Important note: Information in this article was accurate in 2001. The state of the art may have changed since the publication date.
![]()
Reuters newMedia - Monday November 12, 2001
Louis Charbonneau
Dr. Boris Ferko, a member of the Austrian research team, said laboratory mice inoculated with flu viruses laced with material from the HIV/AIDS virus exhibited a significant anti-HIV immunity response.
The material in the flu virus appeared to function as an antigen, a substance alien to the body capable of stimulating an immune response. The details of the institute's study were published in the October 2001 issue of the Journal of Virology.
"The mice appeared to develop an immunity to the HIV virus after getting the modified influenza," Ferko told Reuters on Friday.
There is currently no vaccine for HIV, which has infected an estimated 36 million people worldwide and left 22 million dead from AIDS since 1981. While more than 90 potential vaccines have reached the human trial stage, it remains to be seen whether any of the candidates will prove effective in preventing HIV infection.
Ferko is optimistic and believes there will be a functioning HIV vaccine for humans in the not-too-distant future.
"We think that recombinant influenza viruses are a promising vaccine candidate to help prevent or control various infectious diseases such as HIV," Ferko said, adding that such a vaccine would be perfectly safe. Recombinant viruses are ones that have been genetically altered from the parent viruses. Their genes have been literally recombined to form a new genetic pattern.
HIV has proven especially difficult for vaccine developers because it is an elusive, constantly mutating virus that misleads and systemically destroys the human immune system.
While the research is a good beginning, Ferko said his team had a lot of work to do before they had a flu-based HIV vaccine that could be administered as a routine jab to humans.
The next step in Ferko's research will be to immunize mice with the recombinant influenza/HIV viruses. Afterwards, the mice will be tested with pathogenic, or disease-causing, HIV viruses.
If the mice prove resistant, they will test the vaccine out on a primate. If the vaccine works on primate subjects, Ferko and his colleagues will set to work on producing a human vaccine.
"It could work," said Ferko, adding that the institute hoped to take part in a European Union funded HIV research program with their modified-flu HIV vaccine.
He said that if all went well, the HIV vaccine could be ready for human trials within a year.
011112
RE011117
Copyright © 2001 - Reuters, Ltd. All rights reserved. Republication or redistribution of Reuters content is expressly prohibited without the prior written consent of Reuters. Reuters shall not be liable for any errors or delays in the content, or for any actions taken in reliance thereon. Contact Reuters.
AEGiS is a 501(c)3, not-for-profit, tax-exempt, educational corporation. AEGiS is made possible through unrestricted funding from Broadway Cares/Equity Fights AIDS, Elton John AIDS Foundation, the National Library of Medicine, Pacific Life Foundation and donations from users like you.
Always watch for outdated information. This article first appeared in 2001. This material is designed to support, not replace, the relationship that exists between you and your doctor.
AEGiS presents published material, reprinted with permission and neither endorses nor opposes any material. All information contained on this website, including information relating to health conditions, products, and treatments, is for informational purposes only. It is often presented in summary or aggregate form. It is not meant to be a substitute for the advice provided by your own physician or other medical professionals. Always discuss treatment options with a doctor who specializes in treating HIV.
Copyright ©1980, 2001. AEGiS. All materials appearing on AEGiS are protected by copyright as a collective work or compilation under U.S. copyright and other laws and are the property of AEGiS, or the party credited as the provider of the content. .