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Administration of Recombinant Rhesus Interleukin-12 during Acute Simian Immunodeficiency Virus (SIV) Infection Leads to Decreased Viral Loads Associated with Prolonged Survival in SIVmac251-Infected Rhesus Macaques
- Source :
- The Journal of Virology; February 2002, Vol. 76 Issue: 4 p1731-1743, 13p
- Publication Year :
- 2002
-
Abstract
- ABSTRACTThe ability of recombinant rhesus interleukin-12 (rMamu-IL-12) administration during acute simian immunodeficiency virus SIVmac251 infection to influence the quality of the antiviral immune responses was assessed in rhesus macaques. Group I (n= 4) was the virus-only control group. Group II and III received a conditioning regimen of rMamu-IL-12 (10 and 20 µg/kg, respectively, subcutaneously [s.c.]) on days -2 and 0. Thereafter, group II received 2 µg of IL-12 per kg and group III received 10 µg/kg s.c. twice a week for 8 weeks. On day 0 all animals were infected with SIVmac251 intravenously. While all four group I animals and three of four group II animals died by 8 and 10 months post infection (p.i.), all four group III animals remained alive for >20 months p.i. The higher IL-12 dose led to lower plasma viral loads and markedly lower peripheral blood mononuclear cell and lymph node proviral DNA loads. During the acute viremia phase, the high-IL-12-dose monkeys showed an increase in CD3-CD8a/a+and CD3+CD8 a/a+cells and, unlike the control and low-IL-12-dose animals, did not demonstrate an increase in CD4+CD45RA+CD62L+naive cells. The high-IL-12-dose animals also demonstrated that both CD8a/a+and CD8a/ß+cells produced antiviral factors early p.i., whereas only CD8a/ß+cells retained this function late p.i. Long-term survival correlated with sustained high levels of SIV gag/poland SIV envcytotoxic T lymphocytes and retention of high memory responses against nominal antigens. This is the first study to demonstrate the capacity of IL-12 to significantly protect macaques from SIV-induced disease, and it provides a useful model to more precisely identify correlates of virus-specific disease-protective responses.
Details
- Language :
- English
- ISSN :
- 0022538X and 10985514
- Volume :
- 76
- Issue :
- 4
- Database :
- Supplemental Index
- Journal :
- The Journal of Virology
- Publication Type :
- Periodical
- Accession number :
- ejs57760621
- Full Text :
- https://doi.org/10.1128/JVI.76.4.1731-1743.2002