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Untitled - D Ank Unlimited

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BALT 101 basolateral<br />

A<br />

B<br />

C<br />

H & E<br />

T-cells<br />

B-cells<br />

PA<br />

L<br />

BALT.<br />

300 µm<br />

BALT<br />

See bronchial-associated lymphoid tissue and MALT.<br />

band test<br />

Antigen–antibody deposits at the dermal–epidermal<br />

junctions in patients with lupus erythematosus. They may<br />

consist of IgG, IgM, IgA, and C3. Deposits are not found<br />

in uninvolved areas of the dermal–epidermal junctions in<br />

discoid lupus erythematosus (DLE) but are present in both<br />

involved and uninvolved areas of the junctions in systemic<br />

lupus erythematosus (SLE). Immune complexes at the<br />

dermal–epidermal junction appear in 90 to 95% of SLE<br />

patients. Ninety percent reveal them in skin exposed to sunlight,<br />

and 50% have deposits in skin not exposed to the sun.<br />

Also called lupus band test. Immunofluorescence bands<br />

also occur in some cases of anaphylactoid purpura, atopic<br />

dermatitis, contact dermatitis, autoimmune thyroiditis,<br />

bullous pemphigoid, cold agglutinin syndrome, dermatomyositis,<br />

hypocomplementemic vasculitis, polymorphous light<br />

eruption, rheumatoid arthritis, scleroderma, and a number<br />

of other conditions.<br />

bare lymphocyte syndrome (BLS)<br />

Rare autosomal-recessive disorders in which individuals<br />

manifest little or no expression of human leukocyte antigen<br />

(HLA) major histocompatibility proteins. BLS has been<br />

classified into three types that are of varying severity with<br />

respect to phenotypic HLA expression and loss of immune<br />

C<br />

GC<br />

function. BLS type I patients have little or no expression of<br />

HLA class I molecules on peripheral blood cells. They may<br />

have a broad range of immunodeficiency, with some individuals<br />

even revealing normal immunity. Type II BLS is<br />

characterized by a reduction or complete loss of HLA class<br />

II protein expression on all cells. This disorder is usually<br />

expressed as a severe combined immunodeficiency. In BLS<br />

type III, there is decreased expression of both HLA class I<br />

and class II antigen expression. These patients have severe<br />

immunodeficiency. HLA class I deficiency is sometimes<br />

referred to as type I BLS. It is believed that low expression<br />

of class I molecules may be sufficient for immune responses<br />

against pathogens, whereas complete deficiency would be<br />

lethal. Contrary to type II and III BLS, characterized by<br />

early onset of severe combined immunodeficiency (SCID),<br />

class I antigen deficiencies are not accompanied by specific<br />

pathologic features during the first years of life, although<br />

chronic lung disease develops in late childhood. In contrast<br />

to type II or III BLS, pathology of the gastrointestinal tract<br />

(diarrhea) is not observed. The lack of MHC molecule<br />

expression on the cells is due to a deficiency of the RFX or<br />

CIITA components of the SXY-CITTA regulatory system.<br />

Thus, the syndrome may be attributable to various different<br />

regulatory gene defects leading to severe immune<br />

deficiency.<br />

barrier filter<br />

A device in the eyepiece of an ultraviolet light source<br />

microscope employed for fluorescent antibody techniques<br />

to protect the viewer’s eyes from injury by ultraviolet<br />

radiation. It also facilitates observation of the fluorescence<br />

by blocking light of the wavelength that produces fluorochrome<br />

excitation.<br />

bas<br />

Mutation in an mRNA splicing acceptor site in the rabbit<br />

that leads to diminished expression of the principal type of<br />

immunoglobulin κ light chain (MO-κ-1). Rabbits with the<br />

bas mutation have λ light chains, although a few have the<br />

κ-2 isotype of light chains.<br />

basement membrane<br />

A structure comprised of collagen, laminin, heparan sulfate,<br />

and glycosaminoglycan beneath an overlying epithelial<br />

or endothelial cell layer.<br />

basement membrane antibody<br />

Antibody specific for the basement membranes of various<br />

tissues such as lung basement membranes, glomerular<br />

basement membranes, etc. This antibody is usually<br />

observed by immunofluorescence and less often by immunoperoxidase<br />

technology.<br />

basiliximab (injection)<br />

An immunosuppressive agent that acts as an IL-2 receptor<br />

antagonist by binding with high affinity to the α chain<br />

of the high affinity IL-2 receptor complex and inhibiting<br />

IL-2 binding. It is specific for IL-2Rα, which is expressed<br />

on activated T cell surfaces. High affinity binding of<br />

basiliximab to IL-2Rα inhibits IL-2 mediated activation<br />

of lymphocytes, which is critical in cellular immune<br />

responsiveness in allograft rejection. It blocks responses<br />

of the immune system to antigenic challenges when in the<br />

circulation.<br />

basolateral<br />

The epithelial cell surface that faces the tissue instead of<br />

the lumen.<br />

B

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