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Untitled - D Ank Unlimited

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elative risk (RR) 617 reptile immunity<br />

Relapsing polychondritis.<br />

etiology. Anticollagen antibodies may be demonstrated<br />

in the sera.<br />

relative risk (RR)<br />

Association of a particular disease with a certain HLA antigen.<br />

This represents the chance a person with the diseaseassociated<br />

HLA antigen has of developing the disease<br />

compared with that of a person who does not possess the<br />

antigen. Relative risk is calculated as follows:<br />

p × c<br />

RR =<br />

p × c<br />

+ -<br />

- +<br />

where<br />

p + = number of patients possessing a particular HLA antigen<br />

c – = number of controls not possessing the particular HLA<br />

antigen<br />

p – = number of patients not possessing the particular HLA<br />

antigen<br />

c + = number of controls possessing the particular HLA antigen<br />

The higher the relative risk (above 1), the greater the frequency<br />

of the antigen in the patient population.<br />

relative sibling risk<br />

A comparison of the occurrence of a disease among siblings<br />

with its occurrence in the general population.<br />

released antigen<br />

Antigen derived from trypanosomes during an infection<br />

that may appear in serum. It corresponds to the antigenic<br />

type of the trypanosome infecting the individual.<br />

Remicade ® (infliximab)<br />

A chimeric IgG 1k monoclonal antibody with an approximate<br />

molecular weight of 149,100 Da. It is composed of human<br />

constant and murine variable regions. Infliximab binds<br />

specifically to human tumor necrosis factor α (TNF-α) with<br />

an association constant of 10 10 M –1 . Infliximab is produced<br />

by a recombinant cell line cultured by continuous perfusion<br />

and is purified by a series of steps that includes measures to<br />

inactivate and remove viruses.<br />

remission<br />

Clinically undetectable disease following treatment.<br />

Remission of a hematopoietic neoplasm is defined as a complete<br />

clinical response at least 4 weeks following therapy.<br />

ReoPro ® (abciximab)<br />

The Fab fragment of the chimeric human murine monoclonal<br />

antibody 7E3. Abciximab binds to the glycoprotein<br />

(GP) IIb/IIIa (α IIbβ3) receptors of human platelets and<br />

inhibits platelet aggregation. It also binds to the vitronectin<br />

(α vβ3) receptors found on platelets and vessel wall endothelial<br />

and smooth muscle cells. The chimeric 7E3 antibody<br />

is produced by continuous perfusion in mammalian cell<br />

culture. The 47,615-Da Fab fragment is purified from cell<br />

culture supernatant by a series of steps involving specific<br />

viral inactivation and removal procedures, digestion with<br />

papain, and column chromatography.<br />

reovirus immunity<br />

Most humans acquire a reovirus-specific antibody response<br />

in infancy or early childhood. Reovirus induces strong<br />

humoral and cell-mediated immune responses. Reovirusspecific<br />

antibodies are directed mainly against the outer<br />

capsid protein σ1, yet serum antibodies to other viral proteins<br />

are also induced. Reovirus-specific antibodies to the<br />

σ1 hemagglutinin protein are mainly serotype-specific. By<br />

contrast, reovirus-specific monoclonal antibodies reactive<br />

against other external capsid proteins reveal serotype-nonspecific<br />

neutralizing or hemagglutinin-inhibiting properties.<br />

Reovirus-specific monoclonal antibodies can block<br />

attachment of the virus to host cells and inhibit internalization<br />

and intracellular proteolytic uncoating. Virus-specific<br />

cytotoxic T lymphocytes are also elicited in addition to T<br />

cell-mediated delayed-type hypersensitivity (DTH) reactions.<br />

The DTH response is serotype-specific, whereas<br />

CDLs are mainly serotype-nonspecific. These viruses may<br />

induce antigen-specific and -nonspecific immunosuppression.<br />

Reoviruses can induce specific T cell responses in<br />

systemic tissues. A virus-specific B cell response occurs<br />

in Peyer’s patches, and a cytotoxic T lymphocyte response<br />

occurs in Peyer’s patches. The ability of reovirus to enter<br />

Peyer’s patches via M cells indicates that these viruses<br />

might be used in a mucosal vaccine.<br />

repeating units<br />

Antigens in which macromolecular configurations are<br />

repeated, such as the repeating units of β-1,4-glucose-β-1,3glucuronic<br />

acid in type III pneumococcus polysaccharide.<br />

Polysaccharide antigens in the cell walls of Gram-negative<br />

bacteria also contain repeating structures. Antigens with<br />

such configurations are often thymus-independent.<br />

repertoire<br />

The total antigenic specificity library generated by B or T<br />

cells in response to a foreign antigen.<br />

replicative senescence<br />

Cell death at the conclusion of its predestined number of<br />

divisions.<br />

reptile immunity<br />

Environmental conditions affect the structures and functional<br />

activities of reptile organs including those of the<br />

immune system. The reptilian thymus is the first lymphoid<br />

organ to develop. It is a bilateral organ lying on both sides<br />

of the neck in lizards and anterior to the heart in snakes.<br />

It is frequently multilobed in turtles. The thymus is well<br />

developed in reptiles collected in nature under the correct<br />

R

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