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New role for immune system player may help improve cancer vaccines

Researchers have discovered that a molecule best known for its anti-microbial properties also has the ability to activate key cells in the immune response. This newly discovered function, reported in the Nov. 1, 2002, issue of Science*, suggests the molecule, a peptide called -defensin 2, may be useful in the development of more effective cancer vaccines. Scientists have found that -defensin 2 initiates a chain of events leading to the growth and multiplication of T cells, components of the immune system that recognize and kill foreign cells that have invaded the body.

Defensins are known to be an important component of the body's immediate response to infection. -defensin 2 attacks and destroys a broad range of bacteria as part of the innate immune system, the body's first line of defense against such infections.

The new finding links -defensin 2 to the second arm of the immune system, adaptive immunity. The adaptive immune response combats pathogens that evade the body's initial defense mechanisms. Unlike innate immunity, the adaptive immune system develops specifically in response to an infection, changing as needed to ward off each invader.

"This link between the innate and adaptive immune systems is important for our understanding of the body's ability to detect infection," said Arya Biragyn, Ph.D., National Cancer Institute (NCI) staff scientist and first author of the study. "-defensin 2 is likely to play an important role in the immune system's ability to recognize protein fragments from the body's own cells, including tumor cells."

Working in both mice and laboratory cell cultures, Biragyn and his colleagues found that -defensin 2 directly activates immune cells known as dendritic cells. Once activated, dendritic cells interact with other components of the immune system to stimulate the multiplication of a subset of T cells that will recognize and destroy infected cells. Dendritic cells can also trigger attack of tu
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Contact: NCI Press Office
NCIPressOfficers@mail.nih.gov
301-496-6641
NIH/National Cancer Institute
31-Oct-2002


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