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lood group antigens 110 BLR-1/MDR-15<br />

blood group antigens<br />

Erythrocyte surface molecules that may be detected with<br />

antibodies from other individuals such as ABO blood group<br />

antigens. Various blood group antigen systems including Rh<br />

(Rhesus) may be typed in routine blood banking procedures.<br />

Other blood group antigen systems may be revealed<br />

through cross matching.<br />

blood grouping<br />

The classification of erythrocytes based on their surface<br />

isoantigens. Among the well-known human blood groups<br />

are the ABO, Rh, and MNS systems.<br />

TABelle I<br />

betreffend das blut sechs anscheinend gesunder männer<br />

Sera<br />

Dr. St. – + + + + –<br />

Dr. Plecn. – + + – –<br />

Dr. Sturl. – + – – + –<br />

Dr. Erdh. – + – – + –<br />

Zar. – – + + – –<br />

Landst. – + + + + –<br />

Blutköperchen<br />

von:<br />

Dr. St. Dr. Plecn. Dr. Sturl. Dr. Erdb. Zar. Landst.<br />

Table illustrating ABO blood groups. (From Wien. klin. Wschr., 14, 1132–<br />

1134, 1901.)<br />

TABelle II<br />

betreffend das blut von sechs anscheinend gesunder<br />

puerperae<br />

Sera<br />

Seil – – + – – +<br />

Linsm. + – + + + +<br />

Lust. + – – + + –<br />

Mittelb. – – + – – +<br />

Tomsch. – – + – – +<br />

Graupn. + – – + + –<br />

Blutköperchen<br />

von:<br />

Seil. Linsm. Lust. Mittelb. Tomsch. Graupn.<br />

ABO blood group antigens and antibodies.<br />

Capillary<br />

Capillary<br />

basement<br />

membrane<br />

Antigen<br />

Endothelial<br />

cell<br />

Peri-capillary space<br />

Pericyte Macrophage<br />

Lymphocyte<br />

Epithelial<br />

cell barrier<br />

Interconnecting<br />

epithelial cells<br />

Thymocytes<br />

of cortex<br />

Three levels of lymphocyte protection that form the blood–thymus barrier:<br />

capillary wall, macrophages in pericapillary space, and a wall of<br />

epithelial cells.<br />

blood–thymus barrier<br />

Protects thymocytes from contact with antigen.<br />

Lymphocytes reaching the thymus are prevented from<br />

contact with antigen by a physical barrier. The first level is<br />

represented by the capillary wall endothelial cells inside the<br />

pericytes outside of the lumen. Potential antigenic molecules<br />

that escape the first level of control are taken over<br />

by macrophages present in the pericapillary space. Further<br />

protection is provided by a third level, represented by the<br />

mesh of interconnecting epithelial cells that enclose the<br />

thymocyte population. The effects of thymus and thymic<br />

hormones on the differentiation of T cells is demonstrable<br />

in animals congenitally lacking thymus glands (nu/nu<br />

animals), in neonatal or adult thymectomized animals,<br />

and in subjects with immunodeficiencies involving T cell<br />

function. Differentiation is associated with surface markers<br />

whose presence or disappearance characterizes the different<br />

stages of cell differentiation. Extensive proliferation of the<br />

subcapsular thymocytes occurs. The largest proportion of<br />

these cells die, but remaining cells continue to differentiate.<br />

The differentiating cells become smaller in size and move<br />

through interstices in the thymic medulla. The fully developed<br />

thymocytes pass through the walls of the postcapillary<br />

venules to reach the systemic circulation and seed in the<br />

peripheral lymphoid organs. Some of them recirculate but<br />

do not return to the thymus.<br />

Bloom syndrome (BS)<br />

A very rare clinical entity characterized by a strikingly<br />

small but well-proportioned body size. It is the consequence<br />

of either homozygosity or compound heterozygosity of a<br />

mutation of BLM, a gene that encodes a phylogenetically,<br />

highly conserved nuclear protein. It has been suggested that<br />

this condition should be grouped with the genetically determined<br />

immunodeficiencies. Respiratory tract infections<br />

occur much more commonly in patients with BS than in the<br />

general population; if not treated promptly, these infections<br />

become life threatening, yet 37% of BS patients manifest<br />

no increased tendency to infection of any kind. The disease<br />

is characterized by diminished numbers of T lymphocytes,<br />

decreased antibody levels, and increased susceptibility<br />

to respiratory infections, tumors, and radiation injury.<br />

Mutations in a DNA helicase cause the disorder. Genomic<br />

instability is a characteristic of this rare autosomal recessive<br />

primary immunodeficiency that is attributable to<br />

mutation of the BLM gene associated with the homologous<br />

recombination pathway of DNA repair.<br />

blot<br />

The transfer of DNA, RNA, or protein molecules from an<br />

electrophoretic gel to a nitrocellulose or nylon membrane<br />

by osmosis or vacuum, followed by immersion of the<br />

membrane in a solution containing a complementary (i.e.,<br />

mirror-image) molecule corresponding to the one on the<br />

membrane. This is known as a hybridization blot.<br />

BLR-1/MDR-15<br />

Burkitt’s lymphoma receptor-1/monocyte-derived receptor-15<br />

(BLR-1/MDR-15) is a member of the G proteincoupled<br />

receptor family, the chemokine receptor branch of<br />

the rhodopsin family. It is expressed on B cells and memory<br />

T cells, chronic B lymphoid leukemia and non-Hodgkin<br />

lymphoma cells, peripheral blood monocytes, and lymphocytes.<br />

It is expressed in tonsils and secondary lymphoid<br />

organs and in selected other tissues. Most Burkitt’s

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