the genetic capacity of the<br />

host to respond to, rather than merely upon, the antigenic<br />

properties of an injected immunogen. The term also alludes<br />

to any molecule capable of producing peptides that unite<br />

specifically with T cell receptors. Refer also to epitope.<br />

antigen–antibody complex<br />

The union of antibody with soluble antigen in solution containing<br />

electrolyte. When the interaction takes place in vitro,<br />

it is called the precipitin reaction, but it may also take place<br />

in vivo. The relative proportion in which antigen and antibody<br />

combine varies according to their molar ratio. Excess antigen<br />

may lead to soluble complexes, whereas excess antibody may<br />

lead to insoluble complexes. In vivo, soluble complexes are<br />

more likely to produce tissue injury, whereas larger insoluble<br />

complexes are often removed by reticuloendothelial system<br />

cells. Also called immune complex.<br />

antigen-binding capacity<br />

Assay of the total capacity of antibody of all immunoglobulin<br />

classes to bind antigen. This refers to primary<br />

as opposed to secondary or tertiary manifestations of<br />

the antigen–antibody interaction. Equilibrium dialysis<br />

measures the antigen-binding capacity of antibodies<br />

with the homologous hapten, and the Farr test measures<br />

primary binding of protein antigens with the homologous<br />

antibody.<br />

antigen-binding cell (ABC) assays<br />

The principle of this assay is the binding of cells bearing<br />

receptors for antigen to a gelatin dish in which antigen is<br />

incorporated. After incubation for a specified time and<br />

A

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