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Cancer Immune Therapy Edited by G. Stuhler and P. Walden ...

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384 Glossary<br />

suppressor gene products. Cytolysis <strong>by</strong> cytotoxic T lymphocytes or natural killer cells is<br />

also apoptosis. The typical changes associated with apoptosis involve flipping of<br />

phospholipids in the plasma membrane (Annexin), membrane blebbing <strong>and</strong> fragmentation<br />

of the DNA.<br />

B lymphocyte (B cell)<br />

Antibody-expressing lymphocyte. They evolve from cells which are committed to the<br />

B cell linage but have not yet rearranged their immunoglobulin genes via different<br />

stages of pro-B development to pre-B cells with a partly rearranged immunoglobulin<br />

genome to immature B cells that express IgM, <strong>and</strong> mature B cells that secrete IgM<br />

<strong>and</strong> IgD. Upon contact with antigen <strong>and</strong> antigen-mediated interaction with helper<br />

T cells these mature B cells develop into clonally exp<strong>and</strong>ed, IgG-producing cells that<br />

either terminally differentiate into plasma cells or become memory cells <strong>and</strong>, thus,<br />

form the basis of secondary immune responses. Mature B cells express MHC class I<br />

<strong>and</strong> II molecules, <strong>and</strong> a number of adhesion <strong>and</strong> co-stimulating molcules that qualify<br />

them to serve as antigen-presenting cells. Their antigen receptor allows for a specific accumulation<br />

of their cognate antigen which is thus presented with high efficiency.<br />

Bone marrow transplantation (BMT)<br />

Therapeutic transfer of bone marrow to reconstitute, replace or support the hematopoetic<br />

<strong>and</strong> immune system of the recipients. Generally, the recipient has received<br />

chemotherapy or radio-chemotherapy prior to BMT which has eliminated or substantially<br />

reduced the individual's own hematopoetic system. Two regimens are in<br />

use ± the myeloablative approach (aimed at replacing the recipients bone marrow<br />

with autologous or allogeneic stem cells) <strong>and</strong> the non-myeloablative approach (resulting<br />

in a chimerism of host <strong>and</strong> donor stem cells). Because of incompatibility of<br />

minor or major histocompatibility gene products, continuous immunosuppression<br />

is necessary in most recipients.<br />

Carcinoembryonic antigen (CEA)<br />

Glycoprotein expressed <strong>by</strong> many cell types in the developing fetus <strong>and</strong> <strong>by</strong> adenocarcinomas<br />

of endodermally derived intestinal epithelia, but also breast, lung, <strong>and</strong> some<br />

types of thyroid <strong>and</strong> ovarian cancers. CEA is used as a tumor marker <strong>and</strong> as a target<br />

antigen for cancer immune therapy. It has a molecular weight of 180 000 with about<br />

60 % carbohydrate moieties. In healthy adults, CEA expression may be elevated due<br />

to smoking, inflammation, pancreatitis <strong>and</strong> liver cirrhosis.<br />

CD<br />

Cluster of differentiation, nomenclature of differentiation antigens expressed <strong>by</strong> leukocytes.<br />

Regularly held international workshops allocate CD numbers to these antigens.<br />

CD91<br />

Cell surface receptor for a2-macroglobulin <strong>and</strong> some heat shock proteins (gp96,<br />

HSP90, HSP70 <strong>and</strong> calreticulin). CD91 is expressed <strong>by</strong> monocytes <strong>and</strong> their derivatives<br />

including macrophages <strong>and</strong> dendritic cells <strong>and</strong> erythroblasts/reticulocytes. The

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