Audrey E Rindler, K. Kusejko, H. Kuster, Kathrin Neumann, Christine Leemann, Marius Zeeb, S. E. Chaudron, D. Braun, R. Kouyos, K. Metzner, H. Günthard
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引用次数: 1
Abstract
BACKGROUND
HIV-1 replication capacity (RC) of transmitted/founder viruses may influence the further course of HIV-1 infection.
METHODS
Replication capacities (RCs) of 355 whole genome primary HIV-1 isolates derived from samples acquired during acute and recent primary HIV-1 infection (PHI) were determined using a novel high throughput infection assay in primary cells. The RCs were used to elucidate potential factors that could be associated with RC during PHI.
RESULTS
Increased RC was found to be associated with increased set point viral load (VL), and significant differences in RCs among 13 different HIV-1 subtypes were discerned. Notably, we observed an increase in RCs for primary HIV-1 isolates of HIV-1 subtype B over a 17-year period. Associations were not observed between RC and CD4 count at sample date of RC measurement, CD4 recovery after initiation of antiretroviral treatment (ART), CD4 decline in untreated individuals, and acute retroviral syndrome severity scores.
DISCUSSION
These findings highlight that RCs of primary HIV-1 isolates acquired during the acute and recent phase of infection are more associated with viral factors, i.e., set point VL, than with host factors. Furthermore, we observed a temporal increase in RC for HIV-1 subtype B viruses over a period of 17 years.