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Untitled - D Ank Unlimited

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cellular hypersensitivity 161 c-erb-B2 monoclonal antibody<br />

in women with silicone breast implants. Silicone hypersensitivity<br />

results in high levels of interleukin-1 (IL1) and IL1ra<br />

in the circulation. The silicone immune disease reaction is<br />

associated with the synthesis of autoantibodies to multiple<br />

endocrine organs and is compatible with an immune-mediated<br />

endocrinopathy. Nickel sulfate, potassium dichromate,<br />

cobalt chloride, palladium chloride, and gold sodium thiosulfate<br />

represent metal allergy in patients with symptoms<br />

resulting from dental restoration. Lead and cadmium can<br />

lead to suppression of cell-mediated immunity. Laboratory<br />

methods of assessment include enzyme immunoassay<br />

(EIA), memory lymphocyte immunostimulation assay<br />

(MELISA), and lymphocyte proliferation tests.<br />

cellular hypersensitivity<br />

Refer to delayed-type hypersensitivity, type IV cell-mediated<br />

hypersensitivity, and cell-mediated immunity.<br />

cellular immunity<br />

Refer to cell-mediated immunity.<br />

cellular immunology<br />

The study of cells involved in immune phenomena.<br />

cellular interstitial pneumonia<br />

Inflammation of the lung in which the alveolar walls are<br />

infiltrated by mononuclear cells.<br />

cellular oncogene<br />

Refer to protooncogene.<br />

CEM-15<br />

An RNA/DNA editing enzyme of the host that unites<br />

with HIV polyproteins and is incorporated into virions. It<br />

induces hypermutation of replicating HIV DNA, inhibiting<br />

incorporation into the host cell genome.<br />

centiMorgan (cM)<br />

A chromosomal unit of physical distance that corresponds<br />

to a 1% recombination frequency between two genes that<br />

are closely linked. Also termed a map unit.<br />

central lymphoid organs<br />

Lymphoid organs that are requisite for the development of<br />

the lymphoid and therefore of the immune system. These<br />

include the thymus, bone marrow, and bursa of Fabricius.<br />

Also termed primary lymphoid organs. Sites of lymphocyte<br />

development. Human T lymphocytes mature in the thymus,<br />

whereas B lymphocytes develop in the bone marrow.<br />

central MHC<br />

The location of the MHC’s class III region, between the<br />

class I and class II regions.<br />

central tolerance<br />

The mechanism involved in the functional inactivation of<br />

cells requisite for the initiation of an immune response.<br />

Central tolerance affects the afferent limb of the immune<br />

response, which is concerned with sensitization and cell<br />

proliferation. It is established in lymphocytes developing<br />

in central lymphoid organs and prevents the emergence of<br />

lymphocytes with high affinity receptors for self antigens<br />

present in bone marrow or thymus. Induced by negative<br />

selection in the thymus and bone marrow. Peripheral tolerance<br />

protects self cells from attack by autoreactive cells that<br />

evade central tolerance.<br />

centriole antibodies<br />

Antibodies sometimes detected in blood sera also containing<br />

antibodies against mitotic spindle apparatus (MSA). They are<br />

only rarely found in patients developing connective tissue disease<br />

of the scleroderma category. Selected centriole antibodies<br />

may be directed against the glycolytic enzyme enolase.<br />

centroblasts<br />

Large, rapidly dividing cells in germinal centers. These<br />

cells, in which somatic hypermutation is thought to take<br />

place, give rise to memory and antibody-secreting B cells.<br />

centrocyte<br />

Germinal center B cells that are small and nonproliferating.<br />

They are derived from centroblasts and mature into plasma<br />

cells that secrete antibody or memory B cells or may<br />

undergo apoptosis, depending on the interactions between<br />

their receptors and antigen. They undergo affinity maturation,<br />

isotype switching, and somatic hypermutation.<br />

centromere antibodies<br />

Antibodies specific for centromeres/kinetochores are<br />

detectable in 22% of systemic sclerosis patients, most of<br />

whom have CREST syndrome rather than diffuse scleroderma.<br />

Approximately 12% of primary biliary cirrhosis<br />

patients, half of whom also manifest scleroderma, have<br />

centromere antibodies.<br />

centromere antigen complex<br />

Consists of the antigenic proteins CENP-A (18 kDa),<br />

CENP-B (80 kDa), and CDNP-C (140 kDa).<br />

Centromere autoantibodies<br />

centromere autoantibodies<br />

Autoantibodies against centromeres (CENAs) occur in 22%<br />

of systemic sclerosis patients and in 12% of primary biliary<br />

cirrhosis (PBC) cases, half of whom develop scleroderma.<br />

Limited scleroderma known as CREST occurs in 4 to<br />

18% of primary biliary cirrhosis cases. CENA-positive<br />

patients with limited scleroderma are more likely to have<br />

calcinosis and telangiectasia and less often pulmonary<br />

interstitial fibrosis compared with CENA-negative patients<br />

with limited scleroderma. When patients with Raynaud’s<br />

syndrome become CENA-positive, they may be developing<br />

limited scleroderma. CENAs in patients with silicone breast<br />

implants lead to symptoms associated with connective tissue<br />

types of diseases. Antinuclear antibodies developed in<br />

58% (470/813) of patients studied; antibody levels and clinical<br />

symptoms diminished when the implants were removed.<br />

c-erb-B2 monoclonal antibody<br />

A murine monoclonal antibody against c-erb-B2 oncoprotein<br />

that is expressed by tumor cell membranes at a<br />

level detectable by immunohistochemistry in up to 20%<br />

of adenocarcinomas from various sites, including ovary,<br />

gastrointestinal tract, and breast. Immunohistochemical<br />

staining correlates with gene amplification. In the case of<br />

breast cancer, c-erb-B2 expression has been shown to be<br />

associated with poor prognosis. Between 15 and 30% of<br />

C

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