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Written By: Editorial Team | Updated : April 15, 2015 3:41 PM IST
Scientists for long now have tried to develop methods to prevent HIV but success however, has been elusive. But, a study conducted at the Laboratory of Molecular Immunology at Rockefeller University may just have discovered a new preventive therapy. They conducted a first of its type clinical trial where an experimental antibody therapy showed that it can reduce the amount of virus present in a patient's blood.
According to the researchers, the antibody called 3BNC117, can catch HIV off guard and reduce viral loads. This new antibody belongs to a generation of broadly neutralising antibodies that potently fight a wide range of HIV strains. Marina Caskey, assistant professor of clinical investigation in the Laboratory of Molecular Immunology and co-first author of the study explained that these antibodies have activity against over 80 per cent of HIV strains and they are extremely potent.The antibody 3BN117, which was originally isolated by Johannes Scheid in the Nussenzweig laboratory, targets the CD4 binding site of the HIV envelope, and the CD4 receptor is the primary site of attachment of HIV to host cells, 3BNC117 shows activity against 195 out of 237 HIV strains. Read about the 12 diseases that affect people with HIV/AIDS.
In the new study, uninfected and HIV-infected individuals were intravenously given a single dose of the antibody and monitored for 56 days. At the highest dosage level tested in the study, 30 milligrams per kilogram of weight, all eight infected individuals treated showed up to 300-fold decreases in the amount of virus measured in their blood, with most reaching their lowest viral load one week after treatment. The drop in viral load depended on the individual's starting viral load and also the sensitivity of their particular strains of HIV to the antibody. Read the 11 interesting facts about HIV/AIDS you didn't know.
This is the first time that the new generation of HIV antibodies has been tested in humans. Not only was a single dose of 3BN117 well tolerated and effective in temporarily reducing viral loads, in some individuals it remained active in the body for a long time. In half of the individuals receiving the highest dose, viral loads remained below starting levels even at the end of the 8-week study period and resistance to 3BNC117 did not occur.
Researchers believe that antibodies like 3BNC117 may be able to kill viruses hidden in infected cells, which serve as viral reservoirs inaccessible to current antiretroviral drugs. Most likely, 3BNC117, like other anti-retrovirals, will need to be used in combination with other antibodies or antiretroviral drugs to keep infections under control. One important benefit is the dosing schedule: an antibody therapy for HIV might require treatment just once every few months, compared to daily regimens of antiretroviral drugs that are now the front-line treatment for HIV. The study also raises hopes for an HIV vaccine. If researchers can induce an uninfected person's immune system to generate potent antibodies such as 3BNC117, it might be enough to block the HIV infection before it can be established.
The study is published in the journal Nature.
With inputs from PTI
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