2015
DOI: 10.1097/qad.0000000000000548
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Adenovirus vectors as HIV-1 vaccines

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Cited by 9 publications
(8 citation statements)
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“…The use of persistent replicating viral vectors could be instrumental in safely mimicking attenuated HIV antigenic presentation and helping mature and maintain a protective response via vaccine, as suggested by studies in NHP models using CMV as a vector for SIV genes (23)(24)(25). However, a detailed assessment of the mucosal immune responses induced by these viral vectors, including IA, is warranted if they are to be used as a chimeric vector bearing HIV antigens (26,27). Additionally, it has been shown that an activated immune microenvironment prior to vaccination can HIV coreceptor CCR5, the activation markers CD69 and Ki-67, and markers of cell migration and retention (α 4 β 7 , α 4 β 1 , α E β 7 ) in blood, cervix, and rectum.…”
Section: Introductionmentioning
confidence: 99%
“…The use of persistent replicating viral vectors could be instrumental in safely mimicking attenuated HIV antigenic presentation and helping mature and maintain a protective response via vaccine, as suggested by studies in NHP models using CMV as a vector for SIV genes (23)(24)(25). However, a detailed assessment of the mucosal immune responses induced by these viral vectors, including IA, is warranted if they are to be used as a chimeric vector bearing HIV antigens (26,27). Additionally, it has been shown that an activated immune microenvironment prior to vaccination can HIV coreceptor CCR5, the activation markers CD69 and Ki-67, and markers of cell migration and retention (α 4 β 7 , α 4 β 1 , α E β 7 ) in blood, cervix, and rectum.…”
Section: Introductionmentioning
confidence: 99%
“…There is reasonable consensus that both humoral and T-cell responses will be required for an effective HIV vaccine [1][2][3][4] and vaccine candidates designed to elicit these responses have undergone efficacy trials. Two trials (Step/Phambili) tested an adenovirus serotype-5 (Ad5) vector encoding HIV-1 Gag/Pol/Nef (MRKAd5 HIV-1) designed to induce T-cells to reduce viremia [5][6][7].…”
Section: Introductionmentioning
confidence: 99%
“…119 Therefore, concern regarding preexisting vector immunity prompted the development of other Ad vectors with lower seroprevalence, including Ad26 and Ad35. 120,121 Ad26 and Ad35 studies have shown potential in phase I/II human vaccine trials. [122][123][124][125] A recent randomized, double-blind, placebo-controlled trial in 218 healthy adults using Ad26.…”
Section: New Vectorsmentioning
confidence: 99%