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The human immune system’s ability to mount a robust T cell response against conserved regions in viral proteins like HIV’s Gag/Pol is critical for effective long-term control. By targeting less variable parts of the virus with both cytotoxic and helper functions, this approach aims at minimizing viral escape while maximizing immunological pressure where it most impairs viral replication capacity. This strategy underpins several modern vaccine designs seeking broad efficacy across diverse virus strains.
MHC-restricted recognition of conserved Gag/Pol peptides presented by antigen-presenting cells or infected cells, leading to T cell activation, cytokine production, and cytotoxic killing of infected cells.
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