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Untitled - D Ank Unlimited

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TATA 682 T cell antigen receptors<br />

cells leads to synthesis. Tat protein binds to a transcriptional<br />

enhancer in the long terminal repeat of the provirus,<br />

increasing proviral genome transcription. It activates<br />

proviral DNA transcription by interfering with premature<br />

transcription termination. It also facilitates apoptosis of<br />

infected host cells and hinders survival signaling.<br />

TATA<br />

Abbreviation for tumor-associated transplantation antigen.<br />

TATA box<br />

An oligonucleotide sequence comprised of thymidine–<br />

adenine–thymidine–adenine found in numerous genes that<br />

are transcribed often or rapidly.<br />

tat gene<br />

A retrovirus gene found in HIV-1. The Tat transactivating<br />

protein encoded by this gene gains access to the nucleus<br />

and activates viral proliferation. Additional retroviral genes<br />

become activated. Mesenchymal tumors may be induced by<br />

tat genes in experimental animals.<br />

TB<br />

Abbreviation for tuberculosis.<br />

T–B cell cooperation<br />

Cooperation of B cells and helper T cells that leads to B<br />

cell proliferation and differentiation into plasma cells that<br />

synthesize and secrete specific antibody. B cell immunoglobulin<br />

receptors react with protein antigen, followed by<br />

endocytosis, antigen processing, and presentation to helper<br />

T lymphocytes. Their antigen-specific T cell receptors<br />

recognize processed antigen only in the context of major<br />

histocompatibility complex (MHC) class II molecules on<br />

B cell surfaces during antigen presentation. CD4 + helper<br />

T cells secrete lymphokines, including interleukin-2 (IL2),<br />

T cell activation.<br />

that promote B cell growth and differentiation into plasma<br />

cells that secrete specific antibody. T cells are required for<br />

B cells to be able to switch from forming immunoglobulin<br />

M (IgM) to synthesizing IgG or IgA. B and T lymphocytes<br />

recognize different antigens. B cells may recognize peptides,<br />

native proteins, or denatured proteins. T cell recognition<br />

systems are more complex in that a peptide antigen<br />

may be presented to them only in the context of MHC class<br />

II or class I histocompatibility molecules. Hapten–carrier<br />

complexes have been successfully used in delineating the<br />

different responses of B and T cells to each part of this<br />

complex. Immunization of a rabbit or other animal with a<br />

particular hapten–carrier complex will induce a primary<br />

immune response; a second injection of the same conjugate<br />

will induce a secondary immune response. However, linkage<br />

of the same hapten to a different carrier elicits a much<br />

weaker secondary response in an animal primed with the<br />

original hapten–carrier complex. This is termed the carrier<br />

effect. B lymphocytes recognize the hapten, and T lymphocytes<br />

the carrier.<br />

TBI<br />

Abbreviation for total body irradiation.<br />

T cell activation<br />

Response of mature naïve T cells to antigen presented to<br />

them by professional antigen-presenting cells, resulting in<br />

T lymphocyte proliferation and differentiation into effector<br />

T cells.<br />

T cell antigen receptors<br />

The two types of T cell antigen receptors are TCR1, which<br />

appears first in ontogeny, and TCR2. TCR2 is a heterodimer<br />

of α and β polypeptides. TCR1 consists of γ and δ

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