HIV study identifies key cellular defence mechanism
Monday 7 November
Scientists have moved a step closer to understanding how one of our body’s own proteins helps stop the human immunodeficiency virus (HIV) in its tracks.
The study, carried out by researchers at the Medical Research Council National Institute for Medical Research and The University of Manchester and published in Nature, provides a blueprint for the design of new drugs to treat HIV infection, say the researchers.
Scientists in the United States and France recently discovered that a protein named SAMHD1 was able to prevent HIV replicating in a group of white blood cells called myeloid cells.
Now, crucially, UK researchers have shown how SAMHD1 prevents the virus from replicating itself within these cells, opening up the possibility of creating drugs that imitate this biological process.
Dr Ian Taylor from the MRC National Institute for Medical Research explained: “Our research has given us an insight into the detailed interactions between the HIV virus and a particular protein inside human cells. We now wish to define more precisely, at a molecular level, how the SAMHD1 protein functions. If we can achieve this, it will pave the way for new therapeutic approaches to HIV and even vaccine development.”
Dr Michelle Webb, who led the study in Manchester’s School of Biomedicine at the University of Manchester, said: “HIV is one of the most common chronic infectious diseases on the planet, so understanding its biology is critical to the development of new antiviral compounds. SAMHD1 has been shown to prevent the HIV virus replicating in certain cells but precisely how it does this wasn’t known. Our research has found that SAMHD1 is able to degrade deoxynucleotides, which are the building blocks required for replication of the virus. If we can stop the virus from replicating within these cells we can prevent it from spreading to other cells and halt the progress of the infection.”
The study was funded by the Medical Research Council, the European Union Seventh Framework Programme and the European Leukodystrophy Association.
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Notes for editors:
The paper, ‘HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolase,’ is published in Nature.
