Natural Regulatory T Cells in Malaria: Host or Parasite Allies?

Plasmodium falciparum malaria causes 500 million clinical cases with approximately one million deaths each year. After many years of exposure, individuals living in endemic areas develop a form of clinical immunity to disease known as premunition, which is characterised by low parasite burdens rather than sterilising immunity. The reason why malaria parasites persist under a state of premunition is unknown but it has been suggested that suppression of protective immunity might be a mechanism leading to parasite persistence. Although acquired immunity limits the clinical impact of infection and provides protection against parasite replication, experimental evidence indicates that cell-mediated immune responses also result in detrimental inflammation and contribute to the aetiology of severe disease. Thus, an appropriate regulatory balance between protective immune responses and immune-mediated pathology is required for a favourable outcome of infection. As natural regulatory T (Treg) cells are identified as an immunosuppressive lineage able to modulate the magnitude of effector responses, several studies have investigated whether this cell population plays a role in balancing protective immunity and pathogenesis during malaria. The main findings to date are summarised in this review and the implication for the induction of pathogenesis and immunity to malaria is discussed.

Published in the journal: . PLoS Pathog 6(4): e32767. doi:10.1371/journal.ppat.1000771
Category: Review
doi: 10.1371/journal.ppat.1000771


Plasmodium falciparum malaria causes 500 million clinical cases with approximately one million deaths each year. After many years of exposure, individuals living in endemic areas develop a form of clinical immunity to disease known as premunition, which is characterised by low parasite burdens rather than sterilising immunity. The reason why malaria parasites persist under a state of premunition is unknown but it has been suggested that suppression of protective immunity might be a mechanism leading to parasite persistence. Although acquired immunity limits the clinical impact of infection and provides protection against parasite replication, experimental evidence indicates that cell-mediated immune responses also result in detrimental inflammation and contribute to the aetiology of severe disease. Thus, an appropriate regulatory balance between protective immune responses and immune-mediated pathology is required for a favourable outcome of infection. As natural regulatory T (Treg) cells are identified as an immunosuppressive lineage able to modulate the magnitude of effector responses, several studies have investigated whether this cell population plays a role in balancing protective immunity and pathogenesis during malaria. The main findings to date are summarised in this review and the implication for the induction of pathogenesis and immunity to malaria is discussed.

Natural Regulatory T Cells

Control of infection is the main function of the immune system. Some pathogens are difficult to eradicate and require a potent immune response involving destructive and cytotoxic mediators, which can result in adverse effects and immunopathology. Lymphoid populations exerting immunosuppressive activity, such as natural regulatory T (Treg) cells, have been shown to play a critical role in balancing protective immune responses and immune-mediated pathology [1][4]. This suppressor T cell linage is characterised by expression of high levels of CD25 and CD4 [5], while also expressing low levels of CD127 [6]. Natural Treg cells constitutively express high levels of the T cell inhibitory receptor cytotoxic T lymphocyte–associated molecule 4 (CTLA-4) [7] and the glucocortcoid-inducible tumour necrosis factor receptor (GITR) [8]. Forkhead box P3 (Foxp3) is the only transcription factor required for generation of natural Treg cells [9] and it constitutes the most specific marker for this cell population. Natural Treg cells, initially identified by their capacity to inhibit the development of autoimmune gastritis [10], are now known to prevent other autoimmune conditions such as diabetes [7] and inflammatory bowel disease [2], [11], as well as inhibit anti-tumour immunity [12]. They have been shown to inhibit both IL-2 production and cell proliferation of conventional CD4+ T lymphocytes [13] by contact-dependent mechanisms and/or through the production of anti-inflammatory cytokines such as TGF-β [14] and IL-10 [15]. Although they have limited proliferative capacity and are unable to secrete IL-2, natural Treg cells exert their suppressive function after stimulation through the T cell receptor, a process that appears to require antigen-presenting cells [13]. After activation, natural Treg cells do no require further stimulation and are able to suppress T cell responses in a non-specific manner.

In addition to natural Treg cells, induced Treg cells constitute another subset of suppressor lymphocytes [16]. Unlike naturally occurring Treg cells, which develop in the thymus, induced Treg cells are derived from conventional CD4+ T cells and acquire suppressive activity upon activation and exposure to signals such as immunosuppressive cytokines or immature dendritic cells (DCs).

Why Are Treg Cells Expected to Play a Role in Malaria Infection?

Malaria is one the most serious infectious diseases of humans, infecting 5%–10% of the world's population, with approximately 500 million clinical cases annually. This infection is transmitted to vertebrate hosts by the bite of female Anopheles mosquitos that are infected with protozoan parasites of the genus Plasmodium. Although there are several different species of Plasmodium parasites, most cases of severe disease and fatalities are caused by the blood-stage cycle of Plasmodium falciparum, which is endemic in sub-Saharan Africa and throughout the tropics. The fatalities are associated with a spectrum of discrete and overlapping disease syndromes including acute respiratory distress, coagulopathy, shock, metabolic acidosis, hypoglycaemia, renal failure, pulmonary oedema, and cerebral involvement [17]. In endemic areas, the most susceptible population to symptoms associated with severe malaria are children under the age of 5 who have experienced few parasitic infections. After many years of exposure, individuals living in endemic areas develop clinical immunity to disease, which is characterised by low parasitemia levels rather than sterilising immunity [18], [19]. However, this clinical immunity is known as “premunition”, as it requires ongoing exposure to the pathogen, and is lost quite rapidly in the absence of transmission. The reason why malaria parasites persist under the state of premunition is unknown, but it has been suggested that immunosuppressive mechanisms able to modulate protective immunity might lead to the persistence of parasites. In support of this hypothesis, several immunosuppressive processes have been described accompanying both human and experimental malaria infections, including reduced T cell proliferative and IFN-γ responses to parasite antigens [20], [21] and production of immunosuppressive cytokines such as IL-10 [15], [22] and TGF-β [23]. As natural Treg cells have been shown to mediate their suppressive effects through the production of these cytokines, it has been tempting to postulate that this immunoregulatory lineage could impede induction of immunity to malaria.

Although acquired host immunity limits the clinical impact of malaria infection and provides protection against parasite replication, experimental evidence indicates that cell-mediated immune responses also result in detrimental inflammation and contribute to induction of severe disease. In both P. falciparum infections and rodent malaria models, severe disease syndromes arise in diverse organs (e.g., brain, lungs, placenta) and appear to result from the combined effect of cytoadherence of parasitised red blood cells (pRBCs) in vascular beds and a strong host pro-inflammatory response mediated by cytokines such as TNF-α [24], LT-α [25], and IFN-γ [26], and effector cells such as CD4 [27], [28] and CD8 T cells [29], [30], natural killer (NK) T cells [31], [32], and NK cells [33]. As pro-inflammatory cytokines produced by these cells upregulate the expression of adhesion molecules such as intercellular cell adhesion molecule 1 (ICAM-1) [34], which is involved in the recognition of parasitic proteins expressed on pRBCs [35], it has been proposed that local and/or systemic inflammatory cascades exacerbate parasite sequestration. Furthermore, emerging evidence from both human malaria and experimental animal models [29], [30], [36], [37] has revealed the presence of leukocytes in blood vessels of inflamed tissue, suggesting that in addition to their systemic effects, intravascular infiltration of these cells might result in local inflammation and could also contribute to disease induction. Thus, cell-mediated immune responses appear to play a dual role in malaria: mediating protective immunity on the one hand, and contributing to severe inflammation and pathogenesis on the other. Whether natural Treg cells are involved in promoting a balance between these processes has been the subject of several studies. In this review we have summarised the main findings to date investigating the role of natural Treg cells during malaria, including experimental infection using a variety of murine infection models as well as human field studies. The implication of those findings for the induction of pathogenesis and immunity to malaria is discussed.

Natural Treg Cells and the Control of Parasite Clearance in Rodent Malaria Infection Models

Most of the studies using rodent models of infection have relied on the use of anti-CD25 antibodies for in vivo depletion of natural Treg cells (Table 1). Although this appears to be a standard procedure to effectively deplete natural Treg cells in vivo, one disadvantage of this approach is that CD25 is upregulated in activated T cells, thus making it difficult to specifically target natural Treg cells in experimental models in which conventional lymphocytes are expected to become activated. This potential confounder should be addressed experimentally or taken into consideration for interpretation of experimental results.

Tab. 1. Effect of T<sub>reg</sub> cell depletion in the outcome of malaria in rodent infection models.
Effect of T&lt;sub&gt;reg&lt;/sub&gt; cell depletion in the outcome of malaria in rodent infection models.

Several studies have investigated whether natural Treg cells modulate the induction of immune mechanisms responsible for the control of parasite burden. Experimental infections with malaria species such as Plasmodium chabaudi and Plasmodium yoelii are particularly useful for addressing this question since they result in high parasitemia levels and do not induce T cell–mediated organ-specific disease syndromes (Table 2). There are two sub-strains of P. yoelii 17X. One of them is highly virulent (PyL) and induces lethal infections, whereas the other one (PyNL) results in a self-resolving non-lethal infection. This difference in outcome suggested that while infection with non-lethal parasites induces adaptive immune responses able to limit parasite replication, immunosuppressive mechanisms might operate when mice are infected with the lethal sub-strain, preventing the induction of protective immunity. Two independent studies have investigated whether natural Treg cells play a role in the inhibition of immune responses against P. yoelii 17X. One found that depletion of natural Treg cells protects BALB/c mice from overwhelming parasitemia and death after infection with PyL parasites, raising the possibility that natural Treg cell function provides an essential escape mechanism used by malaria parasites to evade host-mediated immunity [38]. A subsequent study found that Foxp3+ regulatory T cells expand and become activated in response to infection with both PyL and PyNL parasites. However, in vivo depletion experiments failed to recapitulate the initial observations supporting a role for natural Treg cells in the control of parasitemia levels [39]. Moreover, CD4+ CD25 Foxp3CD127 adaptive T cells and not natural Treg cells were found to be the source of IL-10 responsible for downregulation of protective immune responses during P. yoelii lethal infections [39]. The reasons for this inconsistency are unclear. The composition of intestinal flora has been shown to influence the development of natural Treg cells [40]. It is therefore possible that Treg cell depletion in genetically identical mouse strains housed in various animal facilities could lead to different infection outcomes if such mice differ in the composition of bacteria in their gastrointestinal tract.

Tab. 2. Malaria rodent models used to investigate T<sub>reg</sub> cell function.
Malaria rodent models used to investigate T&lt;sub&gt;reg&lt;/sub&gt; cell function.

The impact of natural Treg cell depletion was also evaluated in infection of mice with lethal (DS) and non-lethal (DK) strains of P. chabaudi adami. Treg cell depletion resulted in increased production of IFN-γ and TNF-α in response to both lethal and non-lethal P. chabaudi adami infection. In spite of the enhancement of pro-inflammatory responses, Treg cell depletion did not alter the course of infection in animals challenged with non-lethal parasites [41]. Curiously, Treg cell depletion was found to exacerbate parasite burden and accelerate death in mice infected with the lethal DS strain. The haemolytic anaemia that results from hyperparasitemia was also enhanced in the absence of natural Treg cells. These studies accord with the notion that in experimental models resulting in parasitemia of high density, T helper cell 1 (TH1) responses are not sufficient to control parasite burden, and consistently the Treg cell–dependent modulation of pro-inflammatory responses is not critical in determining infection outcome (Figure 1B).

T<sub>reg</sub> cells in malaria: Lessons learnt from experimental rodent models.
Fig. 1. Treg cells in malaria: Lessons learnt from experimental rodent models.
(A) In murine models characterised by high pro-inflammatory responses to infection, Treg cell depletion may result in a strong and rapid cellular immune response, which could rapidly control parasitemia, in turn reducing parasite-mediated pathology. MØ, macrophage. (B) In an infection setting resulting in poor inflammatory responses to malaria, a lack of Treg cells may improve the induction of such responses but at levels that are not sufficient to control parasite burden or induce immunopathology. (C) In re-infection models, TH1 responses generated in the absence of Treg cells during primary exposure appear to be robust enough to facilitate control of parasitemia in a secondary challenge at the expense of increased immune-mediated severe disease induction.

The effect of natural Treg cell depletion with anti-CD25 antibody was also evaluated in immunised as well as naïve BALB/c mice after infection with P. berghei NK65. Treg cell depletion resulted in a delay in the onset of parasitemia compared to non-depleted controls [42]. Whether Treg cell depletion influenced the development of immune responses involved in the control of parasitemia was not investigated.

The Role of Natural Treg Cells in the Control of Experimental Cerebral Malaria

Although infection of mice with P. yoelii, P. berghei NK65, and P. chabaudi adami results in hyperparasitemia and death of susceptible mice due to haemolytic anaemia, it does not induce T cell–mediated organ-specific immunopathology. Therefore, a contribution of Treg cells to the control of pathogenic immune responses cannot be accurately assessed in those infection models. In contrast, infection of susceptible mouse strains with Plasmodium berghei-ANKA induces cerebral malaria (Table 2). This murine infection has many features in common with the human disease and is thus an accepted model for certain important aspects of clinical malaria [43][46]. It manifests an inflammatory cytokine–dependent encephalopathy associated with upregulation of adhesion molecules on the cerebral microvascular endothelium, which facilitates sequestration of pRBCs and the resulting recruitment of inflammatory CXCR3+ leukocytes [33], [47], [48]. C57BL/6 mice, genetically predisposed towards TH1-dominated responses [49], are susceptible to the murine cerebral malaria syndrome, whereas BALB/c mice, with a genetically determined bias towards TH2 responses, are resistant [50]. Moreover, C57BL/6 and BALB/c mouse strains differ in the expression of molecules encoded by a polymorphic genetic region called the natural killer complex (NKC) [51], and it has been shown that the differential expression of these receptors in NK cells and CD1d-restricted NKT cells influences their immunological behaviour in response to malaria infection and accounts for the degree of susceptibility to severe malaria [31], [32]. C57BL/6 NKC alleles are associated with disease susceptibility and the increased severity to cerebral malaria is associated with a differential immune response to infection, characterised by a significantly enhanced IFN-γ production [32], [52]. Interestingly, anti-inflammatory cytokines such as TGF-β and IL-10 have been found to regulate type-1 responses during infection [23] and to play a protective role against P. berghei–mediated cerebral malaria [22], respectively, suggesting that resistance to disease could be associated with the development of suppressive mechanisms aimed at directly inhibiting pathogenic inflammatory responses. Specifically to test that proposition, we investigated the induction of T cell responses in cerebral malaria–resistant mouse strains. Our main results revealed that CD4+ T cells from cerebral disease–resistant BALB/c mice display a strong inhibition of cell proliferation and IL-2 secretion in response to both parasite-specific and polyclonal stimuli and that natural Treg cells appear to play a role in the inhibition of T cell function occurring during infection [53]. Moreover, anti-CD25 depletion experiments revealed that Treg cells also prevent the development of parasite-specific TH1 memory cells involved in the induction of cerebral malaria during a secondary parasitic challenge, demonstrating a regulatory role for this cell population in the control of pathogenic responses leading to fatal disease [53]. Interestingly, although the lack of natural Treg cells during primary exposure to malaria enhanced TH1 memory responses and increased disease severity during re-infection, it also resulted in improved control of parasite burden. Thus, the results support the notion that although TH1 responses could be beneficial to control malaria re-infection, they should be carefully regulated in order to prevent harmful pathogenesis (Figure 1C).

Two independent studies investigated the effect of natural Treg cell depletion with anti-CD25 antibody in the development of cerebral malaria using the disease-susceptible C57BL/6 mouse strain. Because both CD4 and CD8 T cells have been shown to contribute to the induction of severe malaria in this mouse strain, the use of anti-CD25 antibodies in Treg cell depletion protocols requires careful experimental design to avoid targeting activated T cells, which could confound interpretation of the results. Both studies evaluated susceptibility rates of C57BL/6 mice that had been depleted of natural Treg a day prior to infection with P. berghei-ANKA [54], [55]. Under these experimental conditions, anti-CD25 injection resulted in complete protection from cerebral malaria. To minimize depletion of parasite-specific activated T cells that could be potentially involved in cerebral malaria induction, both studies performed Treg cell depletion several weeks prior to parasitic challenge. Whereas Treg cell depletion 30 days before challenge did not alter parasite burden and susceptibility rates of C57BL/6 mice to cerebral malaria [55], anti-CD25 treatment carried out 14 days before parasitic challenge appeared to protect susceptible mice from fatality [54]. Similar results were obtained when natural Treg cells were depleted under similar conditions in cerebral malaria–susceptible CBA mice [56]. Protection from disease was associated with reduced parasite burden and reduced sequestration of pRBCs in brains of infected mice [54]. The increased resistance to infection correlated with enhanced levels of T cell activation and IFN-γ production in spleens of P. berghei-ANKA-infected mice. These latter data suggest that administration of anti-CD25 antibody does not lead to significant depletion of activated antigen-specific T cells in these experiments. However, a recent study shows that Treg cell depletion in DEREG mice, which are transgenic for a bacterial chromosome expressing a diphtheria toxin (DT) receptor–enhanced GFP fusion protein under the control of the foxp3 locus that allows for selective depletion of Foxp3+ Treg cells by DT injection, did not alter the incidence of cerebral malaria after acute P. bergei-ANKA infection [57].

Thus, the contribution of Treg cells to the induction of cerebral malaria in the C57BL/6 background remains controversial. If a role in acute responses is proven, it might be the case that strong early IFN-γ responses produced in the absence of Treg cells in disease-susceptible C57BL/6 mice facilitate control of parasite burden, resulting in reduced sequestration and protection from cerebral malaria (Figure 1A). The magnitude of inflammatory responses obtained after Treg cell depletion in disease-resistant BALB/c animals (genetically predisposed to produce poor IFN-γ responses to malaria [52]) results in a more modest effect, which only exacerbates disease severity but is not sufficient to control parasitemia or increase fatality rates in a primary infection. In cerebral malaria–resistant animals, the impact of Treg cell depletion becomes evident after re-infection, as TH1 memory responses generated in the absence of Treg cells during initial exposure appear to be robust enough to control re-infection despite increased cerebral malaria induction rates. These considerations imply that natural Treg cell function could be either beneficial or detrimental depending on the timing and magnitude of pro-inflammatory responses to malaria and the genetic background of the host.

Human Studies

A few studies have investigated the role of natural Treg cells in human malaria (Table 3). The implementation of such human studies is quite complex. A variety of different factors, including study design, number of individuals recruited for the study cohort, and use of fresh or cryopreserved samples may all have an impact on the results. These variables should be taken into account when assessing the relevance of conclusions arising from human disease association studies.

Tab. 3. Association between natural T<sub>reg</sub> cells and the outcome of human malaria infections.
Association between natural T&lt;sub&gt;reg&lt;/sub&gt; cells and the outcome of human malaria infections.

Foxp3 mRNA expression levels as well as CD3+CD4+CD25hiCD69 cell numbers were found to become highly upregulated after experimental sporozoite infection of volunteers via mosquito bites. Interestingly, individuals with a high percentage of CD4+ Treg cells amongst their peripheral blood mononuclear cells (PBMCs) were found to reach high parasite densities earlier than those with low Treg cell frequencies, suggesting that the presence of Treg cells in peripheral blood from infected individuals might facilitate blood-stage parasite replication. Reduced production of the pro-inflammatory cytokines IFN-γ, IL6, and IL-12 as well as significantly enhanced production of TGF-β levels were also found to be associated with high parasite burden [58]. Interestingly, monocytes and not Treg cells were found to be the cellular source of TGF-β produced in response to infection. The authors proposed that monocyte-derived TGF-β might favour Treg cell differentiation by inducing Foxp3 expression in naïve peripheral CD4+ T lymphocytes. Increased numbers of natural Treg cells would in turn downregulate pro-inflammatory responses, which could result in enhanced parasite growth [58].

The frequency of natural Treg cells was also investigated in naturally infected individuals in a malaria-endemic region of coastal Kenya. Multivariate analysis showed a significant association between increased CD4+ CD25high numbers in peripheral blood and increased risk of clinical malaria [59]. The majority of CD4+ CD25high cells were found to express Foxp3, suggesting that natural Treg cells may negatively affect natural acquired immunity to malaria.

Interethnic comparative approaches on the susceptibility to malaria performed in West Africa revealed that despite similar levels of exposure, Fulani individuals appear to be more resistant to P. falciparum malaria, as they display reduced parasitemia levels and lower incidence of clinical episodes than other ethnic groups. When the expression of genes involved in immune responses was analysed in PBMCs of Fulani and sympatric Mossi individuals, increased expression of TH1 (IFN-γ, IL-18, TBX21) as well as TH2-related genes (IL-4, IL-9, GATA3) was detected in the more resistant Fulani individuals [60]. Interestingly, the upregulation of immunity-associated genes correlated with reduced frequencies of CD4+ CD25+ Foxp3+ cells in peripheral blood in Fulani compared to Mossi individuals and reduced expression of Treg cell–related products such as CTLA4 and TGF-β. Moreover, whereas in vitro depletion of CD25+ cells enhanced proliferative responses to P. falciparum antigens in PBMCs from Mossi individuals, Treg cell depletion did not alter parasite-specific proliferation rates of the Fulani, suggesting that a functional deficit of natural Treg cells could be involved in the lower susceptibility to malaria of this ethnic group [60].

The role of natural Treg cells in clinical malaria was investigated in children with either severe or uncomplicated malaria [61]. TH1 responses were found to be more elevated in severe compared to uncomplicated malaria cases. However, no significant differences in the absolute number or the frequency of natural Treg cells were detected between these two groups. Moreover, in vitro depletion studies with anti-CD25 resulted in similarly increased cell proliferation to schizont antigen in both severe and uncomplicated malaria cases, suggesting that Treg cells from both groups of patients have similar activity and implying that natural Treg cell function is not sufficient to downregulate the strong TH1 response to infection occurring in children with severe malaria. Interestingly, high FOXP3 mRNA levels at base line were found to be associated with reduced parasite-specific IFN-γ memory responses amongst PBMCs collected form convalescent malaria patients [61]. This result resembles findings obtained in the P. berghei-ANKA mouse model of severe malaria [47]. Whether Treg cells acquired during a primary infection in human malaria are able to modulate TH1 memory responses involved in parasite clearance without inducing immunopathology requires further investigation.

The relationship between Treg cell function and parasite biomass was evaluated in adults with uncomplicated or severe malaria in an endemic area of West Papua [62]. Treg cell numbers increased in malaria cases compared to non-infected controls, indicating that these cells expand in response to infection. In patients with severe but not uncomplicated malaria, Treg cell frequency was correlated with parasite biomass. Phenotypic characterization revealed that Treg cells from severe malaria cases express high levels of TNFRII and constitute a subset of regulatory cells that express high levels of Foxp3 and appear to exert strong immunosuppressive function [62].

Recent in vitro studies using PBMCs from healthy donors stimulated with P. falciparum–infected RBCs have provided interesting insights into the mechanism by which Treg cells are induced by malaria [63]. Stimulation with parasitised RBCs was found to induce expansion of two Treg cell populations expressing different levels of Foxp3. Only cells expressing intermediate (Foxp3int) but not high (Foxp3hi) Foxp3 levels were found to secrete large amounts of effector cytokines. Moreover, high proportions of Foxp3hi cells in the co-culture systems correlated with reduced production of pro-inflammatory cytokines, which suggests that this subset plays a role in inhibition of parasite-induced effector responses. Both malaria-elicited Treg subsets appeared to be derived from conventional CD4+CD25Foxp3 T cells. The parasite-driven upregulation of Foxp3 levels required activated monocytes. However, soluble factors rather than direct contact were found to be responsible for this process. These results suggest a T cell receptor–independent mechanism for bystander activation of CD4+CD25+Foxp3+ T cells during malaria.

Phenotypic characterization of Treg cells in PBMCs of healthy Gambian donors ex vivo revealed a very heterogenous population of Foxp3+ cells in this cohort study, with cells displaying different expression levels of CD25 [64]. In vitro stimulation with crude parasite extracts increased CD25 expression levels. The memory phenotype of CD4+Foxp3+ T cells was also investigated using expression of the chemokine receptors CCR7 and CCR4 to identify central and effector memory cells, respectively [64]. Ex vivo analysis indicated that antigen-experienced (CD45RO+) Foxp3+ cells were predominantly effector memory cells. Moreover, these cells were also found to express high levels of CD95 consistent with a highly pro-apoptotic phenotype.

Only one study has investigated whether Treg cells become activated in response to Plasmodium vivax infection. Similar to association studies in P. falciparum malaria, the percentage of Foxp3+ Treg cells was found to increase in acute P. vivax infection. In vitro elicitation assays confirmed this observation, as the number of Foxp3+ cells amongst PBMCs significantly increases in response to P. vivax antigens [65]. The relevance of these findings in the context of P. vivax malaria needs to be further investigated.

Concluding Remarks

The current evidence from rodent infection models as well as human studies suggests that the natural Treg cell pool becomes activated and expands in response to malaria infection [39], [41], [55], [61], [62], [66]. Whether such expansion results from direct proliferation, cytokine-driven differentiation, and/or recruitment of natural Treg cells to secondary lymphoid organs is not completely understood. In vitro studies provided evidence that Treg cells proliferate in response to malarial antigens [62], [65]. The precise mechanism by which such antigens stimulate natural Treg cells is still unclear. It has been shown that Treg cells express toll-like receptors (TLRs) and proliferate in response to lipopolysaccharide [67], raising the possibility that putative malarial TLR agonists such as GPI [68], [69], [70] or hemozoin-bound DNA [71] might stimulate Treg function during infection. Although it is not known if these molecules can specifically stimulate proliferation upon binding to natural Treg cell–expressing TLRs, a recent study demonstrated that TLR9 engagement in DCs is required for natural Treg cell activation by malaria parasites [72].

Although the available literature does not support a unified model for the role of natural Treg cells in malaria, a common feature emerging from data in experimental models and human association studies appears to be the ability of this suppressive T cell population to modulate acute pro-inflammatory and/or TH1 memory responses to infection. In animal models, the increased inflammatory response resulting from natural Treg cell depletion was not always sufficient to control parasitemia levels, particularly in models of high parasite density in which antibody-mediated responses are known to play an important role in protective immunity. In low parasite density models, though, pro-inflammatory responses generated in the absence of natural Treg cells appeared to be more efficient in controlling acute infection, leading to reduced organ-specific parasite sequestration. Consistent with an immunoregulatory role in chronic conditions [73], [74], evidence arising from rodent re-infection models [53] as well as severe malaria association studies in humans [61] supports the notion that natural Treg cells modulate parasite-specific TH1 memory rather than acute responses involved in disease induction, suggesting that this cell population may limit the risk of immune-mediated pathogenesis upon re-infection. On the other hand, human studies available to date reveal associations between Treg cell frequency and increased parasite densities, which in some cases were found to correlate with increased severity of disease. Overall, the literature suggests that whereas in some settings Treg cells might modulate detrimental inflammation involved in disease induction, in other cases Treg cell–mediated inhibition of immune responses results in increased parasite density, which is also known to be a key determinant of disease severity. As often in malaria, the picture seems to be more complex than initially envisaged, and whether natural Treg cell activation results in a favourable outcome for the parasite or the host depends on a variety of factors, including the timing and magnitude of such pro-inflammatory responses to infection, the level of exposure to the parasite, and the genetic background of the host.

The findings concerning the role of Treg cells in relation to malaria infection thus appear consistent with the growing literature on the role of Treg cells in other infectious diseases, supporting the general view that these cells maintain homeostasis by controlling the magnitude of immune responses. Broadly speaking, in the context of other infectious diseases, Treg cells curtail potent and sometimes over-vigorous effector responses. The selective basis of this activity appears to be the need to limit the significant tissue damage that can arise as a side-consequence of antimicrobial immune responses. For example, reactive oxygen species, while a powerful weapon against microbes, can cause significant damage to the host. In certain circumstances, the need to reduce or prevent serious tissue damage can compromise the ability to control infection. Examples of the role of Treg in reducing immunopathology can be found in the original observation of their role in control of colitis [75], reduction of pulmonary inflammation in Pneumocystis [76], control of hepatic pathology in Schistosoma infections [77] and control of immunopathological leasions in viral infections [78], etc. The evidence for Treg cell–dependent control of immune responses, leading sometimes to failure of the effector arm, comes most clearly from studies on chronic infections e.g., Leishmania major [79]. One outcome of the counter-regulatory activity against the effector response appears to be the promotion of pathogen persistence, as exemplified by Litomosoides [80]. Treg cells may thus play a crucial role in maintaining long-term, balanced host/pathogen relationships, and hence in the promotion of commensalism.

Future Directions

Future directions in Treg cell research of relevance to malaria can be envisaged at several levels. Firstly, the activation of Treg cell or their induction in the periphery appears to result from a wide range of signals, including direct stimulation of TLR or other pattern-recognition receptors, the maturation and activation of DCs and other accessory cells by pathogens through similar pathways, the cellular cytokine milieu and the potential contribution of parasite ligands with direct regulatory roles. For mechanistic studies, much can be attempted with human and murine cells in vitro, and in murine models in vivo, to analyse the molecular signals of parasite origin leading to Treg cell activation, and the other contributory cells of the immune system. Secondly, as exemplified here, the contribution of Treg cells depends upon the kinetics and dynamics of the infection, and much more needs to be done in whole animal models of chronic or repeated infection malaria infection, to test experimentally the contribution of Treg to infection and disease processes during re-exposure. Finally, activation of Treg cells urgently needs to be assessed in the context of longitudinal cohort studies in human populations to further test the association of Treg activation parameters with respect to parasitological and pathophysiological outcome variables. Put together, these three avenues may be required to test the proposition that malaria actively engages in Treg cell activation in order to promote the survival of the pathogen.


1. KullbergMC





2002 Bacteria-triggered CD4+ T regulatory cells suppress Helicobacter hepaticus-induced colitis. J Exp Med 196 505 515

2. MaloyKJ





2003 CD4+CD25+ T(R) cells suppress innate immune pathology through cytokine-dependent mechanisms. J Exp Med 197 111 119

3. HoriS



2002 CD4+CD25+ regulatory T cells suppress CD4+ T cell-mediated pullmonary hyperinflammation driven by Pneumocystis carinii in immunodeficient mice. Eur J Immunol 32 1282 1291

4. MontagnoliC





2002 B7/CD28-dependent CD4+CD25+ regulatory T cells are essential components of the memory-protective immunity to Candida albicans. J Immunol 169 6298 6308

5. SakaguchiS





1995 Immunologic self-tolerance maintained by activated T cells expressing IL-2 receptor alpha-chains (CD25). Breakdown of a single mechanism of self-tolerance causes various autoimmune diseases. J Immunol 155 1151 1164

6. LiuW





2006 CD127 expression inversely correlates with FoxP3 and suppressive function of human CD4+ T reg cells. J Exp Med 203 1701 1711

7. SalomonB





2000 B7/CD28 costimulation is essential for the homeostasis of the CD4+CD25+ immunoregualtory T cells that control autoimmune diabetes. Immunity 12 431 440

8. McHughRS





2002 CD4+CD25+ immunoregulatory T cells: gene expression analysis reveals a functional role for the glucocorticoid-induced TNF receptor. Immunity 16 311 323

9. HoriS



2003 Control of regulatory T cell development by the transcription factor Foxp3. Science 299 1057 1061

10. AsanoM




1996 Autoimmune disease as a consequence of developmental abnormality of a T cell subpopulation. J Exp Med 184 387 396

11. MottetC



2003 Cutting edge: cure of colitis by CD4+CD25+ regulatory T cells. J Immunol 170 3939 3943

12. ShimizuJ



1999 Induction of tumor immunity by removing CD25+CD4+ T cells: a common basis between tumor immunity and autoimmunity. J Immunol 163 5211 5218

13. ThorntonAM


1998 CD4+CD25+ immunoregulatory T cells suppress polyclonal T cell activation in vitro by inhibiting interleukin 2 production. J Exp Med 188 287 296

14. NakamuraK



2001 Cell contact-dependent immunosuppression by CD4+CD25+ regulatory T cells is mediated by cell surface-bound transforming growth factor beta. J Exp Med 194 629 644

15. AssemanC





1999 An essential role for interleukin 10 in the function of regulatory T cells that inhibit intestinal inflammation. J Exp Med 190 995 1004

16. BluestoneJA


2003 Natural versus adaptive regulatory T cells. Nat Rev Immunol 3 253 257

17. WhiteNJ


1992 The pathophysiology of malaria. Adv Parasitol 31 83 173

18. BairdJK

1995 Host age as a determinant of naturally acquired immunity to Plasmodium falciparum. Parasitol Today 11 105 111

19. MarshK


2006 Immune effector mechanisms in malaria. Parasite Immunol 28 51 60

20. BejonP





2007 The induction and persistence of T cell IFN-gamma responses after vaccination or natural exposure is suppressed by Plasmodium falciparum. J Immunol 179 4193 4201

21. PlebanskiM





1999 Interleukin 10-mediated immunosuppression by a variant CD4 T cell epitope of Plasmodium falciparum. Immunity 10 651 660

22. KossodoS





1997 Interleukin-10 modulates susceptibility in experimental cerebral malaria. Immunology 91 536 540

23. OmerFM


1998 Transforming growth factor beta production is inversely correlated with severity of murine malaria infection. J Exp Med 188 39 48

24. GrauGE





1987 Tumor necrosis factor (cachectin) as an essential mediator in murine cerebral malaria. Science 237 1210 1212

25. EngwerdaCR



De SouzaJB


2002 Locally up-regulated lymphotoxin alpha, not systemic tumor necrosis factor alpha, is the principle mediator of murine cerebral malaria. J Exp Med 195 1371 1377

26. GrauGE





1989 Monoclonal antibody against interferon g can prevent experimental cerebral malaria and its associated overproduction of tumor necrosis factor. Proc Natl Acad Sci USA 86 5572 5574

27. GrauGE





1986 L3T4+ T lymphocytes play a major role in the pathogenesis of murine cerebral malaria. J Immunol 137 2348 2354

28. YanezDM




van der HeydeHC

1996 Participation of lymphocyte subpopulations in the pathogenesis of experimental murine cerebral malaria. J Immunol 157 1620 1624

29. NitcheuJ





2003 Perforin-dependent brain-infiltrating cytotoxic CD8+ T lymphocytes mediate experimental cerebral malaria pathogenesis. J Immunol 170 2221 2228

30. BelnoueE




van RooijenN

2002 On the pathogenic role of brain-sequestered alphabeta CD8+ T cells in experimental cerebral malaria. J Immunol 169 6369 6375

31. HansenDS


2004 Regulation of immunity and pathogenesis in infectious diseases by CD1d-restricted NKT cells. Int J Parasitol 34 15 25

32. HansenDS





2003 Regulation of murine cerebral malaria pathogenesis by CD1d-restricted NKT cells and the natural killer complex. Immunity 18 391 402

33. HansenDS




2007 NK cells stimulate recruitment of CXCR3+ T cells to the brain during Plasmodium berghei-mediated cerebral malaria. J Immunol 178 5779 5788

34. BauerPR

Van Der HeydeHC




2002 Regulation of endothelial cell adhesion molecule expression in an experimental model of cerebral malaria. Microcirculation 9 463 470

35. ChakravortySJ


2005 The role of ICAM-1 in Plasmodium falciparum cytoadherence. Eur J Cell Biol 84 15 27

36. TaylorTE





2004 Differentiating the pathologies of cerebral malaria by postmortem parasite counts. Nat Med 10 143 145

37. HearnJ




de SouzaJB

2000 Immunopathology of cerebral malaria: morphological evidence of parasite sequestration in murine brain microvasculature. Infect Immun 68 5364 5376

38. HisaedaH





2004 Escape of malaria parasites from host immunity requires CD4+ CD25+ regulatory T cells. Nat Med 10 29 30

39. CouperKN





2008 IL-10 from CD4CD25Foxp3CD127 adaptive regulatory T cells modulates parasite clearance and pathology during malaria infection. PLoS Pathog 4 e1000004 doi:10.1371/journal.ppat.1000004

40. StrauchUG





2005 Influence of intestinal bacteria on induction of regulatory T cells: lessons from a transfer model of colitis. Gut 54 1546 1552

41. CambosM





2008 Natural regulatory (CD4+CD25+FOXP+) T cells control the production of pro-inflammatory cytokines during Plasmodium chabaudi adami infection and do not contribute to immune evasion. Int J Parasitol 38 229 238

42. LongTT





2003 Influence of CD4+CD25+ T cells on Plasmodium berghei NK65 infection in BALB/c mice. Int J Parasitol 33 175 183

43. Brian de SouzaJ


2002 Cerebral malaria: the contribution of studies in animal models to our understanding of immunopathogenesis. Microbes Infect 4 291 300

44. MillerLH




2002 The pathogenic basis of malaria. Nature 415 673 679

45. SchofieldL


2005 Immunological processes in malaria pathogenesis. Nat Rev Immunol 5 722 735

46. ClarkIA


2000 Pathogenesis of malaria. Parasitol Today 16 451 454

47. NieCQ





2009 IP-10-mediated T cell homing promotes cerebral inflammation over splenic immunity to malaria infection. PLoS Pathog 5 e1000369 doi:10.1371/journal.ppat.1000369

48. MiuJ





2008 Chemokine gene expression during fatal murine cerebral malaria and protection due to CXCR3 deficiency. J Immunol 180 1217 1230

49. ScottP





1989 Role of cytokines and CD4+ T-cell subsets in the regulation of parasite immunity and disease. Immunol Rev 112 161 182

50. KossodoS


1993 Profiles of cytokine production in relation with susceptibility to cerebral malaria. J Immunol 151 4811 4820

51. ScalzoAA





1999 Development of intra-natural killer complex (NKC) recombinant and congenic mouse strains for mapping and functional analysis of NK cell regulatory loci. Immunogenetics 49 238 241

52. HansenDS





2005 The natural killer complex regulates severe malarial pathogenesis and influences acquired immune responses to Plasmodium berghei ANKA. Infect Immun 73 2288 2297

53. NieCQ




2007 CD4+ CD25+ regulatory T cells suppress CD4+ T-cell function and inhibit the development of Plasmodium berghei-specific TH1 responses involved in cerebral malaria pathogenesis. Infect Immun 75 2275 2282

54. AmanteFH





2007 A role for natural regulatory T cells in the pathogenesis of experimental cerebral malaria. Am J Pathol 171 548 559

55. VigarioAM





2007 Regulatory CD4+ CD25+ Foxp3+ T cells expand during experimental Plasmodium infection but do not prevent cerebral malaria. Int J Parasitol 37 963 973

56. RandallLM





2008 Common strategies to prevent and modulate experimental cerebral malaria in mouse strains with different susceptibilities. Infect Immun 76 3312 3320

57. SteegC





2009 Limited Role of CD4+Foxp3+ Regulatory T Cells in the Control of Experimental Cerebral Malaria. J Immunol

58. WaltherM





2005 Upregulation of TGF-beta, FOXP3, and CD4+CD25+ regulatory T cells correlates with more rapid parasite growth in human malaria infection. Immunity 23 287 296

59. TodrykSM





2008 Correlation of memory T cell responses against TRAP with protection from clinical malaria, and CD4 CD25 high T cells with susceptibility in Kenyans. PLoS ONE 3 e2027 doi:10.1371/journal.pone.0002027

60. TorciaMG





2008 Functional deficit of T regulatory cells in Fulani, an ethnic group with low susceptibility to Plasmodium falciparum malaria. Proc Natl Acad Sci U S A 105 646 651

61. WaltherM





2009 Distinct roles for FOXP3 and FOXP3 CD4 T cells in regulating cellular immunity to uncomplicated and severe Plasmodium falciparum malaria. PLoS Pathog 5 e1000364 doi:10.1371/journal.ppat.1000364

62. MinigoG





2009 Parasite-dependent expansion of TNF receptor II-positive regulatory T cells with enhanced suppressive activity in adults with severe malaria. PLoS Pathog 5 e1000402 doi:10.1371/journal.ppat.1000402

63. ScholzenA





2009 Plasmodium falciparum-mediated induction of human CD25Foxp3 CD4 T cells is independent of direct TCR stimulation and requires IL-2, IL-10 and TGFbeta. PLoS Pathog 5 e1000543 doi:10.1371/journal.ppat.1000543

64. FinneyOC





2009 Homeostatic regulation of T effector to Treg ratios in an area of seasonal malaria transmission. Eur J Immunol 39 1288 1300

65. JangpatarapongsaK





2008 Plasmodium vivax parasites alter the balance of myeloid and plasmacytoid dendritic cells and the induction of regulatory T cells. Eur J Immunol 38 2697 2705

66. HisaedaH





2005 Resistance of regulatory T cells to glucocorticoid-induced TNFR family-related protein (GITR) during Plasmodium yoelii infection. Eur J Immunol 35 3516 3524

67. CaramalhoI





2003 Regulatory T cells selectively express toll-like receptors and are activated by lipopolysaccharide. J Exp Med 197 403 411

68. NeblT

De VeerMJ


2005 Stimulation of innate immune responses by malarial glycosylphosphatidylinositol via pattern recognition receptors. Parasitology 130 Suppl S45 62

69. SchofieldL


1996 Regulation of host cell function by glycosylphosphatidylinositols of the parasitic protozoa. Immunol Cell Biol 74 555 563

70. TachadoSD



1999 Specificity in signal transduction among glycosylphosphatidylinositols of Plasmodium falciparum, Trypanosoma brucei, Trypanosoma cruzi and Leishmania spp. Parasite Immunol 21 609 617

71. ParrocheP





2007 Malaria hemozoin is immunologically inert but radically enhances innate responses by presenting malaria DNA to Toll-like receptor 9. Proc Natl Acad Sci U S A 104 1919 1924

72. HisaedaH





2008 Malaria parasites require TLR9 signaling for immune evasion by activating regulatory T cells. J Immunol 180 2496 2503

73. MittruckerHW


2004 Mini-review: regulatory T cells and infection: suppression revisited. Eur J Immunol 34 306 312

74. BelkaidY


2005 Natural regulatory T cells in infectious disease. Nat Immunol 6 353 360

75. PowrieF





1994 Inhibition of Th1 responses prevents inflammatory bowel disease in scid mice reconstituted with CD45RBhi CD4+ T cells. Immunity 1 553 562

76. McKinleyL





2006 Regulatory T cells dampen pulmonary inflammation and lung injury in an animal model of pneumocystis pneumonia. J Immunol 177 6215 6226

77. HesseM





2004 The pathogenesis of schistosomiasis is controlled by cooperating IL-10-producing innate effector and regulatory T cells. J Immunol 172 3157 3166

78. SuvasS





2004 CD4+CD25+ regulatory T cells control the severity of viral immunoinflammatory lesions. J Immunol 172 4123 4132

79. BelkaidY





2002 CD4+CD25+ regulatory T cells control Leishmania major persistence and immunity. Nature 420 502 507

80. TaylorMD





2005 Removal of regulatory T cell activity reverses hyporesponsiveness and leads to filarial parasite clearance in vivo. J Immunol 174 4924 4933

Hygiena a epidemiologie Infekční lékařství Laboratoř

Článek vyšel v časopise

PLOS Pathogens

2010 Číslo 4

Nejčtenější v tomto čísle
Zapomenuté heslo

Nemáte účet?  Registrujte se

Zapomenuté heslo

Zadejte e-mailovou adresu, se kterou jste vytvářel(a) účet, budou Vám na ni zaslány informace k nastavení nového hesla.


Nemáte účet?  Registrujte se