- Open Access
Role of innate signalling pathways in the immunogenicity of alphaviral replicon-based vaccines
© Näslund et al; licensee BioMed Central Ltd. 2011
- Received: 11 November 2010
- Accepted: 24 January 2011
- Published: 24 January 2011
Alphaviral replicon-based vectors induce potent immune responses both when given as viral particles (VREP) or as DNA (DREP). It has been suggested that the strong immune stimulatory effect induced by these types of vectors is mediated by induction of danger signals and activation of innate signalling pathways due to the replicase activity. To investigate the innate signalling pathways involved, mice deficient in either toll-like receptors or downstream innate signalling molecules were immunized with DREP or VREP.
We show that the induction of a CD8+ T cell response did not require functional TLR3 or MyD88 signalling. However, IRF3, converging several innate signalling pathways and important for generation of pro-inflammatory cytokines and type I IFNs, was needed for obtaining a robust primary immune response. Interestingly, type I interferon (IFN), induced by most innate signalling pathways, had a suppressing effect on both the primary and memory T cell responses after DREP and VREP immunization.
We show that alphaviral replicon-based vectors activate multiple innate signalling pathways, which both activate and restrict the induced immune response. These results further show that there is a delicate balance in the strength of innate signalling and induction of adaptive immune responses that should be taken into consideration when innate signalling molecules, such as type I IFNs, are used as vaccine adjuvant.
- Cell Response
- Wild Type Mouse
- Semliki Forest Virus
- TLR3 Pathway
- Post Immunization
Alphaviral replicon-based vectors are attractive vaccine candidates since they induce strong immune responses in various animal models. The alphaviral replicon encodes an alphavirus replicase, an RNA polymerase, which strongly amplifies the replicon encoded transgene RNA resulting in high heterologous antigen production. Initially, the superior immune response induced by these types of vectors was attributed to abundant antigen production [1, 2]. However, the replicase activity also leads to the formation of double stranded RNA (dsRNA), which induces activation and cross-priming of viral associated antigens in CD8α+ dendritic cells (DCs) . Hence, it is now becoming increasingly clear that the immunogenicity of alphaviral replicon-based vectors is due to activation of innate immune responses, rather than increased antigen production.
We have previously used alphaviral replicon-based vaccines administered as viral particles capable of one round of replication (VREPs) . These VREPs, based on Semliki Forest virus (SFV), induce strong antibody and cellular responses in animals [5–10]. SFV, being a RNA virus, may target several innate signalling pathways [11, 12] including toll-like receptor (TLR) 3 and 7, as well as cytoplasmic receptors of the RIG-I-like receptor (RLR) family . We have shown that replication of VREP generates double-stranded (ds) RNA intermediates, and that immunization of mice with VREP infected Vero cells activates the TLR3 pathway leading to enhanced cross-priming . However, immune activation was only partly dependent on TLR3, suggesting that other innate signalling pathways are involved. Other studies with RNA viruses have suggested that the MyD88 and TLR3 pathways are targeted [14–16]. However, recent results indicate that MyD88 and TLR3 pathways may be dispensable for generation of T cell responses after VREP immunization . Thus, it is not clear which innate signalling pathways that are activated after VREP immunization. Engagement of TLRs and RLRs results in production of type I interferon (IFN) and pro-inflammatory cytokines. The release of type I IFN has been shown to amplify the innate immune responses and to be a potent inducer of the adaptive immune response by activation of DCs, T- and B-cells [18–21], and has been suggested to be a crucial signalling molecule for the generation of a potent immune response. We have shown that immunization with VREP also induces type I IFNs . However, the impact of type I IFNs on alphaviral replicon-based immunogens is not clear.
Use of naked DNA for vaccination has gained much attention, in particular following early promising pre-clinical results in mice. However, later experiments performed with non-human primates and the first human clinical trials gave rather disappointing results [23–25]. Conventional DNA (convDNA) vaccines do target a number of innate signalling receptors, including toll-like receptors (TLR9) and various cytoplasmic receptors (e.g. DAI and AIM2) [26, 27], but it may be that at conventional delivery doses, these signals are not strong enough to induce a robust immune response. Inclusion of elements resulting in apoptosis [28–30] or expression of interferon regulatory factors , events normally occurring during viral infections, has been shown to increase the immunogenicity of convDNAs, and suggests that one possible way to improve convDNA vaccines would be by mimicking a virus infection.
In our previous studies we have demonstrated that the immunogenicity of naked DNA is significantly improved by inclusion of the alphaviral replicon into convDNA vectors, constructing an alphavirus replicon-based DNA (DREP) vector [32–37]. This suggests that the viral replicase activity could contribute to the enhanced immunogenicity of the replicon-based vectors. While immunization with VREP particles do target various innate pathways it has not yet been investigated in head-to-head comparisons if these are the same for DREP vaccines. In this study we investigated if innate signalling pathways are important for the immunogenicity of alphaviral replicon-based vector immunization.
In this study we show that many of the innate receptors, at least on their own, are dispensable for induction of CD8+ T cell responses both after DREP and VREP immunization. In contrast, IRF3, an important signalling molecule for the induction of type I IFNs and pro-inflammatory cytokines, is needed for a fullminant immune response. Interestingly, the immune responses are suppressed in both DREP and VREP immunized mice by type I IFNs. In conclusion, the immune response is affected by the TLR and RLR downstream signalling molecule IRF3 and type I IFNs, suggesting that multiple innate receptors are involved after replicon-based vaccine administration.
Mice and immunizations
MyD88 knock-out (KO) , IRF3 KO  and corresponding wild type mice, C57Bl/6, and IFN-AR1 KO  mice and corresponding wild type mice, Sv129, were bred and kept at the animal house at Karolinska Institutet, Sweden. The TLR3 KO mice  and corresponding wild type mice, C57Bl/6:Sv129, were bred and kept at the animal house at the Swedish Institute for Infectious Disease Control, Sweden. Female mice, 6-12 weeks old were immunized intramuscularly (i.m.) under pathogen-free conditions with DREP-OVA (1, 10 or 50 μg), deltaREP-OVA (50 μg) or VREP-OVA (106 infectious units (IU)) in a total volume of 100 μl divided equally between both hind legs. The DREP-OVA and deltaREP-OVA DNA were diluted in sterile physiological 0.9% sodium chloride solution and the VREP-OVA viral particles in sterile PBS (Gibco, Invitrogen, Carlsbad, California). Animal care and treatment were in accordance with standards approved by the local ethics committee (Stockholms norra djurförsöksetiska nämnd).
DNA and viruses
The DREP-OVA construct was made by cloning the ova encoding gene, coding for a cytoplasmic non-secreted form of OVA protein lacking the signal peptide, by BglII and NotI restriction digestion and T4 DNA ligase reaction. The deltaREP-OVA construct was made from the DREP-OVA construct by deletion of the region corresponding to the CMV promotor and the SFV replicase by BamHI restriction digestion, Klenow fill-in reaction and AseI restriction digestion. The CMV promoter from the pBK-LacZ plasmid was inserted into the deltaREP-OVA construct by NheI restriction digestion and Klenow fill-in reaction and AseI restriction digestion. All enzymes were obtained from NE Biolabs, Ipswich, MA. Plasmids were purified with Endotoxin free Mega-prep kit (Qiagen, Hilden, Germany) and preparations with endotoxin levels <0.1EU/μg DNA were used for immunization. The SFV two-helper RNA system has been described previously .
IFN-γ ELISpot analysis was performed on freshly isolated splenocytes as described previously . Splenocyte single-cell suspensions were treated with Red Blood Cell lysing buffer and re-suspended in RPMI media supplemented with 2 mM L-glutamine, 2 mM Penicillin-Streptomycin (all from Sigma-Aldrich, St. Louis, MO) and 10% FCS (Gibco, Invitrogen, Carlsbad, California) (complete media). Splenocytes (2 × 105) from individual mice were added to Multiscreen IP plates (Millipore, Billerica, MA) coated with anti-mouse-IFN-γ monoclonal antibody (AN18) (Mabtech AB, Nacka strand, Sweden) and stimulated with media or 2 μg/ml OVA peptide (SIINFEKL) (Proimmune, Oxford, UK) or 2 μg/ml Concanavalin A (Sigma-Aldrich, St. Louis, MO) for 20 hours. The plates were thereafter developed with biotinylated anti-mouse-IFN-γ monoclonal antibody (R4-6A2) (Mabtech AB, Nacka strand, Sweden), Vectastain Elite ABC kit (Immunkemi F&D AB, Järfälla, Sweden) and AEC substrate (Sigma-Aldrich, St. Louis, MO). The spots were counted using an ELISpot reader (Axioplan 2 Imaging; Zeiss) and expressed as spot forming cells (SFC) per 106 splenocytes. A value equal to or greater than 55 spots per million splenocytes in the peptide wells is regarded a positive IFNγ response. Mice with media responses higher than 50 spots in the IFNγ ELISpot were omitted from further analysis.
Statistical analysis was performed using the GraphPad Prism 5 software (GraphPad Software Inc., La Jolla, CA). To test for statistical significance nonparametric two-tailed Mann-Whitney analysis was performed.
Induction of CD8+ T cell responses after deltaREP and DREP immunization
To compare the immunogenicity of the two DNA vaccines, C57Bl/6 mice were immunized with 50 μg of DNA and the splenic OVA-specific CD8+ T cell responses were measured by IFNγ ELISpot 10 days post immunization. After deltaREP-OVA immunization, only a few mice responded to the Kb-restricted OVA SIINFEKL peptide. In contrast, all mice responded to DREP-OVA immunization, with significantly higher numbers of IFNγ producing CD8+ T cells (p < 0.001) (Figure 1B). This result confirms previous studies that DREP is indeed more immunogenic than deltaREP (convDNA vaccines) [32, 33].
Replicon induced CD8+ T cell responses in the absence of TLR signalling
Another possibility is that TLR7 signalling could be involved, since DREP produces single-stranded RNA in the transfected cell. We therefore employed MyD88 KO mice which abolish signalling through TLR7. Again, we found no differences between wild type and MyD88 KO DREP-OVA immunized mice, suggesting that MyD88 dependent pathways, such as the TLR7 signalling pathway, are not crucial for generation of a strong CD8+ T cell response (Figure 2B). Yet another TLR that is signalling via MyD88 and might be targeted by DREP, since DREP is administered as naked DNA, is TLR9. However, no significant difference was found between wild type and TLR9 deficient mice (data not shown).
Taken together, TLR3 and MyD88-dependent receptors are not crucial for the induction of a CD8+ T cell response after VREP and DREP immunization.
Replicon induced CD8+ T cell responses in the absence of IRF3 signalling
Replicon induced CD8+ T cell responses in the absence of the type I interferon receptor
Since lack of the type I IFN receptor had a pronounced effect on the primary T cell response and several reports have shown that type I IFNs are important for the maintenance of memory cells [48, 49], we next investigated whether lack of the type I IFN receptor had any effect on the memory pool. Wild type and IFN-AR1 KO mice were immunized with DREP-OVA or VREP-OVA and five weeks post immunization, the splenic memory response was analysed by IFNγ ELISpot (Figure 4C). As was the case in the primary response, statistically significantly higher numbers of OVA-specific IFNγ producing CD8+ T cells were detected in IFN-AR1 KO mice in comparison to wild type mice, both after DREP-OVA (p < 0.01) and VREP-OVA (p < 0.001) immunization (Figure 4C). These results indicate, in contrast to what has previously been suggested [48, 49], that the memory CD8+ T cell pool is maintained in the absence of type I IFN signalling.
In conclusion, TLR3 or MyD88-dependent innate signalling pathways are not crucial for the induction and activation of CD8+ T cell responses after DREP and VREP immunization. However, IRF3, downstream of both TLR and RLR signalling pathways and important for the generation of type I IFNs and pro-inflammatory cytokines, was required for a potent T cell response after VREP immunization, with a similar trend in DREP immunized mice. In contrast, type I IFNs has a suppressing effect on the T cell response both after DREP and VREP immunization.
In this study we wanted to characterise what possible innate signals could form the basis of the enhanced immunogenicity of DREP and also to investigate if alphaviral replicons, delivered as DNA (DREP) or as viral particles (VREP), activate the same innate signalling pathways, a comparison that has not previously been done.
DREP vectors have been shown to induce stronger immune responses in comparison to convDNA vectors [32–37]. However, in those studies the different backbones in the vectors were not considered. In this study we constructed two new vectors, DREP-OVA and deltaREP-OVA, containing the same backbone, and compared their immunogenicity in mice. We confirmed that indeed DREP is more immunogenic than deltaREP on a per dose basis, despite the potential advantages for deltaREP, such as size. The size difference is in favour for the deltaREP construct, since a smaller plasmid size generates a higher transfection efficacy, as well as higher numbers of plasmid copies per μg in comparison to a bigger plasmid, such as DREP. Since the superior immune effects induced by DREPs does not depend on unusually high antigen expression levels ([1, 2, 32] and data not shown), it is probably mediated by a more potent activation of innate immune responses.
In this study we found that the CD8+ T cell responses induced by DREP or VREP immunization were similar in wild type, TLR3 and MyD88 deficient mice. In accordance with this, it was recently shown that TLR3 is not crucial for the generation of a CD8+ T cell response after DREP immunization  and this also confirms our earlier results that the T cell responses are not dependent on TLR3, nor MyD88, after VREP immunization [17, 22]. In contrast, we have previously shown that the TLR3 signalling pathway is needed for VREP-infected cells to induce CD8+ T cell responses in vivo. However, these results were obtained in a xenogenic model in which VREP infected Vero cells, lacking type I IFN production, were used for immunization . Hence, our present results suggest that the TLR3 pathway is dispensable in vivo when type I IFN is present, induced by multiple signalling pathways after DREP and VREP immunization.
TLR3 signalling, as well as RLR signalling pathways, lead to activation of IRF3, which is known to play a critical role in antiviral responses [51, 52] and crucial for induction of type I IFNs as well as pro-inflammatory cytokines. Interestingly, the CD8+ T cell response was significantly lower in the absence of IRF3 after VREP immunization, with a similar trend detected after DREP immunization, albeit not statistically significant. These results indicate that replicon induced RNAs are important activators of innate signalling pathways and adaptive immune responses. In accordance, it was recently published that Chikungunya virus, an other alphavirus, activates IRF3 via interferon promoter stimulator 1 (IPS-1), a signalling molecule downstream of the RLRs . It further indicates that multiple innate signalling pathways, compensating for each other, are activated after DREP and VREP immunizations, since the T cell response was not affected in single TLR KOs and/or that RLRs play a bigger role than TLRs in replicon induced immunity. In agreement, it was recently published that adenoviral vaccine vectors, which equally to alphaviral vaccine vectors induce strong immune responses, activate multiple innate signalling pathways . Moreover, yellow fever vaccine 17D (YF-17D) is regarded as one of the most effective live attenuated vaccines available  and has been shown to activate several innate signalling pathways such as TLR2, 7, 8 and 9. Hence, it might very well be that activation of multiple innate signalling pathways is a feature of potent vaccines. The reason why we do detect a significant difference between IRF3KO and wild type mice after VREP-OVA immunization, merely detected as a similar trend after DREP-OVA immunization, is most probably due to differences in transfection/infection efficacy. DREP-OVA is mechanically forced into the muscle cells during injection whereas VREP-OVA is actively infecting the cells, most likely leading to a more effective and more reproducible antigen delivery into the cells by VREP-OVA, generally detected as less variation between the immunized mice.
The signalling of several TLRs (TLR3, 4, 7 and 9) and RLRs converge into a type I IFN response. Type I IFNs encompass a multitude of stimulatory effects on the adaptive T cell response including activation of DC function, promotion of cross-priming and stimulation of memory T cells [18–21]. We have previously shown that VREP is a potent inducer of type I IFN . In the present study we observed that the CD8+ T cell response was stronger in mice lacking a functional type I IFN system, and that this balance was maintained in the memory response. These results indicate that type I IFNs suppress the immune response and that the memory CD8+ T cell pool is maintained in the absence of type I IFN signalling, in contrast to what has previously been suggested [18–21, 48, 49]. Moreover, it has previously been reported that splenocyte cultures from DREP immunized IFN-AR1 KO mice produce lower levels of IFNγ in vitro, in comparison to splenocytes from wild type mice . However, our dose titration experiment showed that the T cell responses linearly increased with higher doses of DREP in the IFN-AR1 KO mice whereas, in the wild type mice, the immune responses did not increase at doses higher than 10 μg of DREP. This suggests that type I IFN is only stimulatory until a certain threshold level has been reached. This is in agreement with earlier findings that type I IFNs has a stimulatory effect on CD8+ T cell responses at low doses, whereas at higher doses the cytotoxic response was suppressed . The IRF3KO mice, in contrast to the IFN-AR1 KO mice, are defective in production of both type I IFNs and pro-inflammatory cytokines. Hence, the lower T cell response detected in the IRF3KO mice could be due to differences in other cytokines than type I IFNs, which compensate for the lack of type I IFNs in the IFN-AR1 KO mice.
The increased T cell response in the IFN-AR1 KO mice could have several explanations, such as abundant antigen production and/or the presence of more innate receptor ligands due to non-restricted RNA replication, as RNA viruses are prone to inhibition of replication by type I IFN. In agreement, plasmid DNA transgene expression has been shown to be inhibited by type I IFNs . During a viral infection type I IFN induces an antiviral state in yet uninfected cells, thus prohibiting further spread of the infecting agent. However, in our case, replication of neither vector (VREP or DREP) results in production of new infectious particles. Thus, type I IFN mediated antigen or RNA replication suppression have to be in an autocrine fashion. However, Vero cells infected with VREPs and treated with type I IFN at different time-points post-infection expressed similar amounts of VREP encoded protein, indicating that type I IFN does not suppress the antigen expression level in the infected cell per se (data not shown). Moreover, we have previously shown that within a few hours after transfection, DREP and VREP replication will result in a type I IFN/PKR mediated shutdown of host protein synthesis, without affecting production of the vector encoded antigen in vitro[59–61]. In addition, we have also shown that replication of a VREP mutant, that induces high levels of type I IFNs, was not suppressed in comparison to wild type VREP in vitro. Moreover, by increasing the DREP-OVA dose, antigen and innate receptor ligand load increase, but nevertheless the immune response does not increase in wild type mice immunized with doses exceeding 10 μg DREP-OVA (Figure 4B). Furthermore, it was recently published that addition of type I IFNs do not inhibit alphaviral replication once RNA replication has been established . Collectively, these data suggest that type I IFN does not act in an autocrine fashion lowering replicon encoded antigen expression.
A role of type I IFNs is to activate negative feedback mechanisms to avoid prolonged cytokine production  and also to induce apoptosis [43, 65]. These regulatory pathways are non-functional in IFN-AR1 KO mice and could explain the increased CD8+ T cell responses in the absence of the type I IFN system. It has previously been shown that replicon induced apoptosis increase uptake of apoptotic bodies and cross-priming by DCs  and by blocking apoptosis, mice were less protected against a subsequent tumour challenge [43, 67]. However, it was recently reported that co-delivery of pro-apoptotic genes reduced the efficacy of DNA vaccines . Hence, type I IFN induced apoptosis could give two effects, either stimulating formation of apoptotic vesicles, thereby stimulating cross-priming, or lowering the antigen level produced, due to premature cell death. If type I IFN induced apoptosis is of importance in our system, the latter scenario must be at play in the wild type mice, lowering the antigen level and hence the immune response.
Despite the incapability of the IFN-AR1 KO mice to respond to type I IFNs they still produce and respond to other cytokines induced after DREP and VREP immunization. Hence, the robust T cell responses established despite the lack of the adjuvant effect from type I IFN is probably due to other effector mechanisms in play in the IFN-AR1 KO mice, sufficient for the induction of an immune response, in combination with lack of the negative feedback loop mediated by the type I IFN. In accordance, it was recently published that TLR ligands both positively and negatively modulate the immune response after viral vector immunization .
In conclusion, DREP immunization results in robust T cell responses even after a single administration and are much stronger than those obtained by immunization with convDNA vaccines. We found that DREP induced T cell responses were quite similar to those induced by VREP, suggesting that both vaccine platforms use the same innate signalling pathways. Even though our results could not conclude a single TLR to be crucial for the adjuvant effect induced by SFV replicons, we could show that IRF3, a signalling molecule downstream of several RNA receptors, was needed for a fullminant T cell response in VREP immunized mice, with a similar trend in DREP immunized mice. Our data suggest that alphaviral replicon-based vectors activate multiple innate signalling pathways contributing to their potent immunogenicity. Moreover, we show that VREP and DREP induced type I IFN restricts both primary and memory CD8+ T cell responses. It would seem that the efficacy of the DREP and VREP vaccines, being RNA replicons sensitive to host cellular responses, are dependent on a balance between stimulatory and inhibitory signals where replicon induced RNAs and type I IFN play an important role.
This work was supported by the Swedish Research Council, the European Union 5th Frame work Program and the Swedish Cancer Society.
We thank Margareta Hagelin, Kenth Andersson, Anna-Karin Persson in the animal house at the Department of Microbiology, Tumour and Cell Biology, Karolinska Institutet and Pia Ekeland in the animal house at the Swedish Institute for Infectious Disease Control, Sweden, for technical assistance.
- Driver DA, Latham EM, Polo JM, Belli BA, Banks TA, Chada S, Brumm D, Chang SM, Mento SJ, Jolly DJ, et al.: Layered amplification of gene expression with a DNA gene delivery system. Ann N Y Acad Sci 1995, 772: 261-264. 10.1111/j.1749-6632.1995.tb44754.xView ArticlePubMedGoogle Scholar
- Herweijer H, Latendresse JS, Williams P, Zhang G, Danko I, Schlesinger S, Wolff JA: A plasmid-based self-amplifying Sindbis virus vector. Hum Gene Ther 1995, 6: 1161-1167. 10.1089/hum.1995.6.9-1161View ArticlePubMedGoogle Scholar
- Schulz O, Diebold SS, Chen M, Naslund TI, Nolte MA, Alexopoulou L, Azuma YT, Flavell RA, Liljestrom P, Reis e Sousa C: Toll-like receptor 3 promotes cross-priming to virus-infected cells. Nature 2005, 433: 887-892. 10.1038/nature03326View ArticlePubMedGoogle Scholar
- Atkins GJ, Fleeton MN, Sheahan BJ: Therapeutic and prophylactic applications of alphavirus vectors. Expert Rev Mol Med 2008, 10: e33. 10.1017/S1462399408000859View ArticlePubMedGoogle Scholar
- Zhou X, Berglund P, Zhao H, Liljeström P, Jondal M: Generation of cytotoxic and humoral immune responses by nonreplicative recombinant Semliki Forest virus. Proc Natl Acad Sci USA 1995, 92: 3009-3013. 10.1073/pnas.92.7.3009PubMed CentralView ArticlePubMedGoogle Scholar
- Berglund P, Fleeton MN, Smerdou C, Liljeström P: Immunization with recombinant Semliki Forest virus induces protection against influenza challenge in mice. Vaccine 1999, 17: 497-507. 10.1016/S0264-410X(98)00224-2View ArticlePubMedGoogle Scholar
- Fleeton MN, Chen M, Berglund P, Rhodes G, Parker SE, Murphy M, Atkins GJ, Liljeström P: Self-replicative RNA vaccines elicit protection against influenza A virus, respiratory syncytial virus, and a tickborne encephalitis virus. J Infect Dis 2001, 183: 1395-1398. 10.1086/319857View ArticlePubMedGoogle Scholar
- Chen M, Hu KF, Rozell B, Orvell C, Morein B, Liljeström P: Vaccination with recombinant alphavirus or immune-stimulating complex antigen against respiratory syncytial virus. J Immunol 2002, 169: 3208-3216.View ArticlePubMedGoogle Scholar
- Hanke T, Barnfield C, Wee EG, Agren L, Samuel RV, Larke N, Liljeström P: Construction and immunogenicity in a prime-boost regimen of a Semliki Forest virus-vectored experimental HIV clade A vaccine. J Gen Virol 2003, 84: 361-368. 10.1099/vir.0.18738-0View ArticlePubMedGoogle Scholar
- Sundbäck M, Douagi I, Dayaraj C, Forsell MN, Nordstrom EK, McInerney GM, Spångberg K, Tjäder L, Bonin E, Sundström M, et al.: Efficient expansion of HIV-1-specific T cell responses by homologous immunization with recombinant Semliki Forest virus particles. Virology 2005, 341: 190-202.View ArticlePubMedGoogle Scholar
- Querec TD, Pulendran B: Understanding the role of innate immunity in the mechanism of action of the live attenuated Yellow Fever Vaccine 17D. Adv Exp Med Biol 2007, 590: 43-53. full_textView ArticlePubMedGoogle Scholar
- Querec TD, Akondy RS, Lee EK, Cao W, Nakaya HI, Teuwen D, Pirani A, Gernert K, Deng J, Marzolf B, et al.: Systems biology approach predicts immunogenicity of the yellow fever vaccine in humans. Nat Immunol 2009, 10: 116-25. 10.1038/ni.1688PubMed CentralView ArticlePubMedGoogle Scholar
- Pichlmair A, Reis e Sousa C: Innate recognition of viruses. Immunity 2007, 27: 370-383. 10.1016/j.immuni.2007.08.012View ArticlePubMedGoogle Scholar
- Zhou S, Kurt-Jones EA, Mandell L, Cerny A, Chan M, Golenbock DT, Finberg RW: MyD88 is critical for the development of innate and adaptive immunity during acute lymphocytic choriomeningitis virus infection. Eur J Immunol 2005, 35: 822-830. 10.1002/eji.200425730View ArticlePubMedGoogle Scholar
- Chen M, Barnfield C, Näslund TI, Fleeton MN, Liljeström P: MyD88 expression is required for efficient cross-presentation of viral antigens from infected cells. J Virol 2005, 79: 2964-2972. 10.1128/JVI.79.5.2964-2972.2005PubMed CentralView ArticlePubMedGoogle Scholar
- Honda K, Yanai H, Negishi H, Asagiri M, Sato M, Mizutani T, Shimada N, Ohba Y, Takaoka A, Yoshida N, Taniguchi T: IRF-7 is the master regulator of type-I interferon-dependent immune responses. Nature 2005, 434: 772-777. 10.1038/nature03464View ArticlePubMedGoogle Scholar
- Hidmark AS, Nordström EK, Dosenovic P, Forsell MN, Liljeström P, Karlsson Hedestam GB: Humoral responses against coimmunized protein antigen but not against alphavirus-encoded antigens require alpha/beta interferon signaling. J Virol 2006, 80: 7100-7110. 10.1128/JVI.02579-05PubMed CentralView ArticlePubMedGoogle Scholar
- Le Bon A, Etchart N, Rossmann C, Ashton M, Hou S, Gewert D, Borrow P, Tough DF: Cross-priming of CD8+ T cells stimulated by virus-induced type I interferon. Nat Immunol 2003, 4: 1009-1015. 10.1038/ni978View ArticlePubMedGoogle Scholar
- Le Bon A, Schiavoni G, D'Agostino G, Gresser I, Belardelli F, Tough DF: Type i interferons potently enhance humoral immunity and can promote isotype switching by stimulating dendritic cells in vivo. Immunity 2001, 14: 461-470. 10.1016/S1074-7613(01)00126-1View ArticlePubMedGoogle Scholar
- Le Bon A, Durand V, Kamphuis E, Thompson C, Bulfone-Paus S, Rossmann C, Kalinke U, Tough DF: Direct stimulation of T cells by type I IFN enhances the CD8+ T cell response during cross-priming. J Immunol 2006, 176: 4682-4689.View ArticlePubMedGoogle Scholar
- Le Bon A, Thompson C, Kamphuis E, Durand V, Rossmann C, Kalinke U, Tough DF: Cutting edge: enhancement of antibody responses through direct stimulation of B and T cells by type I IFN. J Immunol 2006, 176: 2074-2078.View ArticlePubMedGoogle Scholar
- Hidmark AS, McInerney GM, Nordström EK, Douagi I, Werner KM, Liljeström P, Karlsson Hedestam GB: Early alpha/beta interferon production by myeloid dendritic cells in response to UV-inactivated virus requires viral entry and interferon regulatory factor 3 but not MyD88. J Virol 2005, 79: 10376-10385. 10.1128/JVI.79.16.10376-10385.2005PubMed CentralView ArticlePubMedGoogle Scholar
- Sandström E, Nilsson C, Hejdeman B, Bråve A, Bratt G, Robb M, Cox J, Vancott T, Marovich M, Stout R, et al.: Broad immunogenicity of a multigene, multiclade HIV-1 DNA vaccine boosted with heterologous HIV-1 recombinant modified vaccinia virus Ankara. J Infect Dis 2008, 198: 1482-1490.View ArticlePubMedGoogle Scholar
- Lu S, Wang S, Grimes-Serrano JM: Current progress of DNA vaccine studies in humans. Expert Rev Vaccines 2008, 7: 175-191. 10.1586/147605184.108.40.206View ArticlePubMedGoogle Scholar
- Harari A, Bart PA, Stohr W, Tapia G, Garcia M, Medjitna-Rais E, Burnet S, Cellerai C, Erlwein O, Barber T, et al.: An HIV-1 clade C DNA prime, NYVAC boost vaccine regimen induces reliable, polyfunctional, and long-lasting T cell responses. J Exp Med 2008, 205: 63-77. 10.1084/jem.20071331PubMed CentralView ArticlePubMedGoogle Scholar
- Takaoka A, Taniguchi T: Cytosolic DNA recognition for triggering innate immune responses. Adv Drug Deliv Rev 2008, 60: 847-857. 10.1016/j.addr.2007.12.002View ArticlePubMedGoogle Scholar
- Kumagai Y, Takeuchi O, Akira S: TLR9 as a key receptor for the recognition of DNA. Adv Drug Deliv Rev 2008, 60: 795-804. 10.1016/j.addr.2007.12.004View ArticlePubMedGoogle Scholar
- Sasaki S, Amara RR, Oran AE, Smith JM, Robinson HL: Apoptosis-mediated enhancement of DNA-raised immune responses by mutant caspases. Nat Biotechnol 2001, 19: 543-547. 10.1038/89289View ArticlePubMedGoogle Scholar
- Chattergoon MA, Kim JJ, Yang JS, Robinson TM, Lee DJ, Dentchev T, Wilson DM, Ayyavoo V, Weiner DB: Targeted antigen delivery to antigen-presenting cells including dendritic cells by engineered Fas-mediated apoptosis. Nat Biotechnol 2000, 18: 974-979. 10.1038/79470View ArticlePubMedGoogle Scholar
- Chattergoon MA, Muthumani K, Tamura Y, Ramanathan M, Shames JP, Saulino V, Robinson TM, Montaner LJ, Weiner DB: DR5 Activation of Caspase-8 Induces DC Maturation and Immune Enhancement In Vivo. Mol Ther 2008, 16: 419-426. 10.1038/sj.mt.6300373View ArticlePubMedGoogle Scholar
- Sasaki S, Amara RR, Yeow WS, Pitha PM, Robinson HL: Regulation of DNA-raised immune responses by cotransfected interferon regulatory factors. J Virol 2002, 76: 6652-6659. 10.1128/JVI.76.13.6652-6659.2002PubMed CentralView ArticlePubMedGoogle Scholar
- Berglund P, Smerdou C, Fleeton MN, Tubulekas I, Liljeström P: Enhancing immune responses using suicidal DNA vaccines. Nat Biotechnol 1998, 16: 562-565. 10.1038/nbt0698-562View ArticlePubMedGoogle Scholar
- Nordström EK, Forsell MN, Barnfield C, Bonin E, Hanke T, Sundström M, Karlsson GB, Liljeström P: Enhanced immunogenicity using an alphavirus replicon DNA vaccine against human immunodeficiency virus type 1. J Gen Virol 2005, 86: 349-354.View ArticlePubMedGoogle Scholar
- Hariharan MJ, Driver DA, Townsend K, Brumm D, Polo JM, Belli BA, Catton DJ, Hsu D, Mittelstaedt D, McCormack JE, et al.: DNA immunization against herpes simplex virus: enhanced efficacy using a Sindbis virus-based vector. J Virol 1998, 72: 950-958.PubMed CentralPubMedGoogle Scholar
- Leitner WW, Ying H, Driver DA, Dubensky TW, Restifo NP: Enhancement of tumor-specific immune response with plasmid DNA replicon vectors. Cancer Res 2000, 60: 51-55.PubMed CentralPubMedGoogle Scholar
- Ljungberg K, Whitmore AC, Fluet ME, Moran TP, Shabman RS, Collier ML, Kraus AA, Thompson JM, Montefiori DC, Beard C, Johnston RE: Increased immunogenicity of a DNA-launched Venezuelan equine encephalitis virus-based replicon DNA vaccine. J Virol 2007, 81: 13412-13423. 10.1128/JVI.01799-07PubMed CentralView ArticlePubMedGoogle Scholar
- Lundstrom K: Alphavirus-based vaccines. Curr Opin Mol Ther 2002, 4: 28-34.PubMedGoogle Scholar
- Adachi O, Kawai T, Takeda K, Matsumoto M, Tsutsui H, Sakagami M, Nakanishi K, Akira S: Targeted disruption of the MyD88 gene results in loss of IL-1- and IL-18-mediated function. Immunity 1998, 9: 143-150. 10.1016/S1074-7613(00)80596-8View ArticlePubMedGoogle Scholar
- Sato M, Suemori H, Hata N, Asagiri M, Ogasawara K, Nakao K, Nakaya T, Katsuki M, Noguchi S, Tanaka N, Taniguchi T: Distinct and essential roles of transcription factors IRF-3 and IRF-7 in response to viruses for IFN-alpha/beta gene induction. Immunity 2000, 13: 539-548. 10.1016/S1074-7613(00)00053-4View ArticlePubMedGoogle Scholar
- Muller U, Steinhoff U, Reis LF, Hemmi S, Pavlovic J, Zinkernagel RM, Aguet M: Functional role of type I and type II interferons in antiviral defense. Science 1994, 264: 1918-1921. 10.1126/science.8009221View ArticlePubMedGoogle Scholar
- Alexopoulou L, Holt AC, Medzhitov R, Flavell RA: Recognition of double-stranded RNA and activation of NF-kappaB by Toll-like receptor 3. Nature 2001, 413: 732-738. 10.1038/35099560View ArticlePubMedGoogle Scholar
- Smerdou C, Liljeström P: Two-helper RNA system for production of recombinant Semliki forest virus particles. J Virol 1999, 73: 1092-1098.PubMed CentralPubMedGoogle Scholar
- Leitner WW, Hwang LN, deVeer MJ, Zhou A, Silverman RH, Williams BR, Dubensky TW, Ying H, Restifo NP: Alphavirus-based DNA vaccine breaks immunological tolerance by activating innate antiviral pathways. Nat Med 2003, 9: 33-39. 10.1038/nm813PubMed CentralView ArticlePubMedGoogle Scholar
- Pichlmair A, Schulz O, Tan CP, Rehwinkel J, Kato H, Takeuchi O, Akira S, Way M, Schiavo G, Reis e Sousa C: Activation of MDA5 requires higher-order RNA structures generated during virus infection. J Virol 2009, 83: 10761-10769. 10.1128/JVI.00770-09PubMed CentralView ArticlePubMedGoogle Scholar
- Bracci L, La Sorsa V, Belardelli F, Proietti E: Type I interferons as vaccine adjuvants against infectious diseases and cancer. Expert Rev Vaccines 2008, 7: 373-381. 10.1586/147605220.127.116.113View ArticlePubMedGoogle Scholar
- Bramson JL, Dayball K, Hall JR, Millar JB, Miller M, Wan YH, Lin R, Hiscott J: Super-activated interferon-regulatory factors can enhance plasmid immunization. Vaccine 2003, 21: 1363-1370. 10.1016/S0264-410X(02)00694-1View ArticlePubMedGoogle Scholar
- Kwissa M, Amara RR, Robinson HL, Moss B, Alkan S, Jabbar A, Villinger F, Pulendran B: Adjuvanting a DNA vaccine with a TLR9 ligand plus Flt3 ligand results in enhanced cellular immunity against the simian immunodeficiency virus. J Exp Med 2007, 204: 2733-2746. 10.1084/jem.20071211PubMed CentralView ArticlePubMedGoogle Scholar
- Zhang X, Sun S, Hwang I, Tough DF, Sprent J: Potent and selective stimulation of memory-phenotype CD8+ T cells in vivo by IL-15. Immunity 1998, 8: 591-599. 10.1016/S1074-7613(00)80564-6View ArticlePubMedGoogle Scholar
- Marrack P, Kappler J, Mitchell T: Type I interferons keep activated T cells alive. J Exp Med 1999, 189: 521-530. 10.1084/jem.189.3.521PubMed CentralView ArticlePubMedGoogle Scholar
- Diebold SS, Schulz O, Alexopoulou L, Leitner WW, Flavell RA, Reis ESC: Role of TLR3 in the immunogenicity of replicon plasmid-based vaccines. Gene Ther 2008.Google Scholar
- Paun A, Pitha PM: The IRF family, revisited. Biochimie 2007, 89: 744-753. 10.1016/j.biochi.2007.01.014PubMed CentralView ArticlePubMedGoogle Scholar
- Tamura T, Yanai H, Savitsky D, Taniguchi T: The IRF family transcription factors in immunity and oncogenesis. Annu Rev Immunol 2008, 26: 535-584. 10.1146/annurev.immunol.26.021607.090400View ArticlePubMedGoogle Scholar
- White L, Sali T, Alvarado D, Gatti E, Pierre P, Streblow D, Defilippis VR: Chikungunya Virus Induces IPS-1-Dependent Innate Immune Activation and PKR-Independent Translational Shutoff. J Virol 2011, 85: 606-20. 10.1128/JVI.00767-10PubMed CentralView ArticlePubMedGoogle Scholar
- Rhee EG, Blattman JN, Kasturi SP, Kelley RP, Kaufman DR, Lynch DM, La Porte A, Simmons NL, Clark SL, Pulendran B, et al.: Multiple Innate Immune Pathways Contribute to the Immunogenicity of Recombinant Adenoviral Vaccine Vectors. J Virol 2011, 85: 315-23. 10.1128/JVI.01597-10PubMed CentralView ArticlePubMedGoogle Scholar
- Pugachev KV, Guirakhoo F, Monath TP: New developments in flavivirus vaccines with special attention to yellow fever. Curr Opin Infect Dis 2005, 18: 387-394. 10.1097/01.qco.0000178823.28585.adView ArticlePubMedGoogle Scholar
- Leitner WW, Bergmann-Leitner ES, Hwang LN, Restifo NP: Type I Interferons are essential for the efficacy of replicase-based DNA vaccines. Vaccine 2006, 24: 5110-5118. 10.1016/j.vaccine.2006.04.059PubMed CentralView ArticlePubMedGoogle Scholar
- Gehring S, Gregory SH, Kuzushita N, Wands JR: Type 1 interferon augments DNA-based vaccination against hepatitis C virus core protein. J Med Virol 2005, 75: 249-257. 10.1002/jmv.20264View ArticlePubMedGoogle Scholar
- Sellins K, Fradkin L, Liggitt D, Dow S: Type I interferons potently suppress gene expression following gene delivery using liposome(-)DNA complexes. Mol Ther 2005, 12: 451-459. 10.1016/j.ymthe.2005.04.008View ArticlePubMedGoogle Scholar
- Liljeström P, Garoff H: Internally located cleavable signal sequences direct the formation of Semliki Forest virus membrane proteins from a polyprotein precursor. J Virol 1991, 65: 147-154.PubMed CentralPubMedGoogle Scholar
- Liljeström P, Garoff H: A new generation of animal cell expression vectors based on the Semliki Forest virus replicon. Biotechnology (N Y) 1991, 9: 1356-1361.View ArticleGoogle Scholar
- McInerney GM, Kedersha NL, Kaufman RJ, Anderson P, Liljestrom P: Importance of eIF2alpha phosphorylation and stress granule assembly in alphavirus translation regulation. Mol Biol Cell 2005, 16: 3753-3763. 10.1091/mbc.E05-02-0124PubMed CentralView ArticlePubMedGoogle Scholar
- Breakwell L, Dosenovic P, Karlsson Hedestam GB, D'Amato M, Liljeström P, Fazakerley J, McInerney GM: Semliki Forest virus nonstructural protein 2 is involved in suppression of the type I interferon response. J Virol 2007, 81: 8677-8684. 10.1128/JVI.02411-06PubMed CentralView ArticlePubMedGoogle Scholar
- Fros JJ, Liu WJ, Prow NA, Geertsema C, Ligtenberg M, Vanlandingham DL, Schnettler E, Vlak JM, Suhrbier A, Khromykh AA, Pijlman GP: Chikungunya virus nonstructural protein 2 inhibits type I/II interferon-stimulated JAK-STAT signaling. J Virol 2010, 84: 10877-10887. 10.1128/JVI.00949-10PubMed CentralView ArticlePubMedGoogle Scholar
- Lemke G, Rothlin CV: Immunobiology of the TAM receptors. Nat Rev Immunol 2008, 8: 327-336. 10.1038/nri2303PubMed CentralView ArticlePubMedGoogle Scholar
- Tovey MG, Lallemand C, Thyphronitis G: Adjuvant activity of type I interferons. Biol Chem 2008, 389: 541-545. 10.1515/BC.2008.051View ArticlePubMedGoogle Scholar
- Ying H, Zaks TZ, Wang RF, Irvine KR, Kammula US, Marincola FM, Leitner WW, Restifo NP: Cancer therapy using a self-replicating RNA vaccine. Nat Med 1999, 5: 823-827. 10.1038/10548PubMed CentralView ArticlePubMedGoogle Scholar
- Leitner WW, Hwang LN, Bergmann-Leitner ES, Finkelstein SE, Frank S, Restifo NP: Apoptosis is essential for the increased efficacy of alphaviral replicase-based DNA vaccines. Vaccine 2004, 22: 1537-1544. 10.1016/j.vaccine.2003.10.013PubMed CentralView ArticlePubMedGoogle Scholar
- Bergmann-Leitner ES, Leitner WW, Duncan EH, Savranskaya T, Angov E: Molecular adjuvants for malaria DNA vaccines based on the modulation of host-cell apoptosis. Vaccine 2009, 27: 5700-5708. 10.1016/j.vaccine.2009.06.059View ArticlePubMedGoogle Scholar
- Rhee EG, Kelley RP, Agarwal I, Lynch DM, La Porte A, Simmons NL, Clark SL, Barouch DH: TLR4 ligands augment antigen-specific CD8+ T lymphocyte responses elicited by a viral vaccine vector. J Virol 2010, 84: 10413-10419. 10.1128/JVI.00928-10PubMed CentralView ArticlePubMedGoogle Scholar
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