Accelerated heterologous adenovirus prime-boost SIV vaccine in neonatal rhesus monkeys.

Abstract:

:A pediatric human immunodeficiency virus type 1 (HIV-1) vaccine would be desirable to protect infants against HIV-1 transmission from breast-feeding. Such a vaccine would need to induce protective immunity at mucosal surfaces in neonates as soon as possible after birth. Recombinant adenovirus (rAd) vectors have been shown to elicit potent systemic and mucosal virus-specific immune responses in adult nonhuman primates and humans, but these vectors have not previously been comprehensively studied in infants. In this study, we demonstrate that a single injection of rAd26 encoding simian immunodeficiency virus mac239 (SIVmac239) Gag on the day of birth elicited detectable Gag-specific cellular immune responses in rhesus monkeys, but these responses were transient and waned quickly. In contrast, an accelerated heterologous prime-boost regimen involving administration of rAd35 at birth and rAd26 at 4 weeks of life elicited potent and durable Gag-specific cellular and humoral immune responses in neonatal rhesus monkeys, including mucosal responses that remained detectable at 1 year of age. These results suggest the potential of an accelerated heterologous rAd prime-boost regimen as a candidate HIV-1 vaccine for newborns.

journal_name

J Virol

journal_title

Journal of virology

authors

Liu J,Li H,Iampietro MJ,Barouch DH

doi

10.1128/JVI.00512-12

subject

Has Abstract

pub_date

2012-08-01 00:00:00

pages

7829-35

issue

15

eissn

0022-538X

issn

1098-5514

pii

JVI.00512-12

journal_volume

86

pub_type

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