[HTML][HTML] Rapid SIV Env-specific mucosal and serum antibody induction augments cellular immunity in protecting immunized, elite-controller macaques against high …

LJ Patterson, M Daltabuit-Test, P Xiao, J Zhao, W Hu… - Virology, 2011 - Elsevier
LJ Patterson, M Daltabuit-Test, P Xiao, J Zhao, W Hu, U Wille-Reece, E Brocca-Cofano
Virology, 2011Elsevier
Three Indian rhesus macaques, Ad-SIV primed/protein boosted and exposed twice to high-
dose mucosal SIVmac251 challenges, exhibited elite control of viremia over 6.5 years. They
were negative for host factors associated with control of SIV infection. After a third intrarectal
challenge with SIVsmE660, all controlled viremia, with one (macaque# 5) maintaining
undetectable viremia in blood. Acquisition was not blocked, but virus was contained in the
jejunum and draining lymph nodes. Polyfunctional memory T cell responses and high-titered …
Three Indian rhesus macaques, Ad-SIV primed/protein boosted and exposed twice to high-dose mucosal SIVmac251 challenges, exhibited elite control of viremia over 6.5years. They were negative for host factors associated with control of SIV infection. After a third intrarectal challenge with SIVsmE660, all controlled viremia, with one (macaque #5) maintaining undetectable viremia in blood. Acquisition was not blocked, but virus was contained in the jejunum and draining lymph nodes. Polyfunctional memory T cell responses and high-titered neutralizing and non-neutralizing serum and mucosal antibodies were present before and maintained post-challenge. The level of protection seen for animal #5 was predicted from analyses of gene transcription in jejunum 2weeks post-challenge. Macaques #7 and #9, exhibiting lower pre-challenge cellular and humoral immunity, partially controlled the SIVsmE660 challenge. Initial vaccine-induced control by macaque #5 extended to the SIVsmE660 challenge due to multiple immune mechanisms that were boosted and augmented by cryptic SIV exposure.
Elsevier