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Prion Diseases

Variant Creutzfeldt-Jakob Disease

In some cases, TSE diseases appear to be infectious. For example, there is good evidence that a newly discovered TSE disease-variant Creutzfeldt-Jakob Disease (vCJD)-was first spread to humans from cattle infected with BSE. Identifying the transmissible agent is still an ongoing area of research.

A leading hypothesis about the origin of vCJD is that abnormal forms of prion protein ingested through diseased meat may sicken people by causing normal human prion protein to form incorrectly. This change from normal to abnormal prion protein spreads in the brain, where the misshapen protein aggregates in the spaces between brain cells and may produce disease. An alternative hypothesis is that the disease could be transmitted by a virus that subsequently triggers the process of forming abnormal prion protein.

Health officials in the United Kingdom have responded to evidence that beef infected with BSE may have spread vCJD to humans. Since the 1980s, when the BSE epidemic began in the United Kingdom, millions of cattle in Europe have been destroyed. In 1997, the U.S. Department of Agriculture (USDA) then reacted by outlawing feeding meat and bone meal products to cattle intended for U.S. consumption.

As of fall 2006, worldwide, there have been 200 reported cases of vCJD, according to the Centers for Disease Control and Prevention (CDC). All of these cases were among people who ate beef in a country with a BSE outbreak, and nearly all (164 cases) were in the United Kingdom. Three U.S. cases have been reported, though these individuals were likely exposed to BSE agent while in the United Kingdom.

The first North American case of BSE was found in Canada in May 2003. Discovery of the first U.S. case of BSE followed in December 2003 in a Washington State cow. In June 2005, a second cow in the U.S. tested positive for BSE in Texas. USDA ascertained that the cow was born in 2001, 4 years after the 1997 USDA ban. A third BSE-infected cow was found in Alabama in March 2006. No cases of endemic vCJD have been associated with consumption of domestic beef in the United States.

Another human type of TSE, CJD, is similar to vCJD but progresses much more quickly and affects older people. CJD is extremely rare with an estimated 1 case per million individuals. Although a majority of cases occur without a known cause, the disease may be inherited. Rare transmission of CJD through infection also has been documented.

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See Also

  • Breakthrough in Detecting Prion Infections
  • Prion Therapy Inhibits Infection in Mice
  • Prion Disease News Releases
  • View a video explaining NIAID scientist Byron Caughey's research on developing a better test for the proteins responsible for mad cow disease (Windows Media Player Format, SMIL captioned, 3 MB, Credit: ScienCentral, Inc.)
    How do I view captions in Windows Media Player? (PDF)
  • Related Links

    View a list of links for more information about prion diseases.

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    See Also

  • Breakthrough in Detecting Prion Infections
  • Prion Therapy Inhibits Infection in Mice
  • Prion Disease News Releases
  • View a video explaining NIAID scientist Byron Caughey's research on developing a better test for the proteins responsible for mad cow disease (Windows Media Player Format, SMIL captioned, 3 MB, Credit: ScienCentral, Inc.)
    How do I view captions in Windows Media Player? (PDF)
  • Related Links

    View a list of links for more information about prion diseases.