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Untitled - D Ank Unlimited

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sequential determinant 646 serology<br />

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H<br />

G F E D C B A<br />

Example of high resolution DRB1 typing using sequence-specific primer<br />

methodology. Molecular weight ladder of known base pairs for base pair<br />

sizing appears at far left.<br />

and the PCR reaction is initiated under stringent conditions,<br />

a perfectly matched primer pair results in an amplification<br />

product. A mismatch at the 3′ end primer pair will not<br />

provide any amplification product. A positive result (amplification)<br />

defines the specificity of the DNA sample. The PCR<br />

amplification step provides the basis for identifying polymorphism.<br />

The post-amplification processing of the sample<br />

consists only of a simple agarose gel electrophoresis to detect<br />

the presence or absence of amplified product. DNA-amplified<br />

fragments are visualized by ethidium bromide staining and<br />

exposure to ultraviolet light. A separate technique detects<br />

amplified product by color fluorescence. The primer pairs<br />

are selected in such a manner that each allele should have<br />

a unique reactivity pattern with the panel of primer pairs<br />

employed. Appropriate controls must be maintained.<br />

sequential determinant<br />

An epitope whose specificity is determined by the sequence<br />

of several residues within the antigenic determinant rather<br />

than by the molecular configuration of the antigen molecule.<br />

A peptide segment of approximately six amino acid<br />

residues represents the sequential determinant structure.<br />

sequestered antigen<br />

An antigen that is anatomically isolated and not in contact<br />

with the immunocompetent T and B lymphoid cells of the<br />

immune system. Examples include myelin basic protein, sperm<br />

antigens, and lens protein antigens. When a sequestered antigen<br />

is released by one or several mechanisms including viral<br />

inflammation, it can activate immunocompetent T and B cells.<br />

An example of the sequestered antigen release mechanism of<br />

autoimmunity is found in experimental and post-infectious<br />

encephalomyelitis. Cell-mediated injury represents the<br />

principal mechanism in this disease. In vasectomized males,<br />

Host cell<br />

Antigen<br />

processed,<br />

Presented<br />

to T cell<br />

T<br />

Normally sequestered antigen<br />

Cell-mediated<br />

autoimmunity<br />

Signal<br />

Autoantibody to sequestered antigen<br />

Release of sequestered antigen.<br />

antisperm antibodies are known to develop when sperm antigens<br />

become exposed to immunocompetent lymphoid cells.<br />

Likewise, lens protein of the eye that enters the circulation<br />

as a consequence of crushing injury to the eye or exposure of<br />

lens protein to immunocompetent cells inadvertently through<br />

surgical manipulation may lead to an antilens protein immune<br />

response. Autoimmunity induced by sequestered antigens is<br />

relatively infrequent and a rare cause of autoimmune disease.<br />

serial dilution<br />

The successive dilution of antiserum in a row of serological<br />

tubes containing physiologic saline solution as diluent to<br />

yield the greatest concentration of antibody in the first tube<br />

and the lowest in the last tube that contains the highest dilution.<br />

For example, a double quantity of antiserum is placed<br />

in the first tube, half of which is transferred to the second<br />

tube containing an equal volume of diluent. After thorough<br />

mixing with a serological pipette, an equivalent amount is<br />

transferred to the next tube. The process continues and the<br />

volume removed from the last tube in the row is discarded.<br />

This represents a doubling dilution.<br />

serial passage<br />

A method to attenuate a pathogenic microorganism but<br />

retain its immunogenicity by transfer through several animal<br />

hosts, growth media, or tissue culture cells.<br />

serial TC triggering model<br />

A design dependent on the hypothesis that relatively few<br />

pMHC complexes can interact successively with enough T<br />

cell receptors to yield the sustained signaling requisite for<br />

naïve T cell total activation.<br />

seroconversion<br />

The first appearance of specific antibodies against a causative<br />

agent in the blood during the course of an infection or<br />

following immunization.<br />

serological determinants<br />

Epitopes on cells that react with specific antibody and<br />

complement, leading to fatal injuries of cells. Serological<br />

determinants are to be distinguished from lymphocyte<br />

determinants that are epitopes on cell surfaces to which sensitized<br />

lymphocytes are directed, leading to cell destruction.<br />

Although the end result is the same, antibodies and lymphocytes<br />

are directed to different epitopes on cell surfaces.<br />

serological epitope<br />

An antigenic determinant reactive with a specific antibody<br />

or group of antibodies.<br />

serologically defined (SD) antigens<br />

Mammalian cellular membrane epitopes encoded by<br />

major histocompatibility complex genes. Antibodies<br />

detect these epitopes.<br />

serology<br />

The study of the in vitro reactions of antibodies in serum<br />

with antigens (usually those of microorganisms inducing<br />

infectious disease).<br />

B

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