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               <mods:identifier type="citation">Nat Med  . 2020 Sep;26(9):1339-1350.</mods:identifier>
               <mods:identifier type="doi">10.1038/s41591-020-1022-1</mods:identifier>
               <mods:identifier type="e-issn">1546-170X</mods:identifier>
               <mods:identifier type="journal">Nature medicine</mods:identifier>
               <mods:identifier type="pubmedID">32895573</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/12088</mods:identifier>
               <mods:abstract>Therapeutic strategies are being clinically tested either to eradicate latent HIV reservoirs or to achieve virologic control in the absence of antiretroviral therapy. Attaining this goal will require a consensus on how best to measure the numbers of persistently infected cells with the potential to cause viral rebound after antiretroviral-therapy cessation in assessing the results of cure-directed strategies in vivo. Current measurements assess various aspects of the HIV provirus and its functionality and produce divergent results. Here, we provide recommendations from the BEAT-HIV Martin Delaney Collaboratory on which viral measurements should be prioritized in HIV-cure-directed clinical trials.</mods:abstract>
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                  <mods:topic>HIV latency</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>HIV reservoirs</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Viral measurements</mods:topic>
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               <mods:subject>
                  <mods:topic>HIV Cure</mods:topic>
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               </mods:subject>
               <mods:subject>
                  <mods:topic>Replication-competent HIV</mods:topic>
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               <mods:titleInfo>
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