HIV-1 Infected Cell Turnover During Antiretroviral Therapy
Author Information
Author(s): Marek Fischer, Beda Joos, Barbara Niederöst, Philipp Kaiser, Roland Hafner, Viktor von Wyl, Martina Ackermann, Rainer Weber, Huldrych F. Günthard
Primary Institution: University Hospital Zürich
Hypothesis
The study aims to define the in vivo decay kinetics of HIV-1 infected cells during antiretroviral therapy.
Conclusion
The study found that latently HIV-infected cells exhibit biphasic decay kinetics, with rapid initial decreases followed by persistence.
Supporting Evidence
- HIV-RNA+ PBMC can be stratified into four distinct viral transcriptional classes.
- Two overlapping cell-classes of high viral transcriptional activity rapidly declined to undetectable levels.
- Cells expressing HIV-RNA at low and intermediate levels persisted during cART.
Takeaway
This study looked at how HIV-infected cells behave when patients start treatment, finding that some cells disappear quickly while others stick around.
Methodology
The study used patient-matched PCR and limiting dilution analysis to assess HIV-infected cell classes in peripheral blood mononuclear cells over one year.
Potential Biases
Potential biases may arise from the small number of patients and the specific treatment regimen used.
Limitations
The study had a small sample size and limited statistical resolution between different cell classes.
Participant Demographics
Five chronically HIV-1 infected therapy-naïve patients were included.
Statistical Information
P-Value
p = 0.0006
Confidence Interval
95% CI not specified
Statistical Significance
p<0.05
Digital Object Identifier (DOI)
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