News Release

Antibodies from unconventional B cells less likely to neutralize HIV, NIH study finds

Immune cells adapt inefficiently in patients with uncontrolled HIV

Peer-Reviewed Publication

NIH/National Institute of Allergy and Infectious Diseases

WHAT:

Antibodies derived from a type of immune cell found in unusually high numbers in HIV-infected individuals with chronically uncontrolled virus levels are less effective at neutralizing HIV than antibodies derived from a different type of immune cell more common in people without HIV, scientists report. The findings help explain why people infected with HIV cannot sufficiently clear the virus with effective antibodies. The study was supported by the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health.

NIAID scientists and researchers at Yale University and University of Maryland drew these conclusions by studying blood samples from 25 donors with chronic HIV infection. The donors were not taking antiretroviral drugs to suppress the level of HIV in their blood, or viral load, at the time of the study. Like many individuals with persistent levels of HIV, the donors' blood samples had abnormally high numbers of immune cells called tissue-like memory (TLM) B cells, compared with resting memory (RM) B cells, which account for the majority of memory B cells in people without HIV.

To better understand how this abnormal distribution of B cell types in people with uncontrolled HIV affected their immune response to the virus, researchers compared HIV-specific antibodies derived from both TLM and RM B cells. Generally, as B cells divide in response to a pathogen like HIV, genes that produce infection-fighting antibodies mutate, and descendant cells producing the most effective antibodies predominate. Despite the fact that TLM B cells generally divided more frequently than their RM counterparts, researchers found that the antibodies derived from TLM B cells showed genetic evidence of fewer adaptive mutations than those derived from RM B cells. In turn, these antibodies were less likely to effectively neutralize HIV than those derived from RM B cells. The RM B cells, in contrast, showed evidence of generating antibodies with more helpful mutations.

The researchers believe this difference in B cell distribution among those with uncontrolled HIV adds to a list of reasons most people do not make effective antibodies against the virus.

ARTICLE:

E Meffre et al. Maturational characteristics of HIV-specific antibodies in viremic individuals. JCI Insight DOI: 10.1172/jci.insight.84610 (2016).

WHO:

NIAID Director Anthony S. Fauci, M.D., who is a coauthor on the study, is available to comment.

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CONTACT:

To schedule interviews, please contact Judith Lavelle, 301-402-1663, judith.lavelle@nih.gov.

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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