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Untitled - D Ank Unlimited

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steric hindrance 668 Streptococcus immunity<br />

Stem cell.<br />

Striational autoantibodies.<br />

individual cells can differentiate and proliferate under favorable<br />

conditions. Pluripotent stem cells (CFU-S) are capable<br />

of differentiating into committed precursor cells of the granulocyte<br />

and monocyte lineage (CFU-C), of erythropoietic<br />

lineage (CFU-E and BFUE), and of megakaryocyte lineage<br />

(CFU-Mg). Lymphocytes, like other hematopoietic cells,<br />

are generated in bone marrow. The stem cell compartment<br />

is composed of a continuum of cells that includes the most<br />

primitive, with the greatest capacity for self renewal and the<br />

least evidence of cell cycle activity, to the most committed<br />

with a lesser capacity for self renewal and the most evidence<br />

of cell cycle activity. Stem cells are multipotential precursors<br />

with the capacity to yield differentiated cell types with different<br />

functions and phenotypes; however, their proliferative<br />

capacity is limited.<br />

steric hindrance<br />

Interference between the interaction of the paratope of an<br />

antibody molecule with the homologous epitopes on antigen<br />

molecules of varying sizes based on the shapes of the two<br />

reactants. Whereas IgM molecules potentially have an<br />

antigen-binding capacity of ten, only some of these may be<br />

able to interact with relatively large antigen molecules bearing<br />

epitopes because of their shapes. By contrast, relatively<br />

small antigen molecules may permit their epitopes to bind<br />

with more paratopes on IgM molecules. Steric hindrance<br />

also refers to the blocking of ligand binding when a receptor<br />

site is already occupied by another ligand.<br />

steric repulsion<br />

Refer to van der Waals forces and London forces.<br />

steroid cell antibodies<br />

Immunoglobulin G (IgG) antibodies that interact with<br />

antigens in the cytoplasm of cells, producing steroids in the<br />

ovary, testes, placenta, and adrenal cortex. Patients with<br />

Addison’s disease along with ovarian failure or hypoparathyroidism<br />

develop these antibodies that are rarely associated<br />

with primary ovarian failure in which organ-specific<br />

and nonorgan-specific autoantibodies are prominent.<br />

stiff man syndrome (SMS)<br />

Progressive involuntary axial and lower limb rigidity<br />

that disappears during sleep. It results from an imbalance<br />

between descending inhibitory γ amino butyric acid<br />

(GABA)-ergic and excitatory aminergic pathways. Sixty<br />

percent of SMS patients have circulating antibody against<br />

glutamic acid decarboxylase (GAD), an enzyme that has<br />

65- and 67-kDa isoforms. GAD is a major antigenic target<br />

in insulin-dependent diabetes mellitus (IDDM). Antibody<br />

levels to GAD are 100- to 500-fold higher in SMS than in<br />

IDDM. SMS anti-GADs bind to both linear epitopes and<br />

epitopes that depend on protein conformation. SMS is associated<br />

with other autoimmune diseases including myasthenia<br />

gravis, pernicious anemia, vitiligo, autoimmune adrenal<br />

failure, ovarian failure, thyroid disease, and IDDM.<br />

stimulated macrophage<br />

A macrophage activated in vivo or in vitro. Activated macrophage<br />

is the preferred term.<br />

stochastic models<br />

Designs characterized by chance events without external<br />

direction or regulation.<br />

Stormont test<br />

A double intradermal tuberculin test.<br />

strain<br />

Genetically identical animals such as mice or rats used in<br />

medical research.<br />

street virus<br />

A natural or genetically unmodified virus such as rabies<br />

that can be isolated from animals.<br />

streptavidin<br />

A protein isolated from streptomyces that binds biotin. This<br />

property makes streptavidin useful in the immunoperoxidase<br />

reaction used extensively in antigen identification in<br />

histopathologic specimens, especially in surgical pathologic<br />

diagnosis.<br />

Streptobacillus immunity<br />

Although immune responses are induced in subjects<br />

infected with Streptobacillus moniliformis, the exact<br />

mechanisms and relative contribution of antibody remain<br />

to be determined. In mouse experiments, antibody confers<br />

only partial immunity to challenge with the microorganism.<br />

Inactivated S. moniliformis vaccines induce only partial<br />

protection against challenge.<br />

streptococcal M protein<br />

A cell wall protein of virulent Streptococcus pyogenes<br />

microorganisms that interferes with phagocytosis and also<br />

serves as a nephritogenic factor.<br />

Streptococcus immunity<br />

The most effective host resistance against pneumococcal<br />

(Streptococcus pneumoniae) infection is the synthesis of<br />

immunoglobulin G (IgG) or IgM that interacts with capsular<br />

polysaccharide, opsonizing the bacteria for ingestion and<br />

killing by professional phagocytes. Anticapsular antibody<br />

develops following colonization or infection. Most individuals<br />

have low resistance as reflected by their lack of antibodies<br />

to most of the commonly infecting pneumococcal serotypes<br />

even though normal adults may have sufficient antibodies

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