Immunity to Protozoan ParasitesView this Special Issue
Review Article | Open Access
Toll-Like Receptors in Leishmania Infections: Guardians or Promoters?
Protozoa of the genus Leishmania cause a wide variety of pathologies ranging from self-healing skin lesions to visceral damage, depending on the parasite species. The outcome of infection depends on the quality of the adaptive immune response, which is determined by parasite factors and the host genetic background. Innate responses, resulting in the generation of mediators with anti-leishmanial activity, contribute to parasite control and help the development of efficient adaptive responses. Among those, the potential contribution of members of the Toll-like receptors (TLRs) family in the control of Leishmania infections started to be investigated about a decade ago. Although most studies appoint a protective role for TLRs, there is growing evidence that in some cases, TLRs facilitate infection. This review highlights recent advances in TLR function during Leishmania infections and discusses their potential role in restraining parasite growth versus yielding disease.
Infections with parasitic protozoa have been a long-term health issue in the tropical and subtropical regions of the globe. Among those, diseases caused by infections with microbes of the Leishmania genus are one of the most wide-spread infirmities. Leishmania parasites are transmitted to the vertebrate host by the sand fly bite that injects the infective metacyclic forms under the skin. The flagellated parasites are rapidly engulfed by phagocytic cells either resident or recruited to the wound site (i.e., neutrophils, macrophages and dendritic cells), reviewed in . While the passage through neutrophils is believed to be transient, serving as a temporary safe hideaway, the parasites are able to establish productive infections in macrophages, where they differentiate to amastigotes and replicate inside the parasitophorous vacuole. The pathology resulting from the infection is related to the parasite species that can either induce cutaneous (i.e., L. major, L. mexicana, L. guyanensis), mucocutaneous (i.e., L. amazonensis, L. braziliensis), or visceral leishmaniasis (L. donovani, L. chagasi). The outcomes of infections are complex, depending not only on the parasite species but also on the immune status of the host. As an example, although L. amazonensis is primarily associated with cutaneous manifestations, it can also provoke mucocutaneous and/or diffuse cutaneous leishmaniasis. Infections with L. panamensis or L. braziliensis can generate a persistent hyperinflammatory response, where a mixed T-helper 1 (Th1)/T-helper 2 (Th2) response is observed, leading to nonresolving lesions in humans [2, 3]. L. guyanensis can also migrate away from the primary infection site, generating distal secondary lesions similar to those observed with L. braziliensis .
Cutaneous leishmaniasis comprises self-healing skin ulcers in immunocompetent individuals, however, parasite persistence remains, helping to maintain protective immunity . Mucocutaneous leishmaniasis involves parasitic dissemination to the nasopharyngeal area, leading to destructive secondary lesions. It is characterized by a persistent inflammatory response associated with increased expression of proinflammatory mediators that are crucial for the recruitment of cells to the site of infection . About 5 to 10% of individuals asymptomatic or with resolved cutaneous lesions may develop mucocutaneous lesions [7, 8]. Although the development of a type-1 immune response is crucial for the control of parasites, unresolved inflammation can derive from lack of an appropriate modulation of those responses in the case of tegumentary leishmaniasis (reviewed in ). On the other hand, the progression of visceral leishmaniasis is often accompanied by a decay in the type-1 response . In this scenario, increasing immunosuppression contributes to disease progression not only due to the presence of immunoregulatory cytokines but also because of partial destruction of lymphoid tissues [11, 12].
The mouse model for cutaneous leishmaniasis caused by L. major has been largely explored over the years, providing a solid body of data defining the immunological mechanisms involved in mounting innate and adaptive protective responses (reviewed in ). However, those findings cannot be readily extrapolated for models of infections by other Leishmania species, rendering it indispensable to investigate the parameters of immunological responses for each combination of parasite species, host cell, and/or animal model for the disease. Although adaptive immunity is essential for the resolution of infection, there is growing evidence that innate mechanisms make an important contribution to the antiparasitic defenses.
Innate responses develop after the initial sensing of invading microbes, leading to the production of effector molecules that contribute to contain initial infection and to mount the subsequent adaptive immune response . The early immune reaction against L. major, L. braziliensis, and L. infantum during experimental infections has been analyzed in detail, revealing, for example, differential susceptibility to nitric oxide (NO) and reactive oxygen species (ROS) in phagocytes located at distinct organs. While the production of NO is required for the leishmanicidal activity against L. major  and L. braziliensis  in the skin of infected mice, it is dispensable in the spleen and mildly important in the lymph node. Although NO was believed to be important to the control of L. donovani in the liver and spleen of mice , it was later established that neither iNOS nor NADPH oxidase (phox) is essential to restrict parasite replication in the liver [18, 19]. The relative importance of such mediators has been recently covered by Liese and coworkers  and will not be explored in this review.
The potential contribution of Toll-like receptors in fighting parasitic infections has gained attention in the last decade. We will cover the main findings regarding the interplay between Toll-mediated responses and Leishmania infections.
2. Toll-Like Receptors (TLRs) and Leishmania
Toll-like receptors (TLRs) are hallmarks of cellular receptors that recognize pathogen-associated molecules and participate in innate responses to infections (reviewed in ). There are currently 13 mammalian TLRs described, while TLRs 1–9 are functionally conserved between humans and mice, TLR10 seems to be functional in humans but divergent at the C-terminus in the mouse, rendering it inoperant. TLR11 is functional in the mouse but truncated in humans. The conserved TLRs can be divided into extracellular: TLR1-2, TLR4-6, and TLR11  or intracellular: TLR3, TLR7-9 and TLR13 , and those receptors recognize specific groups of ligands either at the cell surface or in the endosomal compartment, respectively . Each TLR detects distinct sets of molecules from viruses, bacteria, fungi, and parasites, and upon binding, they recruit different adaptor proteins such as MyD88 or TRIF . TLRs initiate innate responses in a variety of ways, leading to the production of inflammatory cytokines by macrophages and different subtypes of dendritic cells (DCs) and of type I interferons (IFN) by inflammatory monocytes, macrophages, and DCs . Neutrophils also express the majority of TLR family members and several coreceptors but lack intracellular TLR3 and TLR7 (reviewed in ). In those cells, TLR activation often leads to the generation of reactive oxygen species (ROS), cytokine production, increased cellular survival, receptor expression, and phagocytosis .
The microbial molecules recognized by TLRs are conserved polymers, such as bacterial lipopolysaccharides (LPSs), peptidoglycans, unmethylated bacterial DNA, and double-strand viral RNA, among others. Since protozoans lack most of these structures, TLRs must recognize other groups of molecules in order to sense those microbes. The recognition of Trypanosoma cruzi tGPI (glicosylphosphatidylinositol anchor) by TLR2  and of glycoinositolphospholipids by TLR4 , of Plasmodium hemozoin by TLR9 , and of the profilin-like molecule of Toxoplasma gondii by TLR11  are such examples.
The phagocytosis of Leishmania by macrophages, contrary to the observed with other pathogens, is marked by the absence of many proinflammatory cytokines . Furthermore, infected macrophages become unresponsive to subsequent challenges with the TLR4 ligand LPS, a feature that is associated with parasite phosphoglycans [28, 36]. Since TLR recognition is often associated with the production of proinflammatory cytokines and with the generation of additional effector molecules, it is unquestionably important to determine the implications of TLR activation during Leishmania infections. A few Leishmania-derived molecules have been reported to activate TLRs, and the majority of the studies to date focused on the activation of TLR2, TLR4, and TLR9.
2.1. TLR2 and MyD88
Initial experiments suggesting that Leishmania induces TLR-mediated responses came from studies using cells lacking the adaptor molecule MyD88 . Those analyses showed that L. major activates the promoter region of IL-1α, but not of IL-6, IL-8, or IL-10, through MyD88-dependent pathway in macrophages . It was then reported that MyD88-dependent pathways are required for the development of the protective IL-12-mediated Th1 response against the L. major in C57BL6 resistant mice, since MyD88−/− mice infected with L. major developed a nonprotective Th2 response . The animals had enlarged nonhealing lesions and low IL-12 plasma levels suggesting that TLR-mediated responses were important to develop effective antiparasite immunity. At the same time, it was revealed that the higher susceptibility of MyD88−/− mice to L. major infections correlated with elevated levels of IL-4, despite the lack of ulcerating lesions . L. donovani, L. braziliensis, L. major, and L. mexicana induce the maturation of DCs in vivo and the observation that DC maturation was attenuated in MyD88−/− mice infected with L. donovani implied the involvement of TLRs in DC maturation and T-cell priming . Although the studies using MyD88-deficient mice suggested that TLRs influence the adaptive immune response during Leishmania infections, they did not offer undisputable evidence for the participation of TLRs, mainly because MyD88 can also function as an adaptor protein to the IL-1 receptor . Furthermore, there are pathways downstream of TLR3 and TLR4 which are independent of MyD88, such as the activation of TLR4 through IRF3 leading to the production of type-1 interferons . Therefore, it became crucial to prove the direct involvement of TLRs for the responses observed in the infection models described above.
The direct activation of TLR2 by Leishmania components was subsequently reported. Purified L. major lipophosphoglycan (LPG) induced the upregulation and stimulation of TLR2 on human NK cells, with additional enhancement of TNF-α and IFN-γ . LPGs of L. major, L. mexicana, L. aethiopica, and L. tropica were defined as TLR2 ligands in studies using murine macrophages, although the stimulation with L. tropica LPG was only marginal . At this point, the possibility that species- or strain-specific structural differences in the phosphoglycan chain could contribute to receptor recognition or activation was raised. Those studies revealed that the induction of TNF-α synthesis by L. major LPG required the presence of the lipid anchor and of functional MyD88. Intriguingly, LPG also induced the expression of suppressors of the cytokine signaling family proteins SOCS-1 and SOCS-3 . The finding that negative modulators of cytokine synthesis were also induced by LPG indicated that TLR2 stimulation by L. major can lead to both positive and negative inflammatory signals. The fact that SOCS1 itself directly downmodulates TLR4 signaling pathways  illustrates how the initial stimulation of TLR2 by L. major can ultimately lead to the attenuation of further TLR responses.
More recently, it was shown that LPG stimulates cytokine production by human peripheral blood mononuclear cells via TLR2 as well . Although cellular LPG isolated from promastigotes is structurally similar to soluble LPG present in culture supernatants, they differ in the average number of phosphorylated oligosaccharide repeat units and in glycan composition . In the above-mentioned study, while both forms of LPG induced the production of ROS in a TLR-2-dependent manner, Th1-promoting cytokines were induced solely by soluble LPG, leading to the proposal that the first encounter and recognition of L. major by membrane-derived LPG after interaction with TLR2 provides a cytokine milieu for consequent Th2 differentiation . Later on, the same authors provided evidence that the induction of NO production by macrophage cell lines was achieved with both LPG forms, and was dependent on TLR2, but not on TLR4 signaling . More recently, synthetic oligosaccharides based on the LPG structure were shown to induce IL-12 and Th1 responses in vivo through TLR2, corroborating that TLR2 stimulation by Leishmania LPG potentiates the inflammatory responses in mice . Those findings assign a protective role for TLR2 and MyD88 during L. major infection, in particular, TLR2 seems required to mount an effective Th1 response (Figure 1, left pannel).
The consequences of TLR2 activation to the control of leishmaniasis was further verified using the TLR2 ligand, arabinosylated lipoarabinomannan (Ara-LAM), in a Balb/c model of visceral leishmaniasis . Ara-LAM induced the expression of TLR2 in macrophages infected with L. donovani in vitro, which was accompanied by the production of NO and of proinflammatory cytokines. Mice pre-treated with Ara-LAM and subsequently challenged with L. donovani showed around 80% reduction of infection in the liver and the spleen, paralleled by a strong Th1 response. However, one should take care at interpreting those results since Ara-LAM could exert its effect in vivo through additional mechanisms besides TLR2 activation.
The parasite can also modulate the expression of TLRs, interfering with their availability and/or the subsequent quality of the responses mediated by those receptors. For example, two antigens isolated from L. donovani amastigotes were shown to upregulate TLR2 expression in RAW264 macrophages . The 65 and 98 kDa proteins induced elevated levels of MAPK p38, as well as its phosphorylation in relation to that of ERK1/2, leading the authors to conclude that they induced the activation of TLR signaling proteins. However, one should interpret those conclusions with caution, specific controls for the activation of TLR2 (i.e., neutralizing antibodies or cells derived from knock-out mice) were lacking in this study. Furthermore, the contribution of minor nonproteinaceous contaminants in the preparations cannot be excluded considering that the antigens were isolated by elution from SDS-PAGE gels and were not further purified. In another study, while verifying the expression of TLRs during the infection of Balb/c mice with L. chagasi, attempts were made to correlate upregulation of TLR expression with a potential role for those receptors in generating inflammatory versus anti-inflammatory responses . The authors observed upregulation of TLR2 and TLR4 from day 1 to day 28 postinfection, and increased expression correlated with higher mRNA levels for TNFα, IL-17, IL-10, and TGFβ during early infection. On the other hand, there was an inverse correlation between the expression of TLR2-4 and that of IL-12 or IFN-γ, and parasite load, leading to the proposal that those TLRs are involved in the recognition of the parasite during visceral leishmaniasis. However, while most of those studies evaluated the induction of cytokine mRNA and of mRNA for TLRs, they did not provide direct evidence that TLRs are required for the induction of cytokine synthesis. Increased expression of TLRs might have occurred as a consequence of the inflammatory environment in the spleen, making it difficult to evaluate to what extent the activation of TLRs is implicated in those findings.
L. panamensis was found to induce upregulation of TLR1, TLR2, TLR3, and TLR4 in human primary macrophages . The activities of TLR4 and TLR3 correlated with TNF-α secretion and the leishmanicidal activity of those macrophages . A global analysis of gene expression in IFN-γ-treated THP-1 macrophages infected with L. major showed that genes related to TLR signaling are also differentially expressed upon infection , revealing how the parasite could interfere with the capacity of the host cell to respond via TLR-mediated routes. L. major can also induce the expression of TLR2, TLR7, and TLR9 in polymorphic nuclear cells (PMNs) from C57BL6 mice , evidencing that infection provokes alterations in the levels of several TLRs in multiple cells of the innate system.
Additional parasite molecules were implicated in TLR2 activation. The L. infantum protein related to the silent information regulator 2 (SIR2) family leads to the proliferation of activated B lymphocytes, causing increased expression of major histocompatibility complex (MHC) II and the costimulatory molecules CD40 and CD86, in a TLR2-dependent fashion . The maturation of DCs induced by SIR2, accompanied by the secretion of IL12 and TNF, was also dependent on TLR2, while the activation of macrophages still took place in the absence of TLR2.
Other studies suggest that Leishmania downregulates TLR2-mediated responses and attempted to dissect some of the downstream molecular pathways involved therein. The infection of human THP1-derived macrophages by L. donovani in vitro suppresses TLR2 and TLR4-stimulated IL-12 release, with an increase in IL-10 production, through parasite-dependent contact . Parasites were shown to negatively modulate the TLR2-stimulated signaling pathway by suppressing MAPKp38 phosphorylation and activating extracellular regulated kinase (ERK)1/2 phosphorylation . It was also reported that L. donovani, L. mexicana, and L. major exploit the macrophage tyrosine phosphatase SHP-1 to inactivate kinases involved in TLR signaling . The infection of bone-marrow-derived macrophages in vitro leads to IRAK inactivation, impairing LPS-mediated activation as well as macrophage function .
Studies using TLR2-deficient mice revealed a somewhat contrasting scenarium (Figure 1, right pannel). TLR2 was necessary for the development of lesions in mice infected with L. braziliensis . While MyD88−/− mice developed larger and prolonged lesions compared to those in control mice, the lack of TLR2 resulted in enhanced DC activation and increased IL-12 production after infection. L. braziliensis-infected TLR2-deficient DCs were more competent in priming naïve CD4 T cells in vitro, correlating with increased IFN-γ production in vivo and enhanced resistance to infection. More recently, it was reported that TLR2-deficient mice are also less susceptible to the infection with L. amazonensis than the wild-type C57BL6 counterpart, as evidenced by lower parasite burden and reduced recruitment of inflammatory cells in the first weeks of infection . At the same time, it was described that the activation of the protein kinase PKR during the infection of macrophages by L. amazonensis is crucial for parasite survival . Finally, The engagement of PKR and the subsequent production of type-1 IFNs and of superoxide dismutase (SOD-1) were necessary for effective parasite growth and dependent on TLR2, indicating that this TLR is required for the successful infection of macrophages by L. amazonensis . Those findings suggest that TLR2 plays a role in facilitating the establishment of the disease, depending on the Leishmania species in question.
Besides the direct activation of TLRs by parasite molecules, the engagement of those receptors indirectly by nonparasite ligands during phagocytosis could influence the outcome of infection. Studies using TLR4−/− mice indicated that this receptor plays a protective role in L. major infections . The authors observed diminished parasite load at the skin lesions of infected mice at the initial stages of infection, that is, 24 h, and found increased parasite survival in host cells from TLR4-deficient mice, which correlated with a higher activity of arginase . The same group subsequently showed that the lack of TLR4 results in increased parasite growth during both the innate and adaptive phase of the immune response and in delayed healing of the cutaneous lesions . However, TLR4 does not seem important to define the range of chemokines produced in the skin or in the draining lymph nodes of mice infected with L. major . In agreement with a protective role for TLR4, it was described that the lack of SLAM, a cell surface receptor of macrophages that regulates TLR4-transduced signals, increased the susceptibility of mice to L. major infections . Importantly, this phenotype was attributed to defective macrophage function, suggesting that the activation of host cell TLR4 contributes to the control of parasite growth in vivo. The first potential TLR4 ligand present in Leishmania was described a few years ago in L. pifanoi amastigotes and consists of a proteoglycolipid complex (P8) composed of a cysteine and serine metalloprotease, host-derived ApoE, and four glycolipids [62, 63]. Stimulation of macrophages with P8 or its isolated glycolipids provoked the synthesis of a range of proinflammatory cytokines, including IL1β and TNFα and the responses to intact P8 were dependent on TLR4, MD2, CD14, and MyD88  (Figure 2, left). However, the exact molecular entity serving as the TLR4 ligand in P8 still remains to be determined. More recently, TLR4 was implicated in the mechanism underlying the inhibition of IL-12 production in LPS-treated macrophages infected with L. mexicana. Metacyclic promastigotes were found to greatly increase the phosphorylation of the three major MAP kinases, ERK, p38, and JNK, in a manner dependent on TLR4 but not on TLR2 . Parasites prolonged the induction of iNOS or COX-2 expression in LPS-stimulated macrophages, enhanced PGE2 and NO production, and increased the expression of arginase-1. The induction of iNOS, COX-2, and arginase-1 were also dependent on TLR4, supporting the hypothesis that this TLR plays an anti-inflammatory role in macrophages during L. mexicana infections, ultimately preventing IL-12 production.
On the other hand, the anti-leishmanial role of TLR4 might be exerted by multiple downstream effector molecules. For example, macrophages of the mouse strain SPRE/Ei, which is resistant to LPS, have normal MyD88-mediated signaling pathways but are defective in the production of type-1 IFNs . Those mice were found to be highly susceptible to L. major, a feature that was attributed to the poor induction of IFNβ-dependent genes. These observations suggest that type-1 IFNs pose as effectors that, through a paracrine/autocrine loop, contribute to parasite control downstream of TLR4 stimuli. The cross-talk between TLR4 and additional receptors should also be taken into consideration when viewing anti-leishmanial properties attributed to this TLR. For example, in macrophages, the stimulation of the glucocorticoid receptor by progesterone downmodulates TLR4-induced NO and IL-12 production and reduces the killing of L. donovani by activated macrophages  Likewise, complement-derived C5a negatively regulates TLR4-induced IL-12, IL-23, and IL-27 in macrophages, leading to decreased Th1 responses in vivo . It was found that Th1- enhanced immunity in C5a-receptor−/− mice confers protection against an L. major challenge , exemplifying how other receptors of innate immunity might affect susceptibility to leishmania infections through the modulation of TLR responses.
The engagement of TLRs during the interaction between different cells of the innate system can also dictate the fate of parasites in infected macrophages. It was reported that apoptotic neutrophils from C57B6 mice induce the production of TNF-α by L. major-infected macrophages in vitro, leading to parasite elimination . Later on, the activation of macrophage TLR4 by the neutrophil-derived serine protease, neutrophil elastase (NE), was proposed as the underlying mechanism leading to parasite death  (Figure 2, scheme c). More recently, the phagocytosis of apoptotic neutrophils by bone-marrow-derived macrophages in a proinflammatory context in vitro was found to induce a stable M2b phenotype, rendering those macrophages more permissive to the replication of L. major . The induction of the M2b phenotype, correlating with higher IL10 levels and a Th2-type response, was dependent on TLR4 and NE activities, suggesting that the engagement of TLR4 might be beneficial to the parasite at later stages of infection (Figure 2, scheme b). Indeed, rechallenge of those macrophages with LPS promoted parasite growth and the treatment of C57B6 mice with apoptotic neutrophils 3 days before infection increased parasite burdens, demonstrating how TLR4-mediated signals can contribute to create permissive niches for parasite replication at later stages .
We have recently described that NE present at the surface of murine macrophages can also activate TLR4 during the phagocytosis of L. major, without requirement of neutrophils . Wild-type L. major is able to control NE activity, at least in part, through its endogenous protease inhibitor structurally similar to bacterial ecotins, named ISP2 (inhibitor of serine peptidases) . Parasites lacking ISP2 promptly engage macrophage TLR4 due to uncontrolled NE activity  (Figure 2, scheme a). Furthermore, we found cooperativity between TLR4 and CD11b, a subunit of the complement type 3 receptor (CR3), in facilitating the uptake of L. major by macrophages. TLR4 activation led to the production of ROS, provoking partial elimination of intracellular parasites a few hours after internalization . We found that the cooperativity between CD11b and TLR4 to enhance the phagocytosis of parasites was strictly dependent on the activity of NE, setting another example of how multiple components of innate immunity can act concertedly to improve the defense against invading parasites. The ability of Leishmania to promote the cross-talk between those receptors might exacerbate TLR4 responses in light of the finding that optimal signaling through TLR4 requires multiple cell surface associated molecules such as CD11b and HSP90 . We observed that early engagement of TLR4 can influence how macrophages respond to L. major in at least two fronts: (i) first, by promoting enhanced phagocytosis and early killing of promastigotes (i.e., 24 hrs), and (ii) secondly, by restraining the subsequent growth of amastigotes in the following 2–4 days. Those observations suggest that signals mediated through TLR4 at the parasitophorous vacuole could affect the microenvironment surrounding the parasite, controlling sustained intracellular growth.
Recently, a screen of TLR4 mutations in patients with cutaneous leishmaniasis revealed that certain genotypes were largely favoured in individuals with chronic or acute disease, as compared to asymptomatic donors or noninfected individuals, leading to the proposal that TLR4 polymorphism may lead to increased susceptibility or severity of the disease . Although the consequences of TLR activation in macrophages as a result of Leishmania infections are being widely investigated, we are still lacking information on how TLRs might affect the interaction of the parasites with neutrophils. The mobilization of TLRs in neutrophils, in particular that of TLR4, is known to induce a wide range of responses. Of interest, IRAK4 is crucial for the exocytosis of neutrophil secretory granules induced by TLR4 . In view of the findings that NE affects the outcome of parasite growth in macrophages [69–71], the stimulation of TLR4 in neutrophils could regulate the levels of secreted NE, influencing parasite burden in macrophages.
2.3. TLR9 and TLR3
Studies aiming at improving the therapy for L. major infections using recombinant IL-18 pointed to a potential involvement of the CpG-TLR9 pathway in the protective antiparasite response. While promoting rIL18 expression in infected mice through gene gun delivery, the authors observed a synergistic role of the plasmid vector with rIL18, which was dependent of CpG motifs . The induction of proinflammatory cytokines, in particular of IL-12, by antigen-presenting cells was found to be dependent on TLR9 activation by CpG, indicating that TLR9 stimulation could lead to protective immunity against the parasite. In attempting to define which TLRs were involved in the increased susceptibility of MyD88-deficient mice to Leishmania infections, Liese and coworkers showed that TLR9 was required to induce IL-12 in bone-marrow-derived DCs by either L. major or its DNA . Furthermore, they observed that TLR9−/− mice exhibited more severe skin lesions and higher parasite burdens as compared to C57B6 controls, coupled to a transient increase in IL-4, IL-13, and arginase. Even though there was an increase in Th2 cytokines, they did not observe alterations in the levels of IFNγ in the draining lymph node, concluding that deficiency in TLR9 does not influence the quality of the Th1 response . The same group reported that plasmacytoid DCs responded to L. infantum by secreting IFNs α and β and IL-12 in a TLR9-dependent manner and that NK-induced cytotoxicity was abolished in TLR9−/− mice . Those results were the first to link TLR9, IL-12, and DCs to the activation of NK cells during visceral leishmaniasis. The protective role of NK cells in murine leishmaniasis is now proven to be strictly dependent on IL-12 secreted by myeloid DCs in response to Leishmania via TLR9 (reviewed in ).
The involvement of TLR9 in controlling L. major infection was further investigated in the following studies. Lesion progression and parasite burden were higher in TLR9−/− mice as compared to C57BL/6 controls, which was concomitant with a transient inhibition of a Th1 response . The authors showed that the activation of bone-marrow-derived DCs, or of DCs isolated from the spleen, by L. major or by parasite DNA, followed by IFN-γ production by CD4 T cells, was abolished by treatment with DNAse or by alkalinization of endosomal compartments with chloroquine, supporting a role for TLR9 in DC activation by the parasite  (Figure 3, left panel). Those findings caused some controversy as to the impact of TLR9 deficiency in attenuating the Th1 response . Since in both studies there were delays in the healing of skin lesions in TLR9−/− mice, it is feasible that the Th1 response is at least partially compromised in those mice.
The recognition of Leishmania by TLR3 in endosomal compartments was brought up a few years ago. Experiments using RNA interference provided evidence that in IFN-γ primed macrophages, TLR3 is required for the production of NO and TNF-α induced by infection with L. donovani, besides contributing to parasite phagocytosis  (Figure 3, right panel). Since Leishmania does not contain double-stranded RNA, the standard ligand for TLR3, the origin of the stimulatory factor of TLR3 remained an open question. More recently, an elegant work from Ives and coworkers shed light on this matter, providing evidence that RNA from viruses present in L. guyanensis serve as a source of TLR agonists, promoting inflammatory cytokines and chemokines  (Figure 3, right panel). The elevated cytokine production was dependent on the TLR3-TRIF pathway, and augmented via MyD88-transduced signals. Intriguingly, those responses rendered mice more susceptible to infection, as observed by increased swelling and parasite burden, together with more pronounced metastasis. Those findings add to the growing list of examples where the subversion of TLR responses by Leishmania serves to promote infection instead of playing a protective role.
Additional factors can further influence TLR activation indirectly, affecting the outcome of adaptive immunity. For example, it was found that dyslipidemia inhibits TLR-induced production of IL-12, IL-6, and TNF-α, as well as upregulation of costimulatory molecules by CD8α− DCs, in vivo, leading to impaired Th1 and enhanced Th2 responses. Such dysfunction compromised host resistance to L. major, revealing that a dyslipidemic microenvironment can interfere with DC responses to Leishmania through TLRs .
2.4. TLRs Stimulation in Vaccination and Immunotherapy
The use of TLR activators as adjuvants in formulations to improve the efficacy of experimental vaccination against Leishmania has also been largely explored. Even before the knowledge that TLR stimulation could play a role in the defense against Leishmania, CpG oligodeoxynucleotides (ODNs) were tested as an adjuvant in the immunization of mice with L. major-soluble antigen aiming at inducing a protective Th1 response, leading to improved survival . This observation supported the proposal that TLR agonists could serve as cost-effective alternatives in vaccine formulations against leishmaniasis. Along those lines, the formulation of multisubunit recombinant vaccines with the TLR4 agonist, monophosphoryl lipid A, elicited protective immunity against L. major challenge in Balb/c mice, an approach that could serve as an alternative to the use of recombinant IL12 . An analogue of lipid A was subsequently used as a TLR4 agonist in experimental vaccination with L. amazonensis antigens and was proven beneficial for both immunoprophylaxis and immunotherapy, associated mainly with increased levels of IL12 and IFNγ . CpG (ODN) were throughoutly tested as adjuvants in experimental vaccinations to induce protective responses to L. donovani [87, 88], or to L. major in Balb/c mice, when coencapsulated with antigens in liposomes . CpG also protected Balb/c mice immunized with ribosomal proteins against a second challenge with L. major, being effective in providing long-term immunity [90, 91]. Finally, Cpg ODN improved the clinical outcome of immunized rhesus macaques infected with L. major, supporting the hypothesis that TLR9 stimulation might improve the efficacy of vaccination against cutaneous leishmaniasis . Using a combined approach of costimulation of different TLRs, the immunogenicity of recombinant antigens from L. donovani (iron superoxide dismutase B1 and peroxidoxin 4) was greatly improved by immunization in conjunction with TLR9 or TLR4 agonists, resulting in a Th1-type response in Balb/c mice . The use of ligands for TLR7 and/or TLR8 (imiquimod and the related R848 compound) in the immunization of Balb/c mice with crude L. major antigen induced a Th1 response and was protective against subsequent challenges .
More recently, the formulation of a defined polyprotein anti-Leishmania vaccine candidate in conjunction with TLR4 or TLR9 agonists was evaluated as an immunotherapeutical treatment in a mouse model of cutaneous leishmaniasis . A strong effective T cell response was observed during disease, followed by cured lesions and reduced parasite burden upon immunization with the combination of both agonists, suggesting that TLR synergy may serve as a tool for the treatment of parasite infection. TLR2 stimulation was also proposed as an alternative to revert the loss of CD8 function in patients with diffuse cutaneous leishmaniasis . It was found that, in patients infected with L. mexicana who develop diffuse lesions, the reduced cytotoxicity and proliferation of CD8 cells was typical of cellular exhaustion and could be restored in vitro by stimulation with TLR2 agonists, including Leishmania LPG . The design of CD8 activators based on TLR2 activation could be beneficial in reverting the observed in chronic patients with diffuse lesions. More recently, a more sophisticated vaccination approach was attempted in order to promote protective responses against L. panamensis in a murine model of chronic disease . The strategy of prime-boost, consisting of the priming using a single antigen and heterologous DNA, was combined with the addition of a TLR2/1 agonist (PAM3CSK4) as an adjuvant, leading to an effective protection against L. pananemensis infections . Furthermore, they provided evidence that TLR2 stimulation during priming is essential for the elevation of CD4 and CD8 memory T cell responses and reduction of IL-13 and IL-10 levels, which were required for protection. Those findings were a great step forward in the design of simple and cost-effective vaccines against Leishmania (Viannia) species that are refractory to commonly used strategies to other Leishmania species. It also offers an alternative for DNA-based vaccination schemes in cases where the CD8 T cell activation is crucial.
3. Concluding Remarks
The activation of several members of the TLR family of receptors is observed during the infections of isolated cells or in experimental infections of animals with different Leishmania species. The consequences of such activation are complex and depend on the nature of the TLR, the cell type, the parasite species, and the timing in which those events occur. Although studies using TLR-deficient animals offered the initial picture of how those receptors can act in the protection or promotion of disease, the underlying molecular mechanisms are still obscure. In particular, it is indispensable to identify the parasite factors that contribute to TLR activation and/or negatively regulate their responses in the individual cell types and to evaluate to what extent TLR activation in each of those cells contributes to pathology. While most of the earlier studies focused on the requirement of TLRs for cytokine synthesis and for the development of adaptive immunity, the studies on if and how those receptors contribute to the biogenesis of the parasitophorous vacuole and to the control of parasite intracellular growth are still largely missing. TLR activation has emerged as a promising alternative to improve the efficacy of vaccination with parasite antigens and may also act synergistically with other components during immunotherapy. However, a more detailed study of the consequences of such strategies must be addressed before the combined activation of TLRs can be explored in the future in the treatment of patients with more severe and diffuse lesions.
This work is supported by The Wellcome Trust, FAPERJ and CNPq. A. P. C. A. Lima is a CNPq Fellow.
- P. Kaye and P. Scott, “Leishmaniasis: complexity at the host-pathogen interface,” Nature Reviews Microbiology, vol. 9, no. 8, pp. 604–615, 2011.
- I. Follador, C. Araújo, O. Bacellar et al., “Epidemiologic and immunologic findings for the subclinical form of Leishmania braziliensis infection,” Clinical Infectious Diseases, vol. 34, no. 11, pp. E54–E58, 2002.
- F. Bosque, N. G. Saravia, L. Valderrama, and G. Milon, “Distinct innate and acquired immune responses to Leishmania in putative susceptible and resistant human populations endemically exposed to L. (Viannia) panamensis infection,” Scandinavian Journal of Immunology, vol. 51, no. 5, pp. 533–541, 2000.
- B. Travi, J. Rey-Ladino, and N. G. Saravia, “Behavior of Leishmania braziliensis s.l. in golden hamsters: evolution of the infection under different experimental conditions,” Journal of Parasitology, vol. 74, no. 6, pp. 1059–1062, 1988.
- M. Ameen, “Cutaneous leishmaniasis: advances in disease pathogenesis, diagnostics and therapeutics,” Clinical and Experimental Dermatology, vol. 35, no. 7, pp. 699–705, 2010.
- V. S. Amato, F. F. Tuon, H. A. Bacha, V. A. Neto, and A. C. Nicodemo, “Mucosal leishmaniasis. Current scenario and prospects for treatment,” Acta Tropica, vol. 105, no. 1, pp. 1–9, 2008.
- C. V. David and N. Craft, “Cutaneous and mucocutaneous leishmaniasis,” Dermatologic Therapy, vol. 22, no. 6, pp. 491–502, 2009.
- J. A. de Oliveira Guerra, S. R. Prestes, H. Silveira et al., “Mucosal leishmaniasis caused by leishmania (Viannia) braziliensis and Leishmania (Viannia) guyanensis in the Brazilian Amazon,” PLoS Neglected Tropical Diseases, vol. 5, no. 3, article e980, 2011.
- A. Schriefer, M. E. Wilson, and E. M. Carvalho, “Recent developments leading toward a paradigm switch in the diagnostic and therapeutic approach to human leishmaniasis,” Current Opinion in Infectious Diseases, vol. 21, no. 5, pp. 483–488, 2008.
- P. M. Kaye and T. Aebischer, “Visceral leishmaniasis: immunology and prospects for a vaccine,” Clinical Microbiology and Infection, vol. 17, no. 10, pp. 1462–1470, 2011.
- S. Nylen and S. Gautam, “Immunological perspectives of leishmaniasis,” Journal of Global Infectious Diseases, vol. 2, pp. 135–146, 2010.
- J. E. Dalton, A. Maroof, B. M. J. Owens et al., “Inhibition of receptor tyrosine kinases restores immunocompetence and improves immune-dependent chemotherapy against experimental leishmaniasis in mice,” Journal of Clinical Investigation, vol. 120, no. 4, pp. 1204–1216, 2010.
- D. Sacks and N. Noben-Trauth, “The immunology of susceptibility and resistance to Leishmania major in mice,” Nature Reviews Immunology, vol. 2, no. 11, pp. 845–858, 2002.
- J. Liese, U. Schleicher, and C. Bogdan, “The innate immune response against Leishmania parasites,” Immunobiology, vol. 213, no. 3-4, pp. 377–387, 2008.
- M. Blos, U. Schleicher, F. J. Soares Rocha, U. Meißner, M. Röllinghoff, and C. Bogdan, “Organ-specific and stage-dependent control of Leishmania major infection by inducible nitric oxide synthase and phagocyte NADPH oxidase,” European Journal of Immunology, vol. 33, no. 5, pp. 1224–1234, 2003.
- F. J. S. Rocha, U. Schleicher, J. Mattner, G. Alber, and C. Bogdan, “Cytokines, signaling pathways, and effector molecules required for the control of Leishmania (Viannia) braziliensis in mice,” Infection and Immunity, vol. 75, no. 8, pp. 3823–3832, 2007.
- H. W. Murray and F. Nathan, “Macrophage microbicidal mechanisms in vivo: reactive nitrogen versus oxygen intermediates in the killing of intracellular visceral Leishmania donovani,” Journal of Experimental Medicine, vol. 189, no. 4, pp. 741–746, 1999.
- H. W. Murray, Z. Xiang, and X. Ma, “Short report: responses to Leishmania donovani in mice deficient in both phagocyte oxidase and inducible nitric oxide synthase,” American Journal of Tropical Medicine and Hygiene, vol. 74, no. 6, pp. 1013–1015, 2006.
- H. W. Murray, J. D. Berman, C. R. Davies, and N. G. Saravia, “Advances in leishmaniasis,” Lancet, vol. 366, no. 9496, pp. 1561–1577, 2005.
- R. Pifer, A. Benson, C. R. Sturge, and F. Yarovinsky, “UNC93B1 is essential for TLR11 activation and IL-12-dependent host resistance to Toxoplasma gondii,” Journal of Biological Chemistry, vol. 286, no. 5, pp. 3307–3314, 2011.
- A. L. Blasius and B. Beutler, “Intracellular Toll-like receptors,” Immunity, vol. 32, no. 3, pp. 305–315, 2010.
- T. Kawai and S. Akira, “Toll-like Receptors and Their Crosstalk with Other Innate Receptors in Infection and Immunity,” Immunity, vol. 34, no. 5, pp. 637–650, 2011.
- L. R. Prince, M. K. Whyte, I. Sabroe, and L. C. Parker, “The role of TLRs in neutrophil activation,” Current Opinion in Pharmacology, vol. 11, no. 4, pp. 397–403, 2011.
- F. Hayashi, T. K. Means, and A. D. Luster, “Toll-like receptors stimulate human neutrophil function,” Blood, vol. 102, no. 7, pp. 2660–2669, 2003.
- A.-C. Oliveira, J. R. Peixoto, L. B. De Arrada et al., “Expression of functional TLR4 confers proinflammatory responsiveness to Trypanosoma cruzi glycoinositolphospholipids and higher resistance to infection with T. cruzi,” Journal of Immunology, vol. 173, no. 9, pp. 5688–5696, 2004.
- C. Coban, K. J. Ishii, T. Kawai et al., “Toll-like receptor 9 mediates innate immune activation by the malaria pigment hemozoin,” Journal of Experimental Medicine, vol. 201, no. 1, pp. 19–25, 2005.
- L. Carrera, R. T. Gazzinelli, R. Badolato et al., “Leishmania promastigotes selectively inhibit interleukin 12 induction in bone marrow-derived macrophages from susceptible and resistant mice,” Journal of Experimental Medicine, vol. 183, no. 2, pp. 515–526, 1996.
- Y. Belkaid, B. Butcher, and D. L. Sacks, “Analysis of cytokine production by inflammatory mouse macrophages at the single-cell level: selective impairment of IL-12 induction in Leishmania-infected cells,” European Journal of Immunology, vol. 28, no. 4, pp. 1389–1400, 1998.
- T. R. Hawn, A. Ozinsky, D. M. Underhill, F. S. Buckner, S. Akira, and A. Aderem, “Leishmania major activates IL-1α expression in macrophages through a MyD88-dependent pathway,” Microbes and Infection, vol. 4, no. 8, pp. 763–771, 2002.
- F. Yarovinsky, D. Zhang, J. F. Andersen et al., “Immunology: TLR11 activation of dendritic cells by a protozoan profilin-like protein,” Science, vol. 308, no. 5728, pp. 1626–1629, 2005.
- G. Kavoosi, S. K. Ardestani, and A. Kariminia, “The involvement of TLR2 in cytokine and reactive oxygen species (ROS) production by PBMCs in response to Leishmania major phosphoglycans (PGs),” Parasitology, vol. 136, no. 10, pp. 1193–1199, 2009.
- T. Ilg, Y. D. Stierhof, M. Wiese, M. J. McConville, and P. Overath, “Characterization of phosphoglycan-containing secretory products of Leishmania,” Parasitology, vol. 108, pp. S63–S71, 1994.
- A. Osanya, E.-H. Song, K. Metz et al., “Pathogen-derived oligosaccharides improve innate immune response to intracellular parasite infection,” American Journal of Pathology, vol. 179, no. 3, pp. 1329–1337, 2011.
- M. J. de Veer, J. M. Curtis, T. M. Baldwin et al., “MyD88 is essential for clearance of Leishmania major: possible role for lipophosphoglycan and Toll-like receptor 2 signaling,” European Journal of Immunology, vol. 33, no. 10, pp. 2822–2831, 2003.
- M. A. S. Campos, I. C. Almeida, O. Takeuchi et al., “Activation of toll-like receptor-2 by glycosylphosphatidylinositol anchors from a protozoan parasite,” Journal of Immunology, vol. 167, no. 1, pp. 416–423, 2001.
- D. Piedrafita, L. Proudfoot, A. V. Nikolaev et al., “Regulation of macrophage IL-12 synthesis by leishmania phosphoglycans,” European Journal of Immunology, vol. 29, no. 1, pp. 235–244, 1999.
- E. Muraille, C. De Trez, M. Brait, P. De Baetselier, O. Leo, and Y. Carlier, “Genetically resistant mice lacking MyD88-adapter protein display a high susceptibility to Leishmania major infection associated with a polarized Th2 response,” Journal of Immunology, vol. 170, no. 8, pp. 4237–4241, 2003.
- A. Debus, J. Gläsner, M. Röllinghoff, and A. Gessner, “High levels of susceptibility and T helper 2 response in MyD88-deficient mice infected with Leishmania major are interleukin-4 dependent,” Infection and Immunity, vol. 71, no. 12, pp. 7215–7218, 2003.
- C. De Trez, M. Brait, O. Leo et al., “Myd88-dependent in vivo maturation of splenic dendritic cells induced by Leishmania donovani and other Leishmania species,” Infection and Immunity, vol. 72, no. 2, pp. 824–832, 2004.
- M. Muzio, J. Ni, P. Feng, and V. M. Dixit, “IRAK (Pelle) family member IRAK-2 and MyD88 as proximal mediators of IL- 1 signaling,” Science, vol. 278, no. 5343, pp. 1612–1615, 1997.
- K. Hoshino, T. Kaisho, T. Iwabe, O. Takeuchi, and S. Akira, “Differential involvement of IFN-β in toll-like receptor-stimulated dendritic cell activation,” International Immunology, vol. 14, no. 10, pp. 1225–1231, 2002.
- I. Becker, N. Salaiza, M. Aguirre et al., “Leishmania lipophosphoglycan (LPG) activates NK cells through toll-like receptor-2,” Molecular and Biochemical Parasitology, vol. 130, no. 2, pp. 65–74, 2003.
- R. Nakagawa, T. Naka, H. Tsutsui et al., “SOCS-1 participates in negative regulation of LPS responses,” Immunity, vol. 17, no. 5, pp. 677–687, 2002.
- G. Kavoosi, S. K. Ardestani, A. Kariminia, and M. H. Alimohammadian, “Leishmania major lipophosphoglycan: discrepancy in toll-like receptor signaling,” Experimental Parasitology, vol. 124, no. 2, pp. 214–218, 2010.
- P. Bhattacharya, S. Bhattacharjee, G. Gupta et al., “Arabinosylated lipoarabinomannan-mediated protection in visceral leishmaniasis through up-regulation of Toll-Like receptor 2 signaling: an immunoprophylactic approach,” Journal of Infectious Diseases, vol. 202, no. 1, pp. 145–155, 2010.
- N. Dogra, C. Warburton, and W. R. McMaster, “Leishmania major abrogates gamma interferon-induced gene expression in human macrophages from a global perspective,” Infection and Immunity, vol. 75, no. 7, pp. 3506–3515, 2007.
- Á. D. C. Vivarini, R. D. M. S. Pereira, K. L. D. Teixeira et al., “Human cutaneous leishmaniasis: interferon-dependent expression of double-stranded RNA-dependent protein kinase (PKR) via TLR2,” FASEB Journal, vol. 25, no. 12, pp. 4162–4173, 2011.
- P. Kropf, M. A. Freudenberg, M. Modolell et al., “Toll-like receptor 4 contributes to efficient control of infection with the protozoan parasite Leishmania major,” Infection and Immunity, vol. 72, no. 4, pp. 1920–1928, 2004.
- A. Srivastava, N. Singh, M. Mishra et al., “Identification of TLR inducing Th1-responsive Leishmania donovani amastigote-specific antigens,” Molecular and Cellular Biochemistry, vol. 359, no. 1-2, pp. 359–368, 2011.
- G. A.G. Cezário, L. R.C. de Oliveira, E. Peresi et al., “Analysis of the expression of toll-like receptors 2 and 4 and cytokine production during experimental leishmania chagasi infection,” Memorias do Instituto Oswaldo Cruz, vol. 106, no. 5, pp. 573–583, 2011.
- C. Gallego, D. Golenbock, M. A. Gomez, and N. G. Saravia, “Toll-like receptors participate in macrophage activation and intracellular control of Leishmania (Viannia) panamensis,” Infection and Immunity, vol. 79, no. 7, pp. 2871–2879, 2011.
- M. Charmoy, R. Megnekou, C. Allenbach et al., “Leishmania major induces distinct neutrophil phenotypes in mice that are resistant or susceptible to infection,” Journal of Leukocyte Biology, vol. 82, no. 2, pp. 288–299, 2007.
- R. Silvestre, A. M. Silva, A. Cordeiro-Da-Silva, and A. Ouaissi, “The contribution of Toll-like receptor 2 to the innate recognition of a Leishmania infantum silent information regulator 2 protein,” Immunology, vol. 128, no. 4, pp. 484–499, 2009.
- D. Chandra and S. Naik, “Leishmania donovani infection down-regulates TLR2-stimulated IL-12p40 and activates IL-10 in cells of macrophage/monocytic lineage by modulating MAPK pathways through a contact-dependent mechanism,” Clinical and Experimental Immunology, vol. 154, no. 2, pp. 224–234, 2008.
- I. Abu-Dayyeh, M. T. Shio, S. Sato, S. Akira, B. Cousineau, and M. Olivier, “Leishmania-induced IRAK-1 inactivation is mediated by SHP-1 interacting with an evolutionarily conserved KTIM motif,” PLoS Neglected Tropical Diseases, vol. 2, no. 12, article e305, 2008.
- D. A. Vargas-Inchaustegui, W. Tai, L. Xin, A. E. Hogg, D. B. Corry, and L. Soong, “Distinct roles for MyD88 and toll-like receptor 2 during Leishmania braziliensis infection in mice,” Infection and Immunity, vol. 77, no. 7, pp. 2948–2956, 2009.
- C. S. Guerra, R. M. Macedo Silva, L. O. P. Carvalho, K. D. S. Calabrese, P. T. Bozza, and S. Côrte-Real, “Histopathological analysis of initial cellular response in TLR-2 deficient mice experimentally infected by Leishmania (L.) amazonensis,” International Journal of Experimental Pathology, vol. 91, no. 5, pp. 451–459, 2010.
- R. M. S. Pereira, K. L. D. Teixeira, V. Barreto-de-Souza et al., “Novel role for the double-stranded RNA-activated protein kinase PKR: modulation of macrophage infection by the protozoan parasite Leishmania,” FASEB Journal, vol. 24, no. 2, pp. 617–626, 2010.
- P. Kropf, N. Freudenberg, C. Kalis et al., “Infection of C57BL/10ScCr and C57BL/10ScNCr mice with Leishmania major reveals a role for Toll-like receptor 4 in the control of parasite replication,” Journal of Leukocyte Biology, vol. 76, no. 1, pp. 48–57, 2004.
- S. Antoniazi, H. P. Price, P. Kropf et al., “Chemokine gene expression in Toll-like receptor-competent and -deficient mice infected with Leishmania major,” Infection and Immunity, vol. 72, no. 9, pp. 5168–5174, 2004.
- N. Wang, A. Satoskar, W. Faubion et al., “The cell surface receptor SLAM controls T cell and macrophage functions,” Journal of Experimental Medicine, vol. 199, no. 9, pp. 1255–1264, 2004.
- S. M. Whitaker, M. Colmenares, K. G. Pestana, and D. McMahon-Pratt, “Leishmania pifanoi proteoglycolipid complex P8 induces macrophage cytokine production through Toll-like receptor 4,” Infection and Immunity, vol. 76, no. 5, pp. 2149–2156, 2008.
- M. Colmenares, M. Tiemeyer, P. Kima, and D. McMahon-Pratt, “Biochemical and biological characterization of the protective Leishmania pifanoi amastigote antigen P-8,” Infection and Immunity, vol. 69, no. 11, pp. 6776–6784, 2001.
- M. Shweash, H. Adrienne McGachy, J. Schroeder et al., “Leishmania mexicana promastigotes inhibit macrophage IL-12 production via TLR-4 dependent COX-2, iNOS and arginase-1 expression,” Molecular Immunology, vol. 48, no. 15-16, pp. 1800–1808, 2011.
- T. Mahieu, J. M. Park, H. Revets et al., “The wild-derived inbred mouse strain SPRET/Ei is resistant to LPS and defective in IFN-β production,” Proceedings of the National Academy of Sciences of the United States of America, vol. 103, no. 7, pp. 2292–2297, 2006.
- L. A. Jones, J. P. Anthony, F. L. Henriquez et al., “Toll-like receptor-4-mediated macrophage activation is differentially regulated by progesterone via the glucocorticoid and progesterone receptors,” Immunology, vol. 125, no. 1, pp. 59–69, 2008.
- H. Hawlisch, Y. Belkaid, R. Baelder, D. Hildeman, C. Gerard, and J. Köhl, “C5a negatively regulates toll-like receptor 4-induced immune responses,” Immunity, vol. 22, no. 4, pp. 415–426, 2005.
- F. L. Ribeiro-Gomes, A. C. Otero, N. A. Gomes et al., “Macrophage Interactions with Neutrophils Regulate Leishmania major Infection,” Journal of Immunology, vol. 172, no. 7, pp. 4454–4462, 2004.
- F. L. Ribeiro-Gomes, M. C. A. Moniz-de-Souza, M. S. Alexandre-Moreira et al., “Neutrophils activate macrophages for intracellular killing of Leishmania major through recruitment of TLR4 by neutrophil elastase,” Journal of Immunology, vol. 179, no. 6, pp. 3988–3994, 2007.
- A. A. Filardy, D. R. Pires, M. P. Nunes et al., “Proinflammatory clearance of apoptotic neutrophils induces an IL-12 lowIL-10high regulatory phenotype in macrophages,” Journal of Immunology, vol. 185, no. 4, pp. 2044–2050, 2010.
- M. S. Faria, F. C.G. Reis, R. L. Azevedo-Pereira, L. S. Morrison, J. C. Mottram, and A. P.C.A. Lima, “Leishmania inhibitor of serine peptidase 2 prevents TLR4 activation by neutrophil elastase promoting parasite survival in murine macrophages,” Journal of Immunology, vol. 186, no. 1, pp. 411–422, 2011.
- S. C. P. Eschenlauer, M. S. Faria, L. S. Morrison et al., “Influence of parasite encoded inhibitors of serine peptidases in early infection of macrophages with Leishmania major,” Cellular Microbiology, vol. 11, no. 1, pp. 106–120, 2009.
- P. Y. Perera, T. N. Mayadas, S. Takeuchi et al., “CD11b/CD18 acts in concert with CD14 and Toll-like receptor (TLR) 4 to elicit full lipopolysaccharide and Taxol-inducible gene expression,” Journal of Immunology, vol. 166, no. 1, pp. 574–581, 2001.
- S. Ajdary, M. M. Ghamilouie, M. H. Alimohammadian, F. Riazi-Rad, and S. R. Pakzad, “Toll-like receptor 4 polymorphisms predispose to cutaneous leishmaniasis,” Microbes and Infection, vol. 13, no. 3, pp. 226–231, 2011.
- A. A. Brzezinska, J. L. Johnson, D. B. Munafo, B. A. Ellis, and S. D. Catz, “Signalling mechanisms for Toll-like receptor-activated neutrophil exocytosis: key roles for interleukin-1-receptor-associated kinase-4 and phosphatidylinositol 3-kinase but not Toll/IL-1 receptor (TIR) domain-containing adaptor inducing IFN-β (TRIF),” Immunology, vol. 127, no. 3, pp. 386–397, 2009.
- Y. Li, K. Ishii, H. Hisaeda et al., “IL-18 gene therapy develops Th1-type immune responses in Leishmania major-infected BALB/c mice: is the effect mediated by the CpG signaling TLR9?” Gene Therapy, vol. 11, no. 11, pp. 941–948, 2004.
- J. Liese, U. Schleicher, and C. Bogdan, “TLR9 signaling is essential for the innate NK cell response in murine cutaneous leishmaniasis,” European Journal of Immunology, vol. 37, no. 12, pp. 3424–3434, 2007.
- U. Schleicher, J. Liese, I. Knippertz et al., “NK cell activation in visceral leishmaniasis requires TLR9, myeloid DCs, and IL-12, but is independent of plasmacytoid DCs,” Journal of Experimental Medicine, vol. 204, no. 4, pp. 893–906, 2007.
- F. H. A. Fakher, N. Rachinel, M. Klimczak, J. Louis, and N. Doyen, “TLR9-dependent activation of dendritic cells by DNA from Leishmania major favors TH1 cell development and the resolution of lesions,” Journal of Immunology, vol. 182, no. 3, pp. 1386–1396, 2009.
- C. Bogdan and U. Schleicher, “Comment on “TLR9-dependent activation of dendritic cells by DNA from Leishmania major favors Th1 cell development and the resolution of lesions”,” Journal of Immunology, vol. 183, no. 11, p. 6859, 2009.
- J. F. Flandin, F. Chano, and A. Descoteaux, “RNA interference reveals a role for TLR2 and TLR3 in the recognition of Leishmania donovani promastigotes by interferon-γ-primed macrophages,” European Journal of Immunology, vol. 36, no. 2, pp. 411–420, 2006.
- A. Ives, C. Ronet, F. Prevel et al., “Leishmania RNA virus controls the severity of mucocutaneous leishmaniasis,” Science, vol. 331, no. 6018, pp. 775–778, 2011.
- A. T. Shamshiev, F. Ampenberger, B. Ernst, L. Rohrer, B. J. Marsland, and M. Kopf, “Dyslipidemia inhibits Toll-like receptor-induced activation of CD8α-negative dendritic cells and protective Th1 type immunity,” Journal of Experimental Medicine, vol. 204, no. 2, pp. 441–452, 2007.
- K. J. Stacey and J. M. Blackwell, “Immunostimulatory DNA as an adjuvant in vaccination against Leishmania major,” Infection and Immunity, vol. 67, no. 8, pp. 3719–3726, 1999.
- Y. A. W. Skeiky, R. N. Coler, M. Brannon et al., “Protective efficacy of a tandemly linked, multi-subunit recombinant leishmanial vaccine (Leish-111f) formulated in MPL® adjuvant,” Vaccine, vol. 20, no. 27-28, pp. 3292–3303, 2002.
- M. Calvopina, P. A. Barroso, J. D. Marco et al., “Efficacy of vaccination with a combination of Leishmania amastigote antigens and the lipid A-analogue ONO-4007 for immunoprophylaxis and immunotherapy against Leishmania amazonensis infection in a murine model of New World cutaneous leishmaniasis,” Vaccine, vol. 24, no. 27-28, pp. 5645–5652, 2006.
- P. Tewary, J. Mehta, B. Sukumaran, and R. Madhubala, “Vaccination with Leishmania soluble antigen and immunostimulatory oligodeoxynucleotides induces specific immunity and protection against Leishmania donovani infection,” FEMS Immunology and Medical Microbiology, vol. 42, no. 2, pp. 241–248, 2004.
- P. Tewary, B. Sukumaran, S. Saxena, and R. Madhubala, “Immunostimulatory oligodeoxynucleotides are potent enhancers of protective immunity in mice immunized with recombinant ORFF leishmanial antigen,” Vaccine, vol. 22, no. 23-24, pp. 3053–3060, 2004.
- A. Badiee, M. R. Jaafari, A. Samiei, D. Soroush, and A. Khamesipour, “Coencapsulation of CpG oligodeoxynucleotides with recombinant Leishmania major stress-inducible protein 1 in liposome enhances immune response and protection against leishmaniasis in immunized BALB/c mice,” Clinical and Vaccine Immunology, vol. 15, no. 4, pp. 668–674, 2008.
- S. Iborra, N. Parody, D. R. Abánades et al., “Vaccination with the Leishmania major ribosomal proteins plus CpG oligodeoxynucleotides induces protection against experimental cutaneous leishmaniasis in mice,” Microbes and Infection, vol. 10, no. 10-11, pp. 1133–1141, 2008.
- L. Ramirez, S. Iborra, J. Cortes et al., “BALB/c mice vaccinated with Leishmania major ribosomal proteins extracts combined with CpG oligodeoxynucleotides become resistant to disease caused by a secondary parasite challenge,” Journal of Biomedicine and Biotechnology, vol. 2010, Article ID 181690, 9 pages, 2010.
- M. Puig, A. Grajkowski, M. Boczkowska, C. Ausín, S. L. Beaucage, and D. Verthelyi, “Use of thermolytic protective groups to prevent G-tetrad formation in CpG ODN type D: structural studies and immunomodulatory activity in primates,” Nucleic Acids Research, vol. 34, no. 22, pp. 6488–6495, 2006.
- N. S. Daifalla, A. G. Bayih, and L. Gedamu, “Immunogenicity of Leishmania donovani iron superoxide dismutase B1 and peroxidoxin 4 in BALB/c mice: the contribution of Toll-like receptor agonists as adjuvant,” Experimental Parasitology, vol. 129, no. 3, pp. 292–298, 2011.
- W. W. Zhang and G. Matlashewski, “Immunization with a Toll-like receptor 7 and/or 8 agonist vaccine adjuvant increases protective immunity against Leishmania major in BALB/c mice,” Infection and Immunity, vol. 76, no. 8, pp. 3777–3783, 2008.
- V. S. Raman, A. Bhatia, A. Picone et al., “Applying TLR synergy in immunotherapy: implications in cutaneous leishmaniasis,” Journal of Immunology, vol. 185, no. 3, pp. 1701–1710, 2010.
- J. Hernández-Ruiz, N. Salaiza-Suazo, G. Carrada et al., “CD8 cells of patients with diffuse cutaneous leishmaniasis display functional exhaustion: the latter is reversed, in vitro, by TLR2 agonists,” PLoS Neglected Tropical Diseases, vol. 4, no. 11, article e871, 2010.
- A. Jayakumar, T. M. Castilho, E. Park, K. Goldsmith-Pestana, J. M. Blackwell, and D. McMahon-Pratt, “TLR1/2 activation during Heterologous prime-boost vaccination (DNA-MVA) enhances CD8+ T cell responses providing protection against Leishmania (Viannia),” PLoS Neglected Tropical Diseases, vol. 5, no. 6, article e1204, 2011.
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