Viral proteins are degraded into peptide fragments within the infected cell.
These peptide fragments bind to Class I MHC molecules.
The peptide-MHC complexes are then transported to the cell surface and displayed.
Cytotoxic T Cell (CTL) Interaction
CTLs recognize virus-infected cells by interacting with two key components:
Viral antigen (peptide fragment).
Class I MHC molecule presenting the antigen.
This interaction is crucial for target cell specificity.
Mechanism of Cytotoxicity
Upon recognition, the CTL releases cytotoxins to induce apoptosis (programmed cell death) in the infected cell.
Perforin is released, creating perforations or pores in the infected cell's membrane, leading to cell lysis.
Self-Protein Presentation and Tolerance
Self-proteins are also degraded into fragments and presented via Class I MHC molecules.
However, CTLs do not normally recognize these self-peptide/MHC complexes; this is a mechanism of self-tolerance.
This prevents CTLs from attacking healthy, uninfected cells.
CTL Detachment and Continued Surveillance
After inducing apoptosis or lysis of an infected cell, the CTL detaches.
The CTL remains intact and active, moving on to find and eliminate other target cells displaying the same viral antigen.
Repeated Viral Infection
When a virus infects a cell, the process of peptide fragment presentation via class I MHCs occurs.
Cytotoxic T cells recognize both the antigen and the MHC, and the cytotoxic T cells kill the presented cell by using cytotoxins, which induce apoptosis, and perforin, which perforates the cell membrane.