- Oral presentation
- Open Access
Next-generation LTR-specific Tre-recombinase targets a majority of HIV-1 isolates
© Hauber et al; licensee BioMed Central Ltd. 2014
- Published: 23 May 2014
- Antiviral Activity
- Long Terminal Repeat
- Humanize Mouse
- Human Cell Culture
- Broad Clinical Application
HIV-1 integrates into the host chromosome and persists as a provirus flanked by long terminal repeats (LTR). To date, treatment regimens primarily target the virus enzymes, virus attachment or virus-cell fusion, but not the integrated provirus. Thus, current antiretroviral therapies (i.e. cART) cannot eradicate HIV-1, a fact that highlights the urgency of pursuing new strategies to find a cure for HIV/AIDS.
Previously, we engineered an experimental LTR-specific recombinase (Tre-recombinase) that can effectively excise integrated HIV-1 proviral DNA from infected human cell cultures (Sarkar et al. 2007 Science 316:1912). Subsequently, we demonstrated highly significant antiviral activity of this HIV-1 subtype A-specific Tre in humanized mice (Hauber et al. 2013 PLOS pathogens 9:e1003587). Broad clinical application, however, requires availability of a tre-recombinase that recognizes a majority of clinical HIV-1 isolates.
Here we report LTR target site identification as well as the engineering and functional analysis of a next-generation Tre-recombinase that recognizes the vast majority (e.g. >93% clade B and >80% clade A) of clinical HIV-1 isolates.
It is shown that the HIV-1 LTR harbours a conserved region that may serve as a universal tre recognition site for provirus excision. In fact, targeting this site by next-generation tre-recombinase demonstrates pronounced antiviral activity in the absence of cellular toxicity.
The presented data suggest that next-generation Tre technology may be a valuable component of future antiretroviral therapies to reverse infection and thereby providing a cure for HIV/AIDS.
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