Simian Immunodeficiency Virus (SIV) infects different primate species and is regarded as the origin of the HIV.
In the study by an international research team, including scientists from the German Primate Centre (DPZ), SIV-infected rhesus macaques were treated with an antiretroviral drug for 90 days and in addition they were treated with a specific antibody for 23 weeks.
After finishing this therapy, all macaques showed sustained control of the infection as almost no SI viruses could be detected in the blood and gastro-intestinal tissues.
Two years after finishing the treatment the viral load remained low, the immune system intact, and the rhesus macaques healthy.
The strategy offers a new and promising approach to the therapy of HIV infections in humans, researchers said.
Antiretroviral therapy is currently the most frequently used treatment of HIV infections. The drugs effectively block the proliferation of the HI viruses in the infected cells and thus delay the onset of the disease.
However, these drugs have to be administered permanently since their discontinuation would immediately lead to virus rebound in the body.
The focus of the study conducted in the US under the leadership of scientists from the Emory University School of Medicine and the National Institutes of Health (NIH) was on the MHC class I genes as well as the genes of the killer cell immunoglobulin-like receptors (KIR).
Both gene families are essential for a functional immune system as well as for immunological identity of an organism.
It is administered to patients to treat chronic inflammatory bowel diseases such as Crohn's and ulcerative colitis where the CD4+ T cells also play an important role.
The scientists are seeking to test the new treatment strategy in clinical trials with HIV patients. A phase-I clinical trial is already underway in the US.
The aim is to find out whether a combination of antiretroviral therapy with Vedolizumab has the same effect in humans, researchers said.
The study was published in the journal Science.
Disclaimer: No Business Standard Journalist was involved in creation of this content
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