A role for the JAK-STAT1 pathway in blocking replication of HSV-1 in dendritic cells and macrophages
© Mott et al. 2009
Received: 05 March 2009
Accepted: 13 May 2009
Published: 13 May 2009
Macrophages and dendritic cells (DCs) play key roles in host defense against HSV-1 infection. Although macrophages and DCs can be infected by herpes simplex virus type 1 (HSV-1), both cell types are resistant to HSV-1 replication. The aim of our study was to determine factor (s) that are involved in the resistance of DCs and macrophages to productive HSV-1 infection.
We report here that, in contrast to bone marrow-derived DCs and macrophages from wild type mice, DCs and macrophages isolated from signal transducers and activators of transcription-1 deficient (STAT1-/-) mice were susceptible to HSV-1 replication and the production of viral mRNAs and DNA. There were differences in expression of immediate early, early, and late gene transcripts between STAT1+/+ and STAT1-/- infected APCs.
These results suggest for the first time that the JAK-STAT1 pathway is involved in blocking replication of HSV-1 in DCs and macrophages.
Macrophages and DCs are bone marrow-derived cells that are involved in antigen capture, processing, and presentation and thus play a key role in triggering the immune system against infectious agents [1–6]. Although both macrophages  and DCs  cross-present antigens, only DCs are capable of stimulating naive CD8+ T cells [9, 10]. DCs also play an important role in initiation of NK anti-viral immunity [11, 12]. Similar to DCs, macrophages also play a variety of roles in immune system-mediated defense, including a central role in innate or natural immunity. Macrophages exhibit a wide variety of functions, including phagocytosis, tumor cytotoxicity, cytokine secretion and antigen presentation [13–15]. A number of factors are known that "activate" or engage macrophages in these activities, including viral infection.
Herpes simplex virus (HSV) infections are among the most frequent serious viral infections in the U.S. and are considered to be a major health issue in developed countries [16–19]. Both macrophages and DCs perform crucial roles in linking innate and adaptive immunity and augmenting the immune response to HSV-1 infection. It was previously shown that human blood monocytes are resistant to HSV-1 infection [20–22], although a more recent study reported that immature monocyte-derived human DCs could be moderately infected with HSV-1, resulting in productive infection . Bone marrow-derived macrophages are also resistant to HSV-1 infection [24–28].
The factors involved in the resistance of DCs and macrophages to productive HSV-1 infection are not known. The aim of our study was to determine if STAT1 might play a role in DC and macrophage resistance to HSV-1 replication. We found that DCs and macrophages isolated from STAT1-/- mice lost their resistance to HSV-1 infection. Thus, STAT1 seems to be critically important for allowing DCs and macrophages to resist HSV-1 replication.
Materials and methods
Virus, cells, and mice
Triple plaque purified HSV-1 strains McKrae, KOS, and GFP-VP22 were grown in rabbit skin (RS) cell monolayers in minimal essential media (MEM) containing 5% fetal calf serum. GFP-VP22 (a gift from Peter O'hare; Marie Curie Research Institute, Surrey, United Kingdom) is a recombinant virus that contains the gene encoding a major tegument protein, VP22, linked to green fluorescent protein (GFP) [29, 30]. Six week old female BALB/c (The Jackson Laboratory), 129SVE-STAT1-/-, and 129SVE (Taconic) mice were used as a source of bone marrow (BM) for the generation of mouse DCs and macrophages in cultures. BM cells were isolated by flushing femurs and tibiae with PBS. Pelleted cells were briefly resuspended in water to lyse red blood cells and stabilized by adding complete medium (RPMI 1640, 10% fetal bovine serum, 100 U/ml penicillin, 100 μg/ml streptomycin, 2 mM L-glutamine). The cells were centrifuged and resuspended in complete medium supplemented with either murine Flt3-ligand (100 ng/ml; Peprotech, NJ) or GM-CSF (100 ng/ml; Peprotech, NJ) to enhance replication of DCs . To grow macrophages, the media was supplemented with CSF (100 ng/ml; Peprotech, NJ) instead of Fl3tL or GM-CSF. The cells were plated in non-tissue culture plastic Petri dishes (1 bone per 10 cm dish) for 5 days at 37°C with CO2. After 5 days, the media is removed, the adherent cells were recovered by incubating the cells for 5 min. at 37°C with Versene (Invitrogen, San Diego, CA). Cells were washed, counted, and plated onto tissue-culture dishes for use the following day.
Virus replication in tissue culture
Monolayers of macrophages or DCs were infected with various amounts of HSV-1 strain McKrae ranging from 0.01 to 10 PFU/cell. One hr after infection at 37°C or 4°C, virus was removed and the infected cells were washed three times with fresh media at the appropriate temperature and fresh media was added to each well. The monolayers including media were harvested at various times by freezing at -80°C. Virus was harvested by two cycles of freeze-thawing and infectious virus titers were determined by standard plaque assays on RS cells as we previously described .
Viral RNA and DNA extraction and cDNA preparation in vitro
DCs or macrophages grown in 24-well plates were infected with 10 PFU/cell of HSV-1 strain McKrae. RNA preparation was done as we previously described . Briefly, frozen cells were resuspended in TRIzol and homogenized, followed by addition of chloroform, and subsequent precipitation using isopropanol. The RNA was then treated with DNase I to degrade any contaminating genomic DNA followed by clean-up using a Qiagen RNeasy column as described in the manufacturer's instructions. The RNA yield from all samples was determined by spectroscopy (NanoDrop ND-1000, NanoDrop Technologies, Inc., Wilmington, Delaware). Finally, 1000 ng of total RNA was reverse-transcribed using random hexamer primers and Murine Leukemia Virus (MuLV) Reverse Transcriptase from the High Capacity cDNA Reverse Transcription Kit (Applied Biosystems, Foster City, CA), in accordance with the manufacturer's recommendations.
DNA isolation was done as we previously described . Briefly, cells from each well in tissue culture media were frozen and thawed 2 times at -80°C prior to processing. The lysed cells from each well were transferred to individual microcentrifuge tubes and centrifuged at 3000 rpm to clear cellular debris. The supernatant was recovered and centrifuged in a microcentrifuge at 14,000 rpm to recover the viral DNA pellet. The pellet was digested for 2 hours at 55°C in TE buffer containing 0.1% SDS and 200 μg of Proteinase K. The mixture was extracted with Phenol/Chloroform followed by subsequent viral DNA precipitation using ethanol.
TaqMan Real-Time PCR
The expression levels of several viral genes, along with the expression of the cellular GAPDH gene (internal control) were evaluated using commercially available TaqMan Gene Expression Assays (Applied Biosystems, Foster City, CA) with optimized primer and probe concentrations as we previously described [33, 34]. Primer-probe sets consisted of two unlabeled PCR primers and the FAM™ dye-labeled TaqMan MGB probe formulated into a single mixture. The HSV-1 ICP0, ICP4, TK, and gB primers and probe used were as follows: 1) ICP0: forward primer, 5'-CGGACACGGAACTGTTCGA-3'; reverse primer, 5'-CGCCCCCGCAACTG-3'; and probe, 5'-FAM-CCCCATCCACGCCCTG-3' – Amplicon length = 111 bp; 2) ICP4: forward primer, 5'-GCGTCGTCGAGGTCGT-3'; reverse primer, 5'-CGCGGAGACGGAGGAG-3'; and probe, 5'-FAM-CACGACCCCGACCACC-3' – Amplicon length = 69 bp; 3) TK: forward primer, 5'-CAGTAGCGTGGGCATTTTCTG-3'; reverse primer, 5'-CCTCGCCGGCAACAAAA-3'; and probe, 5'-FAM-CTCCAGGCGGACTTC-3' – Amplicon length = 59 bp; and 4) gB: forward primer, 5'-AACGCGACGCACATCAAG-3', reverse primer, 5'-CTGGTACGCGATCAGAAAGC-3'; and probe, 5'-FAM-CAGCCGCAGTACTACC-3' – Amplicon length = 72 bp. As an internal control, a set of GAPDH primers from Applied Biosystems (ASSAY I.D. m999999.15_G1 – Amplicon Length = 107 bp) was used.
Quantitative real-time PCR was performed as we described previously . Real-time PCR was performed in triplicate for each sample from each time point. Relative gene expression levels were normalized to the expression of the GAPDH housekeeping gene (endogenous loading control).
Flow Cytometric Analysis
Infected or mock infected cells were harvested and stained with anti-CD8a-PerCp (clone 53-6.7), anti-CD11b-APC (clone M1/70), anti-CD11c-FITC (clone HL3), anti-CD45R/B220-PerCP (clone RA3-6B2), anti-CD40-PE (clone 1C10), anti-Gr-1-PE (clone RB6-8C5), anti-CD80-FITC (clone 16-10A1), anti-CD83-APC (clone Michel-19), anti-CD86-PE (clone GL1), anti-CD154-PE (clone MR1), anti-MHC class I-FITC (clone 34-1-2S), anti-MHC class II-APC (clone M5/114.15.2), anti-B7-HI-PE (clone MIH5), B7-DC (clone 122), anti-Annexin-PE, and 7-ADD from BD PharMingen (San Diego, CA) and Biolegend (San Diego, CA) and then analyzed by FACS as we previously described .
Confocal Microscopy and Image Analysis
Macrophages or DCs isolated from STAT1-deficient or control 129SVE mice grown on Lab-Tex chamber slides were infected with HSV-1 GFP-VP22 (ranging from 0.01 to 10 PFU for 24 h) as previously reported [29, 30]. This GFP-expressing recombinant virus allows for direct monitoring of virus infectivity without additional manipulation. We visualized GFP expression together with F4/80 Ag-PE (as a macrophage marker) or CD11c-PE (as a DC marker) immunostaining 24 h after HSV-1 GFP-VP22 infection. Briefly, cells were fixed by incubating slides in methanol for 10 min followed by acetone for 5 min at -20°C. Afterwards, slides were rinsed three times for 5 min each at ambient temperature in PBS containing 0.05% v/v Tween-20 (PBS-T). Slides were then blocked for 30 min at ambient temperature in PBS-T containing 1% w/v BSA (PBS-TB). Immunostaining was done according to a direct method using F4/80 Ag-PE or CD11c-PE antibodies (1:200 in PBS-TB for 1 h at ambient temperature) (Becton Dickinson). After an additional three rinses at ambient temperature in PBS-T for 5 min each, slides were dipped into ddH2O (to remove salt) and mounted in ProLong Gold mounting media containing DAPI (Invitrogen).
Images were captured at 1024 × 1024 pixels (original magnification = 20×) in independent fluorescence channels using a Nikon C1 eclipse inverted confocal microscope. We then exported images (n = 3 per condition) as 8-bit greyscale TIFF files for image analysis using Image J software, release 1.40 g. Quantification of GFP labeling was done by first inverting greyscale images and then using thresholding mode to select positive pixels. Data are represented as % immunolabeled area (positive pixels/total pixels captured × 100%). All analyses were done by a single examiner (T.T.) blinded to sample identities, and code was not broken until the analysis was completed.
Statistics were done by Student's t test or Fisher's exact test using Instat (GraphPad, San Diego, CA). Results were considered to be statistically significant if the p value was < 0.05.
HSV-1 replication in DCs isolated from BALB/c mice
Virus attachment/DC-virus complex formation
To determine if there were possible defects in virus association with DCs, we infected highly permissive RS cells (positive control) and DCs with 10 PFU/cell of McKrae and kept the infected cells at 4°C or 37°C for 1 hr to allow viral attachment. Unbound virus was removed by washing 3× with fresh media at the incubation temperature. The same amount of tissue culture media was added to each cell monolayer in 24 well plates and the cells were frozen at -80°C. After two cycles of freeze-thawing, we determined virus titer by plaque assay. At both 4°C and 37°C, the amount of infectious virus that was detected associated with the DCs was equal to or greater than the amount of infectious virus associated with the RS cells (Fig. 1B). This suggests that the low virus titer in DCs was probably not the result of poor virus attachment to DCs as compared to RS cells.
Replication of HSV-1 in DCs isolated from STAT1-/- mice
Viral DNA in STAT1-/- compared to normal DCs
To further confirm the titration results described above (Fig. 2A), we also determined the amount of gB DNA as a measure of the relative amount of viral genomic DNA (Fig. 2B). Infected STAT1-/- DCs had significantly more gB DNA than the STAT+/+ parental 129SVE DCs (p < 0.05). This was also consistent with reduced HSV-1 replication in wild type DCs compared to STAT1-/- DCs, and suggests that the block in HSV-1 replication in wild type DCs occurs prior to viral DNA replication.
Viral transcription in STAT1-/- compared to normal DCs
Effect of HSV-1 infection on cell surface markers on wild type and STAT1-/- DCs
HSV-1 replication in BM-derived macrophages isolated from BALB/c mice
Macrophages isolated from STAT1-/- mice are susceptible to HSV-1 infection
Macrophages were isolated from STAT1-/- mice and parental 129SVE mice and infected with 10 PFU/cell of HSV-1 strain McKrae. Similar to the results described above for DCs, macrophages from STAT1-/- mice were more susceptible to HSV-1 infection than macrophages from wild-type 129SVE mice as judged by virus yield (Fig. 5A), levels of gB mRNA (Fig. 5B), and the amount of genomic DNA (Fig. 5C). As with DCs from STAT1-/- mice, virus replication in macrophages from these mice approached that seen in highly-susceptible RS cells. Thus, in the absence of STAT1, HSV-1 replication in murine macrophages and DCs was highly efficient.
Detection of GFP expression in infected DCs and macrophages by confocal microscopy
It was previously reported that freshly isolated peripheral blood monocytes and lymphocytes are resistant to HSV infection [20–22]. Similarly, infection of resident peritoneal macrophages with HSV-1 results in an abortive infection in which the viral DNA is not replicated and no infectious virus is produced [24–28]. Another study showed that while both mature and immature monocyte-derived DCs are infected by HSV-1, only immature DCs produce infectious virus, but at ten-fold lower levels than most cell lines, despite the fact that DCs express HSV receptors . However, the mechanism of DC and macrophage resistance to HSV-1 replication is not known. Mature DCs are also resistant to productive infection with influenza virus  and dengue virus . We show here that BM-derived DCs and macrophages isolated from wild type mice, including BALB/c or 129SVE strains and C57BL/6 strain (data not shown) do not support replication of HSV-1 as judged by virus yield, viral mRNA transcription, confocal microscopy of a GFP-viral fusion protein, and viral genomic DNA levels. However, in DCs from STAT1-/- mice, HSV-1 replication approached that seen in RS cells. We report here that HSV-1 attaches as efficiently to DCs as it does to the highly permissive RS cells, suggesting that the DCs non-permissiveness for HSV-1 is not due to a defect in viral attachment. Thus, non-permissiveness of DCs to HSV-1 appears due to either inefficient virus penetration or a block in the virus' replication cycle. Since it seems more likely that STAT1 would affect virus replication, we lean towards this explanation. However, it should be noted that the experiments reported here do not definitively distinguish between a block in virus entry versus a block in virus replication. Since RS cells support very efficient replication of HSV-1, these results suggest that STAT1 plays a key role in the resistance of DCs and macrophages to HSV-1 replication. We would predict that STAT1 may also be involved in resistance of DCs to influenza virus and dengue virus, sinceChlamydia trachomatis also propagates more efficiently in STAT1-null or STAT1 knockdown cells .
STAT1-deficient mice are highly sensitive to infection by microbial pathogens and viruses [40–44] including HSV-1, which replicates to approximately 1000-fold higher titers in the eyes of STAT1-/- mice compared to wt mice . We obtained similar results when STAT1-/- mice were ocularly infected with HSV-1 strain McKrae or KOS (data not shown). The experiments presented here constitute the first report of a virus replicating more efficiently in DCs and macrophages from STAT1 deficient mice. In addition, the increased HSV-1 replication in DCs and macrophages from STAT1-/- mice was approximately 1000-fold higher than in wild type mice, similar to that reported in the eyes of STAT1-/- mice [45, 46]. This raises the possibility that the enhanced sensitivity of STAT1 deficient mice to viruses and particularly the 1000 fold increase in HSV-1 replication in STAT1 deficient mice may be due, at least in part, to increased replication of virus in DCs and macrophages. In this regard, it has been reported that HSV-infected DCs are compromised by the infection process and have reduced T-cell stimulatory capacity [47–49].
The increased replication of HSV-1 in STAT1-/- DCs and macrophages shown here might be an important factor contributing to increased susceptibility of STAT1-/- mice to infection. However, since transfer of BM-derived DCs or macrophages from wild-type mice to STAT1-deficient mice did not reduce the susceptibility of STAT1-deficient mice to HSV-1 infection, even when the avirulent HSV-1 strain KOS was used for ocular challenge (data not shown), additional factors are likely involved. Surprisingly, STAT1-/- and STAT1+/+ mice had similar levels of corneal scarring following ocular HSV-1 infection (data not shown). Thus, the resistance of APCs in STAT1+/+ mice to HSV-1 replication compared to the permissiveness of APCs in STAT1-/- mice to HSV-1 replication, did not appear to play an important role in protecting mice against either death or corneal scarring.
STAT1 is one of the seven members of the mammalian STAT family. STATs participate in gene control and are activated when cells encounter various extracellular polypeptides . Targeted disruption of the STAT1 gene in mice revealed a role for STAT1 in the JAK-STAT signaling pathway . The JAK-STAT signaling pathway is involved in mediating biologic responses induced by many cytokines . STAT1-deficient mice lack responsiveness to IFN-α and IFN-γ [40–44]. Thus, it is possible that the absence of responsiveness to IFN-α or IFN-γ in DCs and macrophages isolated from STAT1-deficient mice contributes to their susceptibility to HSV-1 infection. However, IFN-α production does not appear to correlate with innate protection against HSV-2  and we previously showed that expression of murine IFN-γ by an HSV-1 recombinant virus does not impair virus replication [53, 54]. Furthermore, incubation of STAT1+/+ DCs or macrophages in the presence of anti-IFN-α mAb, anti-IFN-γ mAb, or both mAbs did not increase HSV-1 replication in infected DCs (data not shown).
We have shown here for the first time that STAT1 (likely via the JAK-STAT1 pathway) is involved in suppressing HSV-1 replication in murine DCs and macrophages. In addition, the lack of virus replication in wild-type APCs did not appear to be due to transcriptional blockage of HSV-1 α, β, or γ genes, although viral DNA replication did not occur.
This work was supported by NIH grants EY14966 and EY15557 to HG.
- Pozzi LA, Maciaszek JW, Rock KL: Both dendritic cells and macrophages can stimulate naive CD8 T cells in vivo to proliferate, develop effector function, and differentiate into memory cells. J Immunol 2005,175:2071–2081.PubMed
- Broeke LT, Daschbach E, Thomas EK, Andringa G, Berzofsky JA: Dendritic cell-induced activation of adaptive and innate antitumor immunity. J Immunol 2003,171:5842–5852.PubMed
- Colonna M, Pulendran B, Iwasaki A: Dendritic cells at the host-pathogen interface. Nature Immunol 2006,7:117–120.View Article
- Mellman I, Steinman RM: Dendritic cells: specialized and regulated antigen processing machines. Cell 2001,106:255–258.View ArticlePubMed
- Steinman RM, Witmer MD, Nussenzweig MC, Chen LL, Schlesinger S, Cohn ZA: Dendritic cells of the mouse: identification and characterization. J Invest Dermatol 1980,75:14–16.View ArticlePubMed
- Steinman RM, Cohn ZA: Identification of a novel cell type in peripheral lymphoid organs of mice. I. Morphology, quantitation, tissue distribution. J Exp Med 1973,137:1142–1162.View ArticlePubMed
- Bellone M, Iezzi G, Rovere P, Galati G, Ronchetti A, Protti MP, Davoust J, Rugarli C, Manfredi AA: Processing of engulfed apoptotic bodies yields T cell epitopes. J Immunol 1997,159:5391–5399.PubMed
- Albert ML, Sauter B, Bhardwaj N: Dendritic cells acquire antigen from apoptotic cells and induce class I- restricted CTLs. Nature 1998,392:86–89.View ArticlePubMed
- Ronchetti A, Rovere P, Iezzi G, Galati G, Heltai S, Protti MP, Garancini MP, Manfredi AA, Rugarli C, Bellone M: Immunogenicity of apoptotic cells in vivo: role of antigen load, antigen-presenting cells, and cytokines. J Immunol 1999,163:130–136.PubMed
- Banchereau J, Steinman RM: Dendritic cells and the control of immunity. Nature 1998,392:245–252.View ArticlePubMed
- Piccioli D, Sbrana S, Melandri E, Valiante NM: Contact-dependent stimulation and inhibition of dendritic cells by natural killer cells. J Exp Med 2002,195:335–341.View ArticlePubMed
- Ferlazzo G, Tsang ML, Moretta L, Melioli G, Steinman RM, Munz C: Human dendritic cells activate resting natural killer (NK) cells and are recognized via the NKp30 receptor by activated NK cells. J Exp Med 2002,195:343–351.View ArticlePubMed
- Young HA, Hardy KJ: Role of interferon-gamma in immune cell regulation. J Leukoc Biol 1995,58:373–381.PubMed
- Peters JH, Gieseler R, Thiele B, Steinbach F: Dendritic cells: from ontogenetic orphans to myelomonocytic descendants. Immunol Today 1996,17:273–278.View ArticlePubMed
- Steinman RM, Cohn ZA: The interaction of soluble horseradish peroxidase with mouse peritoneal macrophages in vitro. J Cell Biol 1972,55:186–204.View ArticlePubMed
- Corey L, Spear PG: Infections with herpes simplex viruses (1). N Engl J Med 1986,314:686–691.View ArticlePubMed
- Barron BA, Gee L, Hauck WW, Kurinij N, Dawson CR, Jones DB, Wilhelmus KR, Kaufman HE, Sugar J, Hyndiuk RA,et al.: Herpetic Eye Disease Study. A controlled trial of oral acyclovir for herpes simplex stromal keratitis. Ophthalmology 1994,101:1871–1882.PubMed
- Wilhelmus KR, Dawson CR, Barron BA, Bacchetti P, Gee L, Jones DB, Kaufman HE, Sugar J, Hyndiuk RA, Laibson PR, Stulting RD, Asbell PA: Risk factors for herpes simplex virus epithelial keratitis recurring during treatment of stromal keratitis or iridocyclitis. Herpetic Eye Disease Study Group. Br J Ophthalmol 1996,80:969–972.View ArticlePubMed
- Koelle DM, Ghiasi H: Prospects for developing an effective vaccine against ocular herpes simplex virus infection. Curr Eye Res 2005,30:929–942.View ArticlePubMed
- Albers I, Kirchner H, Domke-Opitz I: Resistance of human blood monocytes to infection with herpes simplex virus. Virology 1989,169:466–469.View ArticlePubMed
- Sarmiento M, Kleinerman ES: Innate resistance to herpes simplex virus infection. Human lymphocyte and monocyte inhibition of viral replication. J Immunol 1990,144:1942–1953.PubMed
- Teute H, Braun R, Kirchner H, Becker H, Munk K: Replication of herpes simplex virus in human T lymphocytes. Intervirology 1983,20:32–41.View ArticlePubMed
- Mikloska Z, Bosnjak L, Cunningham AL: Immature monocyte-derived dendritic cells are productively infected with herpes simplex virus type 1. J Virol 2001,75:5958–5964.View ArticlePubMed
- Morahan PS, Mama S, Anaraki F, Leary K: Molecular localization of abortive infection of resident peritoneal macrophages by herpes simplex virus type 1. J Virol 1989,63:2300–2307.PubMed
- Hendrzak JA, Pinto AJ, Morahan PS: Intrinsic resistance to herpes simplex virus type 1 infection in liver Kupffer cells and peritoneal macrophages from normal and immunomodulator-treated mice. Nat Immun 1992,11:26–33.PubMed
- Wu LX, Anaraki F, Morahan PS, Leary K: Transient expression of virus-specific promoters in murine resident peritoneal macrophages. J Leukoc Biol 1990,48:229–236.PubMed
- Leary K, Connor JR, Morahan PS: Comparison of herpes simplex virus type 1 DNA replication and virus production in murine bone marrow-derived and resident peritoneal macrophages. J Gen Virol 1985,66:1123–1129.View ArticlePubMed
- Sit MF, Tenney DJ, Rothstein JL, Morahan PS: Effect of macrophage activation on resistance of mouse peritoneal macrophages to infection with herpes simplex virus types 1 and 2. J Gen Virol 1988,69:1999–2010.View ArticlePubMed
- Elliott G, O'Hare P: Intercellular trafficking of VP22-GFP fusion proteins. Gene Ther 1999,6:149–151.View ArticlePubMed
- Elliott G, O'Hare P: Live-cell analysis of a green fluorescent protein-tagged herpes simplex virus infection. J Virol 1999,73:4110–4119.PubMed
- Gilliet M, Boonstra A, Paturel C, Antonenko S, Xu XL, Trinchieri G, O'Garra A, Liu YJ: The development of murine plasmacytoid dendritic cell precursors is differentially regulated by FLT3-ligand and granulocyte/macrophage colony-stimulating factor. J Exp Med 2002,195:953–958.View ArticlePubMed
- Ghiasi H, Nesburn AB, Wechsler SL: Vaccination with a cocktail of seven recombinantly expressed HSV-1 glycoproteins protects against ocular HSV-1 challenge more efficiently than vaccination with any individual glycoprotein. Vaccine 1996,14:107–112.View ArticlePubMed
- Mott KR, Osorio Y, Brown DJ, Morishige N, Wahlert A, Jester JV, Ghiasi H: The corneas of naive mice contain both CD4+ and CD8+ T cells. Mol Vis 2007,13:1802–1812.PubMed
- Mott KR, Perng GC, Osorio Y, Kousoulas KG, Ghiasi H: A Recombinant Herpes Simplex Virus Type 1 Expressing Two Additional Copies of gK Is More Pathogenic than Wild-Type Virus in Two Different Strains of Mice. J Virol 2007,81:12962–12972.View ArticlePubMed
- Osorio Y, La Point SF, Nusinowitz S, Hofman FM, Ghiasi H: CD8+-dependent CNS demyelination following ocular infection of mice with a recombinant HSV-1 expressing murine IL-2. Exp Neurol 2005,193:1–18.View ArticlePubMed
- Cunningham AL, Carbone F, Geijtenbeek TB: Langerhans cells and viral immunity. Eur J Immunol 2008,38:2377–2385.View ArticlePubMed
- Cella M, Salio M, Sakakibara Y, Langen H, Julkunen I, Lanzavecchia A: Maturation, activation, and protection of dendritic cells induced by double-stranded RNA. J Exp Med 1999,189:821–829.View ArticlePubMed
- Wu SJ, Grouard-Vogel G, Sun W, Mascola JR, Brachtel E, Putvatana R, Louder MK, Filgueira L, Marovich MA, Wong HK, Blauvelt A, Murphy GS, Robb ML, Innes BL, Birx DL, Hayes CG, Frankel SS: Human skin Langerhans cells are targets of dengue virus infection. Nature Medicine 2000,6:816–820.View ArticlePubMed
- Lad SP, Fukuda EY, Li J, de la Maza LM, Li E: Up-regulation of the JAK/STAT1 signal pathway during Chlamydia trachomatis infection. J Immunol 2005,174:7186–7193.PubMed
- Meraz MA, White JM, Sheehan KC, Bach EA, Rodig SJ, Dighe AS, Kaplan DH, Riley JK, Greenlund AC, Campbell D, Carver-Moore K, DuBois RN, Clark R, Aguet M, Schreiber RD: Targeted disruption of the Stat1 gene in mice reveals unexpected physiologic specificity in the JAK-STAT signaling pathway. Cell 1996,84:431–442.View ArticlePubMed
- Durbin JE, Johnson TR, Durbin RK, Mertz SE, Morotti RA, Peebles RS, Graham BS: The role of IFN in respiratory syncytial virus pathogenesis. J Immunol 2002,168:2944–2952.PubMed
- Karst SM, Wobus CE, Lay M, Davidson J, Virgin HW: STAT1-dependent innate immunity to a Norwalk-like virus. Science 2003,299:1575–1578.View ArticlePubMed
- Johnson LM, Scott P: STAT1 expression in dendritic cells, but not T cells, is required for immunity to Leishmania major. J Immunol 2007,178:7259–7266.PubMed
- Durbin JE, Hackenmiller R, Simon MC, Levy DE: Targeted disruption of the mouse Stat1 gene results in compromised innate immunity to viral disease. Cell 1996,84:443–450.View ArticlePubMed
- Halford WP, Weisend C, Grace J, Soboleski M, Carr DJ, Balliet JW, Imai Y, Margolis TP, Gebhardt BM: ICP0 antagonizes Stat 1-dependent repression of herpes simplex virus: implications for the regulation of viral latency. Virol J 2006,3:44.View ArticlePubMed
- Halford WP, Maender JL, Gebhardt BM: Re-evaluating the role of natural killer cells in innate resistance to herpes simplex virus type 1. Virol J 2005,2:56.View ArticlePubMed
- Kruse M, Rosorius O, Kratzer F, Stelz G, Kuhnt C, Schuler G, Hauber J, Steinkasserer A: Mature dendritic cells infected with herpes simplex virus type 1 exhibit inhibited T-cell stimulatory capacity. J Virol 2000,74:7127–7136.View ArticlePubMed
- Salio M, Cella M, Suter M, Lanzavecchia A: Inhibition of dendritic cell maturation by herpes simplex virus. Eur J Immunol 1999,29:3245–3253.View ArticlePubMed
- Prechtel AT, Turza NM, Kobelt DJ, Eisemann JI, Coffin RS, McGrath Y, Hacker C, Ju X, Zenke M, Steinkasserer A: Infection of mature dendritic cells with herpes simplex virus type 1 dramatically reduces lymphoid chemokine-mediated migration. J Gen Virol 2005,86:1645–1657.View ArticlePubMed
- Darnell JE Jr: STATs and gene regulation. Science 1997,277:1630–1635.View ArticlePubMed
- Schindler C, Levy DE, Decker T: JAK-STAT signaling: from interferons to cytokines. J Biol Chem 2007,282:20059–20063.View ArticlePubMed
- Gill N, Deacon PM, Lichty B, Mossman KL, Ashkar AA: Induction of innate immunity against herpes simplex virus type 2 infection via local delivery of Toll-like receptor ligands correlates with beta interferon production. J Virol 2006,80:9943–9950.View ArticlePubMed
- Ghiasi H, Osorio Y, Hedvat Y, Perng GC, Nesburn AB, Wechsler SL: Infection of BALB/c mice with a herpes simplex virus type 1 recombinant virus expressing IFN-g driven by the LAT promoter. Virology 2002,302:144–154.View ArticlePubMed
- Osorio Y, Ghiasi H: Comparison of adjuvant efficacy of herpes simplex virus type 1 recombinant viruses expressing TH1 and TH2 cytokine genes. J Virol 2003,77:5774–5783.View ArticlePubMed
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.