Researchers at UC Davis have made some surprising discoveries  about the body's initial responses to HIV infection. Studying simian  immunodeficiency virus (SIV), the team found that specialized cells in  the intestine called Paneth cells are early responders to viral invasion  and are the source of gut inflammation by producing a cytokine called  interleukin-1 beta (IL-1β).
Though aimed at the presence of virus, IL-1β causes breakdown of the  gut epithelium that provides a barrier to protect the body against  pathogens. Importantly, this occurs prior to the wide spread viral  infection and immune cell killing. But in an interesting twist, a  beneficial bacterium, Lactobacillus plantarum, helps mitigate the  virus-induced inflammatory response and protects gut epithelial barrier.  The study was published in the journal PLoS Pathogens.
One of the biggest obstacles to complete viral eradication and immune  recovery is the stable HIV reservoir in the gut. There is very little  information about the early viral invasion and the establishment of the  gut reservoir.
"We want to understand what enables the virus to invade the gut,  cause inflammation and kill the immune cells," said Satya Dandekar, lead  author of the study and chair of the Department of Medical Microbiology  and Immunology at UC Davis.
"Our study has identified Paneth cells as initial virus sensors in  the gut that may induce early gut inflammation, cause tissue damage and  help spread the viral infection. Our findings provide potential targets  and new biomarkers for intervening or blocking early spread of viral  infection," she said.
In the study, the researchers detected a very small number of SIV  infected cells in the gut within initial 2.5 days of viral infection;  however, the inflammatory response to the virus was playing havoc with  the gut lining. IL-1β was reducing the production of tight-junction  proteins, which are crucial to making the intestinal barrier impermeable  to pathogens. As a result, the normally cohesive barrier was breaking  down.
Digging deeper, the researchers found the inflammatory response  through IL-1β production was initiated in Paneth cells, which are known  to protect the intestinal stem cells to replenish the epithelial lining.  This is the first report of Paneth cell sensing of SIV infection and  IL-1β production that links to gut epithelial damage during early viral  invasion. In turn, the epithelial breakdown underscores that there's  more to the immune response than immune cells.
"The epithelium is more than a physical barrier," said first author  Lauren Hirao. "It's providing support to immune cells in their defense  against viruses and bacteria."
The researchers found that addition of a specific probiotic strain,  Lactobacillus plantarum, to the gut reversed the damage by rapidly  reducing IL-1β, resolving inflammation, and accelerating repair within  hours. The study points to interesting possibilities of harnessing  synergistic host-microbe interactions to intervene early viral spread  and gut inflammation and to mitigate intestinal complications associated  with HIV infection.
"Understanding the players in the immune response will be important  to develop new therapies," said Hirao. "Seeing how these events play out  can help us find the most opportune moments to intervene."
- Lauren A. Hirao, Irina Grishina, Olivier Bourry, William K. Hu, Monsicha Somrit, Sumathi Sankaran-Walters, Chris A. Gaulke, Anne N. Fenton, Jay A. Li, Robert W. Crawford, Frank Chuang, Ross Tarara, Maria L. Marco, Andreas J. Bäumler, Holland Cheng, Satya Dandekar. Early Mucosal Sensing of SIV Infection by Paneth Cells Induces IL-1β Production and Initiates Gut Epithelial Disruption. PLoS Pathogens, 2014; 10 (8): e1004311 DOI: 10.1371/journal.ppat.1004311
 
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