Abstract
The human cytomegalovirus UL111A gene is expressed during latent and productive infections, and it codes for homologs of interleukin-10 (IL-10). We examined whether viral IL-10 expressed during latency altered differentiation of latently infected myeloid progenitors. In comparison to infection with parental virus or mock infection, latent infection with a virus in which the gene encoding viral IL-10 has been deleted upregulated cytokines associated with dendritic cell (DC) formation and increased the proportion of myeloid DCs. These data demonstrate that viral IL-10 restricts the ability of latently infected myeloid progenitors to differentiate into DCs and identifies an immunomodulatory role for viral IL-10 which may limit the host's ability to clear latent virus.
| Original language | English |
|---|---|
| Pages (from-to) | 7465-7471 |
| Number of pages | 7 |
| Journal | Journal of Virology |
| Volume | 85 |
| Issue number | 14 |
| DOIs | |
| Publication status | Published - 15 Jul 2011 |
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