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Untitled - D Ank Unlimited

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escue graft 618 resting lymphocytes<br />

Reptile immunity.<br />

seasonal temperature and other environmental conditions;<br />

otherwise, it may reveal degrees of degeneration. The<br />

spleen is the most significant peripheral lymphoid organ<br />

in reptiles. It becomes lymphopoietic much later than the<br />

thymus in lizards, snakes, and tortoises; 50 to 70% of reptile<br />

splenic lymphocytes are thymus-derived and located in<br />

thymus-dependent areas. Reptiles do not develop germinal<br />

centers and nodules found in mammalian secondary lymphoid<br />

organs. T and B cell-like cells differ in their sensitivity<br />

to environmental conditions. Gut-associated lymphoid<br />

tissue (GALT) develops in lizards, snakes, and chelonians.<br />

Reptiles do not have tonsils, Peyer’s patches, or appendices;<br />

they have numerous lymphoid aggregates in the mucosa<br />

and submucosa along the gut. In lizards, the esophageal<br />

lymphoid aggregates containing T cell-like lymphocytes<br />

are greatly affected by seasonal and environmental conditions,<br />

whereas the B cell-like cells and GALT in reptiles<br />

are resistant to changes in season. The spleen and GALT<br />

carry out humoral immune mechanisms. Although reptiles<br />

do not have true lymph nodes, their lymphoid systems are<br />

homologous to those of mammals except for high sensitivity<br />

to ambient conditions. Reptile lymphocytes are strongly<br />

responsive to plant mitogens. Lizards and snakes reject skin<br />

grafts in a manner similar to mammals. Reptiles also manifest<br />

major functional markers of the major histocompatibility<br />

complex (MHC). They produce at least two classes<br />

of immunoglobulin (Ig) that resemble IgM and a second<br />

immunoglobulin of lower molecular weight that is antigenically<br />

related to the 7S Ig of birds and amphibians. All<br />

reptiles can mount powerful immune responses to various<br />

antigens that include bacteria, protozoa, erythrocytes, and<br />

proteins. Body temperature is a critical regulator of immune<br />

function. Reptiles, in contrast to fish and amphibians, are<br />

restricted in the temperature range over which immune<br />

responses can occur.<br />

rescue graft<br />

A replacement graft for an original graft that failed.<br />

reservoir<br />

A host or carrier that harbors pathogenic microorganisms<br />

without being injured itself; it serves as a source of infection<br />

for others. Also termed reservoir host or reservoir of infection.<br />

resident macrophage<br />

A macrophage normally present at a tissue location without<br />

being induced to migrate there.<br />

respiratory burst<br />

A process used by neutrophils and monocytes to kill certain<br />

pathogenic microorganisms. It involves increased oxygen<br />

consumption with the generation of hydrogen peroxide<br />

and superoxide anions. This occurs also in macrophages<br />

that kill tumor cells. Respiratory burst is characterized<br />

by an abrupt elevation in oxygen consumption, followed<br />

by metabolic events in neutrophils and mononuclear cells<br />

preceding bacteriolysis. Partial reduction of oxygen by this<br />

process provides microbicidal oxidants. The initial event<br />

is a one-electron reduction of oxygen by membrane-bound<br />

oxidase to form a superoxide. The hexose monophosphate<br />

shunt reaction that accompanies this reduction liberates an<br />

H + that unites with the oxygen to produce H 2O 2. Following<br />

neutrophil degranulation, NADPH-dependent oxidases<br />

fixed to granule membranes activate the formation of inorganic<br />

radicals and myeloperoxidase action, leading to the<br />

generation of hypochlorous acid, causing the oxidation of<br />

nucleic acids, amino acids, and thiols of the microbe. The<br />

respiratory burst is reflected in the increased use of oxygen<br />

by NADPH oxidases to maintain this antimicrobial activity.<br />

respiratory disease viruses<br />

Influenza, paramyxoviruses, rhinoviruses, pneumoviruses,<br />

enteroviruses, coronaviruses, and mastadenoviruses that<br />

induce infections of the respiratory tract in humans.<br />

respiratory syncytial virus (RSV)<br />

A frequent cause of severe chest infections in young children<br />

who develop wheezing; a paramyxovirus.<br />

respiratory syncytial virus (RSV) immunity<br />

RSV is responsible for 70% of bronchiolitis cases, a common<br />

cause of infant hospitalization. Immunoglobulin G<br />

(IgG), IgM, and IgA antibodies are formed and can be<br />

detected by enzyme immunoassay (EIA). Some heterologous<br />

antibody responses occur in primary and recurrent<br />

infections with groups A and B RSV. Diagnosis of acute<br />

RSV infection is made by antigen detection in nasopharyngeal<br />

secretions by fluorescent antibody or EIA methods.<br />

responder animals<br />

Guinea pigs immunized by DNP–PLL or DNP–GL produce<br />

significant amounts of anti-DNP antibodies and develop<br />

delayed-type hypersensitivity reactions to the conjugate.<br />

Conversely, nonresponder animals produce few or no anti-<br />

DNP antibodies and do not develop delayed-type hypersensitivity.<br />

The capacity to respond to DNP–PLL antigen is<br />

a function of a dominant autosomal gene. All guinea pigs<br />

of strain 13 are nonresponders, whereas strain 2 guinea<br />

pigs and (2 × 13) F 1 hybrids are responders. The immune<br />

response gene present in strain 2 but absent in strain 13 is<br />

called the PLL gene.<br />

resting lymphocytes<br />

Under light microscopy, resting lymphocytes appear as a<br />

distinct and homogeneous population of round cells, each<br />

with a large spherical or slightly kidney-shaped nucleus that<br />

occupies most of the cell and is surrounded by a narrow<br />

rim of basophilic cytoplasm with occasional vacuoles. The

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