T cells are a type of white blood cell or lymphocyte that recognize and target pathogen-infected or cancer cells for their elimination. T cells are derived from hematopoietic stem cells in the bone marrow, whose precursors are transported to the thymus for final maturation. T cells are selective so that they tolerate the body's own cells but remain highly sensitive to non-self pathogens.
T lymphocytes can be immunophenotyped on the basis of CD3 expression and subsequently further subdivided (eg, CD8+ killer T cells and CD4+ helper T cells). In addition, T cell phenotypes are flexible and can change with different microenvironments, and phenotypes may also overlap among multiple T cell populations. In addition, the classification of T cell subsets may also be determined by the level of specific cytokines secreted in response to certain stimuli or by phosphorylation of immune signaling proteins such as STAT proteins.
Helper T cells (Th cells: CD4+), which help the immune system fight infection. Th cells recognize and bind disease-causing antigens, resulting in the release of soluble factors (cytokines), which in turn signal to the rest of the immune system to initiate a response. Th cells are divided into different subtypes, including Th1 cells and Th2 cells. Th1 cells bind phagocytic macrophages and dendritic cells. Th2 cells bind and activate B cells, a necessary process for the production of antibodies that guarantee lifelong immunity to specific bacterial or viral infections.
Killer T cells (cytotoxic T lymphocytes: CD8+), which recognize antigens released by pathogens bound to host cells. Killer T cells are able to recognize and interact with different cell types and pathogens. T cell receptors bind foreign antigens, triggering the release of cytotoxins into infected cells, leading to cell death.
Regulatory T cells (Treg cells: CD4+, CD25+, Foxp3+, CD127+), which keep the immune system functioning normally. Once an immune response has occurred, these cells ensure that the response is terminated. This regulatory mechanism suppresses immune activity, thereby preventing excessive immune responses. Properly functioning Treg cells are critical to preventing autoimmune disease.
T cell markers serve as essential tools in the identification, isolation, and characterization of different T cell subsets. These markers are proteins or molecules present on the cell surface or within the cell, which provide valuable insights into the type, function, and activation status of T cells.
T Cells Types | Markers | Localization | Description |
---|---|---|---|
T Cells (all) | CD3 | Cell membrane | Cell membrane receptor |
Killer T cells | CD8 | Cell membrane | Cell membrane receptor |
Killer T cells | IFNγ, TNF | Secretion | Cytokines |
Killer T cells | EOMES | Nucleus | Transcription factor |
Helper T cells | CD4 | Cell membrane | Cell membrane receptor |
Th1 cells | CXCR3 | Cell membrane | Chemokine receptor |
Th1 cells | IFNγ, IL-2, IL-12, IL-18 | Secretion | Cytokines |
Th1 cells | STAT4, STAT1 | Nucleus | Transcription factor |
Th2 cells | CCR4 | Cell membrane | Chemokine receptor |
Th2 cells | IL-2, IL-4 | Secretion | Cytokines |
Treg cells | CD4, CD25, CD127, CD152 | Cell membrane | Cell membrane receptor |
Treg cells | TGFβ, IL-10, IL-12 | Secretion | Cytokines |
Treg cells | FoxP3, STAT5 | Nucleus | Transcription factor |
In conclusion, T cells are vital components of the immune system, contributing to the body's defense against pathogens and diseases. Understanding the different types of T cells and their functions is crucial in unraveling the complexities of immune responses. T cell markers play a pivotal role in identifying, characterizing, and studying T cell subsets, aiding researchers and clinicians in their quest to unravel the mysteries of the immune system.
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