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Scientists create ebola vaccine
OSAC ^ | December 10, 2003 | BBC

Posted on 12/10/2003 10:34:33 AM PST by LurkedLongEnough

Scientists have successfully immunised mice against the deadly ebola virus which has killed thousands in Africa.

They used virus-like particles (VLPs) which are non-infectious but are capable of triggering a strong response by the immune system.

Usually lethal doses of ebola had no impact on the vaccinated mice.

The study, by the US Army Medical Research Institute of Infectious Diseases, is published in Proceedings of the National Academy of Sciences.

It looks like a virus, so you have the protective immune response, but it's basically an empty shell.

The scientists hope their work will lead to a vaccine which will protect humans from the virus, which causes haemorrhagic fever and kills up to 90% of its victims.

Not only is it one of the world's most lethal diseases, terrorism experts fear it could be used as a biological weapon.

Currently there are no available vaccines or therapies.

The researchers created VLPs from two ebola virus proteins. These VLPs resemble the outer covering of infectious viral particles, but lack the genetic material necessary to reproduce themselves.

Mice were vaccinated with VLPs three times at three-week intervals and exposed to the ebola virus six weeks after the last vaccination.

The result was 100% protection with no signs of illness in the immunized mice.

VLPs have already been tested and found efficacious as vaccines for several other viruses, including HIV.

The next stage will be to test the vaccine in primates.

Lead researcher Dr Steve Bavari said: "The beauty of this approach is that VLPs are not a traditional vaccine platform, so you don't have to worry about the recipient building up an immunity to that platform.

"It looks like a virus, so you have the protective immune response, but it's basically an empty shell."

The researchers also believe VLPs could be used to develop new tests to identify ebola-infected samples.

Colonel Erik Henchal, commander of USAMRIID, said: "This is astonishing work.

"The ability to produce self-assembling particles that resemble whole virus will give us a new tool to evaluate the combination of variables required to produce a protective immune response to ebola virus."


TOPICS: Culture/Society; Front Page News; News/Current Events
KEYWORDS: ebola; ebolavaccine; usamriid; vaccine; vhfs

1 posted on 12/10/2003 10:34:33 AM PST by LurkedLongEnough
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To: neverdem
ping - saw your Nov post on what looked like another govt group working on this.
2 posted on 12/10/2003 10:38:11 AM PST by LurkedLongEnough (Oh no, I won't leave no stone un-turned...)
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To: LurkedLongEnough
The next stage will be to test the vaccine in primates.

They go directly from mice to apes? Shouldn't they test on puppy dogs first?

3 posted on 12/10/2003 10:40:30 AM PST by RightWhale (Close your tag lines)
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To: LurkedLongEnough
Thanks for posting this.

This would be wonderful. I hope a vaccine won't cost too much.

4 posted on 12/10/2003 10:41:50 AM PST by syriacus (Schumer's unhappy federal judges have lifetime positions, so he should work to amend that.)
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To: LurkedLongEnough
BTT!
5 posted on 12/10/2003 10:42:27 AM PST by varina davis
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To: RightWhale
Some ebola strains affect apes but not humans. Now that you mention it, ape testing could be a waste of time. Just go right to Al-Qaeda prisoners.
6 posted on 12/10/2003 10:49:08 AM PST by LurkedLongEnough (Oh no, I won't leave no stone un-turned...)
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Comment #7 Removed by Moderator

To: Yehuda
I would like to point out that exposure to Ebola is only 70-90% fatal.

Exposure to Hillary... well, it's guaranteed to make 100% of Americans crazy, in one way or another.

8 posted on 12/10/2003 11:55:21 AM PST by LurkedLongEnough (Oh no, I won't leave no stone un-turned...)
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To: LurkedLongEnough
"VLPs have already been tested and found efficacious as vaccines for several other viruses, including HIV."

To my knowledge, there are no effective HIV/AIDS vaccines.

9 posted on 12/12/2003 1:22:09 PM PST by neverdem (Xin loi, min oi)
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