This news is archived NICHD Archive
Note: Information on this page was accurate at the time of publication.
This page is no longer being updated.

Anti-herpes drug may help control HIV, NIH study finds

Friday, March 13, 2015

Valacyclovir, a drug commonly used to control the virus that causes genital herpes, appears to reduce the levels of HIV in patients who do not have genital herpes, according to a study by researchers from the National Institutes of Health, Case Western Reserve University, Cleveland, Emory University, Atlanta and Lima, Peru.  

The study of 18 patients is the first to show that the drug does not require the presence of herpes simplex virus 2 (HSV-2) to suppress HIV in patients. The researchers hope to confirm their results in a larger study.

“These findings are very encouraging,” said senior author Leonid Margolis, Ph.D., head of the Section on Intercellular Interactions at the NIH’s Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD). “If valacyclovir’s effectiveness against HIV can be confirmed in a larger cohort, it could be added to the mix of drugs used to suppress the virus, and might prove especially helpful in cases in which HIV has developed resistance to other drugs.”

The study, published online today in Clinical Infectious Diseases, was supported by NIH’s Bench to Bedside Program, which funds research teams seeking to translate basic scientific findings into medical practice. The first authors of this paper are Christophe Vanpouille and Andrea Lisco, both with NICHD. Other authors are Michael Lederman (senior author) and Benigno Rodriguez of Case Western Reserve University and Case Medical Center and Hospitals; Leda Bassit, Robert Kauffman, and Raymond F. Schinazi (senior author), Emory University School of Medicine and Veterans Administration Medical Center in Atlanta; and Jorge Sanchez, of The Civic Association for Health and Education in Lima. 

These results follow a 2008 study by the same research team, which showed that acyclovir suppresses HIV in laboratory cultures of human tissues that were infected with various kinds of herpes viruses. Valacyclovir is referred to as a prodrug for acyclovir because it’s structurally similar to acyclovir, and is converted to acyclovir in the body.  For the current study, the researchers used valacyclovir because it remains in the blood longer than acyclovir and so would not need to be taken as often.

Earlier studies have shown that acyclovir reduces HIV levels in patients coinfected with HIV and HSV-2, the virus that causes genital herpes. However, this effect has been attributed to the drug’s anti-HSV-2 activity. The decrease in immune activity results in fewer active immune cells for HIV to infect. 

In contrast, the laboratory results of theresearch team indicated that the drug likely reduced HIV levels by interfering directly with HIV’s reproductive machinery and did not require the presence of HSV-2. HSV-2 chemically alters acyclovir, by attaching chemical groups known as phosphates to it. It is this altered form of the drug that suppresses HSV-2. The researchers believe this form also interferes with HIV’s ability to reproduce. In their earlier study, the researchers found that many other kinds of herpes viruses can also attach phosphate groups to acyclovir. Dr. Margolis noted that these other herpes viruses are widespread and that most people harbor at least one of them.

“We wanted to find out whether such a mechanism could operate in the cells of patients with HIV,” Dr. Margolis said.

The researchers enrolled 18 HIV-infected patients in their study, none of whom were infected with HSV-2, and treated them with valacyclovir. For 12 weeks, half of the enrolled patients took valacyclovir twice a day while the other half received a placebo. After two weeks, the placebo group received valacyclovir while the group originally treated with the drug switched to the placebo.

The researchers found that when the patients took valacyclovir, their blood HIV levels declined significantly. Typically, HIV patients take a cocktail of several anti-HIV drugs because a single drug is not enough to suppress the virus. Multiple HIV medications also hinder the virus’ ability to develop resistance to the drugs. 

The researchers conducted a genetic analysis and found that the HIV in the study volunteers did not develop resistance to valacyclovir. But because HIV has a history of becoming resistant to the drugs used to treat it, the researchers do not discount the possibility that the virus could develop resistance to valacyclovir with longer treatment. Given the ability of the drug to lower HIV levels, however, the researchers believe that valacyclovir could one day be added to the cocktail of drugs given to HIV-infected people.

“Larger randomized trials and cost effectiveness analyses could be warranted to further explore the potential of [valacyclovir] in the context of HIV-1 infection, in particular in combination with other antivirals,” the study authors wrote.

###

About the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD): NICHD sponsors research on development, before and after birth; maternal, child, and family health; reproductive biology and population issues; and medical rehabilitation. For more information, visit the Institute's website at http://www.nichd.nih.gov/.  

About the National Institutes of Health (NIH): NIH, the nation's medical research agency, includes 27 Institutes and Centers and is a component of the U.S. Department of Health and Human Services. NIH is the primary federal agency conducting and supporting basic, clinical, and translational medical research, and is investigating the causes, treatments, and cures for both common and rare diseases. For more information about NIH and its programs, visit http://www.nih.gov.

top of pageBACK TO TOP