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By growing vaginal skin cells outside the body and studying the way they interact with 'good and bad' bacteria, researchers at the University of Texas Medical Branch at Galveston think that they may be able to better identify the good bacteria that protect women from HIV infection and other sexually transmitted infections.
The health of the human vagina depends on a symbiotic/mutually beneficial relationship with 'good' bacteria that live on its surface feeding on products produced by vaginal skin cells. These good bacteria, in turn, create a physical and chemical barrier to bad bacteria and viruses including HIV. A publication released from a team of scientists representing multiple disciplines at UTMB and the Oak Crest Institute of Science in Pasadena, Calif., reports a new method for studying the relationship between the skin cells and the 'good' bacteria.
The researchers are the first to grow human vaginal skin cells in a dish in a manner that creates surfaces that support colonization by the complex good and bad communities of bacteria collected from women during routine gynecological exams. The bacteria communities have never before been successfully grown outside a human. The research group led by Richard Pyles at UTMB reports that by using this model of the human vagina, they discovered that certain bacterial communities alter the way HIV infects and replicates.
Their laboratory model will allow careful and controlled evaluation of the complex community of bacteria to ultimately identify those species that weaken the defenses against HIV. Pyles also indicated that this model 'will provide the opportunity to study the way that these mixed species bacterial communities change the activity of vaginal applicants including over-the-counter products like douches and prescription medications and contraceptives. These types of studies are very difficult or even impossible to complete in women who are participating in clinical trials.'
In fact, the team's report documented the potential for their system to better evaluate current and future antimicrobial drugs in terms of how they interact with 'good and bad' bacteria. The study is published in the journal PLOS One.
Other possible HIV cures
Should we be optimistic or cautious? This isn't the first time that we've been presented with tales that an HIV cure is on its way. The most famous of them are:
The Berlin Patient Case Leukaemia
For a long time researchers believed there was no cure. Even five years ago, a scientist who wanted to work on HIV cure research was laughed at. But all that changed with Timothy Brown aka the Berlin Patient. Brown an HIV-positive man who developed leukaemia. After first-line cancer treatments failed, a bone marrow transplant procedure was done. Two transplants later, not only was his leukaemia in remission, his immune system actually managed to ward off HIV. Brown no longer takes antiretroviral drugs or tests positive for HIV. Essentially, he was cured. Read more
Bee venom to cure HIV?
A study suggested that bee venom might have the potency to kill the human immunodeficiency virus (HIV). Researchers at the Washington University School of Medicine had demonstrated that a toxin called melittin which is found in bee venom is the reason for this. The researchers used nanoparticle technology to target the virus. Particles smaller than HIV were infused with bee venom and since HIV cells are smaller than normal body cells the nanoparticles only targeted HIV.
'Melittin on the nanoparticles fuses with the viral envelope,' said research instructor Joshua L. Hood, MD, PhD. 'The melittin forms little pore-like attack complexes and ruptures the envelope, stripping it off the virus.' Adding, 'We are attacking an inherent physical property of HIV. Theoretically, there isn't any way for the virus to adapt to that. The virus has to have a protective coat, a double-layered membrane that covers the virus.'
Stem cell therapy to overcome HIV?
In a path-breaking breakthrough two American were believed to have overcome HIV after undergoing stem-cell therapy! The news has met with widespread elation with experts believing that a cure might be on the cards. Doctors from the Brigham and Women's Hospital in Boston announced on Wednesday night that two previously HIV-positive patients no longer had detectable virus levels in their blood or tissue after having bone marrow stem-cell transplants to treat cancer between two and four years ago, the Age reported. (Read more )
Aggressive antiretroviral treatment the Mississippi baby case
There were reports in March 2013 of a toddler who was completely cured of the virus after being born of it. She has been cured of the disease after following an aggressive regime of drugs. This was the second documented case of a person being completely cured of the virus after an adult known as the Berlin Patient was cured as a result of bone-marrow transplant. This startling piece of information was discovered when the baby's mother stopped treatment and doctors lost track of the baby who was given a bout of heavy drugs (current procedure suggests only a modest daily dose of antiretroviral treatment) about 30 hours after she was born at a rural Mississippi hospital, doctors said at a medical meeting in Atlanta. However, a doctor poured cold water on cold water on what was termed 'the greatest medical breakthrough of the century'.
In his piece, Dr Siedner pointed out in his column, exposure to HIV doesn't mean that the baby will have HIV. 'We will likely never know if those cells were from the child or maternal cell that has been transmitted during pregnancy or birth.' When a child is born, he or she has some maternal cells in his system so it's impossible to tell whether the child actually had HIV or not, or the tests detected the maternal HIV positive cells.
The MX2 gene
According to a study published in the journal Nature, scientists have discovered a new gene which can inhibit the HIV virus from spreading after it has entered the body. The study was led by Dr Caroline Goujon and Professor Mike Malim at the Department of Infectious Diseases, King's College London. It was conducted by introducing the virus to two separate lines of human cells. On one line, they introduced the MX2 gene along with the virus, while on the other they didn't. The line on which the MX2 gene was introduced, it was seen that the virus had stopped replicating. (Read more.)
With inputs from ANI
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