29. Functions of T lymphocytes. Cytotoxic T lymphocytes. T helpers.
Explains the three T lymphocyte subtypes, then takes cytotoxic T cells through MHC class I antigen recognition, CD8, proteasome and TAP processing, the Fas-FasL and perforin-granzyme killing pathways, and the immune synapse. Helper T cells follow, covering MHC class II presentation, CD4, the invariant chain and CLIP, and the Th1 and Th2 roles. It closes with type IV delayed hypersensitivity and four mnemonics that pair CD8 with MHC I and CD4 with MHC II.
Inside: 6 sections · 1 labelled picture · 9 min
Topic 29 of 64 in the MU Sofia syllabus for Biology (Dental Medicine, Year 1). The free AceMed note covers it in 6 sections, about 1,271 words (9 min of reading).
In this note
Cytotoxic and helper T lymphocytes
Overview of T Lymphocytes
Cytotoxic T Lymphocytes (T Killer Cells)
Helper T Lymphocytes (T Helper Cells)
Subtypes of Helper T Cells
MNEMONICS
Overview of T Lymphocytes
T lymphocytes are a type of white blood cell essential for the adaptive immune response.
They do not attack pathogens directly. Instead, they act on other cells in the body, particularly those that present antigens.
T cells only recognize antigens when these are displayed in combination with the body’s own MHC (Major Histocompatibility Complex) molecules.
There are three main subtypes of T cells:
Cytotoxic T cells (Tc): Also called T killer cells
Helper T cells (Th): Guide and coordinate immune responses
Regulatory T cells (Treg): Modulate and suppress the immune response (not covered in detail here)
Cytotoxic T Lymphocytes (T Killer Cells)
Main Function
Cytotoxic T cells destroy cells that are infected by viruses.
They do this by inducing the infected cells to self-destruct through a process called apoptosis.
Antigen Recognition
Tc cells recognize antigens only when they are presented on MHC class I molecules.
MHC class I molecules are found on the surface of all nucleated cells, making all such cells potential targets for virus infection.
Key Surface Marker
Tc cells express a protein called CD8, which helps them interact specifically with MHC class I molecules.
CD8 serves both as a co-receptor and a marker to identify cytotoxic T cells.
Antigen Processing for Tc Cells
The antigens presented on MHC class I molecules come from proteins that are made inside the cell, such as viral proteins during infection.
These proteins are broken down by a cellular machine called the proteasome into short peptides (8–10 amino acids).
These peptides are transported into the endoplasmic reticulum (ER) by a protein called TAP.
Inside the ER, MHC class I molecules bind these peptides and carry them to the cell surface to be displayed.
Mechanisms of Killing
Tc cells kill infected cells using two main pathways:
1. Fas-FasL pathway:
Tc cells express a protein called FasL.
FasL binds to its receptor Fas on the target cell, triggering a cascade of signals that activates enzymes called caspases which lead to apoptosis.
2. Perforin-Granzymes pathway:
Tc cells release perforins, which create pores in the target cell’s membrane.
Through these pores, granzymes enter the cell and activate the internal machinery that causes apoptosis.
If apoptosis is blocked by a virus, extensive membrane damage from perforins can lead to necrosis, a more chaotic form of cell death.
Specificity and Selectivity
All nucleated cells present many peptide-MHC class I complexes.
Tc cells ignore complexes made of normal self-proteins.
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