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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 ...