Public Release: 

Animal study paints picture of the earliest immune responses to HIV

NIH-funded research provides insights for development of HIV prevention tools

NIH/National Institute of Allergy and Infectious Diseases

New research in monkeys exposed to SIV, the monkey equivalent of HIV, suggests that the virus spreads rapidly in the body and triggers early host responses that suppress antiviral immunity, thus promoting viral replication. The study, published in Cell, provides a detailed view of the period between initial mucosal exposure to the virus and the point at which it becomes detectable in the blood. A better understanding of these early events, which are difficult if not impossible to study in people with HIV, will inform development of strategies to prevent HIV infection. The work was funded by the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health.

Researchers led by Dan H. Barouch, M.D., Ph.D., of Beth Israel Deaconess Medical Center and the Ragon Institute of Massachusetts General Hospital, the Massachusetts Institute of Technology and Harvard, vaginally exposed 44 rhesus monkeys to SIV and then analyzed the animals in detail during the first few days after viral exposure. The scientists found that SIV disseminates rapidly through the body, with viral RNA present in at least one tissue outside the reproductive tract in most monkeys analyzed one day after vaginal exposure.

The researchers also observed an inflammatory immune response in virus-infected tissues as early as one day after exposure to SIV. Increasing amounts of viral RNA correlated with rising amounts of a host protein that suppresses non-specific, or innate, antiviral immunity. Additionally, the scientists detected early activation of a cell-signaling pathway that correlated with lower levels of antiviral T-cell responses and higher levels of SIV replication.

According to the authors, these findings suggest that the window of opportunity to contain or eliminate the virus at its mucosal port of entry is more limited than previously appreciated. Researchers may apply these insights to the continued development of vaccines, microbicides and drugs aimed at preventing HIV infection.

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ARTICLE: DH Barouch et al. Rapid inflammasome activation following mucosal SIV infection of rhesus monkeys. Cell DOI: 10.1016/j.cell.2016.03.021 (2016).

WHO: NIAID Director Anthony S. Fauci, M.D., and Carl Dieffenbach, Ph.D., director of NIAID's Division of AIDS, are available for comment.

CONTACT: To schedule interviews, please contact Hillary Hoffman, (301) 402-1663, hillary.hoffman@nih.gov.

This study represents a collaboration among multiple NIH-funded laboratories, including those led by Dan Barouch, M.D., Ph.D., Beth Israel Deaconess Medical Center; Rafick Sekaly, Ph.D., Case Western Reserve University; and Jeffrey Lifson, M.D., Leidos Biomedical Research, Frederick National Laboratory for Cancer Research.

NIAID conducts and supports research--at NIH, throughout the United States, and worldwide--to study the causes of infectious and immune-mediated diseases, and to develop better means of preventing, diagnosing and treating these illnesses. News releases, fact sheets and other NIAID-related materials are available on the NIAID website.

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/.

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