Scientists may have found a clue to why people living with HIV have double the likelihood of developing heart disease. The findings, made by researchers at the University of Pittsburgh Center for Vaccine Research and National Institutes of Health, also show that an experimental drug may hold promise as a potential treatment.
The increased heart disease risk is driven by a subset of immune cells in people with HIV which continue to express a protein that triggers blood clotting and inflammation even after the HIV virus is under control by medication, the scientists explain in Science Translational Medicine.
Furthermore, the researchers found that Ixolaris, an experimental drug isolated from tick saliva and previously tested to treat blood clots in animals, successfully reduced the inflammation in monkeys infected with SIV, the primate form of HIV.
"People are living long, fruitful lives with HIV thanks to tremendous strides in antiviral treatment regimens, however those lives are being cut short due to perplexingly high rates of heart disease," said co-senior author Ivona Pandrea, M.D., Ph.D., professor of pathology in Pitt's Center for Vaccine Research. "By uncovering one of the cellular mechanisms driving the heart disease, we can look for medications - such as Ixolaris - that specifically target and disrupt that mechanism."
Co-senior author Irini Sereti, M.D., of the NIH's National Institute of Allergy and Infectious Diseases (NIAID), tested blood samples from people without HIV, people with HIV whose infections were well-controlled by antiretroviral therapy and people with HIV who weren't on the medications. The researchers found an elevated number of immune cells called monocytes that expressed high levels of the 'tissue factor' protein, which is associated with blood clotting and other inflammatory proteins, in the blood from people with HIV, regardless of how well their infection was controlled.
These findings were confirmed by Pandrea and her team in monkeys that progress to AIDS after infection with SIV. The same cells isolated from a different species of monkey that usually does not develop heart disease when infected with SIV do not produce tissue factor, thus reinforcing the role of this damaging protein in triggering cardiovascular disease in the HIV/SIV settings.
The scientists then exposed the human blood samples to Ixolaris and observed that the drug blocked the activity of tissue factor. When tested in a small group of monkeys during early SIV infection, the treatment significantly lowered the levels of inflammatory proteins linked to cardiovascular disease.
NIH holds the patent for Ixolaris, which is a small molecule found in the saliva of the tick Ixodes scapularis - commonly known as the deer or blacklegged tick - and was uncovered by study co-author Ivo M. B. Francischetti, M.D., Ph.D., of NIAID. More studies are needed to test the drug's safety and interaction with other drugs that are used for HIV patients. Ixolaris has not been tested in humans and the results could differ, the researchers also cautioned.
"This treatment has the potential to improve the clinical management of HIV-infected patients and help them to live longer, healthier lives with HIV," said Pandrea. "That, and other therapies that may arise from targeting the inflammation pathway we discovered, are exciting avenues for future research."
In addition to Pitt and NIH, co-authors are from the Frederick National Laboratory for Cancer Research; Fundação Oswaldo Cruz and Fundação José Silveira, both in Brazil; the University of Cape Town; Vanderbilt University; University of Vermont; Los Alamos National Laboratory; and Universidade de Lisboa in Portugal.
This research was funded by NIAID's Intramural Research Program and Bench-to-Bedside award R01 HL117715-10S1; NIH contract HHSN261200800001E; NIH grants R01 HL123096, R01 HL117715, R01 AI119346 and R01 AI104373.
Article: Inflammatory monocytes expressing tissue factor drive SIV and HIV coagulopathy, Irini Sereti et al., Science Translational Medicine, doi: 10.1126/scitranslmed.aam5441, published 30 August 2017.