Selective inhibition of HIV replication in primary macrophages but not T lymphocytes by macrophage-derived chemokine
AUTOR(ES)
Cota, Manuela
FONTE
The National Academy of Sciences
RESUMO
Macrophage-derived chemokine (MDC) has been reported to inhibit different HIV-1 strains in activated peripheral blood mononuclear cells (T cell blasts), although other investigators have not confirmed these findings. Here we demonstrate that MDC inhibits the replication of CCR5-dependent (R5) HIV-1BaL in monocyte-derived macrophages (MDM), but not in T cell blasts, although with variable potency depending on donor variability. Analysis of HIV-1BaL proviral DNA synthesis in MDM indicated that the suppressive effect of MDC did not involve inhibition of early events such as entry or reverse transcription. Finally, an inverse correlation was observed between the levels of endogenous MDC secreted by uninfected MDM of different donors and the efficiency of different HIV strains, including two primary isolates with different coreceptor usage, to replicate in these cells. Thus, MDC represents an example of a chemokine inhibiting HIV replication in macrophages acting at one or more postentry levels in the virus life cycle.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=16839Documentos Relacionados
- Possible importance of macrophage-derived mediators in acute malaria.
- Antigen-pulsed dendritic cells expressing macrophage-derived chemokine elicit Th2 responses and promote specific humoral immunity
- Differential induction of macrophage-derived cytokines by live and dead intracellular bacteria in vitro.
- Conversion of soluble immune response suppressor to macrophage-derived suppressor factor by peroxide.
- Macrophage-derived growth factor for osteoblast-like cells and chondrocytes.