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Untitled - D Ank Unlimited

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synthetic polypeptide antigens 675 systemic inflammatory response syndrome (SIRS)<br />

Arthritis<br />

Fever<br />

Butterfly rash<br />

Pleurisy<br />

Pericarditis<br />

Systemic lupus erythematosus (SLE).<br />

Glomerulonephritis<br />

Lymphadenopathy<br />

size is less critical with synthetic antigens than with natural<br />

antigens. Thus, molecules as small as those of p-azobenzenearsonate<br />

coupled to three L-lysine residues (750 kDa<br />

molecular weight) or even of p-azobenzenearsonate-Nacetyl-L-tyrosine<br />

(451 kDa) may be immunogenic. Specific<br />

antibodies are markedly stereospecific, and no cross reaction<br />

occurs (e.g., between poly-D-alanyl and poly-L-alanyl<br />

determinants). Studies employing synthetic antigens demonstrated<br />

the significance of aromatic charged amino acid<br />

residues in proving the ability of synthetic polypeptides to<br />

induce immune responses.<br />

synthetic polypeptide antigens<br />

Antigens having a backbone consisting of amino acids that<br />

usually include lysine. Side chains of different amino acids<br />

are attached directly to the backbone and then elongated<br />

with a homopolymer or attached via the homopolymer.<br />

They have contributed much to our knowledge of epitope<br />

structure and function. They have well defined specificities<br />

determined by the arrangement, number, and nature of the<br />

amino acid components. They may be made more complex<br />

by further coupling to haptens or derivatized with various<br />

compounds. The size of the molecule is less critical with<br />

synthetic antigens than with natural antigens. Molecules as<br />

small as p-azobenzenearsonate coupled to three L-lysine<br />

residues (750 molecular weight) or p-azobenzenearsonate-<br />

N-acetyl-L-tyrosine (451 M.W.) may be immunogenic.<br />

Specific antibodies are markedly stereospecific, and no<br />

cross reaction occurs, for example, between poly-D-alanyl<br />

and poly-L-alanyl determinants. Studies employing synthetic<br />

antigens demonstrated the significance of aromatic<br />

charged amino acid residues in proving the ability of synthetic<br />

polypeptides to induce immune responses.<br />

synthetic vaccines<br />

Substances used for prophylactic immunization against<br />

infectious disease prepared by artificial techniques such as<br />

DNA cloning or peptide synthesis.<br />

systemic acquired resistance (SAR)<br />

An immune state of a plant that enables it to resist attack<br />

by a broad range of pathogens. Elevated concentrations of<br />

nitric oxide (NO), salicylic acid, and pathogenesis-related<br />

(PR) proteins mediate SAR.<br />

systemic anaphylaxis<br />

Type I immediate anaphylactic hypersensitivity mediated by<br />

immunoglobulin E (IgE) antibodies anchored to mast cells<br />

that become cross linked by homologous antigen (allergen),<br />

causing release of the pharmacological mediators of immediate<br />

hypersensitivity and producing lesions in multiple organs<br />

and tissue sites. This is in contrast to local anaphylaxis in<br />

which effects are produced in isolated anatomical locations.<br />

The intravenous administration of a serum product, antibiotic,<br />

or other substance against which the patient has anaphylactic<br />

IgE-type hypersensitivity may lead to the symptoms of<br />

systemic anaphylaxis within seconds and prove lethal.<br />

systemic autoimmune disease<br />

Refer to systemic autoimmunity.<br />

systemic autoimmunity<br />

The formation of antibodies specific for self constituents<br />

leading to type III hypersensitivity in which immune<br />

complexes are deposited in tissues, leading to pathological<br />

sequelae. The prototype for systemic autoimmune disease is<br />

systemic lupus erythematosus (SLE) in which autoantibodies<br />

specific for DNA, RNA, and proteins associated with<br />

nucleic acids form immune complexes deposited in small<br />

blood vessels, fix complement, and incite inflammation,<br />

leading to vascular injury.<br />

systemic immunoblastic proliferation<br />

A condition characterized by gene translocation and<br />

immature lymphocyte proliferation. Patients manifest rash,<br />

dyspnea, hepatosplenomegaly, and lymphadenopathy and<br />

show increased incidence of immunoblastic lymphoma.<br />

systemic inflammatory response syndrome (SIRS)<br />

The systemic effects of disseminated bacterial infection.<br />

Mild and severe forms have been described. The mild form<br />

is characterized by fever, neutrophilia, and an increase in<br />

acute phase reactants. Lipopolysaccharide (LPS) and other<br />

bacterial products may stimulate these changes that are<br />

mediated by innate immune system cytokines. Severe SIRS<br />

is characterized by disseminated intravascular coagulation,<br />

adult respiratory distress syndrome, and septic shock.<br />

Lupus band test.<br />

S

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