-Caveat Lector-

Interim report issued after almost two years of 'mad cow' inquiry

LONDON (AP) - Serum extracted from British cattle was still being used to
manufacture human vaccines up until 1991 - six years after the first case of
so-called "mad cow disease" was discovered, according to a report issued
Thursday.

Pharmaceutical companies stopped using British bovine serum in the early
1990s, the report noted, but it is unclear how long the existing vaccine
stock remained on the shelves.

The 226-page interim report is a summary of expert testimony and information
gathered during the first 22 months of an inquiry into bovine spongiform
encephalopathy, the technical name for "mad cow."

The report shows that bovine materials were used in numerous vaccines before
1991, including children's vaccines for mumps, measles and rubella, and adult
vaccines for diphtheria and tetanus.

In 1990, the government's BSE Working Group said it believed benefits from
the vaccinations outweighed the "very remote risk to the population," the
report noted. Nonetheless, the group asked pharmaceutical manufacturers to
stop using British bovine products "as soon as possible," it said.

The names of the pharmaceutical companies and their products were not
included in the report.

Scientists believe there may be a connection between BSE and a new strain of
Creutzfeldt-Jakob disease, which has been linked to 46 deaths in Britain
since the mid-1980s. The spongiform diseases eat holes in the brains of
victims, and no cure has been discovered.

In August, the European Union lifted a ban on British beef exports that had
been imposed in 1996 because of fears of the new disease.
The BSE inquiry is expected to wrap up Dec. 17 and a final report submitted
to Parliament by the end of March.

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