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adrenal autoantibody (AA) 23 AET rosette test (historical)<br />

Adrenal autoantibody.<br />

adrenal autoantibody (AA)<br />

Autoantibody found in two thirds of idiopathic (autoimmune)<br />

patients with Addison’s disease. Although once the<br />

most common cause of Addison’s disease, tuberculosis is<br />

now only infrequently associated with it. Adrenal autoantibodies<br />

react with the zona glomerulosa of the adrenal cortex.<br />

The autoantigens linked to this disease are cytochrome<br />

P-450 enzyme family members that participate in steroidogenesis<br />

in the adrenal and other steroid-producing organs.<br />

The enzyme autoantigens include P-450 steroid 21 hydroxylase<br />

(21 OH), P-450 side chain cleavage enzyme (P-450<br />

scc), and 17 α-hydroxylase (17-α-OH). Autoantibodies in<br />

adult patients with autoimmune Addison’s disease may<br />

be directed against cytochrome P-450 steroid 21 OH, the<br />

only adrenal-specific enzyme. Other autoantibodies such<br />

as those against P-450 scc present in the adrenals, gonads,<br />

and placenta, and 17-α-OH present in the adrenals and<br />

gonads are found in autoimmune polyglandular syndromes<br />

(APGSs). APGS type I autoimmune polyendocrinopathy–<br />

candidiasis–ectodermal dystrophy (APECED) begins in<br />

early childhood with mucocutaneous candidiasis followed<br />

by Addison’s disease and often gonadal failure in hypoparathyroidism.<br />

APS type II (Schmidt syndrome) is mostly an<br />

adult disease inherited in an autosomal-dominant manner<br />

and is marked by a variable combination of Addison’s<br />

disease, insulin-dependent type I diabetes mellitus (IDDM)<br />

and autoimmune thyroid disorders. It is likened to HLA-<br />

DR3. Steroid cell antibodies have been associated with<br />

autoimmune gonadal failure. They are present in 18% of<br />

patients with Addison’s disease, alone or in association with<br />

APGS. The most frequently encountered autoantigen in<br />

Addison’s disease is the adrenal cytochrome P-450 enzyme<br />

21 OH. Autoantibodies to 17-α-OH are found in 55% of<br />

APTS type I patients and in 33% of APGS type II patients.<br />

Autoantibodies against P-450 scc are found in 45% of<br />

APGS type I patients and 42% of APGS type II patients.<br />

adrenergic receptor agonists<br />

The β2-adrenergic receptor is expressed on Th1 but not on<br />

Th2 clones. An agonist for this receptor selectively suppresses<br />

IFN-γ synthesis in vitro; increases IL-4, IL-5, and IL-10<br />

synthesis in spleen cells from treated mice; and increases IgE<br />

levels in vivo. Epinephrine and norepinephrine inhibit IL-12<br />

synthesis but enhance IL-10 formation. β2-adrenergic receptor<br />

stimulation favors Th2 immune responses.<br />

adrenergic receptors<br />

Structures on the surfaces of various types of cells that are<br />

designated α or β and interact with adrenergic drugs.<br />

adrenocorticotrophic hormone (ACTH) antibody<br />

A polyclonal antibody preparation useful in immunoperoxidase<br />

procedures to stain corticotroph cells of the pituitary<br />

gland and benign and malignant tumors arising from these<br />

cells in formalin-fixed, paraffin-embedded tissue biopsies.<br />

adsorption<br />

The elimination of antibodies from a mixture by adding<br />

particulate antigen or the elimination of particulate antigen<br />

from a mixture by adding antibodies. The incubation of<br />

serum-containing antibodies such as agglutinins with red<br />

blood cells or other particles may allow their removal due to<br />

sticking to the particle surface.<br />

adsorption chromatography<br />

A method to separate molecules based on their adsorptive<br />

characteristics. Fluid is passed over a fixed solid stationary<br />

phase.<br />

adult respiratory distress syndrome (ARDS)<br />

Embarrassed respiratory function as a consequence of<br />

pulmonary edema caused by increased vascular permeability.<br />

adult T cell leukemia lymphoma (ATLL)<br />

A lymphoproliferative neoplasm of mature lymphocytes<br />

that progresses rapidly. It has been linked to the<br />

HTLV-1 retrovirus infection observed in Japan, Africa,<br />

the Caribbean, and southeastern United States. Patients<br />

develop hypercalcemia, progressive skin changes, enlarged<br />

hilar, retroperitoneal, and peripheral lymph nodes without<br />

mediastinal node enlargement. Involvement of the lungs,<br />

gastrointestinal tract, and central nervous system and<br />

opportunistic infections may also be observed. The condition<br />

occurs in five clinical forms.<br />

Cytokeratin cocktail⎯prostate.<br />

AE1/AE3 pan-cytokeratin monoclonal antibody<br />

An antibody that provides the broadest spectrum of keratin<br />

reactivity among the 19 catalogued human epidermal keratins<br />

and produces positive staining in virtually all epithelia.<br />

AET rosette test (historical)<br />

A technique used previously to enumerate human T cells<br />

based upon the formation of sheep red cell rosettes surrounding<br />

them. The use of sheep red cells treated with<br />

aminoethylthiouridium bromide renders the rosettes more<br />

stable than using sheep red cells untreated by this technique.<br />

The rosette test technique was replaced by the use of<br />

anti-CD2 monoclonal antibodies and flow cytometry.<br />

A

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