Journal article

Administration of Panobinostat Is Associated with Increased IL-17A mRNA in the Intestinal Epithelium of HIV-1 Patients

AB Christensen, A Dige, J Vad-Nielsen, CR Brinkmann, M Bendix, L Østergaard, M Tolstrup, OS Søgaard, TA Rasmussen, JR Nyengaard, J Agnholt, PW Denton

Mediators of Inflammation | HINDAWI LTD | Published : 2015

Abstract

Intestinal CD4+ T cell depletion is rapid and profound during early HIV-1 infection. This leads to a compromised mucosal barrier that prompts chronic systemic inflammation. The preferential loss of intestinal T helper 17 (Th17) cells in HIV-1 disease is a driver of the damage within the mucosal barrier and of disease progression. Thus, understanding the effects of new therapeutic strategies in the intestines has high priority. Histone deacetylase (HDAC) inhibitors (e.g., panobinostat) are actively under investigation as potential latency reversing agents in HIV eradication studies. These drugs have broad effects that go beyond reactivating virus, including modulation of immune pathways. We e..

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University of Melbourne Researchers

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Funding Acknowledgements

The authors thank H. Stovring for statistical advice. They thank H. Andersen, T. Meyer, and M. Guldmann-Christensen for their assistance with sectioning samples in paraffin blocks. Lars Ostergaard was supported by the Danish Council for Strategic Research (Grant no. 0603-00521B), Ole S. Sogaard was supported by the Danish Council for Strategic Research, the Danish Research Council (Grant no. 12-133887), and the Lundbeck Foundation (Grant no. R126-2012-12588). The Centre for Stochastic Geometry and Advanced Bioimaging is supported by Villum Foundation.