News Release

'Repliclones' fuel perplexing persistence of HIV in the blood of some patients on therapy

Peer-Reviewed Publication

University of Pittsburgh

John Mellors, M.D.

image: Endowed Chair for Global Elimination of HIV and AIDS, and chief of the Division of Infectious Diseases at Pitt and UPMC. view more 

Credit: UPMC

PITTSBURGH, Oct. 5, 2020 - Increasingly, UPMC's chief of infectious diseases--a well-regarded expert in HIV/AIDS--is contacted by a perplexed physician describing a patient with HIV who insists they are adhering to the daily medication regimen meant to keep the virus in check, but testing says otherwise.

Virus is still showing up in the patient's blood, something clinicians believe can't happen when the infection is controlled with medication. University of Pittsburgh School of Medicine scientists report today that they've solved the mystery--and the answer has clinical implications.

In a study published in the Journal of Clinical Investigation, Pitt infectious disease researchers show that the issue isn't nonadherence to medication or resistance to the drugs. Instead, the patients are victims of what the scientists have dubbed "repliclones"--large clones of HIV-infected cells that produce infectious virus particles.

"We found that repliclones can grow large enough and produce enough virus to make it appear that antiretroviral therapy isn't working completely even when it is," said senior author John Mellors, M.D., who holds the Endowed Chair for Global Elimination of HIV and AIDS, and is chief of the Division of Infectious Diseases at Pitt and UPMC.

HIV replicates by taking over a cell's machinery and using it to produce more virus, which can then go on to infect other cells. Antiretroviral therapy, which is taken daily, prevents the virus from infecting new cells so that even though HIV can't yet be cured, it can be controlled to the point that it isn't detectable in blood tests.

Elias Halvas, Ph.D., research assistant professor in Pitt's Division of Infectious Diseases, and Mellors led a multidisciplinary team of U.S.-based HIV scientists in investigating the medical records and blood from eight patients with non-suppressible HIV viremia--detectable virus in the blood--despite adherence to antiretroviral medications. Repeated samples of each patient's blood revealed identical viral genetic sequences that did not change over time.

"This indicates that, in the individual patients, the virus in their blood was coming from identical cellular factories," said Halvas.

In short, rather than the virus going out and infecting new cells, already infected HIV-producing cells are growing into large clones that make and release virus. Current medications for HIV infection block the virus from infecting new cells but don't affect virus production from cells or clones of cells that are already infected.

"Even though we don't have evidence that the virus produced by these repliclones is then infecting new cells--which would be detrimental to the patient's immune system--they could cause other problems, such as chronic inflammation," said Mellors, who also is Distinguished Professor of Medicine at Pitt. "If the patient were to stop drug therapy, the virus could have a head-start on rebounding. And repliclones are a key barrier to developing a true cure for HIV."

The immediate implication of their discovery, Mellors said, involves informing clinicians and patients that HIV viremia can be caused by repliclones. This can help clinicians in developing disease management plans that may allow continuation of current antiretroviral regimen, knowing that switching the treatment may not suppress the viremia. Instead, the patient can be monitored over time for changes in the level of viremia, which can decline as the repliclone shrinks or sometimes can stay the same or increase slowly. Large increases in viremia should prompt the review of medication adherence again and exclusion of new drug resistance, Mellors added.

For the long-term, scientists must figure out how repliclones escape the immune systems and how they can be efficiently killed to cure the infection. While more research is needed, Mellors and his team speculate that smaller, less easily detected repliclones may be present throughout the body and be responsible for the rapid rebound of HIV in patients who stop their therapy. An added complexity is that all the cells of a repliclone may not all be making virus at the same time and thus remain hidden from the immune system as a latent or invisible reservoir of HIV.

"Many scientists around the globe are working hard to expose the HIV reservoir and destroy it," said Halvas.


Additional authors on this study are Kevin W. Joseph, B.S., Leah D. Brandt, Ph.D., Michele D. Sobolewski, M.S., Jana Jacobs, Ph.D., Camille Tumiotto, M.D., Ph.D., and Joshua C. Cyktor, Ph.D., all of Pitt; Shuang Guo, Ph.D., and Xiaolin Wu, Ph.D., of Leidos Biomedical Research, Inc.; John K. Bui, M.D., of New York-Presbyterian Hospital and Weill Cornell Medical Center; Brandon F. Keele, Ph.D., and Wei Shao, Ph.D., both of the Frederick National Laboratory for Cancer Research; Gene D. Morse, Pharm.D., of the University at Buffalo; Michael J. Bale, M.S., Mary F. Kearney, Ph.D., Stephen H. Hughes, Ph.D., and Jason W. Rausch, Ph.D., all of the National Cancer Institute; and John M. Coffin, Ph.D., of Tufts University.

This research was funded by National Cancer Institute contracts HHSN261200800001E and 75N91019D00024, and subcontract 13XS110; Howard Hughes Medical Institute; Bill & Melinda Gates Foundation award OPP1115715; National Institute for Allergy and Infectious Diseases contract UM1AI126603; Office of AIDS Research; American Cancer Society; and University of Rochester HIV/AIDS Clinical Trials Unit contract UM1 AI069511-8.

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About the University of Pittsburgh School of Medicine

As one of the nation's leading academic centers for biomedical research, the University of Pittsburgh School of Medicine integrates advanced technology with basic science across a broad range of disciplines in a continuous quest to harness the power of new knowledge and improve the human condition. Driven mainly by the School of Medicine and its affiliates, Pitt has ranked among the top 10 recipients of funding from the National Institutes of Health since 1998. In rankings recently released by the National Science Foundation, Pitt ranked fifth among all American universities in total federal science and engineering research and development support.

Likewise, the School of Medicine is equally committed to advancing the quality and strength of its medical and graduate education programs, for which it is recognized as an innovative leader, and to training highly skilled, compassionate clinicians and creative scientists well-equipped to engage in world-class research. The School of Medicine is the academic partner of UPMC, which has collaborated with the University to raise the standard of medical excellence in Pittsburgh and to position health care as a driving force behind the region's economy. For more information about the School of Medicine, see

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