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T lymphocyte antigen receptor (TCR) 707 TNF receptors<br />

afferent limb of the immune response to exogenous antigen<br />

delivered to them by antigen-presenting cells. This stimulates<br />

the synthesis of interleukin-2 (IL2), which activates CD8 + T<br />

cells, natural killer (NK) cells, and B cells, thereby orchestrating<br />

an immune response to the antigen. Thus, they are<br />

termed helper T lymphocytes. They also mediate delayedtype<br />

hypersensitivity reactions. CD8 + T lymphocytes include<br />

cytotoxic and suppressor cell populations. They react to<br />

endogenous antigen and often express their effector function<br />

via a cytotoxic mechanism (e.g., against a virus-infected cell).<br />

Other molecules on mature T cells in humans include the E<br />

rosette receptor CD2 molecule, T cell receptor, pan-T cell<br />

marker termed CD3, and transferrin receptors.<br />

T lymphocyte antigen receptor (TCR)<br />

The two types of T cell antigen receptors are TCR1 (appears<br />

first in ontogeny) and TCR2. TCR2 is a heterodimer of α and<br />

β polypeptides. TCR1 consists of γ and δ polypeptides. Each of<br />

the two polypeptides comprising each receptor has a constant<br />

and a variable region (similar to immunoglobulin). Reminiscent<br />

of the diversity of antibody molecules, T cell antigen receptors<br />

can likewise identify a tremendous number of antigenic<br />

specificities (estimated at 10 15 epitopes). The TCR is composed<br />

of a minimum of seven receptor subunits whose production<br />

is encoded by six separate genes. Following transcription,<br />

these subunits are assembled precisely. Assimilation of the<br />

complete receptor complex is requisite for surface expression<br />

of TCR subunits. Numerous biochemical events are associated<br />

with activation of a cell through the TCR. These events<br />

ultimately lead to receptor subunit phosphorylation. T cells may<br />

be activated by the interaction of antigen in the context of the<br />

major histocompatibility complex (MHC) with T cell receptors,<br />

involving transmission of a signal to the interior through the<br />

CD3 protein to activate cells.<br />

T lymphocyte–B lymphocyte cooperation<br />

The association of T and B cells through a number of<br />

receptor–ligand interactions at the surfaces of both cell<br />

types, culminating in the synthesis by B cells of antibody<br />

specific for thymus-dependent antigens.<br />

T lymphocyte clone<br />

Daughter cells of one T lymphocyte derived from the blood<br />

or spleen that are added to culture medium and activated by<br />

antigen. T cells stimulated by the antigen form blasts that<br />

can be separated from the remaining T cells by density gradient<br />

centrifugation. T cells that have responded to antigen<br />

are diluted, and aliquots are dispensed into tissue culture<br />

plates to which antigen and interleukin-2 (IL2) are added.<br />

Each well contains a single lymphocyte. This method provides<br />

individual T cell clones.<br />

T lymphocyte-conditioned medium<br />

A cell culture medium containing multiple lymphokines<br />

released from T cells stimulated by antigens or lectins.<br />

T lymphocyte hybridoma<br />

Produced by fusing a murine splenic T cell and an AKR<br />

strain BW5147 thymoma cell using polyethylene glycol<br />

(PEG). The hybrid cell clone is immortal and releases<br />

interleukin-2 (IL2) when activated by antigen provided by<br />

an antigen-presenting cell.<br />

T lymphocyte receptor<br />

Refer to T lymphocyte antigen receptor.<br />

T lymphocyte subpopulation<br />

A subset of T cells that have a specific function and express<br />

a specific cluster of differentiation (CD) markers or other<br />

antigens on their surfaces. Examples include the CD4 +<br />

helper T lymphocyte subset and the CD8 + suppressor/cytotoxic<br />

T lymphocyte subset.<br />

T lymphocytes<br />

Synonym for T cells. T lymphocyte precursors are detectable<br />

in a human fetus at 7 weeks of gestation. Between<br />

weeks 7 and 14 of gestation, thymic changes begin to<br />

imprint thymic lymphocytes as T cells. The maturation<br />

(mediated by hormones such as thymosin, thymulin, and<br />

thymopoietin II) may be followed by identification of<br />

surface (cluster of differentiation [CD]) markers detectable<br />

by immunophenotyping. CD3, a widespread T cell marker,<br />

serves as a signal transducer from the antigen receptor to<br />

the cell interior. Thus, CD3 is intermittently associated<br />

with the T cell receptor for antigen. T lymphocytes in the<br />

medulla initially express both CD4 and CD8 class markers<br />

but these cells later differentiate into CD4 + helper cells or<br />

CD8 + suppressor cells. The CD4 + cells characterized by<br />

55-kDa surface markers communicate with macrophages<br />

and B cells bearing major histocompatibility complex<br />

(MHC) class II molecules during antigen presentation.<br />

The CD8 + suppressor/cytotoxic cells interact with antigenpresenting<br />

cells bearing MHC class I molecules.<br />

T lymphocyte–T lymphocyte cooperation<br />

Signals from one T lymphocyte subpopulation to another,<br />

e.g., isotype class switching in the regulation of immunologic<br />

responsiveness.<br />

Tm<br />

Membrane immunoglobulin heavy chain tail (C terminal)<br />

polypeptide.<br />

T6 marker<br />

A chromosome of CBA/H-T6 inbred mice discovered in an<br />

irradiated male. It has been used as a cell marker to trace<br />

cells transferred to other mice. Its length is abbreviated and<br />

it has a secondary constriction adjacent to the centromere.<br />

TNF<br />

Abbreviation for tumor necrosis factor.<br />

TNF-<br />

Abbreviation for tumor necrosis factor α.<br />

TNF-<br />

Abbreviation for tumor necrosis factor β.<br />

TNF receptor-associated factors (TRAFs)<br />

Adaptor molecules that interact with cytoplasmic domains<br />

in TNF receptor molecules. This family includes tumor<br />

necrosis factor (TNF)-RII, lymphotoxin (LT) β receptor,<br />

and CD40. Cytoplasmic motifs in these receptors bind<br />

separate TRAFs that interact with other signaling molecules,<br />

resulting in transcription factor AP-1 and NF-κB<br />

transcription factors.<br />

TNF receptor-associated periodic syndrome (TRAPS)<br />

A primary autoinflammatory immunodeficiency defined<br />

by repeated episodes of severe localized inflammation and<br />

extended bouts of fever. Attributable to TNGR1 mutations<br />

that lead to uncontrolled activation of the TNRF1 pathway.<br />

TNF receptors<br />

Tumor necrosis factor (TNF) receptors interact with three<br />

structurally related ligands: TNF-α, lymphotoxin α (LTα)<br />

or TNF-β, and LTβ. Two of the three have the designations<br />

CD120a (type I, p55 or p60 receptor) and CD120b (type II,<br />

p75 or p80 receptor). The third is designated LTβ receptor<br />

(LTβ-R), type III TNF receptor, or TNFR-RP. TNF receptors<br />

may be cell-bound or soluble. CD120a and CD120b<br />

T

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