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

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

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Glossary<br />

Dendritic cell (DC)<br />

Migratory mononuclear cell found in nearly all tissues <strong>and</strong> characterized <strong>by</strong> typical<br />

filiform processes. DCs are highly efficient antigen-presenting cells <strong>and</strong> particularly<br />

important for the primary induction of immune responses. They are thought to harvest<br />

antigens in the tissues <strong>and</strong>, upon activation <strong>by</strong> inflammatory processes, for instance,<br />

migrate to the draining lymph nodes. These mature DCs express high levels<br />

of MHC class I <strong>and</strong> II molecules, <strong>and</strong> co-stimulatory molecules, <strong>and</strong> efficiently activate<br />

T lymphocytes. In man, two types of DCs have been described, the plasmocytoid DCs<br />

<strong>and</strong> the myeloid DCs. Myeloid DCs are derived from or related to monocytes. Plasmacytoid<br />

DCs, in addition to specific DC markers, express a set of cell surface molecules<br />

that are also found on cells of lymphatic lineage <strong>and</strong> synthesize type I interferons.<br />

Plasmacytoid <strong>and</strong> myeloid DCs express different sets of Toll-like receptors, <strong>and</strong>,<br />

thus, respond differently to pathogenic microorganisms.<br />

Donor lymphocyte infusion (DLI)<br />

Therapeutic strategy of infusing into a patient subsequently to allogeneic bone marrow<br />

transplantation immune-competent T lymphocytes from the same donor. This<br />

therapy aims at induction of a graft-versus-leukemia (GvL) or graft-versus-tumor<br />

(GvT) effect of the donor lymphocytes.<br />

Effector cell<br />

cell with fully developed cytolytic capacity, usually activated CD8 + cytotoxic T lymphocytes<br />

or natural killer cells.<br />

Epitope<br />

Portion of an antigen that is actually bound <strong>by</strong> the immune receptors, antibodies or<br />

T cell receptors (TCR). For antibodies, epitopes may be continuous stretches of the primary<br />

sequence of a protein antigen (continuous epitopes) or composed of elements<br />

of different parts of the antigen (discontinuous epitopes). In addition to peptides,<br />

any small residue such as a hapten or a hapten in the context of a peptide can form<br />

an epitope for antibodies. Epitopes for T lymphocytes are always peptides derived<br />

from proteins <strong>by</strong> limited proteolysis that must be bound to MHC molecules for recognition<br />

<strong>by</strong> the TCR.<br />

Fas (APO-1, CD95)<br />

Cell surface receptor of 43 kDa of the tumor necrosis factor (TNF) receptor superfamily<br />

which is one of the main triggers of receptor-mediated apoptosis. Fas is expressed<br />

in thymus, liver, heart <strong>and</strong> ovary, <strong>and</strong> <strong>by</strong> activated T lymphocytes <strong>and</strong> some<br />

tumors. It carries an intracellular death domain that, after engagement of Fas with<br />

its lig<strong>and</strong> (FasL), binds FADD, an intracellular adaptor molecule that initiates caspase-mediated<br />

pathways of apoptosis. FasL (CD95L), also a member of the TNF<br />

superfamily, is expressed predominantly <strong>by</strong> activated T lymphocytes. However, some<br />

tumors also express FasL <strong>and</strong>, thus, can induce apoptosis in cytotoxic T lymphocytes<br />

that attack the tumor. The actual role of receptor-mediated apoptosis in the control of<br />

tumors in patients has not yet been clarified.<br />

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