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Untitled - D Ank Unlimited

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plaque-forming cells 575 plasma cells<br />

antibody on their surface will be lysed. Circular areas of<br />

hemolysis appear in the gel medium. If viewed under a<br />

microscope, a single antibody-forming cell can be identified<br />

in the center of the lytic area. This assay has several modifications<br />

since antibodies other than IgM may fix complement<br />

less efficiently. In order to enhance the effects, an antiglobulin<br />

antibody called developing antiserum is added to the<br />

mixture. The latter technique is called indirect PFC assay.<br />

plaque-forming cells<br />

The antibody-producing cells in the centers of areas of hemolysis<br />

observed microscopically during a hemolytic plaque<br />

assay. The antibodies they form are specific for red blood<br />

cells suspended in the gel medium surrounding them. Once<br />

complement is added, the antibody-coated erythrocytes lyse,<br />

producing clear areas of hemolysis surrounding the antibodyforming<br />

cells. The antibody produced may be specific both<br />

for red blood cell surface antigens and also for soluble antigens<br />

deliberately coated on their surfaces for assay purposes.<br />

plaque technique<br />

Refer to hemolytic plaque assay and phage neutralization assay.<br />

plasma<br />

A transparent yellow material that constitutes 50 to 55%<br />

of blood volume. It is 92% fluid and 7% protein. Inorganic<br />

salts, hormones, sugars, lipids, and gases comprise the<br />

remaining 1%. Plasma from which fibrinogen and clotting<br />

factors have been removed is known as serum.<br />

plasmablast<br />

An immature cell of the plasma cell lineage that reveals distinctive,<br />

clumped nuclear chromatin, developing endoplasmic<br />

reticulum, and a Golgi apparatus; a B lymphocyte in a<br />

lymph node that is beginning to reveal plasma cell features.<br />

Manifests increased rough endoplasmic reticulum, Golgi<br />

apparatus, and ribosomes.<br />

plasma cell antigen<br />

A murine plasmacyte membrane alloantigen. It may be<br />

designated PC-1 or PC-2.<br />

plasma cell dyscrasias<br />

Lymphoproliferative disorders in which monoclonal plasma<br />

cell proliferation leads to such conditions as multiple<br />

myeloma or to the less ominous extramedullary plasmacytoma.<br />

A diverse assemblage of neoplastic diseases characterized<br />

by proliferation of a single cell clone producing<br />

an M component, a monoclonal immunoglobulin, or<br />

immunoglobulin fragment. The cells often have plasma cell<br />

morphology but may resemble lymphocytic or lymphoplasmacytic<br />

cells.<br />

plasma cell leukemia<br />

A malignancy associated with plasma cells in the circulating<br />

blood that constitute greater than 20% of the leukocytes.<br />

The absolute plasma cell number is more than 2000<br />

per cubic millimeter of blood. Advanced cases reveal<br />

extensive infiltration of the tissue with plasma cells and<br />

replacement of the marrow. Reactive plasmacytosis must be<br />

considered in the diagnosis.<br />

plasma cells<br />

Terminally differentiated antibody-producing B cells that fail<br />

to express MHC class II or mIg and are incapable of receiving<br />

further T cell help. Immunoglobulins are present<br />

in their cytoplasm, and secretion of immunoglobulin by<br />

plasma cells has been directly demonstrated in vitro. Increased<br />

levels of immunoglobulins in some pathologic conditions<br />

are associated with increased numbers of plasma cells and<br />

14–20 µm.<br />

Diagram of a plasma cell.<br />

Plasma cell in peripheral blood.<br />

Plasma cell in peripheral blood.<br />

Plasma cells in peripheral blood smear.<br />

conversely their number at antibody-producing sites increases<br />

following immunization. Plasma cells develop from B cells<br />

and are large, spherical, or ellipsoidal cells, 10 to 20 μm in<br />

P

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