Boosting SIV-specific CD8+ T cell responses prior to ART interruption extends time to SIVmac239 rebound.

Additionally, fewer SIVmac239M viral barcode clonotypes contributed to post-ART viremia early after ART discontinuation in mRNA/SIVgag-vaccinated RMs compared with controls, though this difference did not reach statistical significance ( P = 0.153) ( Figure 4B and Supplemental Figure 5 ).

also in 111,027 other papers