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T cell antigen-specific suppressor factor 683 T cell development<br />

Plasma<br />

membrane<br />

Antigen binding site<br />

α<br />

β<br />

T Cell receptor<br />

heterodimer<br />

γ<br />

polypeptides. Each of the two polypeptides comprising each<br />

receptor has a constant and a variable region (similar to<br />

immunoglobulin). Reminiscent of the diversity of antibody<br />

molecules, T cell antigen receptors can likewise identify a<br />

tremendous number of antigenic specificities (estimated to<br />

be able to recognize 10 15 epitopes). The TCR is comprised<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<br />

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

events ultimately lead to receptor subunit phosphorylation.<br />

T cells may be activated by the interaction of antigen, in<br />

the context of MHC, with the T cell receptor. This involves<br />

transmission of a signal to the interior through the CD3<br />

protein to activate the cell.<br />

T cell antigen-specific suppressor factor<br />

A soluble substance produced by a suppressor T cell after it<br />

has been activated. This suppressor factor has been claimed<br />

δ<br />

CD3 Proteins<br />

T cell antigen receptor.<br />

Large<br />

pre- B cell<br />

Small<br />

B cell<br />

Intermediate<br />

B cell<br />

Mature<br />

B cell<br />

Immunoblast<br />

ε<br />

Early B<br />

lineage<br />

precursor<br />

ζ ζ ζ<br />

η<br />

Lymphoid<br />

stem cell<br />

Active<br />

B cell<br />

to bind antigen and cause the immune response to be suppressed<br />

in an antigen-specific manner.<br />

T cell areas<br />

Regions of secondary tissues occupied predominantly by<br />

T lymphocytes.<br />

T cell chemotactic factor<br />

Former term for interleukin-8 (IL8).<br />

T cell clonal expansion<br />

Clonal expansion of T lymphocytes after initial encounter<br />

with antigen is a critical mechanism of the effector limb of<br />

the immune response. This permits the immune system to<br />

respond to a broad spectrum of pathogens. Clonal expansion<br />

is closely regulated to prevent inappropriate responses.<br />

Increased clonal expansion is desirable during the early<br />

course of an infection and in the prevention of growth and<br />

survival of T cells mediating autoimmune disease.<br />

T-cell-dependent (TD) antigen<br />

An immunogen that is much more complex than the<br />

T-cell-independent (TI) antigens. TD antigens are usually<br />

proteins, protein–nuclear protein conjugates, glycoproteins,<br />

or lipoproteins. They stimulate all five classes of<br />

immunoglobulin, elicit anamnestic or memory responses,<br />

and are present in most pathogenic microorganisms. These<br />

properties ensure that an effective immune response can be<br />

generated in a host infected with these pathogens.<br />

T cell development<br />

Stem cells in the bone marrow that are destined to develop<br />

into T cells migrate to the thymus, where they undergo<br />

maturation and development. These precursors of T cells<br />

possess unrearranged T cell receptor (TCR) genes and do<br />

not express CD4 or CD8 markers. Thymocytes (developing<br />

T cells) are found first in the outer cortex, where their<br />

numbers increase; the TCR genes are rearranged; and<br />

CD3, CD4, CD8, and TCR molecules are expressed on<br />

the surface. During maturation, these cells pass from the<br />

CD4<br />

Suppressor/<br />

Inducer<br />

T cell<br />

Helper<br />

T cell<br />

Subcortical<br />

thymocyte<br />

Thymus cell differentation⎯T cell maturation.<br />

CD8<br />

Cytotoxic<br />

T cell<br />

Activated T cell<br />

Suppressor<br />

T cell<br />

Bone marrow<br />

Thymus<br />

Blood<br />

Lymph node<br />

T

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