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Poster Exhibition - International AIDS Society

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we need to comprehensively characterize all cell types that may contribute to it, as<br />

each cell type may have unique mechanisms of latency and persistence.<br />

In poster 7, Zink et al., identify macrophages as another potential cell type that may<br />

be contributing to the HIV reservoir within the CNS. In poster 8, Ruel et al., studied<br />

pediatric cART cases in Uganda and identified that the HIV reservoir is most<br />

pronounced in naïve CD4+ T-cells and is predominantly established by CXCR4-tropic<br />

virus. This work highlights important considerations for strategies aimed at virus<br />

eradication because of the differences that may exist between viral reservoirs in<br />

adults and children. Finally, in poster 9, Donahue et al., proposed superinfection of<br />

latently infected cells as a potential mechanism for the emergence of multi-drug<br />

resistant virus.<br />

3. Determine the origins of immune activation and inflammation in the presence of<br />

ART and their consequences for HIV persistence<br />

It’s well known that chronic immune activation and inflammation caused by HIV<br />

plays a central role in premature ageing, bone disease, heart disease and several<br />

other debilitating conditions. However, their role in the establishment and<br />

maintenance of viral reservoirs is less well understood. In posters 10-14, the authors<br />

identify several new immune mediators that may play a key role in HIV persistence.<br />

In poster 11, Naicker et al., propose polymorphisms in IL-10 as a potential mediator<br />

of altered cytokine production that may act as a driver of chronic HIV infection and<br />

HIV persistence. In poster 13, Reece et al., studied an SIV model confirming that viral<br />

reservoirs are established early and highlighting the need for early interventions to<br />

restrict their expansion. Additionally, they suggested that eliminating cells while<br />

under high turnover would achieve the greatest impact in reducing viral reservoirs.<br />

4. Determine host and immune mechanisms that control infection but allow viral<br />

persistence<br />

Numerous studies have investigated the correlates of protection and viral control<br />

against HIV, highlighting strong CTL responses and broad neutralizing antibodies.<br />

However, their relationship to viral persistence remains to be determined. In posters<br />

15-16, the authors attempt to dissect this relationship and in the process uncover<br />

some interesting findings. In poster 16, Conceicao et al., undertook genome wide<br />

expression studies of patients pre- and post-cART and compared these against a<br />

panel of long-term non-progressors (LTNP). Their findings suggest that LTNP have a<br />

block in apoptosis pathways which in turn favors strong immune responses that<br />

assists in controlling viremia.<br />

5. Study, compare and validate assays to measure persistent infection<br />

<strong>Poster</strong> 17 studied viral replication in human M1-MDM (monocyte-derived<br />

macrophage). They showed a transient but robust restriction of HIV replication in<br />

those cells compared to M2-MDM. In <strong>Poster</strong> 18 the role of Vacc-4x, a p24 peptidebased<br />

HIV therapeutic vaccine, was evaluated in 135 patients. The authors showed

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