Skip to main content

Targeted blockade in lethal West Nile virus encephalitis indicates a crucial role for very late antigen (VLA)-4-dependent recruitment of nitric oxide-producing macrophages


Infiltration of Ly6Chi monocytes from the blood is a hallmark of viral encephalitis. In mice with lethal encephalitis caused by West Nile virus (WNV), an emerging neurotropic flavivirus, inhibition of Ly6Chi monocyte trafficking into the brain by anti-very late antigen (VLA)-4 integrin antibody blockade at the time of first weight loss and leukocyte influx resulted in long-term survival of up to 60% of infected mice, with subsequent sterilizing immunity. This treatment had no effect on viral titers but appeared to be due to inhibition of Ly6Chi macrophage immigration. Although macrophages isolated from the infected brain induced WNV-specific CD4+ T-cell proliferation, T cells did not directly contribute to pathology, but are likely to be important in viral control, as antibody-mediated T-cell depletion could not reproduce the therapeutic benefit of anti-VLA-4. Instead, 70% of infiltrating inflammatory monocyte-derived macrophages were found to be making nitric oxide (NO). Furthermore, aminoguanidine-mediated inhibition of induced NO synthase activity in infiltrating macrophages significantly prolonged survival, indicating involvement of NO in the immunopathology. These data show for the first time the therapeutic effects of temporally targeting pathogenic NO-producing macrophages during neurotropic viral encephalitis.


During autoimmune or infectious inflammation of the central nervous system (CNS), inflammatory monocytes migrate into the brain, where they can differentiate into microglia, macrophages, and even dendritic cells [13]. The major function of infiltrating inflammatory monocytes is to initiate and amplify the immune response [46], but we have recently shown that immigration of these cells into the brain infected with West Nile virus (WNV) contributes directly to the immune pathology of the disease [2]. Inhibition of migration of these cells by anti-chemokine (C-C motif) ligand 2 (CCL2) antibody resulted in a short prolongation of survival in WNV-infected animals [2]. In this report, we extend these findings to show that inflammatory monocyte-derived macrophages not only migrate into the WNV-infected CNS, utilizing very late antigen (VLA)-4, but play a significant role in driving the immune-mediated pathology, at least in part through sustained production of NO in the symptomatic stages of disease. Importantly, for potential clinical translation, we show that pulsed anti-VLA-4 therapy during acute disease increases the survival of infected animals.


Ethics approval

All procedures were conducted with approval from the animal ethics committee of Sydney University.


Female C57BL/6 mice were intranasally inoculated with 6 × 104 or 6 × 103 plaque-forming units (PFU) WNV (Sarafend; Generated as described in 2) or phosphate buffered saline (PBS; Sham control) under anesthesia at 8 weeks old, as previously described [2, 7]. For in vivo antibody treatments, mice were injected daily with 100 μg anti-CD49d (VLA-4), CD11a (lymphocyte function-associated antigen-1; LFA-1), CD4, CD8 or isotype control antibodies (Biolegend, San Diego, CA, USA intraperitoneally from day 6 post-infection (p.i.) titrated for maximal effect. For in vivo NO inhibition, mice were injected with 300 mg/kg aminoguanidine hemisulfate (Sigma) intraperitoneally from day 6 p.i. For in vivo cathespin labeling, mice were intravenously injected with 2 nmol/l of a fluorescent agent (ProSense; VisEn Medical, Bedford, MA, USA) on day 6 p.i. Mice were killed on day 7 p.i. by cardiac perfusion under anesthesia, as previously described [7]. To determine virus titers, plaque assays using homogenized brain on baby hamster kidney cell monolayers were conducted as previously described [7]. For immunohistology, brains were cut into 8 μm sections and stained with anti-CD54 (intercellular adhesion molecule-1; ICAM-1), CD106 (vascular cell adhesion molecule 1; VCAM-1), isotype control antibodies (Biolegend), or anti-iNOS (Neomarkers Inc., Fremont, CA, USA), using a previously described immunohistochemical protocol [2]. In situ hybridization for NOS2 was conducted as previously described [7], using a P33-labeled cRNA probe. For flow-cytometry analysis, leukocytes isolated from the brain and blood were incubated with CD16/32 antibody and then labeled with fluorochrome-conjugated CD45, CD11b, Ly6C, Ly6G, F4/80, CD3, CD4, CD8, major histocompatibility complex (MHC)-II, CD80, CD86, CD49d (VLA-4), CD11a (LFA-1) or isotype control antibodies (Biolegend), using a previously described flow-cytometry protocol [2]. For detection of intracellular NO, cells were incubated with 5 μmol/l of a green fluorescent marker that is activated by NO (4-amino-5-methylamino-2',7'-difluorofluorescein diacetate (DAF-FM); Invitrogen Corp., Carlsbad, CA, USA) for 30 minutes as previously described [8]. Fluorescence was measured, and cell sorting carried out (FACS ARIA; Becton Dickinson, Franklin Lakes, NJ, USA) and analyzed using flow-cytometry software (FlowJo; TreeStar Inc., Ashland, OR, USA). For T-cell proliferation assays, Ly6Chi macrophages, Ly6C microglia and CD4+ T cells were sorted from the brains of colony-stimulating factor 1 receptor (cFMS)-enhanced green fluorescent protein (EGFP) chimeras (described previously [2]) and spleens of C57BL/6 mice on day 7 p.i. cFMS-EGFP is the promoter for CD115 (the macrophage colony-stimulating factor receptor), thus, in these mice, macrophages express EGFP. Assays using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assays were conducted in accordance with the manufacturer’s instructions (Invitrogen Corp.), with cells plated at the indicated ratios and incubated for a total of 72 hours.

Statistical analysis

Statistical analysis was conducted using one-way ANOVA with a Tukey-Kramer post hoc test, and statistical analysis of survival was conducted using the log-rank (Mantel-Cox) test. Data shown are means ± standard deviations. P < 0.05 was considered significant.

Results and discussion

Expression of integrins and cellular adhesion molecules

Previously, we have shown that WNV infection triggers significant limbic-seizure responses that occur immediately preceding death [7]. In addition, acute weight loss correlates with the infiltration of T cells (14%) and neutrophils (3%), but the most striking infiltration (by both number and percentage) are Ly6C-expressing inflammatory macrophages (~50%) (Figure 1A). This infiltration occurs between days 5 and 7 p.i. (Figure 1A) and without detectable blood–brain barrier disruption in most mice [2]. We could not isolate any from sham-infected mice (Figure 1A) [2]. The mechanism by which inflammatory monocytes enter the brain during WNV infection has not been addressed. LFA-1 and VLA-4 are integrins important for trans-endothelial migration [9], and were expressed on blood monocytes in WNV-infected and sham-infected mice (Figure 1B). Although a trend toward increased VLA-4 expression on monocytes from WNV-infected mice was seen, it was not significant. Furthermore, expression of the respective ligands for these integrins, ICAM-1 and VCAM-1, was upregulated in the WNV-infected brain. Expression of both ligands was found on platelet endothelial cell adhesion molecule-positive cerebrovascular endothelium (Figure 1C). To investigate the functional role of these integrins, we injected VLA-4-blocking antibody intraperitoneally into WNV-infected mice on day 6 p.i. Although T-cell numbers decreased, the most dramatic reduction was seen in inflammatory monocyte-derived Ly6Chi macrophages. This reduction was significantly greater in mice treated with anti-VLA-4 than in those treated with anti-LFA-1 (Figure 1D). VLA-4 antibody blockade resulted in reduced encephalitic symptoms, including a reduction in the incidence of seizures (not shown), culminating in enhanced long-term survival of 10 to 60% of mice (P < 0.001), with subsequent immunity to virus rechallenge, depending on the inoculating dose of virus used (Figure 1E). By contrast, LFA-1 blockade had no effect on the disease course (Figure 1F). Neutralization of LFA-1 or VLA-4 had no effect on viral titers in the brain on day 7 p.i. (Figure 1G), suggesting that survival is not the result of reductions in viral burden or virus cytotoxicity. However, the data support our previous findings suggesting that increased survival is the direct result of decreased inflammatory monocyte trafficking into the brain [2].

Figure 1
figure 1

VLA-4 is the primary integrin for inflammatory monocyte derived macrophages. Analysis at day 7 p.i. showed (A) CD4+ and CD8+ T cells, Ly6G+ neutrophils (~6%, 7% and 3%, respectively, of all infiltrating leukocytes), and large numbers of Ly6C+ macrophages (~50% of infiltrating leukocytes, of which >90% were Ly6Chi) infiltrating into the brain from day 5 p.i., and (B) lymphocyte function-associated antigen (LFA)-1 and very late antigen (VLA)-4 was expressed on Ly6Clo and Ly6Chi blood monocytes. (C) Immunohistochemical staining for intercellular adhesion molecule (ICAM)-1 and vascular cell adhesion molecule (VCAM)-1 performed on day 7 p.i. on the sham-infected and WNV-infected brains of C57BL/6 mice showed significant widespread upregulation of both molecules in WNV-infected mice and co-localized with CD31. Treatment with 100 μg anti-VLA-4 antibody from day 6 p.i. onwards resulted in reduced neutrophil and T cell recruitment into day 7 p.i. WNV-infected brains. A 66% reduction was seen in the CD45+/CD11b+/Ly6G/Ly6Chi macrophage compartment. (D) By contrast, LFA-1 blockade reduced Ly6Chi macrophage infiltration by 33%. (E) VLA-4 blockade resulted in increased survival of 10 to 60%, depending on the inoculation dose (P < 0.001), whereas (F) LFA-1 blockade did not increase survival. (G) Viral titers in the brain at day 7 p.i. were similar in all treatment groups. Data are representative of at least three independent experiments with at least four mice per group. Antibody-mediated effects on the disease course were determined on four separate occasions with at least ten mice per group. Data shown are the mean ± standard deviation. Statistical analysis was conducted using one-way ANOVA with a Tukey-Kramer post hoc test. Statistical analysis of survival was conducted using the log-rank (Mantel-Cox) test. * P < 0.05; **P < 0.001; ***P < 0.001. The inoculation dose used was 6 × 103 plaque-forming units, unless otherwise noted.

The mechanism by which these cells contribute to the pathogenesis of disease is unresolved. To address this, we initially investigated the ability of these cells to process and present antigen to T cells, as CNS macrophages exhibited cathepsin activity and expressed MHC-II and CD86 (Figure 2A-C), and we hypothesized that infiltrating macrophages might exert their pathogenic effects indirectly acting as antigen presenting cells (APC), via T-cell stimulation. Using naive and activated CD4+ T cells, we tested from day 7 p.i. the capacity of immigrant brain macrophages and resident microglia to stimulate T-cell proliferation (Figure 2D). Whereas the control Ly6C (resident) microglia failed to stimulate T-cell proliferation, inflammatory monocyte-derived macrophages were capable of inducing proliferation of activated T cells, supporting previous studies showing that macrophages can stimulate anti-WNV T-cell responses [10]. It is tempting to speculate from these data that inflammatory monocyte-derived macrophages may cause immunopathology via their influence on T cells [11]; however, deletion of either CD4+ or CD8+ T cells, or both, did not increase survival time in these mice (Figure 2E). When considered with the reduced number of T cells seen after anti-VLA-4 treatment, these data potentially argue against a role for T cells in causing the observed immune pathology in WNV-infected mice. Indeed, previous studies have shown that in concert with neuronal intracellular antiviral defenses, T cells are important for viral clearance [1214]. Examination of these pathways in VLA-4 treated mice will be needed to clarify these viral eradication mechanisms precisely.

Figure 2
figure 2

Assessment of macrophages isolated from the West Nile virus (WNV) infected brain. (A, B) Macrophages isolated from day 7 p.i. brain tissue infected with West Nile virus expressed major histocompatability complex (MHC)-II and CD86. (C) More than 70% of Ly6Chi macrophages in the WNV-infected brain were positive for fluorescent agent (ProSense; VisEn Medical, Bedford, MA, USA), indicative of cathepsin activity. (D) The ability of macrophages (CD45+/CD11b+/Ly6G/GFP+/CD11c/Ly6Chi) and resident microglia (CD45lo/int/CD11b+/GFP/CD11c/Ly6Chi), isolated from WNV-infected colony-stimulating factor 1 receptor (cFMS)-enhanced green fluorescent protein (EGFP) chimeric mice [2] to stimulate naïve and activated CD3+/CD4+ T cells from sham-infected and WNV-infected mice, respectively, was measured. Except at the highest antigen-presenting cell (APC):CD4 ratios, neither population was capable of stimulating naive T-cell proliferation, as measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. (E) Notwithstanding the apparent APC capabilities, depletion of CD8+ or CD4+ or CD4+ and CD8+ had no effect on overall survival in this model. All experiments were performed at least twice with four to five mice per group. Cells were sorted from 10 pooled cFMS-EGFP chimeric mice, and data represent the mean of triplicate wells and the standard deviation of absorbance. T-cell depletion was performed at least twice with eight to ten mice per group. Statistical analysis was conducted using one-way ANOVA with a Tukey-Kramer post hoc test. * Indicates significance of comparison of CD4+ T-cell proliferation between wells with macrophages and wells with CD4+ T cells only. * P < 0.05; **P < 0.001; ***P < 0.001. Mice infected with 6 ×104 plaque-forming units were used to obtain APC populations.

Because NO production during viral infection has been shown to be protective in some instances, and pathogenic in others, we investigated the possible pathogenic role of NO production by macrophages [1518]. In situ hybridization and immunohistochemistry for inducible NO synthase (NOS)-2 showed significant expression in the WNV-infected brain at day 7 p.i. (Figure 3A-F). Flow cytometry using the NO marker DAF-FM diacetate [8], which becomes fluorescent when it reacts with NO, showed that 72% of macrophages in the WNV-infected brain expressed NO, compared with only 24% of resident microglia (CD45Lo/Ly6C) (Figure 3G). Furthermore, intraperitoneal administration of aminoguanidine from day 6 p.i. resulted in an increased survival of up to 4 days for infected mice (Figure 3H), with the percentage of DAF-FM + macrophages decreasing to less than 12% (Figure 3G). Furthermore, increased survival in VLA-4- treated mice correlated with a significant reduction in NO+ macrophages in the brain (Figure 3I) at day 7 p.i. Taken together, these data show that inhibition of Ly6Chi monocyte-derived NO, either by reducing the immigration of these cells into the brain, or by inhibiting NO, promotes survival in WNV encephalitis.

Figure 3
figure 3

Macrophages produce NO, which is pathogenic during WNV infection. (A-E) Analysis of sections from sham-infected and West Nile virus (WNV)-infected mice at day 7 p.i. showed significant upregulation of nitric oxide synthase (NOS)-2 message in the WNV-infected brains. (C, F) Furthermore, immunohistochemical staining for NOS-2 protein (red) and lectin (green) showed that most cells expressing NOS-2 in the WNV-infected brain parenchyma at day 7 p.i. were lectin-positive. (G) Using the dye 4-amino-5-methylamino-2',7'-difluorofluorescein diacetate (DAF-FM), which, in the presence of NO becomes fluorescent, flow cytometry showed that more than 70% of macrophages (CD45hi/CD11b+/CD11c/Ly6C+) expressed NO compared with approximately 25% of resident microglia (CD45lo/int/CD11b+/CD11c/Ly6C), and treatment of mice with aminoguanidine resulted in a significant reduction in macrophages expressing NO. (H) Inhibition of NO with aminoguanidine did not increase survival when used over the entire infectious period, but it had a demonstrably protective effect given at day 6 p.i. (P < 0.05). (I) A significant reduction in DAF-FM-positive macrophages was seen from day 7 p.i. in the brains of WNV-infected mice that had been treated with anti-VLA-4 neutralizing antibodies on day 6 p.i. In situ hybridization was performed on sagittal brain sections from at least six mice per group. DAF-FM data are representative of three experiments with at least three mice per group. Aminoguanidine therapy was performed four times with at least ten mice per group. Values shown are means ± SD. Statistical analysis was conducted using one-way ANOVA with Tukey-Kramer post hoc test. * P < 0.05; **P < 0.001; ***P < 0.001. Statistical analysis of survival was determined using the log-rank (Mantel-Cox) test. *P < 0.05 was considered significant.

Although the production of other pro-inflammatory mediators is also likely to occur via inflammatory monocyte-derived macrophages, these data provide one potential lethal effector function for pathogenic macrophages that infiltrate into the WNV-infected brain. The production of NO by macrophages is integral to clearance of many invading pathogens and mediates viral clearance in models of HSV-2, Ectromelia and Vaccinia virus infection [16]. Over-exuberant NO production can be pathogenic, as exemplified by infection by another flavivirus, Murray Valley encephalitis virus, in which experimental inhibition of NO attenuated disease and prolonged survival [15]. During WNV encephalitis, more than 70% of the inflammatory monocyte-derived macrophages in the WNV-infected brain produced NO. Importantly, whereas inhibition of NO with aminoguanidine over the entire course of infection had no effect on disease outcome, inhibiting NO on day 6 p.i. resulted in enhanced survival of WNV-infected mice. This apparently paradoxical effect suggests that NO may be important in the early control of WNV infection, whereas later, the sustained production of NO by large numbers of infiltrating macrophages becomes poorly regulated and thus pathogenic. This is supported by previous macrophage-depletion studies, which show that early prolonged macrophage depletion can result in brain infection in mice infected with a non-encephalogenic WNV strain [19]. It is important to consider that although NOS-2 in situ hybridization studies support a role for macrophages in NO production during WNV encephalitis, NO may also be produced by neurons (neuronal NOS; NOS-1) and endothelium (endothelial NOS; NOS-3). Because arginine is required as a substrate for the production of NO by all forms of NOS, and aminoguanidine competes with arginine at all these sites, we cannot determine with certainty that the effect we found after aminoguanidine administration is due to the inhibition of NO within macrophages, endothelium, or neurons. In addition, in the brain, NO modulates neurotransmission. Because WNV infection of the brain causes severe seizures, and other studies have implicated NO in the modulation of neuronal function [7], the ability of NO inhibition at day 6 p.i. to enhance survival of infected mice may also be the result of aminoguanidine interactions that stabilize neurons within the WNV-infected brain. The lack of seizures seen in interferon- γ (IFN-γ−/−) mice, as previously described [7], supports this hypothesis. This is because mice deficient in IFN-γ have reduced ability to produce NO and do not develop seizures [7]. However, in IFN-γ−/− mice, only the NO produced via NOS-2 is reduced. Similar survival kinetics were reported with WNV-infected IFN-γ−/− mice [7] compared with wild-type mice receiving aminoguanidine from day −1 p.i. throughout the disease course. Together this strongly suggests that the antiviral effects of NOS-2-induced NO are important early during infection and contrasts with its evident pathogenic function, probably via similar mechanisms, late in the disease.

In conclusion, we show here that macrophages derived from Ly6Chi inflammatory monocytes predominantly utilize VLA-4 to enter the CNS. Abrogation of this migration by integrin blockade resulted in long-term survival and immunity in an otherwise lethal model. Finally, these data show the crucial contribution by inflammatory macrophages, within in a narrow, temporally defined window, to the immunopathogenesis of disease. This should inform interventional approaches that can ameliorate immunopathology by targeting a specific myeloid subset(s) in the short term, while enabling virus clearance and host survival.



Antigen presenting cell


Central nervous system


Chemokine ligand


Cluster of differentiation


colony-stimulating factor 1 receptor-enhanced green fluorescent protein (Mac Green mouse)


4-amino-5-methylamino-2’,7’-diflourofluorescein diacetate


Intercellular adhesion molecule


Inducible nitric oxide synthase


Lymphocyte function associated antigen-1


3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide


Nitric oxide


Plaque-forming units


vascular cell adhesion molecule


Very late antigen-4


West Nile virus.


  1. D'Agostino PM, Kwak C, Vecchiarelli HA, Toth JG, Miller JM, Masheeb Z, McEwen BS, Bulloch K: Viral-induced encephalitis initiates distinct and functional CD103+ CD11b+ brain dendritic cell populations within the olfactory bulb. Proc Natl Acad Sci U S A 2012, 109:6175–6180.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Getts DR, Terry RL, Getts MT, Muller M, Rana S, Shrestha B, Radford J, Van Rooijen N, Campbell IL, King NJ: Ly6c+ "inflammatory monocytes" are microglial precursors recruited in a pathogenic manner in West Nile virus encephalitis. J Exp Med 2008, 205:2319–2337.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. King IL, Dickendesher TL, Segal BM: Circulating Ly-6C+ myeloid precursors migrate to the CNS and play a pathogenic role during autoimmune demyelinating disease. Blood 2009, 113:3190–3197.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Bailey SL, Schreiner B, McMahon EJ, Miller SD: CNS myeloid DCs presenting endogenous myelin peptides 'preferentially' polarize CD4+ T(H)-17 cells in relapsing EAE. Nat Immunol 2007, 8:172–180.

    Article  CAS  PubMed  Google Scholar 

  5. Cros J, Cagnard N, Woollard K, Patey N, Zhang SY, Senechal B, Puel A, Biswas SK, Moshous D, Picard C, et al.: Human CD14dim monocytes patrol and sense nucleic acids and viruses via TLR7 and TLR8 receptors. Immunity 2010, 33:375–386.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Geissmann F, Auffray C, Palframan R, Wirrig C, Ciocca A, Campisi L, Narni-Mancinelli E, Lauvau G: Blood monocytes: distinct subsets, how they relate to dendritic cells, and their possible roles in the regulation of T-cell responses. Immunol Cell Biol 2008, 86:398–408.

    Article  CAS  PubMed  Google Scholar 

  7. Getts DR, Matsumoto I, Muller M, Getts MT, Radford J, Shrestha B, Campbell IL, King NJ: Role of IFN-gamma in an experimental murine model of West Nile virus-induced seizures. J Neurochem 2007, 103:1019–1030.

    Article  CAS  PubMed  Google Scholar 

  8. Ponomarev ED, Shriver LP, Maresz K, Pedras-Vasconcelos J, Verthelyi D, Dittel BN: GM-CSF production by autoreactive T cells is required for the activation of microglial cells and the onset of experimental autoimmune encephalomyelitis. J Immunol 2007, 178:39–48.

    Article  CAS  PubMed  Google Scholar 

  9. Ley K, Laudanna C, Cybulsky MI, Nourshargh S: Getting to the site of inflammation: the leukocyte adhesion cascade updated. Nat Rev Immunol 2007, 7:678–689.

    Article  CAS  PubMed  Google Scholar 

  10. Kulkarni AB, Mullbacher A, Blanden RV: Functional analysis of macrophages, B cells and splenic dendritic cells as antigen-presenting cells in West Nile virus-specific murine T lymphocyte proliferation. Immunol Cell Biol 1991,69(Pt 2):71–80.

    Article  PubMed  Google Scholar 

  11. McGavern DB, Truong P: Rebuilding an immune-mediated central nervous system disease: weighing the pathogenicity of antigen-specific versus bystander T cells. J Immunol 2004, 173:4779–4790.

    Article  CAS  PubMed  Google Scholar 

  12. Samuel MA, Whitby K, Keller BC, Marri A, Barchet W, Williams BR, Silverman RH, Gale M Jr, Diamond MS: PKR and RNase L contribute to protection against lethal West Nile virus infection by controlling early viral spread in the periphery and replication in neurons. J Virol 2006, 80:7009–7019.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Shrestha B, Diamond MS: Role of CD8+ T cells in control of West Nile virus infection. J Virol 2004, 78:8312–8321.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Wang Y, Lobigs M, Lee E, Mullbacher A: CD8+ T cells mediate recovery and immunopathology in West Nile virus encephalitis. J Virol 2003, 77:13323–13334.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Andrews DM, Matthews VB, Sammels LM, Carrello AC, McMinn PC: The severity of murray valley encephalitis in mice is linked to neutrophil infiltration and inducible nitric oxide synthase activity in the central nervous system. J Virol 1999, 73:8781–8790.

    CAS  PubMed  PubMed Central  Google Scholar 

  16. Karupiah G, Xie QW, Buller RM, Nathan C, Duarte C, MacMicking JD: Inhibition of viral replication by interferon-gamma-induced nitric oxide synthase. Science 1993, 261:1445–1448.

    Article  CAS  PubMed  Google Scholar 

  17. Noda S, Tanaka K, Sawamura S, Sasaki M, Matsumoto T, Mikami K, Aiba Y, Hasegawa H, Kawabe N, Koga Y: Role of nitric oxide synthase type 2 in acute infection with murine cytomegalovirus. J Immunol 2001, 166:3533–3541.

    Article  CAS  PubMed  Google Scholar 

  18. Presti RM, Popkin DL, Connick M, Paetzold S, Virgin HW: Novel cell type-specific antiviral mechanism of interferon gamma action in macrophages. J Exp Med 2001, 193:483–496.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Ben-Nathan D, Huitinga I, Lustig S, van Rooijen N, Kobiler D: West Nile virus neuroinvasion and encephalitis induced by macrophage depletion in mice. Arch Virol 1996, 141:459–469.

    Article  CAS  PubMed  Google Scholar 

Download references


We thank Barbara Hernandez for expert histological advice. In addition we thank Ben Roediger and Wolfgang Weninger for the provision of anti-CD31 antibody. This work was funded by NH&MRC grants 512413 to NJCK and ILC and 1030897 to NJCK and DRG.

Author information

Authors and Affiliations


Corresponding author

Correspondence to Nicholas JC King.

Additional information

Competing interests

The authors have no competing interest to report.

Authors’ contributions

DG & NJC designed infection experiments, performed flow cytometry, immunohistochemistry and drafted the manuscript. MT, RT & CD assisted with experimental design, flow cytomtry and antibody/drug treatments. TMA & JR, optimized and performed immunohistochemistry. MM & MH designed and completed in-situ hybridizations experiments. ILC designed in-situ primers and assisted with manuscript drafting. All authors read and approved the final manuscript.

Rights and permissions

Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Getts, D.R., Terry, R.L., Getts, M.T. et al. Targeted blockade in lethal West Nile virus encephalitis indicates a crucial role for very late antigen (VLA)-4-dependent recruitment of nitric oxide-producing macrophages. J Neuroinflammation 9, 246 (2012).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: