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Live-attenuated SIV expressing interleukin-4 stimulate immune response.

Vaccine Weekly

| April 02, 2003 | COPYRIGHT 2003 NewsRX. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

2003 APR 2 - (NewsRx.com & NewsRx.net) -- Live-attenuated simian immunodeficiency viruses expressing interleukin-4 or interferon-gamma stimulated an immune response in macaques.

According to recent research from Germany, "Nef deletion mutants of SIV-expressing interleukin-4 (SIV-IL4) or interferon-gamma (SIV-IFN) were constructed to study the effect of interferon-gamma (IFN-gamma) and interleukin-4 (IL-4) on viral load, immunogenicity, and protective properties. Four rhesus monkeys were infected with SIV-IL4 and four were infected with SIV-IFN. During the acute phase of infection, the cell-associated viral load, but not the plasma viral RNA load, was approximately 10-fold lower in SIV-IFN-infected macaques than in SIV-IL4-infected rhesus monkeys."

"The viral load declined to hardly detectable levels 4 months postinfection in all animals," said Christiane Stahl-Hennig and collaborators at Ruhr-University Bochum, Universitat Erlangen-Nuernberg, and the Deutsches Primatenzentrum. "SIV antibody titers and the affinity of these antibodies were higher in SIV-IL4-infected macaques than in SIV-IFN-infected animals, consistent with a stimulation of T helper cell type 2 immune responses by IL-4. At peak viremia, there was a trend to higher interleukin-12 and perforin mRNA levels of the lymph nodes in the SIV-IFN-infected macaques than in the SIV-IL4-infected monkeys. Deletion of the viral IFN gene, but not the viral IL-4 gene, after the development of antiviral immune responses suggests a repressive ...

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