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eosinophil cationic protein (ECP) 251 eotaxin<br />

(BALF) of selected patients with asthma. ECA induces<br />

early atopic dermatitis lesions and is induced by transepidermal<br />

permeation of mite allergen. Eosinophils also participate<br />

in renal and liver allograft rejection, as reflected by<br />

eosinophil cationic protein assays. Eosinophil major basic<br />

protein interacts with interleukin-1 (IL1) and transforming<br />

growth factor β (TGF-β) to upregulate lung fibroblasts<br />

to synthesize IL6 cytokine. When stimulated by C5a,<br />

eosinophils produce increased levels of H 2O 2, as assayed by<br />

chemiluminescence (CL). Eosinophil activation may also<br />

be assayed by flow cytometry. Defective adherence and the<br />

migration of neutrophils can be a cause of increased susceptibility<br />

to bacterial infection in neonates. The chemotactic<br />

cytokine, neutrophil-activating ENA-78 is a proinflammatory<br />

polypeptide that shares sequence similarity with IL8<br />

and GRO-α. ENA-78 is a powerful upregulator of MAC-1<br />

cell-surface expression. It is found in cystic fibrosis lung,<br />

and its mRNA levels are elevated in human pulmonary<br />

inflammation. Flow cytometry and nitroblue tetrazolium<br />

reduction can be used to access neutrophil activation.<br />

eosinophil cationic protein (ECP)<br />

An eosinophil, granule, basic, single-chain, zinc-containing<br />

protein that manifests cytotoxic, helminthotoxic, ribonuclease,<br />

and bactericidal properties. ECP, major basic protein<br />

(MBP), eosinophil-derived neurotoxin (EDN), and eosinophil<br />

peroxidase (EPO) are the four main eosinophil granule<br />

proteins. ECP and MBP induce the release of preformed<br />

histamine and synthesis of vasoactive and proinflammatory<br />

mediators (PGD 2) from activated human heart mast cells.<br />

Acute graft rejection and atopic dermatitis patients manifest<br />

provated ECP, whereas systemic sclerosis patients develop<br />

increased serum levels of MBP. MBP can act as a cell<br />

stimulant and as a toxin. ECP, EPO, EDN, and MBP are<br />

versatile in their biological activities that include the capacity<br />

to activate other cells including basophils, neutrophils,<br />

and platelets. Both enzyme immunoassay (EIA) and flow<br />

cytometry have been used to assay intracellular eosinophil<br />

proteins in eosinophils from bone marrow and peripheral<br />

blood.<br />

eosinophil chemotactic factor<br />

Mast cell granule peptides that induce eosinophil chemotaxis.<br />

These include two tetrapeptides: Val–Gly–Ser–Glu and Ala–<br />

Gly–Ser–Glu. Histamine also induces eosinophil chemotaxis.<br />

eosinophil differentiation factor (EDF)<br />

A 20-kDa cytokine synthesized by some activated CD4 +<br />

T lymphocytes and byb-activated mast cells. Formerly it<br />

was called T cell replacing factor or B cell growth factor<br />

II. It facilitates B cell growth and differentiation into cells<br />

that secrete immunoglobulin A (IgA). It is a costimulator<br />

with interleukin-2 (IL2) and IL4 of B cell growth and<br />

differentiation. IL5 also stimulates eosinophil growth and<br />

differentiation. It activates mature eosinophils to render<br />

them capable of killing helminths. Through IL5, T lymphocytes<br />

exert regulatory effects on inflammation mediated by<br />

eosinophils. Because of its action in promoting eosinophil<br />

differentiation, it has been called eosinophil differentiation<br />

factor (EDF). IL5 can facilitate B cell differentiation into<br />

plaque-forming cells of IgM and IgG classes. In parasitic<br />

diseases, IL5 leads to eosinophilia.<br />

eosinophil granule major basic protein (EGMBP)<br />

A polypeptide rich in arginine released from eosinophil<br />

granules. It is a powerful toxin for helminths and selected<br />

mammalian cells and plays a significant role in latephase<br />

reactions in allergy and asthma and in late-phase<br />

skin reactions to allergens such as dust mites. EGMBP<br />

is believed to be significant in endomyocardial injury<br />

inducted by cardiac localization of eosinophil granule<br />

proteins. Interleukin-3 (IL3), granulocyte–macrophage<br />

colony-stimulating factor (GM-CSF), and IL5 are<br />

eosinophilopoietic cytokines that activate eosinophils and<br />

facilitate their survival. These cytokines enhance eosinophil<br />

activation in the airways of patients with bronchial<br />

asthma which leads to epithelial injury. IFN-α inhibits<br />

the release of EGMBP in hypereosinophilic syndrome<br />

patients. Immunohistochemistry is used to measure<br />

EGMBP from eosinophils infiltrating skin lesions of<br />

atopic dermatitis.<br />

eosinophilia<br />

Elevated number of eosinophils in the blood. It occurs in<br />

immediate, type I hypersensitivity reactions, including<br />

anaphylaxis and atopy, and is observed in patients with<br />

parasitic infestations, especially by nematodes.<br />

eosinophilic granuloma<br />

A subtype of a macrophage lineage (histiocytosis X) tumor<br />

that contains eosinophils, especially in bone.<br />

eosinophilic myalgia syndrome (EMA)<br />

An intoxication syndrome observed in persons in the<br />

United States that appeared to be linked to the consumption<br />

of l-tryptophan, proposed by some health advocates as an<br />

effective treatment for various disorders such as insomnia,<br />

premenstrual syndrome, etc. It was associated with a<br />

strain of Bacillus amyloliquefaciens employed to produce<br />

tryptophan commercially. The inducing agent was apparently<br />

an altered amino acid, DTAA (ditryptophan aminal<br />

acetaldehyde), a contaminant introduced during manufacture.<br />

Clinical manifestations of the syndrome included<br />

arthralgia, myopathy, angioedema, alopecia, mobiliform<br />

rash, oral ulcers, sclerodermoid lesions, restricted lung<br />

disease, fever, lymphadenopathy, and dyspnea, among<br />

other features, accompanied by a significant eosinophilia.<br />

Interleukin-5 (IL5) was believed to have a role in injury to<br />

tissues. Histopathologic examination revealed arteriolitis<br />

and sclerosing skin lesions.<br />

eotaxin<br />

A β chemokine family (CC) purified from bronchoalveolar<br />

lavage fluid proteins. It has 53% homology with human<br />

monocyte chemoattractant protein-1 (MCP-1), 44% with<br />

guinea pig MCP-1, 31% with human MIP-1α, and 26%<br />

with human RANTES. It is induced locally following<br />

transplantation of interleukin-4 (IL4)-secreting tumor cells,<br />

suggesting that it may contribute to eosinophil recruitment<br />

and antitumor activity of IL4. It has a known human<br />

homolog. Eotaxin is expressed by mouse endothelial cells,<br />

alveolar macrophages, lung, intestine, stomach, heart,<br />

thymus, spleen, liver, testes, and kidney; the target cells<br />

are eosinophils. It is constitutively expressed in guinea pig<br />

lungs. Its level is increased within 30 minutes after challenge<br />

of sensitized guinea pigs with aerosolized antigen<br />

in association with eosinophil infiltration. Eotaxin protein<br />

can induce accumulation of eosinophils but not neutrophils<br />

following intradermal injection. Eotaxin protein administered<br />

to guinea pigs in aerosolized form induces eosinophil<br />

but not neutrophil accumulation in bronchalveolar fluid. It<br />

facilitates chemotaxin eosinophils.<br />

E

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