Human ocular-derived virus-specific CD4+ T cells control Varicella zoster virus replication in human retinal pigment epithelial cells
PURPOSE. Varicella zoster virus (VZV)-induced retinitis is characterized by the presence of virus-infected cells in the retinal layer and the ocular infiltration of VZV-specific T cells. Herein, the susceptibility of human retinal pigment epithelial (RPE) cells to VZV infection and the ability of virus-specific CD4+T cells to control VZV infection in RPE cells in vitro is addressed. METHODS. Human primary RPE cell cultures (n = 2) were infected with a VZV strain expressing green fluorescent protein. The infection and viability of infected RPE cells was monitored by flow cytometry or by a fluorescent imager on RPE monolayers. RPE cells, pretreated with or without interferon-γ (IFN-γ), were infected with VZV and subsequently cultured with VZV-specific CD4+T-cell clones (TCCs; n = 3) recognizing disparate VZV proteins presented by different HLA class II alleles. IFN-γ production and cytotoxicity of the TCCs in response to VZV-infected RPE cells was determined by flow cytometry. RESULTS. Human RPE cells are permissive to a productive VZV infection. VZV-infected RPE cells presented the cognate antigen to the CD4+TCCs only if the RPE cells were pretreated with IFN-γ and expressed the appropriate HLA class II allele. VZV-specific TCCs inhibited productive VZV infection in RPE cells, which was in part attributed to TCC-mediated killing of the VZV-infected RPE cells. CONCLUSIONS. The results presented suggest that RPE cells may play a role as retina-resident antigen-presenting cells in the intraocular, VZV-specific, T cell-mediated inflammatory response of VZV-induced uveitis.
|Persistent URL||dx.doi.org/10.1167/iovs.08-2611, hdl.handle.net/1765/25298|
|Journal||Investigative Ophthalmology & Visual Science|
Milikan, J.C, Baarsma, G.S, Kuijpers, R.W.A.M, Osterhaus, A.D.M.E, & Verjans, G.M.G.M. (2009). Human ocular-derived virus-specific CD4+ T cells control Varicella zoster virus replication in human retinal pigment epithelial cells. Investigative Ophthalmology & Visual Science, 50(2), 743–751. doi:10.1167/iovs.08-2611