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Exhausted B Cells Hamper Immune Response To HIV

Date:
July 14, 2008
Source:
NIH/National Institute of Allergy and Infectious Diseases
Summary:
Recent studies have shown that HIV causes a vigorous and prolonged immune response that eventually leads to the exhaustion of key immune system cells -- CD4+ and CD8+ T-cells -- that target HIV. These tired cells become less able to fight the virus. Now, researchers have shown that a similar type of exhaustion strikes another important brigade of immune system soldiers: the B cells that make virus-fighting proteins called antibodies.

Recent studies have shown that HIV causes a vigorous and prolonged immune response that eventually leads to the exhaustion of key immune system cells--CD4+ and CD8+ T-cells--that target HIV. These tired cells become less and less able to fight the virus, and the cells' fatigue contributes to the inability of an HIV-infected person's immune system to clear the virus from the body.

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Now, researchers at the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health, have shown that a similar type of exhaustion strikes another important brigade of immune system soldiers: the B cells that make virus-fighting proteins called antibodies.

In most HIV-infected individuals not receiving antiretroviral therapy, the virus replicates continuously, causing systemic disturbances that include changes in certain subsets of B cells that circulate in the blood. One of these subsets, known as "tissue-like memory B cells," is abundant in HIV-infected individuals who do not control their viral burden. These particular cells show signs of premature exhaustion and a reduced ability to make the high-quality antibodies needed to fight HIV.

As with studies of exhausted CD4+ and CD8+ T cells, these new findings related to exhausted B cells help illuminate the complex immune system damage caused by HIV, and the challenges to rebuilding or bolstering an HIV-infected person's immune system.

NIAID's HIV vaccine research program aims to increase the understanding of B cells to help inform the development of an effective vaccine, and this study contributes to this effort. The authors note that the design of a therapeutic vaccine designed to slow HIV disease progression will need to overcome or circumvent the challenge posed by the inability of certain exhausted B cells to make high-quality antibodies.


Story Source:

The above story is based on materials provided by NIH/National Institute of Allergy and Infectious Diseases. Note: Materials may be edited for content and length.


Journal Reference:

  1. S Moir et al. Evidence for HIV-associated B cell exhaustion in a dysfunctional memory B cell compartment in HIV-infected viremic individuals. Journal of Experimental Medicine, (in press) DOI: 10.1084/jem.20072683

Cite This Page:

NIH/National Institute of Allergy and Infectious Diseases. "Exhausted B Cells Hamper Immune Response To HIV." ScienceDaily. ScienceDaily, 14 July 2008. <www.sciencedaily.com/releases/2008/07/080714092726.htm>.
NIH/National Institute of Allergy and Infectious Diseases. (2008, July 14). Exhausted B Cells Hamper Immune Response To HIV. ScienceDaily. Retrieved April 21, 2015 from www.sciencedaily.com/releases/2008/07/080714092726.htm
NIH/National Institute of Allergy and Infectious Diseases. "Exhausted B Cells Hamper Immune Response To HIV." ScienceDaily. www.sciencedaily.com/releases/2008/07/080714092726.htm (accessed April 21, 2015).

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