00:00 / 00:00
of complete
of complete
2024
2023
2022
2021
naive T-cell activation p. 101
T cell dysfunction p. 114
T cells and p. 99
T cells and p. 409
T-cell differentiation p. 99
activation p. 101
adaptive immunity p. 97
anergy p. 108
cell surface proteins p. 108
corticosteroid effects p. 118
cytokine production p. 99, 106
cytotoxic p. 100
delayed (type IV) hypersensitivity p. 99
differentiation and maturation p. 96, 99
disorders of p. 114, 115
functions p. 99
helper p. 98
leflunomide effects p. 495
lymph nodes p. 94
major functions of p. 99
neoplasms p. 435
regulatory p. 100
sirolimus effect p. 118
spleen p. 96
thymus p. 96
untreated HIV p. 173
T cell selection in p. 100
T cell origination in p. 409
B- and T-cell disorders p. 115
T cells, also known as T lymphocytes are a type of lymphocyte that play a central role in cell-mediated immunity. The process of T-cell development begins with the migration of immature T-cell precursors from the bone marrow to the thymus gland, where they undergo a series of steps to become fully mature T-cells. In the thymus, T-cells are exposed to a diverse array of self-antigens and undergo positive and negative selection to ensure that only T-cells that recognize foreign antigens but not self-antigens are allowed to leave the thymus and enter the bloodstream.
During positive selection, T-cells that recognize self-antigens displayed by thymic stromal cells receive survival signals, allowing them to continue their development. During negative selection, T-cells that recognize self-antigens too strongly undergo apoptosis to prevent the development of autoimmunity. Once T-cells have successfully completed positive and negative selection, they leave the thymus and enter the bloodstream, where they travel to various organs and tissues to carry out their functions.
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