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Untitled - D Ank Unlimited

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elephantiasis 245 ENA antibodies<br />

Staphylococcal<br />

Antitoxin<br />

Plasma-agar plate showing<br />

staphylocoagulase effect<br />

inhibited by commercial antitoxin<br />

Elek plate.<br />

to a streak of the microorganisms on the agar plate. Toxin<br />

formation by the growing microbes interacts with antitoxin in<br />

the filter paper to form a line of precipitation.<br />

elephantiasis<br />

Enlargement of extremities by lymphedema caused by lymphatic<br />

obstruction during granulomatous reactivity in filariasis.<br />

elevated IgE, defective chemotaxis, recurrent<br />

infection, and eczema<br />

Individuals with the third disorder may manifest several<br />

bacterial infections, eczema, abscesses, and pneumonia<br />

associated with group A β hemolytic streptococci and<br />

Staphylococcus aureus. They demonstrate normal functions<br />

of both B and T cell limbs of the immune response,<br />

although their IgE levels are strikingly elevated, reaching<br />

values that are tenfold those of normal individuals. Only<br />

chemotactic function is defective, with other parameters of<br />

phagocytic cell function within normal limits. No treatment<br />

other than antibiotic therapy is available.<br />

elicitation<br />

An overactive, abnormal, secondary response to a sensitizing<br />

agent that leads to inflammatory tissue injury. Also<br />

referred to as an effector stage. Refer to hypersensitivity<br />

and types I through IV hypersensitivities.<br />

ELISA (enzyme-linked immunosorbent assay)<br />

Refer to enzyme-linked immunosorbent assay.<br />

ELISPOT assay<br />

A modification of the enzyme-linked immunosorbent assay<br />

(ELISA) that involves the capture of products secreted from<br />

cells placed in contact with antigen or antibody fixed to a<br />

plastic surface. An enzyme-linked antibody is then used<br />

to identify the captured products by cleaving a colorless<br />

substrate to yield a colored spot.<br />

eluate<br />

In immunology, a substance such as an antibody obtained<br />

by physical or chemical treatment of an antigen–antibody<br />

complex. By allowing particulate antigens such as erythrocytes<br />

to interact with antibody followed by heating the<br />

antibody particle or cell complex to 56°C, the antibody can<br />

be dissociated from the particulate antigen and is present in<br />

the eluate.<br />

embryonic antigens<br />

Protein or carbohydrate antigens synthesized during<br />

embryonic and fetal life that are either absent or formed in<br />

only minute quantities in normal adult subjects. Aberrant<br />

expression by a tumor cell can render it a tumor-associated<br />

antigen. α-Fetoproteins (AFPs) and carcinoembryonic antigens<br />

(CEAs) are fetal antigens that may be synthesized once<br />

again in large amounts in individuals with certain tumors.<br />

Their detection and level during the course of the disease<br />

and following surgery to remove a tumor, reducing the substance,<br />

may serve as a diagnostic and prognostic indicator<br />

of the disease process. Blood group antigens, such as iI, that<br />

are reversed in their levels of expression in the fetus and in<br />

the adult may show a re-emergence of i antigen in adults<br />

with thalassemia and hypoplastic anemia. Cold autoagglutinins<br />

specific for i may be found in infectious mononucleosis<br />

patients. Common acute lymphoblastic leukemia<br />

antigen (CD10) is rarely found on peripheral blood cells of<br />

normal subjects, whereas CALLA + cells coexpressing IgM<br />

and CD19 molecules may be found in fetal bone marrow<br />

and peripheral blood samples. CD10 may be expressed in<br />

children with common acute lymphoblastic leukemia.<br />

embryonic stem (ES) cells<br />

Murine embryonic cells that are immortal in culture and<br />

retain the capacity to give rise to all cell lineages. They may<br />

be altered genetically in vitro and introduced into mouse<br />

blastocysts to give rise to mutant murine lines. Genes may be<br />

deleted in ES cells by homologous recombination to produce<br />

mutant ES cells that can give rise to gene knockout mice.<br />

emerging infectious disease<br />

An infection potentially capable of impacting the world population<br />

because it is induced by a pathogenic microorganism<br />

that has recently emerged or is undergoing alteration.<br />

EMF-1<br />

Embryo fibroblast protein-1 is a chemokine of the α (CXC)<br />

family. It has been found in chicken fibroblasts and mononuclear<br />

cells, yet no human or murine homolog is known.<br />

Cultured chick embryo fibroblasts (CEFs) abundantly<br />

express the avian gene 9E3/CEF-4. The EMF-1 gene was<br />

isolated from RSV-transformed CEFs identified by differential<br />

screening of a cDNA library. EMF-1 is characterized<br />

as a chemokine because its sequence resembles that of<br />

CTAP-III and PF4. RSV-infected cells represent the tissue<br />

source. Fibroblasts in mononuclear cells are the target cells.<br />

Expression of EMF-1 together with high collagen levels and<br />

its presence in wounded tissues suggest that it has a role in<br />

wound response and/or repair. EMF-1 is chemotactic for<br />

chicken peripheral blood mononuclear cells.<br />

EMIT<br />

Acronym for enzyme-multiplied immunoassay technique.<br />

emperipolesis<br />

The intrusion or penetration of a lymphocyte into the<br />

cytoplasm of another cell followed by passage through the<br />

cell. Emperipolesis also describes the movement of one cell<br />

within the cytoplasm of another cell.<br />

ENA-78 (epithelial-derived neutrophil attractant-78)<br />

A chemokine of the α family (CXC family). ENA-78 is<br />

related to NAP-2, GRO-α, and IL-8. Tissue sources include<br />

epithelial cells and platelets. Neutrophils are the target<br />

cells. ENA-78 is increased in peripheral blood, synovial<br />

fluid, and synovial tissue from rheumatoid arthritis patients.<br />

ENA-78 mRNA levels are elevated in acutely rejecting<br />

human renal allografts compared with renal allografts that<br />

are not being rejected.<br />

ENA antibodies<br />

Antibodies against extractable nuclear antigens. This<br />

category includes antibodies to ribonucleoprotein (RNP),<br />

E

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