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BlyS 111 booster injection<br />

lymphoma cell lines express the receptor. Interleukin-4<br />

(IL-4) and IL-6 downregulate BLR-1. The receptor is also<br />

downregulated by monoclonal antibodies against CD40<br />

and CD3. Jurkat cells expressing BLR-1 do not bind known<br />

chemokines. Also called BLR-1 and MDR-15.<br />

BlyS<br />

A tumor necrosis factor (TNF) cytokine family molecule<br />

that is secreted by T lymphocytes and is critical in the<br />

formation of germinal centers and plasma cells and may be<br />

significant in maturation of dendritic cells.<br />

bm mutants<br />

Mouse H-2 bm mutants have served as elegant genetic tools<br />

for performing detailed analyses of the H-2 gene structure and<br />

its relationship to functions of the gene products. The mutants<br />

are especially useful when intact animals are needed to investigate<br />

a particular process. These mutants have aided in the<br />

assignment of diverse biological and immunologic functions<br />

to single H-2 genes. They also influence mating preferences,<br />

as evidenced by the ability of mice to use urine odor to distinguish<br />

parental animals from those carrying bm mutations.<br />

BMT<br />

Abbreviation for bone marrow transplantation.<br />

Bombay phenotype<br />

The O h phenotype is an ABO blood group antigen variant<br />

on human erythrocytes in rare subjects. These red blood<br />

cells do not possess A, B, or H antigens on their surfaces,<br />

even though the subject’s serum contains anti-A, anti-B,<br />

and anti-H antibodies. The Bombay phenotype may cause<br />

difficulties in crossmatching for transfusion.<br />

bombesin<br />

A neuropeptide of 14 residues analogous to a gastrin-releasing<br />

peptide that is synthesized in the gastrointestinal (GI)<br />

tract and induces GI smooth muscle contraction and the<br />

release of stomach acid and the majority of GI hormones,<br />

with the exception of secretin. Bombesin injection into<br />

the brain may induce hyperglucagonemia, hyperglycemia,<br />

analgesia, and hypothermia. Bombesin facilitates bronchial<br />

epithelial cell proliferation and pancreas and small cell<br />

carcinoma. Antibombesin antibodies may prove useful in<br />

the future for the treatment of small cell lung carcinoma,<br />

the cells of which bear bombesin receptors.<br />

bone marrow<br />

Soft tissue within bone cavities that contains hematopoietic<br />

precursor cells and hematopoietic cells that are maturing<br />

into erythrocytes, the five types of leukocytes, and<br />

thrombocytes. Whereas red marrow is hematopoietic and is<br />

present in developing bone, ribs, vertebrae, and long bones,<br />

some of the red marrow may be replaced by fat and become<br />

yellow marrow. In mammals, the bone marrow is the site of<br />

B cell development and the source of stem cells from which<br />

T lymphocytes develop following migration to the thymus,<br />

where they mature. A stromal framework comprised of<br />

fibroblasts, fat cells, endothelial cells and fibers supports<br />

the developing hematopoietic cells. Bone marrow transplantation<br />

may supply all of the cellular elements of the blood,<br />

including those needed for adaptive immunity.<br />

bone marrow cell<br />

Stem cells from which the formed elements of the blood,<br />

including erythrocytes, leukocytes, and platelets, are<br />

derived. B lymphocyte and T lymphocyte precursors are<br />

abundant. The B lymphocytes and pluripotent stem cells<br />

in bone marrow are important for reconstitution of an<br />

irradiated host. Bone marrow transplants are useful in the<br />

treatment of aplastic anemias, leukemias, and immunodeficiencies.<br />

Patients may donate their own marrow for<br />

subsequent bone marrow autotransplantation if they are to<br />

receive intensive doses of irradiation.<br />

bone marrow chimera<br />

The inoculation of an irradiated recipient mouse with bone<br />

marrow from an unirradiated donor mouse which ensures<br />

that lymphocytes and other cellular elements of the blood will<br />

be of donor genetic origin. The technique has been useful in<br />

demonstrating lymphocyte and other blood cell development.<br />

bone marrow transplantation<br />

The inoculation of a recipient with donor bone marrow<br />

including stem cells that serve as precursors for all mature<br />

cellular elements of the blood including lymphocytes; a<br />

procedure used to treat both nonneoplastic and neoplastic<br />

conditions not amenable to other forms of therapy. It has<br />

been especially used in cases of aplastic anemia, acute lymphoblastic<br />

leukemia, and acute nonlymphoblastic leukemia.<br />

A high degree of histocompatibility between donor and<br />

recipient is required. Using an HLA-matched donor, 750 mL<br />

of bone marrow are removed from the iliac crest. Following<br />

appropriate treatment of the marrow to remove bone spicules,<br />

the cell suspension is infused intravenously into an appropriately<br />

immunosuppressed recipient who has received<br />

whole-body irradiation and immunosuppressive drug therapy.<br />

Bone marrow cells derived from a patient during disease<br />

remission may be held frozen in liquid nitrogen for a future<br />

autologous bone marrow transplant that will permit the subject<br />

to receive his or her own cells. Graft-vs.-host episodes,<br />

acute graft-vs.-host disease, or chronic graft-vs.-host disease<br />

may follow bone marrow transplantation in selected subjects.<br />

The immunosuppressed patients are highly susceptible to<br />

opportunistic infections. See graft-vs.-host disease.<br />

Bony fish (teleosts)<br />

T and B lymphocyte functions become separate and distinctive,<br />

NK cells appear, and important cytokines such as<br />

IL-2 and IFN appear in bony fish. A polymorphic major<br />

histocompatibility complex (MHC) system resembling<br />

mammalian MHC is demonstrable in zebrafish.<br />

booster<br />

A second administration of immunogen to an individual<br />

primed months or years previously by a primary injection of<br />

the same immunogen. The purpose is to deliberately induce<br />

a secondary or anamnestic or memory immune response to<br />

facilitate protection against an infectious disease agent.<br />

booster injection<br />

The administration of a second inoculation of an immunizing<br />

preparation, such as a vaccine, to which an individual<br />

has been previously exposed. The booster inoculation elicits<br />

B

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