Year: 2017
Type: article
Abstract: the pre-ART plasma phylogeny, but did not specifically align within rebound lineages.Expanded clones comprised 30% to 95% of participants' reservoirs, with similar frequencies pre-and post-ATI.Thus, sequences showed no evidence for enrichment of rebound viruses post-trial and pre-trial QVOA viruses failed to predict the identity of rebound virus.Pre-ART, rebound and QVOA Envs for each participant had similar IC50s to VRC01.Conclusions: Quantitative and phylogenetic analyses suggest a brief ATI does not expand the latent reservoir.While clonal QVOA populations comprised a substantial fraction of replication competent peripheral latent virus, they did not rebound in vivo upon ATI despite similar VRC01 sensitivities.Results provide reassurance for participants of clinical trials employing ATI and highlight the challenge of accurately characterizing the full range of the replication competent latent reservoir that reactivates in vivo.
Source: Journal of Virus Eradication
Language: English
Topic: HIV Research and Treatment
Subfield: Virology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,950
OpenAlex ID: W3041573612
