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Untitled - D Ank Unlimited

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anti-Clq antibody 50 anti-double-stranded DNA (anti-dsDNA)<br />

antibodies. The antibodies do not affect survival and pulmonary<br />

hypertension in patients with limited scleroderma;<br />

however, survival is much longer in anticentromere-positive<br />

patients with limited scleroderma than in anti-Scl-<br />

70-positive diffuse scleroderma patients.<br />

anti-Clq antibody<br />

Present in the majority of patients with hypocomplementemic<br />

urticarial vasculitis syndrome (HUVS) and in 30 to<br />

60% of systemic lupus erythematosus (SLE) patients. Clq<br />

is strikingly decreased in the blood sera of HUVS patients,<br />

even though their Clr and Cls levels are within normal<br />

limits and C5 to C9 are slightly activated.<br />

Cytomegalovirus (CMV)⎯placenta.<br />

anticomplementary<br />

The action of any agent or treatment that interferes with complement<br />

fixation through removal or inactivation of complement<br />

components or cascade reactants. Multiple substances<br />

may exhibit anticomplementary activity. These are especially<br />

significant in complement fixation serology, as anticomplementary<br />

agents may impair the evaluation of test results.<br />

anticytomegalovirus (CMV) antibody<br />

A mouse monoclonal antibody that reacts with CMVinfected<br />

cells giving a nuclear staining pattern with early<br />

antigen and a nuclear and cytoplasmic reaction with the late<br />

viral antigen. The antibody shows no crossreactivity with<br />

other herpesviruses or adenoviruses.<br />

anticytoplasmic antibody<br />

Antineutrophil cytoplasmic antibody occurring in 84 to 100%<br />

of active generalized Wegener’s granulomatosis patients. This<br />

antibody is assayed by flow cytometry and indirect fluorescence<br />

microscopy. HIV-1 infected patients may be biologically<br />

false-positive for neutrophil cytoplasmic antibody.<br />

anti-D antibody<br />

Antibody against the Rh blood group D antigen. This<br />

antibody is stimulated in the RhD – mother by fetal RhD +<br />

red blood cells that enter her circulation at parturition.<br />

Anti-D antibodies become a problem usually with the third<br />

pregnancy, resulting from the booster immune response<br />

against the D antigen to which the mother was previously<br />

exposed. IgG antibodies pass across the placenta, leading to<br />

hemolytic disease of the newborn (erythroblastosis fetalis).<br />

Anti-D antibody (Rhogam ® ) administered up to 72 hours<br />

following parturition may combine with the RhD + red blood<br />

cells in the mother’s circulation, thereby facilitating their<br />

removal by the reticuloendothelial system. This prevents<br />

maternal immunization against the RhD antigen.<br />

Rh D<br />

antigen<br />

Anti-D, IgG<br />

antibodies<br />

+ Complement<br />

“D” red blood cell<br />

RBC<br />

Lysis<br />

Complement-mediated lysis of RhD antigen-positive red blood cells<br />

through doublets of anti-D, IgG antibodies on the red cell surface.<br />

antidesmin antibody<br />

A mouse monoclonal antibody (clone DE-R-11) raised<br />

against purified porcine desmin that reacts with the<br />

53-kDa intermediate filament desmin protein. This<br />

reagent may be used to aid in the identification of cells of<br />

myocyte lineage. The antibody is intended for qualitative<br />

staining in sections of formalin-fixed, paraffin-embedded<br />

tissue. Antidesmin primary antibody specifically binds to<br />

antigens located in the cytoplasm of myocytic cells. The<br />

clinical interpretation of any staining or its absence must<br />

be complemented by morphological studies and evaluation<br />

of proper controls.<br />

anti-DEX antibodies<br />

Murine α1–3 dextran specific antibodies.<br />

Anti-dsDNA (rim pattern).<br />

Anti-dsDNA.<br />

anti-double-stranded DNA (anti-dsDNA)<br />

Antibodies present in the blood sera of systemic lupus erythemastosus<br />

(SLE) patients. Among the detection methods<br />

is an immunofluorescence (IFT) technique using Crithidia<br />

luciliae as the substrate. Fluorescence of the kinetoplast<br />

containing mitochondrial DNA signals the presence of<br />

anti-dsDNA antibodies. This technique is useful for assaying<br />

SLE serum, which is usually positive in patients with active

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