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Untitled - D Ank Unlimited

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pFc′ fragment 568 phagocyte<br />

Platelets and megakaryocytes represent the tissue source.<br />

Fibroblasts, platelets, adrenal microvascular pericytes, mast<br />

cells, basophils, and megakaryocytes are the target cells. PF4<br />

levels increase during cardiopulmonary bypass surgery, in arterial<br />

thrombosis, following surgery, in acute myocardial infarction,<br />

during acute infections, and during inflammation.<br />

pFc′ fragment<br />

A fragment of pepsin digestion of immunoglobulin G (IgG)<br />

or the Fc fragment that yields low molecular weight peptides<br />

and a pFc′ fragment that is still capable of binding to<br />

an Fc receptor on a macrophage or monocyte. It is a 27-kDa<br />

dimer without a covalent bond composed of two C H3<br />

domains, the carboxyl terminal 116-amino acid residues<br />

of each chain. Unlike the Fc′ fragment, it has the basic N<br />

terminal and C terminal peptides of this immunoglobulin<br />

domain.<br />

PFC (plaque-forming cell)<br />

An in vitro technique in which antibody-synthesizing cells<br />

derived from the spleen of an animal immunized with a<br />

specific antigen produce antibodies that lyse red blood cells<br />

coated with the corresponding antigen in the presence of<br />

complement in a gel medium. The reaction bears some<br />

resemblance to β hemolysis produced by streptococci on a<br />

blood agar plate. When examined microscopically, a single<br />

antibody-producing cell can be detected in the center of the<br />

plaque-forming unit.<br />

Richard Pfeiffer.<br />

Pfeiffer, Richard (1858–1945)<br />

Pfeiffer was a colleague of Robert Koch in Berlin. He observed<br />

that Vibrio cholerae organisms were lysed in the peritoneum<br />

of immunized guinea pigs and showed the same process in<br />

vitro. This became known as Pfeiffer’s phenomenon.<br />

Pfeiffer’s phenomenon<br />

The rapid lysis of Vibrio cholerae microorganisms injected<br />

into the peritoneal cavities of guinea pigs immunized<br />

against them. The microorganisms are first rendered nonmotile,<br />

followed by complement-induced lysis in the presence<br />

of antibody. Immune bacteriolysis in vivo involving<br />

Vibrio cholera became known as Pfeiffer’s phenomenon.<br />

PFU<br />

Abbreviation for plaque-forming unit. An assay of plaques that<br />

develop in hemolytic plaque assays and related techniques.<br />

PHA<br />

Abbreviation for phytohemagglutinin. PHA is principally<br />

a T lymphocyte mitogen, producing a greater stimulatory<br />

effect on CD4 + helper/inducer T lymphocytes than on CD8<br />

suppressor/cytotoxic T cells. It has a weaker mitogenic<br />

effect on B lymphocytes.<br />

phacoanaphylactic endophthalmitis<br />

Introduction of lens protein into the circulation following<br />

an acute injury of the eye involving the lens may result in<br />

chronic inflammation of the lens as a consequence of autoimmunity<br />

to lens protein.<br />

phacoanaphylaxis<br />

Hypersensitivity to lens protein of the eye following an<br />

injury that introduces lens protein, normally a sequestered<br />

antigen, into the circulation. The immune system does not<br />

recognize it as self and responds to it as it would any other<br />

foreign antigen.<br />

phage display<br />

A technique that permits expression of the humoral immune<br />

system in vitro by phage display technology and antibody<br />

engineering. Large libraries of antibody fragments are<br />

displayed on the surfaces of bacteriophage particles. Phages<br />

expressing desirable antibody specificity must be selected<br />

and expanded. Favorable mutations in the genes encoding<br />

a selected antibody specificity must be selected. Antibody<br />

fragments are selected from large libraries constructed from<br />

B cells or assembled in vitro from the genetic elements<br />

encoding antibodies. This technique is rapid and unaffected<br />

by the immunogenicity of the target antigen. Selection<br />

procedures permit the isolation of antibodies specific for<br />

membrane molecules and epitopes. Antibody fragments<br />

can be tailored to have the desired avidity, pharmacokinetic<br />

properties, and biological effector functions. Monoclonal<br />

antibodies prepared from phage display libraries formed<br />

from human V regions constitute a molecule especially<br />

amenable for immunotherapy in humans.<br />

phage antibody library<br />

Cloned antibody variable region gene sequences that may<br />

be expressed as Fab or svFv fusion proteins with bacteriophage<br />

coat proteins. They can be exhibited on phage<br />

surfaces. The phage particle contains the gene encoding a<br />

monoclonal recombinant antibody and can be selected from<br />

the library by binding of the phage to specific antigen.<br />

phage display library<br />

Antibody-like phage produced by cloning immunoglobulin<br />

V region genes and filamentous phage which results in<br />

their expressing antigen-binding domains on their surfaces.<br />

Antigen-binding phage can be replicated in bacteria and<br />

used like antibodies. This method can be employed to<br />

develop antibodies of any specificity.<br />

phage neutralization assay<br />

A laboratory test in which bacteriophage is combined<br />

with antibodies specific for it to diminish its capacity to<br />

infect a host bacterium. This neutralization of infectivity<br />

may be quantified by showing the decreased numbers of<br />

plaques produced when the phage that has been incubated<br />

with specific antibody is plated on appropriate bacteria.<br />

The technique is sensitive and can demonstrate even weak<br />

antibody activity.<br />

phagocyte<br />

A cell capable of phagocytosis, for example, mononuclear<br />

phagocytes and polymorphonuclear neutrophils that ingest

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