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Untitled - D Ank Unlimited

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venom 740 V gene<br />

Ileum<br />

Lumen<br />

the first 2 weeks after the transplant. The incidence may<br />

be higher among older patients with diagnoses of acute<br />

myelogenous leukemia (AML) or chronic myelogenous<br />

leukemia (CML) and hepatitis. The mortality rate of VOD<br />

is relatively high at 32%.<br />

venom<br />

A poisonous substance produced by selected species such<br />

as snakes, arthropods, and bees. The poison is transmitted<br />

by bite or sting. At least 100 species of fish inject venoms<br />

that are hazardous to humans including sharks, rays, catfish,<br />

weever fish, scorpion fish, and stargazers.<br />

vermiform appendix<br />

A lymphoid organ situated at the ileocecal junction of the<br />

gastrointestinal tract.<br />

very late activation antigens (VLA molecules)<br />

β 1 integrins that have the CD19 β chain in common. They<br />

were originally described on T lymphocytes grown in longterm<br />

culture and subsequently found on additional types of<br />

leukocytes and on cells other than blood cells. VLA proteins<br />

facilitate leukocyte adherence to vascular endothelium<br />

and extracellular matrix. Resting T lymphocytes<br />

express VLA-4, VLA-5, and VLA-6. VLA-4 is expressed<br />

on multiple cells that include thymocytes, lymphocytes in<br />

blood, B and T cell lines, monocytes, natural killer (NK)<br />

cells, and eosinophils. The extracellular matrix ligand<br />

for VLA-4 and VLA-5 is fibronectin, and for VLA-6 it is<br />

laminin. The binding of these molecules to their ligands<br />

gives T lymphocytes costimulator signals. VLA-5 is present<br />

on monocytes, memory T lymphocytes, platelets, and<br />

fibroblasts. It facilitates B and T cell binding to fibronectin.<br />

VLA-6, found on platelets, T cells, thymocytes,<br />

and monocytes, mediates platelet adhesion to laminin.<br />

VLA-3 is a laminin receptor, binds collagen, and identifies<br />

fibronectin. It is present on B cells, the thyroid, and<br />

the renal glomeruli. Platelet VLA-2 binds to collagen only.<br />

Endothelial cell VLA-2 combines with collagen and laminin.<br />

Lymphocytes bind through VLA-4 to high endothelial<br />

venules and endothelial cell surface proteins (VCAM-1) in<br />

areas of inflammation. VLA-1 present on activated T cells,<br />

monocytes, melanoma cells, and smooth muscle cells binds<br />

collagen and laminin.<br />

Vermiform appendix.<br />

Germinal center<br />

Lymphoid<br />

follicles<br />

Crypts of<br />

Lieberkühn<br />

Cross-sectional view<br />

of appendix<br />

TCR<br />

MHC<br />

Autoreactive<br />

T-cell<br />

Veto cell<br />

Veto effect.<br />

Self epitope<br />

vesiculation<br />

Development of minute intraepidermal fluid-filled spaces,<br />

i.e., vesicles seen in contact dermatitis.<br />

veto cells<br />

A proposed population of cells suggested to facilitate<br />

maintenance of self tolerance through veto of autoimmune<br />

responses by T cells. A veto cell would neutralize the function<br />

of an autoreactive T lymphocyte. A T cell identifies<br />

itself as an autoreactive lymphocyte by recognizing the<br />

surface antigen on the veto cell. No special receptors with<br />

specificity for the autoreactive T lymphocyte are required<br />

for the veto cell to render the T lymphocyte nonfunctional.<br />

Contemporary research suggests the existence of a veto cell<br />

that can eliminate cytotoxic T lymphocyte (CTL) precursors<br />

reactive against allogeneic major histocompatibility<br />

complex (MHC) class I molecules or antigens presented in<br />

association with self MHC class I molecules.<br />

V gene<br />

Gene encoding the variable region of immunoglobulin<br />

light or heavy chains. Although it is not in proximity to the

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