New 'armour' developed to avoid infection from AIDS virus

Key points
- The scientific community continues to strive to find the formula that will halt the advance of one of the viruses that has sparked most scientific interest over recent years.
- The research study lays down the bases of possible future pharmaceutical drugs that will enable combating the AIDS virus at its initial phase and has been published in the prestigious journal Chemistry & Biology of the Cell Group.
- The study provides a new, hitherto unexplored focus on scientific research.
- This pioneering contribution on the AIDS virus is based on the regulation of the fluidity of the cell membranes and seeks to avoid the phenomenon known as the fusion of membranes, a consequence of contact between the cell membranes and the membrane of the virus itself.
The doors are closing on the AIDS virus. The scientific community continues to strive to find the formula that will halt the advance of one of the viruses that has sparked most scientific interest over recent years. A study by the Consejo Superior de Investigaciones Científicas (CSIC) and led by Mr Félix Goñi, director of the Biophysics Unit at the CSIC-University of the Basque Country Mixed Centre, has developed a method of attack against the AIDS virus The method involves creating a prevention system, i.e. an ‘armour’ in the cells that are likely to be infected and thus impede, de facto, the virus from accessing them and starting to act on their immunological system.
The research study lays down the bases of possible future pharmaceutical drugs that will enable combating the AIDS virus at its initial phase and has been published in the prestigious journal Chemistry & Biology of the Cell Group. Participating in the research, apart from Mr Goñi, was a team from the National Biotechnology Centre (CSIC-Universidad Autónoma de Madrid) and another from the Institute of Applied Chemistry of Cataloniaa (CSIC, Barcelona). The article is entitled “Dihydrosphingomyelin impairs HIV-1 infection by rigidifying liquid-ordered membrane domains”.
The study provides a new, hitherto unexplored focus on scientific research.
This pioneering contribution on the AIDS virus is based on the regulation of the fluidity of the cell membranes and seeks to avoid the phenomenon known as the fusion of membranes, a consequence of contact between the cell membranes and the membrane of the virus itself.
The membrane is the “coating” of the cell cytoplasm and which protects it from the outside, and which has a structure similar to that of the membranes of the AIDS virus. When both membranes come into contact, and due to the fact that the cell membrane is very “fragile”, an orifice is created and fusion occurs – and a route is opened for the AIDS virus to enter, connect to a specific “receptor” of the cell and commence its viral activity.
What the researchers are seeking with this study is to strengthen the membrane structure, making it more rigid, in order to avoid this fusion of membranes and, thus, the inoculation of the cell by the AIDS virus.
Practically all treatment for the AIDS virus currently being applied is based on halting the progress of the virus once it is inside the host cell. There is but one treatment, commercially known as Enfurvitide, which attempts to stop the virus actually entering the cell. The research published in Chemistry & Biology comes to the same conclusion, but by a totally different and novel route.
“For the cell membranes and the virus to come together and this orifice be opened to allow the entrance of the virus, the membranes have to have a certain degree of fluidity, of mobility. We discovered a procedure to make the cell membranes more rigid. This could well give rise to a new pharmaceutical drug which makes the membranes more rigid and impede the entrance of the AIDS virus. Instead of the membrane being flexible, a kind of armour is established which makes the cell impenetrable”, explained Félix Goñi.
Written and revised by
David Cohen, M.D.
Our doctors write and review articles for accuracy and keep them up to date.
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