Overexpression of CD6 and PD-1 Identifies Dysfunctional CD8(+) T-Cells During Chronic SIV Infection of Rhesus Macaques

Effective CD8(+) T-cell responses play an important role in determining the course of SIV/HIV viral infection. Here we identified a unique population of dysfunctional CD8(+) T-cells in lymphoid tissues and bronchoalveolar lavage (BAL) of rhesus macaques with chronic SIV infection characterized by co-expression of CD6 and PD-1. The frequency of CD6 and PD-1 co-expressing CD8(+) T-cells was significantly increased in lymphoid tissues and BAL during chronic SIV infection compared to pre-infection levels. These CD6(+)PD-1(+)CD8(+) T-cells displayed impaired proliferation, cytokine secretion and cytotoxicity compared to their CD6(−)PD-1(+)CD8(+) T cell counterparts. The frequency of CD8(+)PD-1(+) and CD8(+)CD6(−)PD-1(+) T-cells in the lymph node and bone marrow did not correlate with SIV viral load, whereas the frequency of CD8(+)CD6(+)PD-1(+) T-cells positively correlated with SIV viral load in these tissues highlighting the contribution of CD6 to disease progression. CD6(+)PD-1(+)CD8(+) T-cells expressed elevated levels of SHP2 phosphatase compared to CD6(−)PD-1(+)CD8(+) T-cells providing a potential mechanism by which CD6 may induce T-cell dysfunction during chronic SIV infection. Combined targeting of CD6 and PD-1 effectively revived the CD8(+) T-cell proliferative response in vitro suggesting a strategy for potential therapeutic benefit.