Differential Impact of Magnitude, Polyfunctional Capacity, and Specificity of HIV-Specific CD8 + T Cell Responses on HIV Set Point

Abstract

Defining the characteristics of HIV-specific CD8 + T cell responses that lead to viral control is crucial for vaccine development. We evaluated the differential impact of magnitude, polyfunctional capacity, and specificity of the CD8 + response at approximately 6 months postinfection on the viral set point at 12 months in a cohort of HIV-infected individuals. High frequencies of Gag and Nef responses endowed with four functions were the best predictors of a low viral set point.